SG11202001684PA - Inhibiting ubiquitin specific peptidase 30 - Google Patents
Inhibiting ubiquitin specific peptidase 30Info
- Publication number
- SG11202001684PA SG11202001684PA SG11202001684PA SG11202001684PA SG11202001684PA SG 11202001684P A SG11202001684P A SG 11202001684PA SG 11202001684P A SG11202001684P A SG 11202001684PA SG 11202001684P A SG11202001684P A SG 11202001684PA SG 11202001684P A SG11202001684P A SG 11202001684PA
- Authority
- SG
- Singapore
- Prior art keywords
- ubiquitin specific
- specific peptidase
- inhibiting ubiquitin
- inhibiting
- peptidase
- Prior art date
Links
- 101000748132 Homo sapiens Ubiquitin carboxyl-terminal hydrolase 30 Proteins 0.000 title 1
- 102100040052 Ubiquitin carboxyl-terminal hydrolase 30 Human genes 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C261/00—Derivatives of cyanic acid
- C07C261/04—Cyanamides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
- C07D231/40—Acylated on said nitrogen atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/04—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/14—Nitrogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/82—Nitrogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/135—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/04—Systems containing only non-condensed rings with a four-membered ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201762569177P | 2017-10-06 | 2017-10-06 | |
PCT/US2018/054520 WO2019071073A1 (en) | 2017-10-06 | 2018-10-05 | Inhibiting ubiquitin specific peptidase 30 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11202001684PA true SG11202001684PA (en) | 2020-03-30 |
Family
ID=65995221
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11202001684PA SG11202001684PA (en) | 2017-10-06 | 2018-10-05 | Inhibiting ubiquitin specific peptidase 30 |
Country Status (15)
Country | Link |
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US (2) | US11247987B2 (en) |
EP (1) | EP3692028B1 (en) |
JP (2) | JP2020536863A (en) |
KR (1) | KR20200067850A (en) |
CN (1) | CN111148743B (en) |
AU (1) | AU2018346597B2 (en) |
BR (1) | BR112020003725A2 (en) |
CA (1) | CA3072362A1 (en) |
EA (1) | EA202090871A1 (en) |
ES (1) | ES2950757T3 (en) |
IL (1) | IL272838B2 (en) |
MX (1) | MX2020003671A (en) |
SG (1) | SG11202001684PA (en) |
WO (1) | WO2019071073A1 (en) |
ZA (1) | ZA202001057B (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG11202001684PA (en) | 2017-10-06 | 2020-03-30 | Forma Therapeutics Inc | Inhibiting ubiquitin specific peptidase 30 |
ES2945834T3 (en) | 2018-10-05 | 2023-07-07 | Forma Therapeutics Inc | Fused pyrrolines that act as inhibitors of ubiquitin-specific protease 30 (USP30) |
EP3902533A1 (en) * | 2018-12-26 | 2021-11-03 | Forma Therapeutics, Inc. | Inhibiting ubiquitin specific peptidase 9x |
GB201905371D0 (en) | 2019-04-16 | 2019-05-29 | Mission Therapeutics Ltd | Novel compounds |
GB201905375D0 (en) | 2019-04-16 | 2019-05-29 | Mission Therapeutics Ltd | Novel compounds |
GB201912674D0 (en) | 2019-09-04 | 2019-10-16 | Mission Therapeutics Ltd | Novel compounds |
CA3166630A1 (en) | 2020-01-03 | 2021-07-08 | Berg Llc | Polycyclic amides as ube2k modulators for treating cancer |
CA3171349A1 (en) | 2020-04-08 | 2021-10-14 | Mission Therapeutics Limited | N-cyanopyrrolidines with activity as usp30 inhibitors |
KR20230016674A (en) | 2020-05-28 | 2023-02-02 | 미션 테라퓨틱스 엘티디 | N-(1-cyanopyrrolidin-3-yl)-5-(3-(trifluoromethyl)phenyl)oxazole-2-carboxamide derivatives and corresponding Oxadiazole derivatives |
BR112022019722A2 (en) | 2020-06-04 | 2022-12-20 | Mission Therapeutics Ltd | N-CYANOPYRROLIDINES WITH ACTIVITY AS USP30 INHIBITORS |
JP2023528087A (en) | 2020-06-08 | 2023-07-03 | ミッション セラピューティクス リミティド | 1-(5-(2-cyanopyridin-4-yl)oxazole-2-carbonyl)-4-methylhexahydropyrrolo[3] as USP30 inhibitors used in the treatment of mitochondrial dysfunction, cancer, and fibrosis ,4-b]pyrrole-5(1H)-carbonitrile |
GB202016800D0 (en) | 2020-10-22 | 2020-12-09 | Mission Therapeutics Ltd | Novel compounds |
WO2023099561A1 (en) | 2021-12-01 | 2023-06-08 | Mission Therapeutics Limited | Substituted n-cyanopyrrolidines with activity as usp30 inhibitors |
Family Cites Families (186)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030191279A1 (en) | 1999-08-27 | 2003-10-09 | Goldstein Steven Wayne | Urea derivatives useful as anticancer agents |
US6576632B1 (en) | 1999-08-27 | 2003-06-10 | Pfizer Inc | Biaryl compounds useful as anticancer agents |
US6632815B2 (en) | 1999-09-17 | 2003-10-14 | Millennium Pharmaceuticals, Inc. | Inhibitors of factor Xa |
MX228790B (en) | 1999-09-17 | 2005-06-30 | Millennium Pharm Inc | Inhibitors of factor xa. |
CZ2002961A3 (en) | 1999-09-17 | 2002-08-14 | Millennium Pharmaceuticals, Inc. | Benzamides and related compounds for inhibition of Xa factor |
CA2387892A1 (en) | 1999-10-18 | 2001-04-26 | University Of Connecticut | Pyrazole derivatives as cannabinoid receptor antagonists |
WO2003020217A2 (en) | 2001-08-31 | 2003-03-13 | University Of Connecticut | Novel pyrazole analogs acting on cannabinoid receptors |
AU2001250783A1 (en) | 2000-02-29 | 2001-09-12 | Cor Therapeutics, Inc. | Benzamides and related inhibitors of factor xa |
US6835727B2 (en) | 2000-04-06 | 2004-12-28 | Merck Frosst Canada & Co. | Cathepsin cysteine protease inhibitors |
DE60126143T2 (en) | 2000-12-06 | 2007-11-15 | Sanofi-Aventis Deutschland Gmbh | GUANIDINE AND AMIDINE COMPOUNDS, AND THEIR USE AS FACTOR XA INHIBITORS |
EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
AU2002317377A1 (en) | 2001-07-20 | 2003-03-03 | Cancer Research Technology Limited | Biphenyl apurinic/apyrimidinic site endonuclease inhibitors to treat cancer |
KR101116627B1 (en) | 2002-06-27 | 2012-10-09 | 노보 노르디스크 에이/에스 | Aryl carbonyl derivatives as therapeutic agents |
NZ538339A (en) | 2002-08-09 | 2007-01-26 | Astrazeneca Ab | Oxadiazoles as modulators of metabotropic glutamate receptor-5 |
MXPA05001590A (en) | 2002-08-09 | 2005-05-23 | Astrazeneca Ab | Compounds having an activity at metabotropic glutamate receptors. |
AU2004220225B2 (en) | 2003-03-14 | 2010-06-17 | Ono Pharmaceutical Co., Ltd. | Nitrogen-containing heterocyclic derivatives and drugs containing the same as the active ingredient |
AR043633A1 (en) | 2003-03-20 | 2005-08-03 | Schering Corp | CANABINOID RECEIVERS LINKS |
JP4847868B2 (en) | 2003-05-14 | 2011-12-28 | ニューロジェネティック ファーマシューティカルズ、 インコーポレイテッド | Compounds and their use in the regulation of amyloid beta |
GB0315111D0 (en) | 2003-06-27 | 2003-07-30 | Cancer Rec Tech Ltd | Substituted 5-membered ring compounds and their use |
WO2005019200A2 (en) | 2003-08-14 | 2005-03-03 | Icos Corporation | Aryl piperidine derivatives as vla-1 integrin antagonists and uses thereof |
GB0325956D0 (en) | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
TWI316955B (en) | 2003-11-19 | 2009-11-11 | Chisso Corp | Photo-polymerization liquid composition,polymer or polymer co mposition and optical compensation device thereof |
WO2005077345A1 (en) | 2004-02-03 | 2005-08-25 | Astrazeneca Ab | Compounds for the treatment of gastro-esophageal reflux disease |
WO2005077368A2 (en) | 2004-02-03 | 2005-08-25 | Astrazeneca Ab | Treatment of gastro-esophageal reflux disease (gerd) |
WO2005077373A2 (en) | 2004-02-03 | 2005-08-25 | Astrazeneca Ab | Treatment of gastro-esophageal reflux disease (gerd) |
US7585881B2 (en) | 2004-02-18 | 2009-09-08 | Astrazeneca Ab | Additional heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
CN101018779A (en) | 2004-02-18 | 2007-08-15 | 阿斯利康(瑞典)有限公司 | Triazole compounds and their use as metabotropic glutamate receptor antagonists |
AU2005221678B2 (en) | 2004-03-09 | 2008-10-09 | National Health Research Institutes | Pyrrolidine compounds |
WO2005112540A2 (en) | 2004-05-21 | 2005-12-01 | Merck Patent Gmbh | Liquid crystal compounds, liquid crystal medium and liquid crystal display |
WO2005115382A1 (en) | 2004-05-29 | 2005-12-08 | 7Tm Pharma A/S | Crth2 receptor ligands for medicinal uses |
WO2005115374A1 (en) | 2004-05-29 | 2005-12-08 | 7Tm Pharma A/S | Crth2 receptor ligands for therapeutic use |
WO2006015279A1 (en) | 2004-07-28 | 2006-02-09 | Neurogen Corporation | Heterocyclic diamine compounds as ligands of the melanin concentrating hormone receptor useful for the treatment of obesity, diabetes, eating and sexual disorders |
PL382308A1 (en) | 2004-08-25 | 2007-08-20 | Targegen, Inc. | Heterocyclic compounds and the manners of use |
WO2006027076A1 (en) | 2004-09-06 | 2006-03-16 | Merck Patent Gmbh | Polymerisable liquid crystal material |
DE102004051277A1 (en) | 2004-10-21 | 2006-04-27 | Merck Patent Gmbh | Heterocyclic carbonyl compounds |
DE102004054666A1 (en) | 2004-11-12 | 2006-05-18 | Bayer Cropscience Gmbh | New substituted pyrazol-3-carboxamide derivatives useful to combat harmful plants and for growth regulation of plants |
WO2006063113A2 (en) | 2004-12-07 | 2006-06-15 | Portola Pharmaceuticals, Inc. | Ureas as factor xa inhibitors |
EP1844020B1 (en) | 2005-01-10 | 2017-09-06 | Exelixis, Inc. | Heterocyclic carboxamide compounds as steroid nuclear receptor ligands |
AU2006203845A1 (en) | 2005-01-10 | 2006-07-13 | Alexandros Makriyannis | Novel heteropyrrole analogs acting on cannabiniod receptors |
GB2424881B (en) | 2005-04-07 | 2010-11-24 | Merck Patent Gmbh | Halophenyl derivatives of bisalkylfluorene |
EP1879881A2 (en) | 2005-04-14 | 2008-01-23 | Bristol-Myers Squibb Company | Inhibitors of 11-beta hydroxysteroid dehydrogenase type i |
CA2608419A1 (en) | 2005-05-13 | 2006-11-23 | Eli Lilly And Company | Substituted n-arylpyrrolidines as selective androgen receptor modulators |
GB0510139D0 (en) | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds B1 |
WO2007024744A2 (en) | 2005-08-21 | 2007-03-01 | Exelixis, Inc. | Heterocyclic carboxamide compounds as steroid nuclear receptor ligands |
EP1948614A2 (en) | 2005-11-18 | 2008-07-30 | Takeda San Diego, Inc. | Glucokinase activators |
WO2008035209A2 (en) | 2006-05-30 | 2008-03-27 | Methylgene Inc. | Inhibitors of protein tyrosine kinase activity |
BRPI0712332A2 (en) | 2006-06-09 | 2012-12-18 | Icos Corp | pharmaceutically acceptable compound and derivatives thereof, pharmaceutical composition, method of antagonizing a dp-2 receptor, and use of a compound |
TW200815438A (en) | 2006-06-13 | 2008-04-01 | Bayer Schering Pharma Ag | Substituted pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
TW200815437A (en) | 2006-06-13 | 2008-04-01 | Bayer Schering Pharma Ag | Substituted aminopyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
JP5606736B2 (en) | 2006-09-02 | 2014-10-15 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | Particle beam method for orienting reactive mesogens. |
RU2452484C2 (en) | 2006-12-08 | 2012-06-10 | Милленниум Фармасьютикалз, Инк. | Standard drug preparations and methods of treating thrombosis by oral administration of factor xa inhibitor |
EP2125808A2 (en) | 2006-12-15 | 2009-12-02 | Bayer Schering Pharma Aktiengesellschaft | 3-h-pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same |
AU2007338792B2 (en) | 2006-12-20 | 2012-05-31 | Amgen Inc. | Substituted heterocycles and methods of use |
AU2008253118B2 (en) | 2007-05-22 | 2013-11-21 | Madrigal Pharmaceuticals, Inc. | Diacylglycerol acyltransferase inhibitors |
KR101077417B1 (en) | 2007-06-12 | 2011-10-26 | 주식회사 엘지화학 | Retardation film and polarizing plate and liquid crystal display comprising the same |
EP2017264A1 (en) | 2007-07-16 | 2009-01-21 | Bayer Cropscience Ag | Substituted phenyl propargyl compounds, method for their manufacture and their use as herbicides and plant growth regulators |
US20090069288A1 (en) | 2007-07-16 | 2009-03-12 | Breinlinger Eric C | Novel therapeutic compounds |
JP5057056B2 (en) | 2007-08-03 | 2012-10-24 | Jsr株式会社 | Liquid crystal aligning agent, method for producing liquid crystal aligning film, polyamic acid, polyimide and diamine compound |
JP5570424B2 (en) | 2007-10-10 | 2014-08-13 | ビーエーエスエフ ソシエタス・ヨーロピア | Sulfonium salt initiator |
JP2009108152A (en) | 2007-10-29 | 2009-05-21 | Sumitomo Chemical Co Ltd | Polymerizable compound and optical film |
WO2009078992A1 (en) | 2007-12-17 | 2009-06-25 | Amgen Inc. | Linear tricyclic compounds as p38 kinase inhibitors |
JP2009149754A (en) | 2007-12-20 | 2009-07-09 | Sumitomo Chemical Co Ltd | Polymerizable compound and optical film produced by polymerizing the polymerizable compound |
US20090270418A1 (en) | 2008-01-09 | 2009-10-29 | Marianne Sloss | Pyrazole pyrazine amine compounds as kinase inhibitors, compositions thereof and methods of treatment therewith |
JP5219583B2 (en) | 2008-03-31 | 2013-06-26 | 住友化学株式会社 | Composition, optical film and method for producing the same, optical member and display device |
CL2009000915A1 (en) | 2008-04-18 | 2010-04-16 | Glaxo Group Ltd | Compounds derived from 1-cyano-3-pyrrolidinyl-benzenesulfonamides, cathepsin c inhibitors; pharmaceutical composition comprising said compound; and use of the compound for the treatment of a chronic obstructive pulmonary disease (copd). |
KR20110025224A (en) | 2008-06-27 | 2011-03-09 | 아빌라 테라퓨틱스, 인크. | Heteroaryl compounds and uses thereof |
JP5443720B2 (en) | 2008-09-05 | 2014-03-19 | 住友化学株式会社 | Composition, optical film and method for producing the same, optical member, and display device |
JP2010066630A (en) | 2008-09-12 | 2010-03-25 | Sumitomo Chemical Co Ltd | Method for manufacturing optical film, and optical film |
WO2010048149A2 (en) | 2008-10-20 | 2010-04-29 | Kalypsys, Inc. | Heterocyclic modulators of gpr119 for treatment of disease |
CN102264737A (en) | 2008-12-23 | 2011-11-30 | 雅培制药有限公司 | Anti-viral compounds |
JP5899607B2 (en) | 2009-03-16 | 2016-04-06 | 住友化学株式会社 | Compound, optical film and method for producing optical film |
CN101838264B (en) | 2009-03-16 | 2014-12-03 | 住友化学株式会社 | Compound, optical film and process for producing optical film |
JP2011006360A (en) | 2009-06-26 | 2011-01-13 | Sumitomo Chemical Co Ltd | Compound, optical film and method for producing optical film |
KR101256018B1 (en) | 2009-08-20 | 2013-04-18 | 한국과학기술연구원 | 1,3,6-Substituted indole derivatives having inhibitory activity for protein kinase |
JP2011042606A (en) | 2009-08-20 | 2011-03-03 | Sumitomo Chemical Co Ltd | Compound, optical film and process for producing optical film |
WO2011025706A2 (en) | 2009-08-26 | 2011-03-03 | Schering Corporation | Heterocyclic amide compounds as protein kinase inhibitors |
EP2475254A4 (en) | 2009-09-11 | 2013-05-22 | Enanta Pharm Inc | Hepatitis c virus inhibitors |
WO2011053825A2 (en) | 2009-10-30 | 2011-05-05 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Compositions and methods for the treatment or prevention of mitochondrial diseases |
US8431575B2 (en) | 2010-02-18 | 2013-04-30 | Transtech Pharma, Inc. | Phenyl-heteroaryl derivatives and methods of use thereof |
CN104940200B (en) | 2010-03-30 | 2019-06-28 | 维颂公司 | Inhibitor of the polysubstituted aromatic compounds as fibrin ferment |
EP2569302A1 (en) | 2010-05-13 | 2013-03-20 | Amgen, Inc | Heteroaryloxyheterocyclyl compounds as pde10 inhibitors |
GB201010359D0 (en) | 2010-06-21 | 2010-08-04 | Univ Nottingham | Compounds for treating proliferative disorders |
PT2598483T (en) | 2010-07-29 | 2020-10-12 | Rigel Pharmaceuticals Inc | Ampk-activating heterocyclic compounds and methods for using the same |
KR101931224B1 (en) | 2010-12-08 | 2018-12-20 | 더 유나이티드 스테이츠 오브 어메리카, 애즈 리프리젠티드 바이 더 세크러테리, 디파트먼트 오브 헬쓰 앤드 휴먼 서비씨즈 | Substituted pyrazolopyrimidines as glucocerebrosidase activators |
JP5728921B2 (en) | 2010-12-10 | 2015-06-03 | コニカミノルタ株式会社 | Optical film, polarizing plate using the same, and liquid crystal display device |
US20150232455A1 (en) | 2010-12-15 | 2015-08-20 | Allan C. Krueger | Anti-viral compounds |
EP2651920A4 (en) | 2010-12-15 | 2014-12-17 | Abbvie Inc | Anti-viral compounds |
WO2012129562A2 (en) | 2011-03-24 | 2012-09-27 | The Scripps Research Institute | Compounds and methods for inducing chondrogenesis |
EP2697210B1 (en) | 2011-04-13 | 2017-03-01 | Merck Sharp & Dohme Corp. | 5-substituted iminothiazines and their mono-and dioxides as bace inhibitors, compositions, and their use |
RU2013156864A (en) | 2011-05-23 | 2015-06-27 | Санофи | METHOD FOR PRODUCING DEUTERED COMPOUNDS CONTAINING N-ALKYL GROUPS |
DK2713722T3 (en) | 2011-05-31 | 2017-07-03 | Celgene Int Ii Sarl | Newly known GLP-1 receptor stabilizers and modulators |
CN103929961A (en) | 2011-06-20 | 2014-07-16 | 美国阿尔茨海默病研究所公司 | Compounds and therapeutic uses thereof |
JP6061922B2 (en) | 2011-06-22 | 2017-01-18 | ザ ジェネラル ホスピタル コーポレイション | How to treat proteinopathy |
CA2849995A1 (en) | 2011-09-27 | 2013-04-04 | Novartis Ag | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh |
EP2763532B1 (en) | 2011-10-05 | 2018-09-19 | The Board of Trustees of the Leland Stanford Junior University | Pi-kinase inhibitors with broad spectrum anti-infective activity |
EP2788332A1 (en) | 2011-12-07 | 2014-10-15 | Amgen, Inc. | Bicyclic aryl and heteroaryl sodium channel inhibitors |
WO2013106678A1 (en) | 2012-01-12 | 2013-07-18 | Envivo Pharmaceuticals, Inc. | Tetrasubstituted benzenes |
TW201348231A (en) | 2012-02-29 | 2013-12-01 | Amgen Inc | Heterobicyclic compounds |
JP5798066B2 (en) | 2012-03-08 | 2015-10-21 | 富士フイルム株式会社 | Compound, liquid crystal composition, polymer material and film |
US9013997B2 (en) | 2012-06-01 | 2015-04-21 | Broadcom Corporation | System for performing distributed data cut-through |
EP2671885A1 (en) | 2012-06-05 | 2013-12-11 | Ares Trading S.A. | Imidazo-oxadiazole and Imidazo-thiadiazole derivatives |
FR2992317B1 (en) | 2012-06-22 | 2016-05-13 | Diverchim | PROCESS FOR THE PREPARATION OF CHIRAL PEPTIDES |
WO2014000846A1 (en) | 2012-06-26 | 2014-01-03 | dedeMERCK PATENT GMBH | Method of preparing a birefringent polymer film |
CA2883480A1 (en) | 2012-09-17 | 2014-03-20 | F. Hoffmann-La Roche Ag | Usp30 inhibitors and methods of use |
US20150291554A1 (en) | 2012-11-02 | 2015-10-15 | Pfizer Inc. | Bruton's Tyrosine Kinase Inhibitors |
JP6293161B2 (en) | 2012-11-07 | 2018-03-14 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Triazolo compounds |
CN103012428A (en) | 2013-01-08 | 2013-04-03 | 中国药科大学 | 4-(five-membered heterocycle pyrimidin/substituted pyridine) amino-1H-3-pyrazolecarboxamide CDK (cyclin dependent kinase)/Aurora dual inhibitor and application thereof |
AU2014248568B2 (en) | 2013-03-12 | 2017-07-13 | Curegenix, Inc. | Compounds for treatment of cancer |
CN104045552B (en) | 2013-03-13 | 2019-06-11 | 江苏先声药业有限公司 | Medicinal compound as neuroprotective agent |
CN105120867A (en) | 2013-03-14 | 2015-12-02 | 广州源生医药科技有限公司 | Compounds for treatment of fibrosis diseases |
EP2970116A1 (en) | 2013-03-15 | 2016-01-20 | F. Hoffmann-La Roche AG | ARYL SULFAMIDE AND SULFAMATE DERIVATIVES AS RORc MODULATORS |
US9393244B2 (en) | 2013-03-15 | 2016-07-19 | Georgetown University | Increasing parkin activity by administering a deubiquitinating enzyme inhibitor |
JP2014232188A (en) | 2013-05-29 | 2014-12-11 | コニカミノルタ株式会社 | Cellulose acylate film, circularly polarizing plate and image display device |
US20160145304A1 (en) | 2013-07-12 | 2016-05-26 | Helmholtz-Zentrum für Infektionsforschung GmbH | Cystobactamides |
WO2015010297A1 (en) | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
WO2015011284A2 (en) | 2013-07-25 | 2015-01-29 | Fondazione Telethon | Inhibitors of fapp2 and uses thereof |
KR101715090B1 (en) | 2013-08-28 | 2017-03-13 | 한국화학연구원 | Novel compound or pharmaceutically acceptable salt thereof and pharmaceutical composition for prevention or treatment of disease caused by influenza virus infection containing the same as an active ingredient |
US20150087673A1 (en) | 2013-09-26 | 2015-03-26 | Rigel Pharmaceuticals, Inc. | Methods for using and biomarkers for ampk-activating compounds |
SG11201602070TA (en) | 2013-09-30 | 2016-04-28 | Beijing Synercare Pharma Tech Co Ltd | Substituted nicotinimide inhibitors of btk and their preparation and use in the treatment of cancer, inflammation and autoimmune disease |
DK3060550T3 (en) | 2013-10-21 | 2019-07-22 | Merck Patent Gmbh | HETEROARYL COMPOUNDS AS BTK INHIBITORS AND USES THEREOF |
US9663718B2 (en) | 2013-10-21 | 2017-05-30 | Merck Patent Gmbh | Method of preparing a birefringent polymer film |
WO2015085238A1 (en) | 2013-12-05 | 2015-06-11 | The Regents Of The University Of California, A California Corporation | Inhibitors of lpxc |
US9745324B2 (en) | 2013-12-18 | 2017-08-29 | Merck Sharp & Dohme Corp. | Iminothiadiazepane dioxide compounds as BACE inhibitors, compositions, and their use |
WO2015106292A1 (en) | 2014-01-13 | 2015-07-16 | Coferon, Inc. | Bcr-abl tyrosine-kinase ligands capable of dimerizing in an aqueous solution, and methods of using same |
DK3110420T3 (en) | 2014-02-25 | 2019-05-13 | Board Of Regents Univ Of Texas System | SALT OF HETEROCYCLIC MODULATORS OF HIF ACTIVITY FOR TREATMENT OF DISEASES |
DK3143011T3 (en) | 2014-05-13 | 2021-05-03 | Hoffmann La Roche | Deuterated heterocyclic compounds and their use as imaging agents |
KR102412045B1 (en) | 2014-05-22 | 2022-06-22 | 놀스 차이나 파마수티칼 컴퍼니., 엘티디. | Hydrazide compound as blood coagulation factor xa inhibitor |
US9511142B2 (en) | 2014-06-11 | 2016-12-06 | VenatoRx Pharmaceuticals, Inc. | Beta-lactamase inhibitors |
GB201410653D0 (en) | 2014-06-14 | 2014-07-30 | Mission Therapeutics Ltd | Methodologies for measuring isopeptidase activity in biological samples in a high throughput manner |
CN106065009B (en) | 2014-06-28 | 2019-03-01 | 广东东阳光药业有限公司 | Application as the compound of hepatitis c inhibitor and its in drug |
US10005724B2 (en) | 2014-07-07 | 2018-06-26 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
EP3169683A4 (en) | 2014-07-16 | 2017-11-22 | Novogen Ltd. | Functionalised and substituted indoles as anti-cancer agents |
US9290457B2 (en) | 2014-07-31 | 2016-03-22 | Boehringer Ingelheim International Gmbh | Substituted dihydropyrimidinones and their use as inhibitors of neutrophil elastase activity |
WO2016019237A2 (en) * | 2014-07-31 | 2016-02-04 | Pharmacyclics Llc | Inhibitors of bruton's tyrosine kinase |
CN106687563B (en) | 2014-09-05 | 2023-03-14 | 默克专利有限公司 | Preparation and electronic device |
WO2016040449A1 (en) | 2014-09-10 | 2016-03-17 | Raze Therapeutics, Inc. | 3-phosphoglycerate dehydrogenase inhibitors and uses thereof |
GB201416754D0 (en) * | 2014-09-23 | 2014-11-05 | Mission Therapeutics Ltd | Novel compounds |
JP2016115940A (en) | 2014-12-12 | 2016-06-23 | 出光興産株式会社 | Organic electroluminescent element and electronic apparatus |
CN104557862B (en) | 2014-12-15 | 2017-05-17 | 苏州云轩医药科技有限公司 | Heterocyclic compound having Wnt signal channel inhibitory activity |
EP3954685A1 (en) | 2014-12-29 | 2022-02-16 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Small molecule inhibitors of lactate dehydrogenase and methods of use thereof |
WO2016156816A1 (en) * | 2015-03-30 | 2016-10-06 | Mission Therapeutics Limited | 1-cyano-pyrrolidine compounds as usp30 inhibitors |
US11040976B2 (en) | 2015-04-24 | 2021-06-22 | President And Fellows Of Harvard College | Substrate selective inhibitors of insulin-degrading enzyme (IDE) and uses thereof |
WO2017002120A1 (en) | 2015-07-02 | 2017-01-05 | Yeda Research And Development Co. Ltd. | Selective inhibitors of senescent cells and uses thereof |
WO2017010399A1 (en) | 2015-07-10 | 2017-01-19 | 塩野義製薬株式会社 | COMPOUNDS HAVING RORγt INHIBITORY EFFECTS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME |
ES2773046T3 (en) | 2015-07-14 | 2020-07-09 | Mission Therapeutics Ltd | Cyanopyrrolidines as DUB inhibitors for cancer treatment |
WO2017019817A1 (en) | 2015-07-29 | 2017-02-02 | Medivation Technologies, Inc. | Methods and compositions for targeted therapeutics |
WO2017019822A1 (en) | 2015-07-29 | 2017-02-02 | Medivation Technologies, Inc. | Pellet composition containing repair cells |
WO2017019830A1 (en) | 2015-07-29 | 2017-02-02 | Medivation Technologies, Inc. | Methods and compositions for targeted therapeutics |
EP3350181B1 (en) | 2015-09-02 | 2023-11-01 | The Regents of The University of California | Her3 ligands and uses thereof |
US9661853B2 (en) | 2015-09-04 | 2017-05-30 | Dow Agrosciences Llc | Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto |
WO2017066705A1 (en) | 2015-10-14 | 2017-04-20 | Aquinnah Pharmaceuticals, Inc. | Compounds, compositions and methods of use against stress granules |
GB201521109D0 (en) | 2015-11-30 | 2016-01-13 | Mission Therapeutics Ltd | Novel compounds |
EP3386976A1 (en) | 2015-12-09 | 2018-10-17 | Research Triangle Institute, International | Improved apelin receptor (apj) agonists and uses thereof |
GB201522267D0 (en) | 2015-12-17 | 2016-02-03 | Mission Therapeutics Ltd | Novel compounds |
GB201522768D0 (en) | 2015-12-23 | 2016-02-03 | Mission Therapeutics Ltd | Novel compounds |
CN106986859B (en) | 2016-01-20 | 2020-02-11 | 广东东阳光药业有限公司 | Indole derivatives and uses thereof |
GB201602854D0 (en) | 2016-02-18 | 2016-04-06 | Mission Therapeutics Ltd | Novel compounds |
GB201603779D0 (en) | 2016-03-04 | 2016-04-20 | Mission Therapeutics Ltd | Novel compounds |
EP4219449A3 (en) | 2016-03-16 | 2023-10-11 | Kura Oncology, Inc. | Substituted indole derivatives and methods of preparation thereof |
GB201604647D0 (en) | 2016-03-18 | 2016-05-04 | Mission Therapeutics Ltd | Novel compounds |
GB201604638D0 (en) | 2016-03-18 | 2016-05-04 | Mission Therapeutics Ltd | Novel compounds |
JP6959252B2 (en) | 2016-03-24 | 2021-11-02 | ミッション セラピューティクス リミティド | 1-Cyanopyrrolidine derivative as a DUB inhibitor |
CN107226805A (en) | 2016-03-24 | 2017-10-03 | 北京天诚医药科技有限公司 | Aromatic amides analog derivative, its preparation method and its in application pharmaceutically |
TW201811759A (en) | 2016-06-29 | 2018-04-01 | 加拿大蒙特利爾大學 | Biarylmethyl heterocycles |
CN107619388A (en) | 2016-07-13 | 2018-01-23 | 南京天印健华医药科技有限公司 | Heterocyclic compound as FGFR inhibitor |
CN107619384B (en) | 2016-07-13 | 2020-07-28 | 江苏恒瑞医药股份有限公司 | Benzo-heterocycle derivative, preparation method and application thereof in medicine |
CN107674013B (en) | 2016-08-02 | 2022-05-24 | 上海迪诺医药科技有限公司 | Polycyclic compound, preparation method, pharmaceutical composition and application thereof |
BR112019003659B1 (en) | 2016-08-30 | 2022-05-03 | Dow Global Technologies Llc | Method for producing a treated mixture, treated mixture and article of manufacture |
WO2018060689A1 (en) | 2016-09-27 | 2018-04-05 | Mission Therapeutics Limited | Cyanopyrrolidine derivatives with activity as inhibitors of usp30 |
GB201616511D0 (en) | 2016-09-29 | 2016-11-16 | Mission Therapeutics Limited | Novel compounds |
GB201616627D0 (en) | 2016-09-30 | 2016-11-16 | Mission Therapeutics Limited | Novel compounds |
TWI771327B (en) | 2016-10-05 | 2022-07-21 | 英商使命醫療公司 | Novel compounds |
WO2018106820A1 (en) | 2016-12-07 | 2018-06-14 | Kura Oncology, Inc. | Methods of promoting beta cell proliferation |
WO2018106818A1 (en) | 2016-12-07 | 2018-06-14 | Kura Oncology, Inc. | Methods of promoting beta cell proliferation |
RU2764980C2 (en) | 2017-01-20 | 2022-01-24 | Лео Фарма А/С | Bicyclic amines as new inhibitors of jak kinase |
CA3051765C (en) | 2017-02-08 | 2020-08-18 | Helmholtz-Zentrum Dresden - Rossendorf E.V. | In vivo stable hg-197(m) compounds, method for the production thereof and use thereof in nuclear medical diagnostics and endoradionuclide therapy (theranostics) |
US10744213B2 (en) | 2017-02-14 | 2020-08-18 | Colossus Biopharma Consultants Company, Limited | Fluorescent compounds for imaging of blood vessels and blood flow, and an in vivo screen for pro- and anti-angiogenic agents |
WO2018160891A1 (en) | 2017-03-01 | 2018-09-07 | Achillion Pharmaceutical, Inc. | Pharmaceutical compounds for treatment of medical disorders |
US11136324B2 (en) | 2017-03-03 | 2021-10-05 | Jiangsu Hansoh Pharmaceutical Group Co., Ltd. | Substituted imidazoles as apoptosis signal regulating kinase 1 inhibitors |
US10968172B2 (en) | 2017-05-15 | 2021-04-06 | Mitobridge, Inc. | USP30 inhibitors |
GB201708652D0 (en) | 2017-05-31 | 2017-07-12 | Mission Therapeutics Ltd | Novel compounds and uses |
EP3642196B1 (en) | 2017-06-20 | 2022-08-17 | Mission Therapeutics Limited | Substituted cyanopyrrolidines with activity as dub inhibitors |
SG11202001684PA (en) | 2017-10-06 | 2020-03-30 | Forma Therapeutics Inc | Inhibiting ubiquitin specific peptidase 30 |
GB2571731A (en) | 2018-03-06 | 2019-09-11 | Mission Therapeutics Ltd | Novel compounds and uses |
CA3098628A1 (en) | 2018-05-17 | 2019-11-21 | Forma Therapeutics, Inc. | Fused bicyclic compounds useful as ubiquitin-specific peptidase 30 inhibitors |
ES2945834T3 (en) | 2018-10-05 | 2023-07-07 | Forma Therapeutics Inc | Fused pyrrolines that act as inhibitors of ubiquitin-specific protease 30 (USP30) |
-
2018
- 2018-10-05 SG SG11202001684PA patent/SG11202001684PA/en unknown
- 2018-10-05 AU AU2018346597A patent/AU2018346597B2/en active Active
- 2018-10-05 IL IL272838A patent/IL272838B2/en unknown
- 2018-10-05 CN CN201880063763.7A patent/CN111148743B/en active Active
- 2018-10-05 KR KR1020207012361A patent/KR20200067850A/en not_active Application Discontinuation
- 2018-10-05 MX MX2020003671A patent/MX2020003671A/en unknown
- 2018-10-05 US US16/753,439 patent/US11247987B2/en active Active
- 2018-10-05 WO PCT/US2018/054520 patent/WO2019071073A1/en unknown
- 2018-10-05 BR BR112020003725-7A patent/BR112020003725A2/en not_active Application Discontinuation
- 2018-10-05 JP JP2020519048A patent/JP2020536863A/en active Pending
- 2018-10-05 ES ES18864076T patent/ES2950757T3/en active Active
- 2018-10-05 CA CA3072362A patent/CA3072362A1/en active Pending
- 2018-10-05 EA EA202090871A patent/EA202090871A1/en unknown
- 2018-10-05 EP EP18864076.7A patent/EP3692028B1/en active Active
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2020
- 2020-02-19 ZA ZA2020/01057A patent/ZA202001057B/en unknown
-
2021
- 2021-12-21 US US17/557,215 patent/US20220185806A1/en active Pending
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2023
- 2023-06-20 JP JP2023100583A patent/JP2023123613A/en active Pending
Also Published As
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EP3692028B1 (en) | 2023-04-26 |
CA3072362A1 (en) | 2019-04-11 |
BR112020003725A2 (en) | 2020-11-03 |
IL272838B1 (en) | 2023-05-01 |
CN111148743B (en) | 2023-12-15 |
IL272838A (en) | 2020-04-30 |
AU2018346597A1 (en) | 2020-02-27 |
JP2023123613A (en) | 2023-09-05 |
ZA202001057B (en) | 2023-10-25 |
EA202090871A1 (en) | 2020-07-03 |
US11247987B2 (en) | 2022-02-15 |
ES2950757T3 (en) | 2023-10-13 |
MX2020003671A (en) | 2020-08-03 |
EP3692028A1 (en) | 2020-08-12 |
AU2018346597B2 (en) | 2023-07-13 |
EP3692028A4 (en) | 2021-10-13 |
CN111148743A (en) | 2020-05-12 |
WO2019071073A1 (en) | 2019-04-11 |
IL272838B2 (en) | 2023-09-01 |
JP2020536863A (en) | 2020-12-17 |
KR20200067850A (en) | 2020-06-12 |
US20200317658A1 (en) | 2020-10-08 |
US20220185806A1 (en) | 2022-06-16 |
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