Α-Chlorocodide
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IUPAC name 6β-Chloro-3-methoxy-17-methyl-7,8-didehydro-4,5α-epoxymorphinan | |
Systematic IUPAC name (4R,4aR,7R,7aR,12bS)-7-Chloro-9-methoxy-2,3,4,4a,7,7a-hexahydro-1H-4,12-methano[1]benzofuro[3,2-e]isoquinoline | |
Other names 6β-Chloro-6-deoxycodeine 6-Chloro-6-deoxyisocodeine | |
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Properties | |
Chemical formula | C18H20ClNO2 |
Molar mass | 317.81 g·mol−1 |
Melting point | 151 to 154 °C (304 to 309 °F; 424 to 427 K)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
α-Chlorocodide is an opioid analog that is a derivative of codeine in which the 6-hydroxy group has been replaced by chlorine.[1]
See also
- Chloromorphide
References
- ^ a b Stork, Gilbert; Clarke, Frank H. (1956). "The SN2' Reaction. III. Structure and SN2' Reactions of the Halocodides". Journal of the American Chemical Society. 78 (18): 4619–4624. doi:10.1021/ja01599a026.
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Opioid receptor modulators
(MOR)
(DOR)
(KOR)
(NOP)
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Antagonists |
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- Enkephalinase inhibitors: Amastatin
- BL-2401
- Candoxatril
- D -Phenylalanine
- Dexecadotril (retorphan)
- Ecadotril (sinorphan)
- Kelatorphan
- Racecadotril (acetorphan)
- RB-101
- RB-120
- RB-3007
- Opiorphan
- Selank
- Semax
- Spinorphin
- Thiorphan
- Tynorphin
- Ubenimex (bestatin)
- Propeptides: β-Lipotropin (proendorphin)
- Prodynorphin
- Proenkephalin
- Pronociceptin
- Proopiomelanocortin (POMC)
- Others: Kyotorphin (met-enkephalin releaser/degradation stabilizer)
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