HRP20030330A2 - Triazole derivatives and pharmaceutical compositions comprising them - Google Patents
Triazole derivatives and pharmaceutical compositions comprising themInfo
- Publication number
- HRP20030330A2 HRP20030330A2 HR20030330A HRP20030330A HRP20030330A2 HR P20030330 A2 HRP20030330 A2 HR P20030330A2 HR 20030330 A HR20030330 A HR 20030330A HR P20030330 A HRP20030330 A HR P20030330A HR P20030330 A2 HRP20030330 A2 HR P20030330A2
- Authority
- HR
- Croatia
- Prior art keywords
- formula
- acid
- methoxy
- dimethoxy
- solvates
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title description 3
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 title description 3
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- 238000000034 method Methods 0.000 claims description 25
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- 150000003839 salts Chemical class 0.000 claims description 18
- 239000012453 solvate Substances 0.000 claims description 18
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- IQIUBXJCJXNJNP-UHFFFAOYSA-N benzyl 6-methoxy-1-(3-methoxy-3-oxopropyl)-4,5-dimethylindole-2-carboxylate Chemical compound C=1C2=C(C)C(C)=C(OC)C=C2N(CCC(=O)OC)C=1C(=O)OCC1=CC=CC=C1 IQIUBXJCJXNJNP-UHFFFAOYSA-N 0.000 description 1
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 1
- 210000000941 bile Anatomy 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
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- 230000015572 biosynthetic process Effects 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
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- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
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- 201000001883 cholelithiasis Diseases 0.000 description 1
- 210000002932 cholinergic neuron Anatomy 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
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- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
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- 238000002050 diffraction method Methods 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- SXZIXHOMFPUIRK-UHFFFAOYSA-N diphenylmethanimine Chemical compound C=1C=CC=CC=1C(=N)C1=CC=CC=C1 SXZIXHOMFPUIRK-UHFFFAOYSA-N 0.000 description 1
- 235000014632 disordered eating Nutrition 0.000 description 1
- 229960003638 dopamine Drugs 0.000 description 1
- 229940052760 dopamine agonists Drugs 0.000 description 1
- 239000003136 dopamine receptor stimulating agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 230000008918 emotional behaviour Effects 0.000 description 1
- HVJJYOAPXBPQQV-UHFFFAOYSA-N ethyl 2-azidoacetate Chemical compound CCOC(=O)CN=[N+]=[N-] HVJJYOAPXBPQQV-UHFFFAOYSA-N 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 210000000744 eyelid Anatomy 0.000 description 1
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- 230000002349 favourable effect Effects 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- YFHXZQPUBCBNIP-UHFFFAOYSA-N fura-2 Chemical compound CC1=CC=C(N(CC(O)=O)CC(O)=O)C(OCCOC=2C(=CC=3OC(=CC=3C=2)C=2OC(=CN=2)C(O)=O)N(CC(O)=O)CC(O)=O)=C1 YFHXZQPUBCBNIP-UHFFFAOYSA-N 0.000 description 1
- 208000001130 gallstones Diseases 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 201000001421 hyperglycemia Diseases 0.000 description 1
- 230000002631 hypothermal effect Effects 0.000 description 1
- 238000005417 image-selected in vivo spectroscopy Methods 0.000 description 1
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- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000012739 integrated shape imaging system Methods 0.000 description 1
- 230000008991 intestinal motility Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
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- 208000023060 memory loss Diseases 0.000 description 1
- CWWARWOPSKGELM-SARDKLJWSA-N methyl (2s)-2-[[(2s)-2-[[2-[[(2s)-2-[[(2s)-2-[[(2s)-5-amino-2-[[(2s)-5-amino-2-[[(2s)-1-[(2s)-6-amino-2-[[(2s)-1-[(2s)-2-amino-5-(diaminomethylideneamino)pentanoyl]pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-5-oxopentanoyl]amino]-5 Chemical compound C([C@@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)OC)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@@H](N)CCCN=C(N)N)C1=CC=CC=C1 CWWARWOPSKGELM-SARDKLJWSA-N 0.000 description 1
- JPZYUHLBRMMAPC-UHFFFAOYSA-N methyl 3-[2-[[1-(2-cyclohexylethyl)-5-(2,5-dimethoxy-4-methylphenyl)-1,2,4-triazol-3-yl]carbamoyl]-6-methoxy-4,5-dimethylindol-1-yl]propanoate Chemical compound C=1C2=C(C)C(C)=C(OC)C=C2N(CCC(=O)OC)C=1C(=O)NC(=NN1CCC2CCCCC2)N=C1C1=CC(OC)=C(C)C=C1OC JPZYUHLBRMMAPC-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- UVEWQKMPXAHFST-UHFFFAOYSA-N n,1-diphenylmethanimine Chemical group C=1C=CC=CC=1C=NC1=CC=CC=C1 UVEWQKMPXAHFST-UHFFFAOYSA-N 0.000 description 1
- JIKUXBYRTXDNIY-UHFFFAOYSA-N n-methyl-n-phenylformamide Chemical compound O=CN(C)C1=CC=CC=C1 JIKUXBYRTXDNIY-UHFFFAOYSA-N 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 230000001537 neural effect Effects 0.000 description 1
- 201000001119 neuropathy Diseases 0.000 description 1
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- 239000002858 neurotransmitter agent Substances 0.000 description 1
- 210000001009 nucleus accumben Anatomy 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229940005483 opioid analgesics Drugs 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 208000033808 peripheral neuropathy Diseases 0.000 description 1
- 229940124531 pharmaceutical excipient Drugs 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 210000001187 pylorus Anatomy 0.000 description 1
- 230000003979 response to food Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 201000000980 schizophrenia Diseases 0.000 description 1
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- 229940076279 serotonin Drugs 0.000 description 1
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- 230000009329 sexual behaviour Effects 0.000 description 1
- 208000015891 sexual disease Diseases 0.000 description 1
- 235000021055 solid food Nutrition 0.000 description 1
- NHXLMOGPVYXJNR-ATOGVRKGSA-N somatostatin Chemical compound C([C@H]1C(=O)N[C@H](C(N[C@@H](CO)C(=O)N[C@@H](CSSC[C@@H](C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2C3=CC=CC=C3NC=2)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N1)[C@@H](C)O)NC(=O)CNC(=O)[C@H](C)N)C(O)=O)=O)[C@H](O)C)C1=CC=CC=C1 NHXLMOGPVYXJNR-ATOGVRKGSA-N 0.000 description 1
- 229960000553 somatostatin Drugs 0.000 description 1
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- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU0004153A HUP0004153A3 (en) | 2000-10-26 | 2000-10-26 | 3-amino-triazole derivatives with medicinal applicability, process for their preparation and pharmaceutical compositions containing them and their use |
FR0013728A FR2815963B1 (fr) | 2000-10-26 | 2000-10-26 | Nouveaux derives du triazole et les compositions pharmaceutiques les contenant |
PCT/EP2001/012984 WO2002034743A1 (en) | 2000-10-26 | 2001-10-25 | Triazole derivatives and pharmaceutical compositions comprising them |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20030330A2 true HRP20030330A2 (en) | 2003-06-30 |
Family
ID=89978697
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20030330A HRP20030330A2 (en) | 2000-10-26 | 2003-04-28 | Triazole derivatives and pharmaceutical compositions comprising them |
Country Status (21)
Country | Link |
---|---|
US (1) | US20040019091A1 (no) |
EP (1) | EP1335914A1 (no) |
JP (1) | JP2004512334A (no) |
KR (1) | KR20030042035A (no) |
CN (1) | CN1471525A (no) |
AR (1) | AR031042A1 (no) |
AU (1) | AU2002226330A1 (no) |
BG (1) | BG107642A (no) |
BR (1) | BR0114888A (no) |
CA (1) | CA2420727A1 (no) |
EA (1) | EA200300238A1 (no) |
EE (1) | EE200300161A (no) |
HR (1) | HRP20030330A2 (no) |
IL (1) | IL155055A0 (no) |
IS (1) | IS6734A (no) |
NO (1) | NO20031841L (no) |
NZ (1) | NZ524437A (no) |
PL (1) | PL365328A1 (no) |
SK (1) | SK5172003A3 (no) |
WO (1) | WO2002034743A1 (no) |
YU (1) | YU18803A (no) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005035793A2 (en) * | 2003-10-09 | 2005-04-21 | Decode Genetics Ehf. | Cckar markers and haplotypes associated with extreme weight conditions |
JP4892915B2 (ja) * | 2005-10-04 | 2012-03-07 | 大日本印刷株式会社 | エパルレスタット製造法 |
CA2731097A1 (en) * | 2008-07-15 | 2010-01-21 | Novartis Ag | Organic compounds |
US20130179356A1 (en) * | 2012-01-05 | 2013-07-11 | General Electric Company | Method and system for maintenance of turbomachinery |
CN104130243B (zh) * | 2014-07-08 | 2016-05-25 | 河北美星化工有限公司 | 取代对卤苯基三唑环取代氟化烟酰胺化合物及合成方法 |
BR112022006546A2 (pt) | 2019-10-07 | 2022-08-30 | Kallyope Inc | Agonistas de gpr119 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2701708B1 (fr) * | 1993-02-19 | 1995-05-19 | Sanofi Elf | Dérivés de 2-amido-4-phénylthiazoles polysubstitués, procédé de préparation, composition pharmaceutique et utilisation de ces dérivés pour la préparation d'un médicament. |
FR2703995B1 (fr) * | 1993-04-16 | 1995-07-21 | Sanofi Elf | 5-acylamino 1,2,4-thiadiazoles, leur preparation et compositions pharmaceutiques en contenant. |
FR2763337B1 (fr) * | 1997-05-13 | 1999-08-20 | Sanofi Sa | Nouveaux derives du triazole, un procede pour leur preparation et compositions pharmaceutiques les contenant |
-
2001
- 2001-10-25 US US10/398,858 patent/US20040019091A1/en not_active Abandoned
- 2001-10-25 KR KR10-2003-7005772A patent/KR20030042035A/ko not_active Application Discontinuation
- 2001-10-25 WO PCT/EP2001/012984 patent/WO2002034743A1/en not_active Application Discontinuation
- 2001-10-25 EA EA200300238A patent/EA200300238A1/ru unknown
- 2001-10-25 SK SK517-2003A patent/SK5172003A3/sk unknown
- 2001-10-25 NZ NZ524437A patent/NZ524437A/en not_active Application Discontinuation
- 2001-10-25 EE EEP200300161A patent/EE200300161A/xx unknown
- 2001-10-25 CN CNA018181236A patent/CN1471525A/zh active Pending
- 2001-10-25 EP EP01988716A patent/EP1335914A1/en not_active Withdrawn
- 2001-10-25 PL PL01365328A patent/PL365328A1/xx not_active Application Discontinuation
- 2001-10-25 AR ARP010104990A patent/AR031042A1/es unknown
- 2001-10-25 YU YU18803A patent/YU18803A/sh unknown
- 2001-10-25 BR BR0114888-5A patent/BR0114888A/pt not_active Application Discontinuation
- 2001-10-25 IL IL15505501A patent/IL155055A0/xx unknown
- 2001-10-25 AU AU2002226330A patent/AU2002226330A1/en not_active Abandoned
- 2001-10-25 JP JP2002537734A patent/JP2004512334A/ja not_active Withdrawn
- 2001-10-25 CA CA002420727A patent/CA2420727A1/en not_active Abandoned
-
2003
- 2003-02-28 IS IS6734A patent/IS6734A/is unknown
- 2003-03-18 BG BG107642A patent/BG107642A/xx unknown
- 2003-04-24 NO NO20031841A patent/NO20031841L/no not_active Application Discontinuation
- 2003-04-28 HR HR20030330A patent/HRP20030330A2/hr not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CA2420727A1 (en) | 2002-05-02 |
NO20031841L (no) | 2003-06-19 |
KR20030042035A (ko) | 2003-05-27 |
NO20031841D0 (no) | 2003-04-24 |
NZ524437A (en) | 2004-10-29 |
YU18803A (sh) | 2006-05-25 |
CN1471525A (zh) | 2004-01-28 |
SK5172003A3 (en) | 2003-10-07 |
EE200300161A (et) | 2003-06-16 |
BR0114888A (pt) | 2003-12-09 |
WO2002034743A1 (en) | 2002-05-02 |
BG107642A (en) | 2003-11-28 |
JP2004512334A (ja) | 2004-04-22 |
AU2002226330A1 (en) | 2002-05-06 |
IL155055A0 (en) | 2003-10-31 |
PL365328A1 (en) | 2004-12-27 |
US20040019091A1 (en) | 2004-01-29 |
AR031042A1 (es) | 2003-09-03 |
EP1335914A1 (en) | 2003-08-20 |
EA200300238A1 (ru) | 2003-10-30 |
IS6734A (is) | 2003-02-28 |
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