| 词条 | Cogazocine |
| 释义 |
| IUPAC_name = 3-(cyclobutylmethyl)-6-ethyl-11,11-dimethyl-1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocin-8-ol | image = Cogazocine.svg | image2 = Cogazocine-3D-balls-by-AHRLS-2012.png | CAS_number = 57653-29-9 | ATC_prefix = None | ATC_suffix = | UNII = 6GKB767I3M | PubChem = 198576 | ChEMBL = 2104583 | ChemSpiderID = 171872 | C = 21 | H = 31 | N = 1 | O = 1 | molecular_weight = 313.477 g/mol | smiles = Oc1ccc4c(c1)C2(C(C(N(CC2)CC3CCC3)C4)(C)C)CC | StdInChI = 1S/C21H31NO/c1-4-21-10-11-22(14-15-6-5-7-15)19(20(21,2)3)12-16-8-9-17(23)13-18(16)21/h8-9,13,15,19,23H,4-7,10-12,14H2,1-3H3 | StdInChIKey = IUUBFDSJJHOTDI-UHFFFAOYSA-N | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | pregnancy_category = | legal_status = | routes_of_administration = }}Cogazocine (INN) is an opioid analgesic of the benzomorphan family which was never marketed.[1][2] See also
References1. ^{{cite web | url = http://whqlibdoc.who.int/hq/2004/WHO_EDM_QSM_2004.5.pdf | author = World Health Organization | title = The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substance | year = 2004 | format = PDF}} {{Analgesics}}{{Opioidergics}}2. ^{{cite journal |vauthors=James RW, Heywood R, Crook D | title = Reversible suppression of spermiogenesis in beagle dogs following overdosage with the narcotic analgesic cogazocine lactate | journal = Toxicology | volume = 16 | issue = 3 | pages = 193–203 | year = 1980 | pmid = 6106974 | doi = 10.1016/0300-483x(80)90116-x| url = }} 5 : Alcohols|Analgesics|Benzazocines|Opioids|Cyclobutanes |
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