Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C21H20O12 |
Molecular Weight | 464.3763 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@H]1O[C@@H](OC2=C(OC3=C(C2=O)C(O)=CC(O)=C3)C4=CC=C(O)C(O)=C4)[C@H](O)[C@@H](O)[C@H]1O
InChI
InChIKey=OVSQVDMCBVZWGM-DTGCRPNFSA-N
InChI=1S/C21H20O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-18,21-27,29-30H,6H2/t13-,15+,17+,18-,21+/m1/s1
Molecular Formula | C21H20O12 |
Molecular Weight | 464.3763 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
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In silico prediction of pregnane X receptor activators by machine learning approaches. | 2007 Jan |
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The mechanism of hyperoside protection of ECV-304 cells against tert-butyl hydroperoxide-induced injury. | 2008 |
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Antioxidant and enzyme inhibition activities and chemical profiles of Polygonum sachalinensis F.Schmidt ex Maxim (Polygonaceae). | 2010 Mar |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 20:40:32 GMT 2023
by
admin
on
Fri Dec 15 20:40:32 GMT 2023
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Record UNII |
8O1CR18L82
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Record Status |
Validated (UNII)
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Record Version |
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DSLD |
1394 (Number of products:104)
Created by
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DSLD |
4101 (Number of products:1)
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admin on Fri Dec 15 20:40:32 GMT 2023 , Edited by admin on Fri Dec 15 20:40:32 GMT 2023
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8O1CR18L82
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1335202
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5281643
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207-580-6
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DTXSID501028789
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482-36-0
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67486
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407304
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C021304
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HYPEROSIDE
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admin on Fri Dec 15 20:40:32 GMT 2023 , Edited by admin on Fri Dec 15 20:40:32 GMT 2023
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Related Record | Type | Details | ||
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PARENT -> CONSTITUENT ALWAYS PRESENT | |||
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PARENT -> CONSTITUENT ALWAYS PRESENT |
USP
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PARENT -> CONSTITUENT ALWAYS PRESENT | |||
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PARENT -> CONSTITUENT ALWAYS PRESENT | |||
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PARENT -> CONSTITUENT ALWAYS PRESENT | |||
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PARENT -> CONSTITUENT ALWAYS PRESENT |
Secondary metabolite detected in developing cacao seeds.
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