Norhydrocodone

Norhydrocodone
Clinical data
Other names	(5α)-3-Methoxy-4,5-epoxymorphinan-6-one
Dependence; liability	High
Identifiers
	IUPAC name (4R,4aR,7aR,12bS)-9-Methoxy-2,3,4,4a,5,6,7a,13-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7-one;
CAS Number	5083-62-5;
PubChem CID	13001738;
ChemSpider	32698944;
UNII	18NB5F1JT4;
CompTox Dashboard (EPA)	DTXSID70198862 ;
Chemical and physical data
Formula	C17H19NO3
Molar mass	285.343 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES COC1=C2C3=C(C[C@@H]4[C@H]5[C@]3(CCN4)[C@@H](O2)C(=O)CC5)C=C1;
	InChI InChI=1S/C17H19NO3/c1-20-13-5-2-9-8-11-10-3-4-12(19)16-17(10,6-7-18-11)14(9)15(13)21-16/h2,5,10-11,16,18H,3-4,6-8H2,1H3/t10-,11+,16-,17-/m0/s1; Key:JGORUXKMRLIJSV-YNHQPCIGSA-N;

Norhydrocodone is the major metabolite of the opioid analgesic hydrocodone. It is formed from hydrocodone in the liver via N-demethylation predominantly by CYP3A4. Unlike hydromorphone, a minor metabolite of hydrocodone, norhydrocodone is described as inactive. However, norhydrocodone is actually an agonist of the μ-opioid receptor with similar potency to hydrocodone, but has been found to produce only minimal analgesia when administered peripherally to animals. This is likely due to poor blood-brain-barrier and thus central nervous system penetration.

Clinical data

Other names	(5α)-3-Methoxy-4,5-epoxymorphinan-6-one
Dependence liability	High
Identifiers
IUPAC name (4R,4aR,7aR,12bS)-9-Methoxy-2,3,4,4a,5,6,7a,13-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7-one
CAS Number	5083-62-5
PubChem CID	13001738
ChemSpider	32698944
UNII	18NB5F1JT4
CompTox Dashboard (EPA)	DTXSID70198862
Chemical and physical data
Formula	C₁₇H₁₉NO₃
Molar mass	285.343 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES COC1=C2C3=C(C[C@@H]4[C@H]5[C@]3(CCN4)[C@@H](O2)C(=O)CC5)C=C1
InChI InChI=1S/C17H19NO3/c1-20-13-5-2-9-8-11-10-3-4-12(19)16-17(10,6-7-18-11)14(9)15(13)21-16/h2,5,10-11,16,18H,3-4,6-8H2,1H3/t10-,11+,16-,17-/m0/s1 Key:JGORUXKMRLIJSV-YNHQPCIGSA-N