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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H19NO3.ClH
Molecular Weight 333.809
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ORIPAVINE HYDROCHLORIDE

SMILES

Cl.[H][C@@]12OC3=C(O)C=CC4=C3[C@@]15CCN(C)[C@]([H])(C4)C5=CC=C2OC

InChI

InChIKey=OGVCGIJVSVSIEL-HIMTYSBHSA-N
InChI=1S/C18H19NO3.ClH/c1-19-8-7-18-11-4-6-14(21-2)17(18)22-16-13(20)5-3-10(15(16)18)9-12(11)19;/h3-6,12,17,20H,7-9H2,1-2H3;1H/t12-,17+,18+;/m1./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C18H19NO3
Molecular Weight 297.3484
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparison of pharmacological activities of buprenorphine and norbuprenorphine: norbuprenorphine is a potent opioid agonist.
2001 May
Characterization of opiates, neuroleptics, and synthetic analogs at ORL1 and opioid receptors.
2001 Sep 28
Separation of opiate alkaloids by electrokinetic chromatography with sulfated-cyclodextrin as a pseudo-stationary phase.
2003 Jan 24
RNAi-mediated replacement of morphine with the nonnarcotic alkaloid reticuline in opium poppy.
2004 Dec
Analgesia: morphine-pathway block in top1 poppies.
2004 Sep 23
Submolecular partitioning of morphine hydrate based on its experimental charge density at 25 K.
2005 Aug
BU74, a complex oripavine derivative with potent kappa opioid receptor agonism and delayed opioid antagonism.
2005 Feb 21
A rapid and reliable solid-phase extraction method for high-performance liquid chromatographic analysis of opium alkaloids from papaver plants.
2005 Nov
WHO Expert Committee on Drug Dependence.
2006
Thienorphine: receptor binding and behavioral effects in rhesus monkeys.
2007 Apr
Differentiation of opium and poppy straw using capillary electrophoresis and pattern recognition techniques.
2007 Dec 12
Determination of opiate alkaloids in process liquors using capillary electrophoresis.
2007 Feb 19
Rapid determination of Papaver somniferum alkaloids in process streams using monolithic column high-performance liquid chromatography with chemiluminescence detection.
2007 Jul 30
Cinnamoyl derivatives of 7alpha-aminomethyl-6,14-endo-ethanotetrahydrothebaine and 7alpha-aminomethyl-6,14-endo-ethanotetrahydrooripavine and related opioid ligands.
2007 Oct 18
Live cell monitoring of mu-opioid receptor-mediated G-protein activation reveals strong biological activity of close morphine biosynthetic precursors.
2007 Sep 14
Designation of oripavine as a basic class of controlled substance. Final rule.
2007 Sep 24
A hybrid FIA/HPLC system incorporating monolithic column chromatography.
2007 Sep 26
Isolation and identification of unique marker compounds from the Tasmanian poppy Papaver somniferum N. Implications for the identification of illicit heroin of Tasmanian origin.
2008 Mar 5
Biochemistry and occurrence of o-demethylation in plant metabolism.
2010
N-demethylation of N-methyl alkaloids with ferrocene.
2010 Aug 1
No hyperalgesia following opioid withdrawal after the oripavine derivative etorphine compared to remifentanil and sufentanil.
2010 Feb
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:28:52 GMT 2023
Edited
by admin
on Sat Dec 16 10:28:52 GMT 2023
Record UNII
HRR7PQ2JHN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ORIPAVINE HYDROCHLORIDE
Common Name English
MORPHINAN-3-OL, 6,7,8,14-TETRADEHYDRO-4,5.ALPHA.-EPOXY-6-METHOXY-17-METHYL-, HYDROCHLORIDE
Systematic Name English
MORPHINAN-3-OL, 6,7,8,14-TETRADEHYDRO-4,5-EPOXY-6-METHOXY-17-METHYL-, HYDROCHLORIDE, (5.ALPHA.)-
Systematic Name English
MORPHINAN-3-OL, 6,7,8,14-TETRADEHYDRO-4,5-EPOXY-6-METHOXY-17-METHYL-, HYDROCHLORIDE (1:1), (5.ALPHA.)-
Systematic Name English
(4R,7AR,12BS)-7-METHOXY-3-METHYL-2,4,7A,13-TETRAHYDRO-1H-4,12-METHANOBENZOFURO(3,2-E)ISOQUINOLIN-9-OL;HYDROCHLORIDE
Systematic Name English
Code System Code Type Description
FDA UNII
HRR7PQ2JHN
Created by admin on Sat Dec 16 10:28:52 GMT 2023 , Edited by admin on Sat Dec 16 10:28:52 GMT 2023
PRIMARY
CAS
6153-40-8
Created by admin on Sat Dec 16 10:28:52 GMT 2023 , Edited by admin on Sat Dec 16 10:28:52 GMT 2023
PRIMARY
PUBCHEM
66760524
Created by admin on Sat Dec 16 10:28:52 GMT 2023 , Edited by admin on Sat Dec 16 10:28:52 GMT 2023
PRIMARY
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