Anazocine

Anazocine
Clinical data
ATC code	None;
Identifiers
	IUPAC name 9-methoxy-3-methyl-9-phenyl-3-azabicyclo[3.3.1]nonane;
CAS Number	15378-99-1 ; 21650-02-2 (citrate);
PubChem CID	27213;
ChemSpider	25327;
ChEMBL	ChEMBL2105792;
Chemical and physical data
Formula	C16H23NO
Molar mass	245.360 g/mol g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O(C2(c1ccccc1)C3CCCC2CN(C3)C)C;
	InChI InChI=1S/C16H23NO/c1-17-11-14-9-6-10-15(12-17)16(14,18-2)13-7-4-3-5-8-13/h3-5,7-8,14-15H,6,9-12H2,1-2H3; Key:YFFNPIAPUDUYAU-UHFFFAOYSA-N;

Anazocine (INN; CS-307), also known as azabicyclane, is an opioid analgesic of the morphan/benzomorphan family developed in the middle 1960s in the United States which was never marketed.^[1]^[2] It is listed by some sources as a teratogen.^[3]

The structure and properties of several related a- and ß-azabicyclane opioids was explored.^[4] Anazocine's chemical and structural relatives include opioid partial agonists, mixed agonist-antagonists, pure agonists, antagonists, and atypical non-opioid analgesics. It was tested in pigeons and in other experiments which contrasted and compared its analgesic effects to those of the phenazepine opioid ethoheptazine and the phenalkoxam open chain opioid propoxyphene,^[5] and pethidine as well.^[6]

References

^ F.. Macdonald (1997). Dictionary of Pharmacological Agents. CRC Press. p. 146. ISBN 978-0-412-46630-4. Retrieved 22 April 2012.
^ Kobayashi S, Hasegawa K, Oshima T, Takagi H (September 1970). "The pharmacology of azabicyclane, a new analgesic agent". Toxicology and Applied Pharmacology. 17 (2): 344–54. doi:10.1016/0041-008X(70)90191-2. PMID 5528556.
^ https://www.purdue.edu/ehps/rem/ih/terat.htm
^ "Conformational properties of ?- and ?-azabicyclane opiates. The effect of conformation on pharmacological activity". Journal of Computational Chemistry. 5: 291–298. doi:10.1002/jcc.540050403.
^ Kobayashi S, Hasegawa K, Oshima T, Takagi H (September 1970). "The pharmacology of azabicyclane, a new analgesic agent". Toxicol. Appl. Pharmacol. 17: 344–54. doi:10.1016/0041-008X(70)90191-2. PMID 5528556.
^ "Effects of propoxyphene, ethoheptazine, and azabicyclane on schedule-controlled responding: Attenuation by pentobarbital but not naloxone". Psychopharmacology. 66: 19–22. doi:10.1007/BF00431983.

[Macdonald1997-1] F.. Macdonald (1997). Dictionary of Pharmacological Agents. CRC Press. p. 146. ISBN 978-0-412-46630-4. Retrieved 22 April 2012.

[pmid5528556-2] Kobayashi S, Hasegawa K, Oshima T, Takagi H (September 1970). "The pharmacology of azabicyclane, a new analgesic agent". Toxicology and Applied Pharmacology. 17 (2): 344–54. doi:10.1016/0041-008X(70)90191-2. PMID 5528556.

[3] ttps://www.purdue.edu/ehps/rem/ih/terat.htm

[4] "Conformational properties of ?- and ?-azabicyclane opiates. The effect of conformation on pharmacological activity". Journal of Computational Chemistry. 5: 291–298. doi:10.1002/jcc.540050403.

[5] Kobayashi S, Hasegawa K, Oshima T, Takagi H (September 1970). "The pharmacology of azabicyclane, a new analgesic agent". Toxicol. Appl. Pharmacol. 17: 344–54. doi:10.1016/0041-008X(70)90191-2. PMID 5528556.

[6] "Effects of propoxyphene, ethoheptazine, and azabicyclane on schedule-controlled responding: Attenuation by pentobarbital but not naloxone". Psychopharmacology. 66: 19–22. doi:10.1007/BF00431983.

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See also

References