Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C17H24O |
| Molecular Weight | 244.3719 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCC\C=C/CC#CC#C[C@H](O)C=C
InChI
InChIKey=UGJAEDFOKNAMQD-QXPKXGMISA-N
InChI=1S/C17H24O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)4-2/h4,10-11,17-18H,2-3,5-9,12H2,1H3/b11-10-/t17-/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Anti-mycobacterial diynes from the Canadian medicinal plant Aralia nudicaulis. | 2012-03-06 |
|
| Panaxynol protects cortical neurons from ischemia-like injury by up-regulation of HIF-1alpha expression and inhibition of apoptotic cascade. | 2010-01-05 |
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| Antiproliferative effect of panaxynol on RASMCs via inhibition of ERK1/2 and CREB. | 2008-02-15 |
Patents
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| Code System | Code | Type | Description | ||
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Falcarinol
Created by
admin on Mon Mar 31 19:03:16 GMT 2025 , Edited by admin on Mon Mar 31 19:03:16 GMT 2025
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DTXSID50415266
Created by
admin on Mon Mar 31 19:03:16 GMT 2025 , Edited by admin on Mon Mar 31 19:03:16 GMT 2025
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8P1DJD416I
Created by
admin on Mon Mar 31 19:03:16 GMT 2025 , Edited by admin on Mon Mar 31 19:03:16 GMT 2025
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7070
Created by
admin on Mon Mar 31 19:03:16 GMT 2025 , Edited by admin on Mon Mar 31 19:03:16 GMT 2025
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21852-80-2
Created by
admin on Mon Mar 31 19:03:16 GMT 2025 , Edited by admin on Mon Mar 31 19:03:16 GMT 2025
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8P1DJD416I
Created by
admin on Mon Mar 31 19:03:16 GMT 2025 , Edited by admin on Mon Mar 31 19:03:16 GMT 2025
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5281149
Created by
admin on Mon Mar 31 19:03:16 GMT 2025 , Edited by admin on Mon Mar 31 19:03:16 GMT 2025
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PRIMARY |
SUBSTANCE RECORD
