Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C18H19NO3 |
| Molecular Weight | 297.3484 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C2[C@H]3CC4=CC=C(O)C5=C4[C@@]2(CCN3C)[C@H]1O5
InChI
InChIKey=ZKLXUUYLEHCAMF-UUWFMWQGSA-N
InChI=1S/C18H19NO3/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/t12-,17+,18+/m1/s1
| 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 |
|
| Submolecular partitioning of morphine hydrate based on its experimental charge density at 25 K. | 2005 Aug |
|
| 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 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:08:23 GMT 2025
by
admin
on
Mon Mar 31 22:08:23 GMT 2025
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| Record UNII |
575AOU51CR
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Common Name | English | ||
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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DEA NO. |
9330
Created by
admin on Mon Mar 31 22:08:23 GMT 2025 , Edited by admin on Mon Mar 31 22:08:23 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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467-04-9
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PRIMARY | |||
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DTXSID10196908
Created by
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PRIMARY | |||
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m8232
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admin on Mon Mar 31 22:08:23 GMT 2025 , Edited by admin on Mon Mar 31 22:08:23 GMT 2025
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PRIMARY | Merck Index | ||
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5462306
Created by
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PRIMARY | |||
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8324
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admin on Mon Mar 31 22:08:23 GMT 2025 , Edited by admin on Mon Mar 31 22:08:23 GMT 2025
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PRIMARY | |||
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ORIPAVINE
Created by
admin on Mon Mar 31 22:08:23 GMT 2025 , Edited by admin on Mon Mar 31 22:08:23 GMT 2025
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PRIMARY | |||
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207-385-6
Created by
admin on Mon Mar 31 22:08:23 GMT 2025 , Edited by admin on Mon Mar 31 22:08:23 GMT 2025
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PRIMARY | |||
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575AOU51CR
Created by
admin on Mon Mar 31 22:08:23 GMT 2025 , Edited by admin on Mon Mar 31 22:08:23 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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SALT/SOLVATE -> PARENT |
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> IMPURITY | |||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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PARENT -> IMPURITY |
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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