AR106041A1 - Moduladores de la proteína core de la hepatitis b - Google Patents
Moduladores de la proteína core de la hepatitis bInfo
- Publication number
- AR106041A1 AR106041A1 ARP160102820A ARP160102820A AR106041A1 AR 106041 A1 AR106041 A1 AR 106041A1 AR P160102820 A ARP160102820 A AR P160102820A AR P160102820 A ARP160102820 A AR P160102820A AR 106041 A1 AR106041 A1 AR 106041A1
- Authority
- AR
- Argentina
- Prior art keywords
- 6alkyl
- group
- halogen
- optionally substituted
- 6alkoxy
- Prior art date
Links
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
- C07D417/12—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
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/554—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one sulfur as ring hetero atoms, e.g. clothiapine, diltiazem
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/38—[b, e]- or [b, f]-condensed with six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/02—Seven-membered rings
- C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D267/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D267/16—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D267/20—[b, f]-condensed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D281/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D281/02—Seven-membered rings
- C07D281/04—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D281/08—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D281/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D281/16—[b, f]-condensed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D413/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D417/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Abstract
Se proveen, en parte, compuestos que tienen propiedades efectoras alostéricas contra la Cp del virus de la Hepatitis B. También se proveen métodos de tratamiento de infecciones virales, tal como la hepatitis B, que comprenden administrar a un paciente que lo necesita uno de los compuestos divulgados. Reivindicación 1: Un compuesto caracterizado porque está representado mediante la fórmula (1), donde Y se selecciona del grupo que consiste en S(O)ʸ, C=O, C(R¹¹)₂, NRY y O donde y es 0, 1, ó 2; R¹¹ es H o C₁₋₆alquilo, RY se selecciona del grupo que consiste en H, metilo, etilo, propilo, proprenilo, butilo, fenilo y bencilo, donde RY, cuando no es H, puede estar opcionalmente sustituido con hidroxilo; RZ se selecciona del grupo que consiste en H, metilo, etilo, propilo, fenilo y bencilo; Rᵐ y Rᵐ se seleccionan en forma independiente entre sí del grupo que consiste en H y C₁₋₆alquilo (opcionalmente sustituido con uno, dos o tres sustituyentes seleccionados cada uno de forma independiente entre halógeno e hidroxilo); R²¹ se selecciona en cada caso del grupo que consiste en H, halógeno, y C₁₋₆alquilo; q es 0, 1, ó 2; R²² se selecciona en cada caso del grupo que consiste en H, halógeno, hidroxilo, nitro, ciano, carboxi, C₁₋₆alquilo, C₂₋₆alquenilo, C₂₋₆alquinilo, C₁₋₆alcoxi, NRR, -C(O)-C₁₋₆alquilo, -C(O)-C₁₋₆alcoxi, -C(O)-NRR, -C(=NH)-NRR, X²-fenilo (opcionalmente sustituido con uno, dos o tres sustituyentes representados mediante R⁶³), fenilo (opcionalmente sustituido con uno, dos o tres sustituyentes representados mediante R⁶³), heteroarilo, monocíclico de 5 - 6 miembros (opcionalmente sustituido con uno, dos o tres sustituyentes representados mediante R⁶³), heteroarilo bicíclico de 9 - 10 miembros (opcionalmente sustituido con uno, dos o tres sustituyentes representados mediante R⁷³), C₃₋₆cioloalquilo, -S(O)ʷ-C₁₋₆alquilo (donde w es 0, 1 ó 2), -S(O)ʷ-NRR (donde w es 0, 1 ó 2), y -NR-S(O)ʷ (donde w es 0, 1 ó 2); R se selecciona, en forma independiente en cada caso, entre H, metilo, etilo, y propilo; R se selecciona, en forma independiente en cada caso, entre H, metilo, etilo, propilo, butilo, -C(O)-metilo y -C(O)-etilo, o R y R tomados junto con el nitrógeno al cual están unidos pueden formar un heterociclo de 4 - 7 miembros; cada una de las porciones R⁴, R⁵, R⁶, R⁷, R⁸, R⁸, y R¹⁰ se selecciona en forma independiente en cada caso entre el grupo que consiste en hidrógeno, C₁₋₆alquilo, C₂₋₆alquinilo, C₂₋₆alquenilo, halógeno, hidroxilo, nitro, ciano, y NRR; R⁶³ se selecciona en forma independiente en cada caso entre el grupo que consiste en H, halógeno, hidroxilo, nitro, ciano, carboxi, C₁₋₆alquilo, -C(O)-O-C₁₋₆alquilo, heterociclo (opcionalmente sustituido con halógeno o NRR), -C(O)-NRR, -C(=NH)-NRR, heteroarilo, fenilo, bencilo, C₂₋₆alquenilo, C₂₋₆alquinilo, C₁₋₆alcoxi, carboxi, NRR, -C(O)-C₁₋₆alquilo, -C(O)-C₁₋₆alcoxi, C₃₋₆cicloalquilo, -S(O)ʷ-C₁₋₆alquilo (donde w es 0, 1 ó 2), -S(O)ʷ-NRR (donde w es 0, 1 ó 2), -NR-S(O)ʷ-C₁₋₆alquilo (donde w es 0, 1 ó 2), X²-R⁶⁹; R⁶⁹ se selecciona del grupo que consiste en H, halógeno, hidroxilo, nitro, ciano, C₁₋₆alquilo, -C(O)-O-C₁₋₆alquilo, heterociclo (opcionalmente sustituido con halógeno o NRR), -C(O)-NRR, -C(=NH)-NRR, heteroarilo, fenilo, C₂₋₆alquenilo, C₂₋₆alquinilo, C₁₋₆alcoxi, carboxi, NRR, -C(O)-C₁₋₆alquilo, -C(O)-C₁₋₆alcoxi, C₃₋₆cicloalquilo, -S(O)ʷ-C₁₋₆alquilo (donde w es 0, 1 ó 2), -S(O)ʷ-NRR (donde w es 0, 1 ó 2), y -NR-S(O)ʷ-C₁₋₆ alquilo (donde w es 0, 1 ó 2), X² se selecciona entre S(O)ʷ (donde w es 0, 1, o 2), O, CH₂, o NR; donde en cada caso, C₁₋₆alquilo puede estar opcionalmente sustituido con uno, dos, tres o más sustituyentes seleccionados del grupo que consiste en halógeno, hidroxilo, nitro, ciano, carboxi, C₂₋₆alquenilo, C₂₋₆alquinilo, C₁₋₆alcoxi, NRR, -NR-S(O)ʷ-C₁₋₆alquilo (donde w es 0, 1 ó 2), y S(O)ʷ-NRR (donde w es 0, 1 ó 2); C₁₋₆alcoxi puede estar opcionalmente sustituido con uno, dos, tres o más sustituyentes seleccionados del grupo que consiste en halógeno, hidroxilo, nitro, ciano, carboxi, C₁₋₆alquilo, NRR, -NR-S(O)ʷ-C₁₋₆ alquilo (donde w es 0, 1 ó 2), y S(O)ʷ-NRR (donde w es 0, 1 ó 2); y sales aceptables farmacéuticamente del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201562218815P | 2015-09-15 | 2015-09-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR106041A1 true AR106041A1 (es) | 2017-12-06 |
Family
ID=58289869
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP160102819A AR106040A1 (es) | 2015-09-15 | 2016-09-15 | Moduladores de la proteína core de la hepatitis b |
ARP160102816A AR106037A1 (es) | 2015-09-15 | 2016-09-15 | Moduladores de la proteína core de la hepatitis b |
ARP160102820A AR106041A1 (es) | 2015-09-15 | 2016-09-15 | Moduladores de la proteína core de la hepatitis b |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP160102819A AR106040A1 (es) | 2015-09-15 | 2016-09-15 | Moduladores de la proteína core de la hepatitis b |
ARP160102816A AR106037A1 (es) | 2015-09-15 | 2016-09-15 | Moduladores de la proteína core de la hepatitis b |
Country Status (28)
Country | Link |
---|---|
US (6) | US10766890B2 (es) |
EP (4) | EP3349580B1 (es) |
JP (4) | JP7023838B2 (es) |
KR (3) | KR20180053363A (es) |
CN (4) | CN108348529A (es) |
AR (3) | AR106040A1 (es) |
AU (4) | AU2016323297A1 (es) |
CA (3) | CA2998803A1 (es) |
CL (2) | CL2018000684A1 (es) |
CY (1) | CY1123570T1 (es) |
DK (1) | DK3349580T3 (es) |
DO (1) | DOP2018000074A (es) |
EA (3) | EA201890731A1 (es) |
ES (2) | ES2905950T3 (es) |
HK (3) | HK1258761A1 (es) |
HR (1) | HRP20201812T1 (es) |
HU (1) | HUE051872T2 (es) |
IL (3) | IL258099A (es) |
LT (1) | LT3349580T (es) |
MX (4) | MX2018003206A (es) |
PH (3) | PH12018500573A1 (es) |
PT (1) | PT3349580T (es) |
RS (1) | RS61064B1 (es) |
SG (1) | SG10202011103UA (es) |
SI (1) | SI3349580T1 (es) |
TW (4) | TW201720802A (es) |
WO (3) | WO2017048954A1 (es) |
ZA (1) | ZA201802456B (es) |
Families Citing this family (60)
Publication number | Priority date | Publication date | Assignee | Title |
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RS59430B1 (sr) | 2014-03-13 | 2019-11-29 | Univ Indiana Res & Tech Corp | Alosterni modulatori proteina jezgra hepatitisa b |
TW201720802A (zh) * | 2015-09-15 | 2017-06-16 | 艾森伯利生物科學公司 | B型肝炎核心蛋白質調節劑 |
WO2018053157A1 (en) * | 2016-09-15 | 2018-03-22 | Assembly Biosciences, Inc. | Hepatitis b core protein modulators |
SG10201914029RA (en) | 2016-10-14 | 2020-03-30 | Precision Biosciences Inc | Engineered meganucleases specific for recognition sequences in the hepatitis b virus genome |
US10821103B2 (en) | 2016-11-07 | 2020-11-03 | Arbutus Biopharma Corporation | Substituted pyridinone-containing trycyclic compounds, and methods using same |
HUE054822T2 (hu) | 2017-02-23 | 2021-10-28 | Fujian Cosunter Pharmaceutical Co Ltd | Triciklusos vegyület és ennek alkalmazásai |
JP2020511436A (ja) | 2017-03-02 | 2020-04-16 | アッセンブリー バイオサイエンシズ,インコーポレイテッド | 環状スルファミド化合物およびその使用方法 |
EP3596070A1 (en) * | 2017-03-13 | 2020-01-22 | Assembly Biosciences, Inc. | Process for making hepatitis b core protein modulators |
WO2018172852A1 (en) | 2017-03-21 | 2018-09-27 | Arbutus Biopharma Corporation | Substituted dihydroindene-4-carboxamides and analogs thereof, and methods using same |
JP2021501764A (ja) | 2017-11-02 | 2021-01-21 | アイクリス ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディトゲゼルシャフト | B型肝炎ウイルス(hbv)に対して有効な新規高活性アミノチアゾール置換インドール−2−カルボキサミド |
US11236087B2 (en) | 2017-11-02 | 2022-02-01 | Aicuris Gmbh & Co. Kg | Highly active pyrazolo-piperidine substituted indole-2-carboxamides active against the hepatitis B virus (HBV) |
WO2019123339A1 (en) | 2017-12-20 | 2019-06-27 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 2'3' cyclic dinucleotides with phosphonate bond activating the sting adaptor protein |
CA3084569A1 (en) | 2017-12-20 | 2019-06-27 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3'3' cyclic dinucleotides with phosphonate bond activating the sting adaptor protein |
CN111788204B (zh) | 2018-02-26 | 2023-05-05 | 吉利德科学公司 | 作为hbv复制抑制剂的取代吡咯嗪化合物 |
US10870691B2 (en) | 2018-04-05 | 2020-12-22 | Gilead Sciences, Inc. | Antibodies and fragments thereof that bind hepatitis B virus protein X |
TWI818007B (zh) | 2018-04-06 | 2023-10-11 | 捷克科學院有機化學與生物化學研究所 | 2'3'-環二核苷酸 |
EP3774832A1 (en) | 2018-04-06 | 2021-02-17 | Institute of Organic Chemistry and Biochemistry ASCR, V.V.I. | 3'3'-cyclic dinucleotides |
TW202005654A (zh) | 2018-04-06 | 2020-02-01 | 捷克科學院有機化學與生物化學研究所 | 2,2,─環二核苷酸 |
US11142750B2 (en) | 2018-04-12 | 2021-10-12 | Precision Biosciences, Inc. | Optimized engineered meganucleases having specificity for a recognition sequence in the Hepatitis B virus genome |
EP3787631A4 (en) * | 2018-05-03 | 2022-01-19 | Emory University | ORPHAN NUCLEAR RECEPTOR MODULATORS FOR NASH AND OTHER METABOLIC DISORDERS |
US20190359645A1 (en) | 2018-05-03 | 2019-11-28 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 2'3'-cyclic dinucleotides comprising carbocyclic nucleotide |
TWI815887B (zh) * | 2018-05-15 | 2023-09-21 | 美商愛彼特生物製藥股份有限公司 | 經取代的2,2'-雙嘧啶基化合物、其類似物及其使用方法 |
WO2020028097A1 (en) | 2018-08-01 | 2020-02-06 | Gilead Sciences, Inc. | Solid forms of (r)-11-(methoxymethyl)-12-(3-methoxypropoxy)-3,3-dimethyl-8-0x0-2,3,8,13b-tetrahydro-1h-pyrido[2,1-a]pyrrolo[1,2-c] phthalazine-7-c arboxylic acid |
SG11202103839UA (en) | 2018-10-31 | 2021-05-28 | Gilead Sciences Inc | Substituted 6-azabenzimidazole compounds as hpk1 inhibitors |
TW202136261A (zh) | 2018-10-31 | 2021-10-01 | 美商基利科學股份有限公司 | 經取代之6-氮雜苯并咪唑化合物 |
UY38439A (es) | 2018-11-02 | 2020-05-29 | Aicuris Gmbh & Co Kg | Novedosas urea 6,7-dihidro-4h-pirazolo[4,3-c]piridinas activas contra el virus de la hepatitis b (vhb) |
UY38435A (es) | 2018-11-02 | 2020-05-29 | Aicuris Gmbh & Co Kg | Nuevas urea 6,7-dihidro-4h-pirazol[1,5-a] pirazinas activas contra el virus de la hepatitis b (vhb) |
UY38434A (es) | 2018-11-02 | 2020-05-29 | Aicuris Gmbh & Co Kg | Nuevas 6,7-dihidro-4h-pirazolo[1,5-a]pirazin indol-2-carboxamidas activas contra el virus de la hepatitis b (hbv) |
TW202031666A (zh) | 2018-11-02 | 2020-09-01 | 德商艾庫瑞斯公司 | 對抗b型肝炎病毒(hbv)之新穎6,7-二氫-4h-噻唑并[5,4-c]吡啶脲活性劑 |
UY38437A (es) | 2018-11-02 | 2020-05-29 | Aicuris Gmbh & Co Kg | Nuevas urea 6,7-dihidro-4h-pirazolo[1,5-a]pirazinas activas contra el virus de la hepatitis b (hbv) |
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