NO20052379L - New antitumoral compounds - Google Patents
New antitumoral compoundsInfo
- Publication number
- NO20052379L NO20052379L NO20052379A NO20052379A NO20052379L NO 20052379 L NO20052379 L NO 20052379L NO 20052379 A NO20052379 A NO 20052379A NO 20052379 A NO20052379 A NO 20052379A NO 20052379 L NO20052379 L NO 20052379L
- Authority
- NO
- Norway
- Prior art keywords
- antitumoral compounds
- new antitumoral
- new
- compounds
- kahalalide
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
- C07D207/09—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4748—Tumour specific antigens; Tumour rejection antigen precursors [TRAP], e.g. MAGE
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/50—Cyclic peptides containing at least one abnormal peptide link
- C07K7/54—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring
- C07K7/56—Cyclic peptides containing at least one abnormal peptide link with at least one abnormal peptide link in the ring the cyclisation not occurring through 2,4-diamino-butanoic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/64—Cyclic peptides containing only normal peptide links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Abstract
The present invention is directed to new kahalalide antitumoral compounds, in particular to analogues of kahalalide F, useful as antitumoral, antiviral, antifungal agents and in the treatment of psoriasis.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/GB2002/004735 WO2003033012A1 (en) | 2001-10-19 | 2002-10-18 | Kahalalide compounds for use in cancer therapy |
GBGB0304367.6A GB0304367D0 (en) | 2003-02-26 | 2003-02-26 | Methods for treating psoriasis |
GB0314725A GB0314725D0 (en) | 2003-06-24 | 2003-06-24 | New antitumoral compounds |
PCT/US2003/033207 WO2004035613A2 (en) | 2002-10-18 | 2003-10-20 | 4-methylhexanoic kahalaide f compound |
Publications (3)
Publication Number | Publication Date |
---|---|
NO20052379D0 NO20052379D0 (en) | 2005-05-13 |
NO20052379L true NO20052379L (en) | 2005-07-15 |
NO333448B1 NO333448B1 (en) | 2013-06-10 |
Family
ID=35276268
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20052379A NO333448B1 (en) | 2002-10-18 | 2005-05-13 | New 4-methylhexanoic acid kahalalide F compounds, methods for their preparation, their use for the preparation of a drug preferably for the treatment of cancer, pharmaceutical compositions comprising the compounds, and a kit containing a pharmaceutical composition comprising the compounds. |
Country Status (12)
Country | Link |
---|---|
KR (2) | KR20110114690A (en) |
AT (1) | ATE490975T1 (en) |
AU (1) | AU2003285911B2 (en) |
CY (1) | CY1111319T1 (en) |
DE (1) | DE60335292D1 (en) |
DK (1) | DK1572726T3 (en) |
HK (1) | HK1082261A1 (en) |
IL (1) | IL167724A (en) |
NO (1) | NO333448B1 (en) |
PL (1) | PL209129B1 (en) |
PT (1) | PT1572726E (en) |
SI (1) | SI1572726T1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0321066D0 (en) * | 2003-09-09 | 2003-10-08 | Pharma Mar Sau | New antitumoral compounds |
GB0408958D0 (en) * | 2004-04-22 | 2004-05-26 | Pharma Mar Sa | Convergent synthesis for kahalalide compounds |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9302046D0 (en) * | 1993-02-03 | 1993-03-24 | Pharma Mar Sa | Antiumoral compound-v |
HUP0600031A3 (en) * | 2000-10-31 | 2012-02-28 | Pharma Mar | Kahalalide formulations and their use |
WO2003033012A1 (en) * | 2001-10-19 | 2003-04-24 | Pharma Mar, S.A. | Kahalalide compounds for use in cancer therapy |
-
2003
- 2003-10-20 PT PT03779140T patent/PT1572726E/en unknown
- 2003-10-20 KR KR1020117020121A patent/KR20110114690A/en not_active Application Discontinuation
- 2003-10-20 AU AU2003285911A patent/AU2003285911B2/en not_active Ceased
- 2003-10-20 KR KR1020057006480A patent/KR101149095B1/en not_active IP Right Cessation
- 2003-10-20 DE DE60335292T patent/DE60335292D1/en not_active Expired - Lifetime
- 2003-10-20 AT AT03779140T patent/ATE490975T1/en active
- 2003-10-20 DK DK03779140.7T patent/DK1572726T3/en active
- 2003-10-20 SI SI200331948T patent/SI1572726T1/en unknown
- 2003-10-20 PL PL377056A patent/PL209129B1/en unknown
-
2005
- 2005-03-29 IL IL167724A patent/IL167724A/en not_active IP Right Cessation
- 2005-05-13 NO NO20052379A patent/NO333448B1/en not_active IP Right Cessation
-
2006
- 2006-03-08 HK HK06102999.1A patent/HK1082261A1/en not_active IP Right Cessation
-
2011
- 2011-03-08 CY CY20111100265T patent/CY1111319T1/en unknown
Also Published As
Publication number | Publication date |
---|---|
HK1082261A1 (en) | 2006-06-02 |
PL209129B1 (en) | 2011-07-29 |
KR20050070056A (en) | 2005-07-05 |
ATE490975T1 (en) | 2010-12-15 |
SI1572726T1 (en) | 2011-04-29 |
DE60335292D1 (en) | 2011-01-20 |
PT1572726E (en) | 2011-02-14 |
NO20052379D0 (en) | 2005-05-13 |
AU2003285911A1 (en) | 2004-05-04 |
IL167724A (en) | 2012-01-31 |
AU2003285911B2 (en) | 2009-11-19 |
KR20110114690A (en) | 2011-10-19 |
NO333448B1 (en) | 2013-06-10 |
DK1572726T3 (en) | 2011-03-28 |
PL377056A1 (en) | 2006-01-23 |
CY1111319T1 (en) | 2015-08-05 |
KR101149095B1 (en) | 2012-05-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM1K | Lapsed by not paying the annual fees |