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7-Spiroindanyloxymorphone
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| Systematic (IUPAC) name | |
| (4aR-(4aα,7aα,8α,9cα))-1',3',7,7a,8,9-Hexahydro-3,7a-dihydroxy-12-methylspiro(6H-8,9c-(iminoethano)phenanthro(4,5-bcd)furan-6,2'-(2H)inden)-5(4aH)-one | |
| Identifiers | |
| CAS number | |
| ATC code | ? |
| PubChem | |
| Chemical data | |
| Formula | C25H25NO4 |
| Mol. mass | 403.470 g/mol |
| SMILES | & |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | ? |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
? |
| Legal status | |
| Routes | ? |
7-Spiroindanyloxymorphone (SIOM) is a drug which is used in scientific research. It is a selective δ-opioid agonist.[1][2][3][4][5]
References
- ^ Portoghese PS, Moe ST, Takemori AE. A selective delta 1 opioid receptor agonist derived from oxymorphone. Evidence for separate recognition sites for delta 1 opioid receptor agonists and antagonists. Journal of Medicinal Chemistry. 1993 Aug 20;36(17):2572-4. PMID 8394935
- ^ Fang X, Larson DL, Portoghese PS. 7-spirobenzocyclohexyl derivatives of naltrexone, oxymorphone, and hydromorphone as selective opioid receptor ligands. Journal of Medicinal Chemistry. 1997 Sep 12;40(19):3064-70. PMID 9301669
- ^ Ohkawa S, DiGiacomo B, Larson DL, Takemori AE, Portoghese PS. 7-Spiroindanyl derivatives of naltrexone and oxymorphone as selective ligands for delta opioid receptors. Journal of Medicinal Chemistry. 1997 May 23;40(11):1720-5. PMID 9171881
- ^ Kshirsagar TA, Fang X, Portoghese PS. 14-Desoxy analogues of naltrindole and 7-spiroindanyloxymorphone: the role of the 14-hydroxy group at delta opioid receptors. Journal of Medicinal Chemistry. 1998 Jul 2;41(14):2657-60. PMID 9651172
- ^ Shenderovich MD, Liao S, Qian X, Hruby VJ. A three-dimensional model of the delta-opioid pharmacophore: comparative molecular modeling of peptide and nonpeptide ligands. Biopolymers. 2000 Jun;53(7):565-80. PMID 10766952
Wikipedia content modification information:
- This page was last modified on 26 June 2008, at 08:13.
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