Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C18H17NO3 |
| Molecular Weight | 295.3325 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1CCC2=CC3=C(OCO3)C4=C2[C@H]1CC5=C4C(O)=CC=C5
InChI
InChIKey=IKMXUUHNYQWZBC-GFCCVEGCSA-N
InChI=1S/C18H17NO3/c1-19-6-5-11-8-14-18(22-9-21-14)17-15(11)12(19)7-10-3-2-4-13(20)16(10)17/h2-4,8,12,20H,5-7,9H2,1H3/t12-/m1/s1
| Molecular Formula | C18H17NO3 |
| Molecular Weight | 295.3325 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Native New Zealand plants with inhibitory activity towards Mycobacterium tuberculosis. | 2010-06-10 |
|
| The antinociceptive and anti-inflammatory activities of caulerpin, a bisindole alkaloid isolated from seaweeds of the genus Caulerpa. | 2009-11-26 |
|
| Vascular activity of (-)-anonaine, (-)-roemerine and (-)-pukateine, three natural 6a(R)-1,2-methylenedioxyaporphines with different affinities for alpha1-adrenoceptor subtypes. | 2004-07 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:24:38 GMT 2025
by
admin
on
Mon Mar 31 23:24:38 GMT 2025
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| Record UNII |
Z9Y5O2QUPA
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID00331801
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Z9Y5O2QUPA
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m9315
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81-67-4
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442340
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