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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
Structure of SPARASSOL

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

HIDE SMILES / InChI

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

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
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
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:42:49 GMT 2023
Edited
by admin
on Sat Dec 16 09:42:49 GMT 2023
Record UNII
49LGW9K0EH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SPARASSOL
MI  
Common Name English
BENZOIC ACID, 2-HYDROXY-4-METHOXY-6-METHYL-, METHYL ESTER
Systematic Name English
METHYL EVERNINATE
Common Name English
2-HYDROXY-4-METHOXY-6-METHYLBENZOIC ACID METHYL ESTER
Systematic Name English
METHYL 4-METHOXY-6-METHYLSALICYLATE
Systematic Name English
SPARASSOL [MI]
Common Name English
Code System Code Type Description
WIKIPEDIA
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
PRIMARY
CAS
520-43-4
Created by admin on Sat Dec 16 09:42:49 GMT 2023 , Edited by admin on Sat Dec 16 09:42:49 GMT 2023
PRIMARY
PUBCHEM
596344
Created by admin on Sat Dec 16 09:42:49 GMT 2023 , Edited by admin on Sat Dec 16 09:42:49 GMT 2023
PRIMARY
EPA CompTox
DTXSID901028412
Created by admin on Sat Dec 16 09:42:49 GMT 2023 , Edited by admin on Sat Dec 16 09:42:49 GMT 2023
PRIMARY
MERCK INDEX
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
PRIMARY Merck Index
FDA UNII
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
PRIMARY
Related Record Type Details
ACTIVE MOIETY