Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H12O4 |
Molecular Weight | 196.1999 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)C1=C(C)C=C(OC)C=C1O
InChI
InChIKey=PFVPJOAAHSOENR-UHFFFAOYSA-N
InChI=1S/C10H12O4/c1-6-4-7(13-2)5-8(11)9(6)10(12)14-3/h4-5,11H,1-3H3
Molecular Formula | C10H12O4 |
Molecular Weight | 196.1999 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Sparassol is a naturally occurring antibiotic and antifungal compound which can be isolated from Sparassis crispa. It has also shown insecticidal activity against Drosophila suzukii, and nematicidal activity against Bursaphelenchus xyphilus. There has been limited interest in biological or pharmacological effects on humans and animals.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Unselective phenolic coupling of methyl 2-hydroxy-4-methoxy-6-methylbenzoate--a valuable tool for the total synthesis of natural product families. | 2003 Feb 24 |
|
Insecticidal and Enzyme Inhibitory Activities of Sparassol and Its Analogues against Drosophila suzukii. | 2016 Jul 13 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:42:49 GMT 2023
by
admin
on
Sat Dec 16 09:42:49 GMT 2023
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Record UNII |
49LGW9K0EH
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Record Status |
Validated (UNII)
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Record Version |
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-
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Code System | Code | Type | Description | ||
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Sparassol
Created by
admin on Sat Dec 16 09:42:49 GMT 2023 , Edited by admin on Sat Dec 16 09:42:49 GMT 2023
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520-43-4
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596344
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DTXSID901028412
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admin on Sat Dec 16 09:42:49 GMT 2023 , Edited by admin on Sat Dec 16 09:42:49 GMT 2023
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m10131
Created by
admin on Sat Dec 16 09:42:49 GMT 2023 , Edited by admin on Sat Dec 16 09:42:49 GMT 2023
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PRIMARY | Merck Index | ||
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49LGW9K0EH
Created by
admin on Sat Dec 16 09:42:49 GMT 2023 , Edited by admin on Sat Dec 16 09:42:49 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |