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
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
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
Title | Date | PubMed |
---|---|---|
Comparison of pharmacological activities of buprenorphine and norbuprenorphine: norbuprenorphine is a potent opioid agonist. | 2001 May |
|
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 |
|
Thienorphine: receptor binding and behavioral effects in rhesus monkeys. | 2007 Apr |
|
Cinnamoyl derivatives of 7alpha-aminomethyl-6,14-endo-ethanotetrahydrothebaine and 7alpha-aminomethyl-6,14-endo-ethanotetrahydrooripavine and related opioid ligands. | 2007 Oct 18 |
|
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 |
|
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 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:28:52 GMT 2023
by
admin
on
Sat Dec 16 10:28:52 GMT 2023
|
Record UNII |
HRR7PQ2JHN
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
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 | |||
|
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 | |||
|
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 |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
|