Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C15H14O6 |
| Molecular Weight | 290.2681 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C1=CO[C@@H]2O[C@@H]3[C@]4(OC(=O)\C3=C\C)C=C[C@H]1[C@H]24
InChI
InChIKey=VFXXNAVZODKBIW-JKXVGBJFSA-N
InChI=1S/C15H14O6/c1-3-7-11-15(21-13(7)17)5-4-8-9(12(16)18-2)6-19-14(20-11)10(8)15/h3-6,8,10-11,14H,1-2H3/b7-3+/t8-,10-,11+,14-,15+/m1/s1
| Molecular Formula | C15H14O6 |
| Molecular Weight | 290.2681 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 1 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Anti-mycobacterial activity of plumericin and isoplumericin against MDR Mycobacterium tuberculosis. | 2013-06 |
|
| HIV-1 and HIV-2 reverse transcriptases: a comparative study of sensitivity to inhibition by selected natural products. | 1992-05-29 |
|
| Evaluation of natural products as inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. | 1991-01-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:44:22 GMT 2025
by
admin
on
Mon Mar 31 22:44:22 GMT 2025
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| Record UNII |
L0126U506Z
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| Record Status |
Validated (UNII)
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| Record Version |
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