Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H25NO4 |
| Molecular Weight | 355.4275 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12CC3=CC(OC)=C(OC)C=C3C4=C1C(CCN2C)=CC(OC)=C4OC
InChI
InChIKey=RUZIUYOSRDWYQF-HNNXBMFYSA-N
InChI=1S/C21H25NO4/c1-22-7-6-12-9-18(25-4)21(26-5)20-14-11-17(24-3)16(23-2)10-13(14)8-15(22)19(12)20/h9-11,15H,6-8H2,1-5H3/t15-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Central action of glaucine in rodents. | 1994 |
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| Antipoliovirus structure-activity relationships of some aporphine alkaloids. | 1998 Apr |
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| Seasonal variation of the chemical constituents from Croton species. | 2001 May-Jun |
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| Behavioural evidence of agonist-like effect of isoteoline at 5-HT1B serotonergic receptors in mice. | 2003 Jan |
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| A novel alkaloid from Mitrephora maingayi. | 2005 Jun |
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| Identification and quantification of isoquinoline alkaloids in the genus Sarcocapnos by GC-MS. | 2005 Sep-Oct |
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| Ascorbic acid and tetrahydrobiopterin potentiate the EDHF phenomenon by generating hydrogen peroxide. | 2009 Nov 1 |
|
| The antinociceptive and anti-inflammatory activities of caulerpin, a bisindole alkaloid isolated from seaweeds of the genus Caulerpa. | 2009 Nov 26 |
|
| Screening of antinociceptive components in Corydalis yanhusuo W.T. Wang by comprehensive two-dimensional liquid chromatography/tandem mass spectrometry. | 2010 Mar |
Patents
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| Code System | Code | Type | Description | ||
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C005004
Created by
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100000078186
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207-501-5
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SUB13972MIG
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1368876
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5373
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GLAUCINE
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475-81-0
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DTXSID8031100
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NU19306XA7
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16754
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34396
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m5741
Created by
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PRIMARY | Merck Index | ||
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NU19306XA7
Created by
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)
SALT/SOLVATE (PARENT)
SALT/SOLVATE (PARENT)
