Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C17H22O5 |
Molecular Weight | 306.3536 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 6 / 6 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12[C@H](C)C(=O)O[C@]1([H])[C@]3([H])C(C=C[C@@]3(C)O)=C(C)C[C@@H]2OC(C)=O
InChI
InChIKey=SYTRJRUSWMMZLV-VQGWEXQJSA-N
InChI=1S/C17H22O5/c1-8-7-12(21-10(3)18)13-9(2)16(19)22-15(13)14-11(8)5-6-17(14,4)20/h5-6,9,12-15,20H,7H2,1-4H3/t9-,12-,13+,14-,15-,17+/m0/s1
Molecular Formula | C17H22O5 |
Molecular Weight | 306.3536 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 5 / 6 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
On the absolute configuration of matricin. | 2001 Apr |
|
Absolute stereochemistry of guaianolides, of matricin and its epimers, of yarrow proazulenes, and of chamazulene carboxylic acid. | 2001 Jul |
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Supercritical carbon dioxide extraction of chamomile flowers: extraction efficiency, stability, and in-line inclusion of chamomile-carbon dioxide extract in beta-cyclodextrin. | 2004 Jul-Aug |
|
Chamazulene carboxylic acid and matricin: a natural profen and its natural prodrug, identified through similarity to synthetic drug substances. | 2006 Jul |
|
Ethnoveterinary medicines used for ruminants in British Columbia, Canada. | 2007 Feb 26 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:30:15 GMT 2023
by
admin
on
Sat Dec 16 09:30:15 GMT 2023
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Record UNII |
O034C3549S
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Record Status |
Validated (UNII)
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Record Version |
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O034C3549S
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92265
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29041-35-8
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Matricin
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249-384-3
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DTXSID50951639
Created by
admin on Sat Dec 16 09:30:15 GMT 2023 , Edited by admin on Sat Dec 16 09:30:15 GMT 2023
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Related Record | Type | Details | ||
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PARENT -> CONSTITUENT ALWAYS PRESENT |