Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C20H18O6 |
| Molecular Weight | 354.3533 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)=CCC1=C(O)C2=C(OC=C(C2=O)C3=CC=C(O)C=C3O)C=C1O
InChI
InChIKey=MMPVAPMCVABQPS-UHFFFAOYSA-N
InChI=1S/C20H18O6/c1-10(2)3-5-13-16(23)8-17-18(19(13)24)20(25)14(9-26-17)12-6-4-11(21)7-15(12)22/h3-4,6-9,21-24H,5H2,1-2H3
| Molecular Formula | C20H18O6 |
| Molecular Weight | 354.3533 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Regioselective synthesis of 6-alkyl- and 6-prenylpolyhydroxyisoflavones and 6-alkylcoumaronochromone derivatives. | 2004 Nov |
|
| Sucrose-induced lupine defense against Fusarium oxysporum. Sucrose-stimulated accumulation of isoflavonoids as a defense response of lupine to Fusarium oxysporum. | 2005 Apr |
|
| LC-MSMS profiling of flavonoid conjugates in wild Mexican lupine, Lupinus reflexus. | 2010 Jul 23 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:09:36 UTC 2023
by
admin
on
Fri Dec 15 19:09:36 UTC 2023
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| Record UNII |
FU3E0232IF
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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| Name | Type | Language | ||
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| Code System | Code | Type | Description | ||
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5281797
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FU3E0232IF
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27917
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41743-56-0
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DTXSID00194574
Created by
admin on Fri Dec 15 19:09:37 UTC 2023 , Edited by admin on Fri Dec 15 19:09:37 UTC 2023
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LUTEONE (ISOFLAVONE)
Created by
admin on Fri Dec 15 19:09:37 UTC 2023 , Edited by admin on Fri Dec 15 19:09:37 UTC 2023
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> CONSTITUENT ALWAYS PRESENT |
Original source: FUKUI H, NEW ISOFLAVONE WITH ANTIFUNGAL ACTIVITY FROM IMMATURE FRUITS OF LUPINUS-LUTEUS, Agricultural and Biological Chemistry, 37(2)417 -421, 1973
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