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词条 Otenabant
释义

  1. See also

  2. References

{{Drugbox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 417842381
| IUPAC_name = 1-[8-(2-chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-yl]-4-(ethylamino)piperidine-4- carboxamide
| image = Otenabant.svg
| tradename =
| pregnancy_AU =
| pregnancy_US =
| pregnancy_category =
| legal_AU =
| legal_CA =
| legal_UK =
| legal_US =
| legal_status =
| routes_of_administration =
| bioavailability =
| protein_bound =
| metabolism =
| elimination_half-life =
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| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 686344-29-6
| ATC_prefix = none
| ATC_suffix =
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank =
| UNII_Ref = {{fdacite|changed|FDA}}
| UNII = J8211Y53EF
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D09362
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 562668
| PubChem = 10052040
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 8227602
| chemical_formula =
| C=25 | H=25 | Cl=2 | N=7 | O=1
| molecular_weight = 510.4 g/mol
| smiles = CCNC1(CCN(CC1)C2=NC=NC3=C2N=C(N3C4=CC=C(C=C4)Cl)C5=CC=CC=C5Cl)C(=O)N
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C25H25Cl2N7O/c1-2-31-25(24(28)35)11-13-33(14-12-25)22-20-23(30-15-29-22)34(17-9-7-16(26)8-10-17)21(32-20)18-5-3-4-6-19(18)27/h3-10,15,31H,2,11-14H2,1H3,(H2,28,35)
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = UNAZAADNBYXMIV-UHFFFAOYSA-N
}}Otenabant (CP-945,598) is a drug which acts as a potent and highly selective CB1 antagonist.[1] It was developed by Pfizer for the treatment of obesity,[2] but development for this application has been discontinued following the problems seen during clinical use of the similar drug rimonabant.[3]

See also

  • Cannabinoid receptor antagonist

References

1. ^{{Citation |last= Kim |first= M.|title= Design, chemical synthesis, and biological evaluation of novel triazolyl analogues of taranabant (MK-0364), a cannabinoid-1 receptor inverse agonist |journal= Tetrahedron |volume= 64 |issue= 48 |pages= 10802–10809 |year= 2008 |url=http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THR-4TJ1HGJ-9-2&_cdi=5289&_user=713789&_orig=search&_coverDate=11%2F24%2F2008&_sk=999359951&view=c&wchp=dGLbVzb-zSkWA&md5=2e8fe6fab24adb1087bd17bbcd3544a7&ie=/sdarticle.pdf |doi= 10.1016/j.tet.2008.09.057 |display-authors=etal}}
2. ^Woods SC. The endocannabinoid system: novel pathway for cardiometabolic Risk-factor reduction. Journal of the American Academy of Physician Assistants. 2007 Nov;Suppl Endocannabinoid:7-10. {{PMID|18047036}}
3. ^http://www.pfizer.com
{{Anorectics}}{{Cannabinoids}}{{Cannabinoidergics}}{{cannabinoid-stub}}

8 : Cannabinoids|Purines|Piperidines|Carboxamides|Chloroarenes|Pfizer|Pfizer products|CB1 receptor antagonists

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