SI1572726T1 - 4-methylhexanoic kahalalide f compound - Google Patents
4-methylhexanoic kahalalide f compoundInfo
- Publication number
- SI1572726T1 SI1572726T1 SI200331948T SI200331948T SI1572726T1 SI 1572726 T1 SI1572726 T1 SI 1572726T1 SI 200331948 T SI200331948 T SI 200331948T SI 200331948 T SI200331948 T SI 200331948T SI 1572726 T1 SI1572726 T1 SI 1572726T1
- Authority
- SI
- Slovenia
- Prior art keywords
- kahalalide
- methylhexanoic
- compound
- antitumoral
- antiviral
- Prior art date
Links
- -1 kahalalide f compound Chemical class 0.000 title 1
- 230000000259 anti-tumor effect Effects 0.000 abstract 2
- RCGXNDQKCXNWLO-WLEIXIPESA-N (2r)-n-[(2s)-5-amino-1-[[(2r,3r)-1-[[(3s,6z,9s,12r,15r,18r,19s)-9-benzyl-15-[(2r)-butan-2-yl]-6-ethylidene-19-methyl-2,5,8,11,14,17-hexaoxo-3,12-di(propan-2-yl)-1-oxa-4,7,10,13,16-pentazacyclononadec-18-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-1-oxopent Chemical class N([C@@H](CCCN)C(=O)N[C@H]([C@H](C)CC)C(=O)N[C@H]1C(N[C@@H](C(=O)N[C@@H](C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)NC(/C(=O)N[C@H](C(=O)O[C@H]1C)C(C)C)=C\C)C(C)C)[C@H](C)CC)=O)C(=O)[C@H]1CCCN1C(=O)[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](NC(=O)CCCC(C)C)C(C)C)[C@@H](C)O)C(C)C)C(C)C RCGXNDQKCXNWLO-WLEIXIPESA-N 0.000 abstract 1
- 201000004681 Psoriasis Diseases 0.000 abstract 1
- 230000000840 anti-viral effect Effects 0.000 abstract 1
- 229940121375 antifungal agent Drugs 0.000 abstract 1
- 239000003429 antifungal agent Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229930194861 kahalalide Natural products 0.000 abstract 1
Classifications
-
- 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
- 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Immunology (AREA)
- Toxicology (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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 (5)
| 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 |
| EP03779140A EP1572726B1 (en) | 2002-10-18 | 2003-10-20 | 4-methylhexanoic kahalalide f compound |
| PCT/US2003/033207 WO2004035613A2 (en) | 2002-10-18 | 2003-10-20 | 4-methylhexanoic kahalaide f compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SI1572726T1 true SI1572726T1 (en) | 2011-04-29 |
Family
ID=35276268
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI200331948T SI1572726T1 (en) | 2002-10-18 | 2003-10-20 | 4-methylhexanoic kahalalide f compound |
Country Status (11)
| Country | Link |
|---|---|
| KR (2) | KR101149095B1 (en) |
| AT (1) | ATE490975T1 (en) |
| AU (1) | AU2003285911B2 (en) |
| CY (1) | CY1111319T1 (en) |
| DE (1) | DE60335292D1 (en) |
| DK (1) | DK1572726T3 (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 |
| ES2256305T3 (en) * | 2000-10-31 | 2006-07-16 | Pharma Mar, S.A. | FORMULATIONS OF KAHALALIDE F. |
| EP1435990A1 (en) * | 2001-10-19 | 2004-07-14 | Pharma Mar, S.A. | Kahalalide compounds for use in cancer therapy |
-
2003
- 2003-10-20 SI SI200331948T patent/SI1572726T1/en unknown
- 2003-10-20 KR KR1020057006480A patent/KR101149095B1/en not_active Expired - Fee Related
- 2003-10-20 DE DE60335292T patent/DE60335292D1/en not_active Expired - Lifetime
- 2003-10-20 AT AT03779140T patent/ATE490975T1/en active
- 2003-10-20 PT PT03779140T patent/PT1572726E/en unknown
- 2003-10-20 DK DK03779140.7T patent/DK1572726T3/en active
- 2003-10-20 KR KR1020117020121A patent/KR20110114690A/en not_active Ceased
- 2003-10-20 PL PL377056A patent/PL209129B1/en unknown
- 2003-10-20 AU AU2003285911A patent/AU2003285911B2/en not_active Ceased
-
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
-
2011
- 2011-03-08 CY CY20111100265T patent/CY1111319T1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL167724A (en) | 2012-01-31 |
| NO20052379L (en) | 2005-07-15 |
| NO20052379D0 (en) | 2005-05-13 |
| HK1082261A1 (en) | 2006-06-02 |
| DE60335292D1 (en) | 2011-01-20 |
| AU2003285911A1 (en) | 2004-05-04 |
| KR101149095B1 (en) | 2012-05-30 |
| PL377056A1 (en) | 2006-01-23 |
| DK1572726T3 (en) | 2011-03-28 |
| ATE490975T1 (en) | 2010-12-15 |
| AU2003285911B2 (en) | 2009-11-19 |
| KR20110114690A (en) | 2011-10-19 |
| PT1572726E (en) | 2011-02-14 |
| NO333448B1 (en) | 2013-06-10 |
| PL209129B1 (en) | 2011-07-29 |
| CY1111319T1 (en) | 2015-08-05 |
| KR20050070056A (en) | 2005-07-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MXPA04003796A (en) | Substituted thioacetamides. | |
| DE60332137D1 (en) | Cyclohexyl-sulphone als gamma-sekretase-inhibitoren | |
| MXPA02011288A (en) | Substituted thioacetamides. | |
| GB0225474D0 (en) | Therapeutic agents | |
| MXPA05009682A (en) | Methods of radiofluorination of biologically active vectors. | |
| WO2003099266A3 (en) | Acetamides and benzamides that are useful in treating sexual dysfunction | |
| ZA200802848B (en) | Potassium channel inhibitors | |
| SG167670A1 (en) | Aminocyclohexyl ether compounds and uses thereof | |
| MXPA05004133A (en) | 4-methylhexanoic kahalaide f compound. | |
| TW200701982A (en) | Novel use of peptide compounds for treating pain in trigeminal neuralgia | |
| ATE486915T1 (en) | AZEOTROP-LIKE COMPOSITION OF 1,2-DICHLORO-3,3,3-TRIFLUOROPROPENE AND HYDROGEN FLUORIDE | |
| GB0216001D0 (en) | Process and composition | |
| ATE549024T1 (en) | QUINAZOLINE POTASSIUM CHANNEL INHIBITORS | |
| MXPA02011039A (en) | Fungicidal combinations of active agents. | |
| IL157457A0 (en) | Benzimidazoles that are useful in treating sexual dysfuction | |
| IL135825A0 (en) | Use of mirtazapine for treating sleep apneas | |
| ATE372330T1 (en) | N-SULFONYLUREA APOPTOSIS PROMOTER | |
| SI1572726T1 (en) | 4-methylhexanoic kahalalide f compound | |
| AU2001247241A1 (en) | Biologically active analogs of discodermolide | |
| MXPA05012605A (en) | Compositions comprising gastrin compounds and their use in diabetes. | |
| MX2008001548A (en) | Antitumoral compounds. | |
| ATE423780T1 (en) | MACROCYCLES FOR THE TREATMENT OF CANCER DISEASES | |
| IL142295A0 (en) | Use of acylcarnitines as antitumour agents | |
| LT2002131A (en) | New use of fir oil for cosmetic | |
| TW200607493A (en) | Potassium channel inhibitors |