Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H16O7 |
Molecular Weight | 344.3154 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(O)C2=C(OC(=CC2=O)C3=CC=C(O)C=C3)C(OC)=C1OC
InChI
InChIKey=SAMBWAJRKKEEOR-UHFFFAOYSA-N
InChI=1S/C18H16O7/c1-22-16-14(21)13-11(20)8-12(9-4-6-10(19)7-5-9)25-15(13)17(23-2)18(16)24-3/h4-8,19,21H,1-3H3
Molecular Formula | C18H16O7 |
Molecular Weight | 344.3154 |
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 |
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Distribution of 8-oxygenated leaf-surface flavones in the genus Ocimum. | 2001 Mar |
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Inhibitory effect of xanthomicrol and 3 alpha-angeloyloxy-2 alpha-hydroxy-13,14Z-dehydrocativic acid from Brickellia paniculata on the contractility of guinea-pig ileum. | 2002 May |
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Chemical profiling of Ocimum americanum using external flavonoids. | 2003 Jul |
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Antiplatelet activity of Varthemia iphionoides. | 2004 Dec |
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A new chromone from Ficus lyrata. | 2005 Feb |
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Bioactive constituents from Dracocephalum subcapitatum (O. Kuntze) Lipsky. | 2005 Jan-Feb |
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Xanthomicrol is the main cytotoxic component of Dracocephalum kotschyii and a potential anti-cancer agent. | 2005 Jul |
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Relaxant effect of xanthomicrol and 3alpha-angeloyloxy-2alpha-hydroxy-13,14z-dehydrocativic acid from Brickellia paniculata on rat uterus. | 2006 Jul |
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In vivo anti-inflammatory and antinociceptive activity evaluation of phenolic compounds from Sideritis stricta. | 2007 Jul-Aug |
|
Sonoran propolis: chemical composition and antiproliferative activity on cancer cell lines. | 2007 Nov |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:44:30 GMT 2023
by
admin
on
Fri Dec 15 19:44:30 GMT 2023
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Record UNII |
3IN82Y8CAA
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Record Status |
Validated (UNII)
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Record Version |
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