U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C8H8O3
Molecular Weight 152.1473
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6-METHYLSALICYLIC ACID

SMILES

CC1=C(C(O)=O)C(O)=CC=C1

InChI

InChIKey=HCJMNOSIAGSZBM-UHFFFAOYSA-N
InChI=1S/C8H8O3/c1-5-3-2-4-6(9)7(5)8(10)11/h2-4,9H,1H3,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C8H8O3
Molecular Weight 152.1473
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Polyketide biosynthesis: a millennium review.
2001 Aug
Production of 6-methylsalicylic acid by expression of a fungal polyketide synthase activates disease resistance in tobacco.
2001 Jun
Yeast hydroxy fatty acids and fungal polyketides: lessons learned from the Konrad Bloch laboratory.
2002 Apr 19
Genetic characterization of the chlorothricin gene cluster as a model for spirotetronate antibiotic biosynthesis.
2006 Jun
Yeast cell factories for fine chemical and API production.
2008 Aug 7
Heteroatom-containing antibacterial phenolic metabolites from a terrestrial Ampelomyces fungus.
2008 Jul
Production of the polyketide 6-MSA in yeast engineered for increased malonyl-CoA supply.
2008 Sep
Ancient horizontal gene transfer from bacteria enhances biosynthetic capabilities of fungi.
2009
Determination of the extent of phosphopantetheinylation of polyketide synthases expressed in Escherichia coli and Saccharomyces cerevisiae.
2009 Nov 1
Cloning and characterization of novel methylsalicylic acid synthase gene involved in the biosynthesis of isoasperlactone and asperlactone in Aspergillus westerdijkiae.
2009 Oct
Deciphering pactamycin biosynthesis and engineered production of new pactamycin analogues.
2009 Sep 4
Biosynthesis and toxicological effects of patulin.
2010 Apr
Functional analysis of fungal polyketide biosynthesis genes.
2010 May
Hidden function of catalytic domain in 6-methylsalicylic acid synthase for product release.
2010 May 14
Insights into bacterial 6-methylsalicylic acid synthase and its engineering to orsellinic acid synthase for spirotetronate generation.
2010 May 28
Marine myxobacteria as a source of antibiotics--comparison of physiology, polyketide-type genes and antibiotic production of three new isolates of Enhygromyxa salina.
2010 Sep 3
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:17:27 GMT 2023
Edited
by admin
on Fri Dec 15 18:17:27 GMT 2023
Record UNII
L5352FE23Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
6-METHYLSALICYLIC ACID
Systematic Name English
2-HYDROXY-6-METHYLBENZOIC ACID
Systematic Name English
NSC-403256
Code English
6-MSA
Common Name English
6-HYDROXY-O-TOLUIC ACID
Common Name English
BENZOIC ACID, 2-HYDROXY-6-METHYL-
Common Name English
2,6-CRESOTIC ACID
Common Name English
Code System Code Type Description
WIKIPEDIA
6-Methylsalicylic acid
Created by admin on Fri Dec 15 18:17:27 GMT 2023 , Edited by admin on Fri Dec 15 18:17:27 GMT 2023
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FDA UNII
L5352FE23Y
Created by admin on Fri Dec 15 18:17:27 GMT 2023 , Edited by admin on Fri Dec 15 18:17:27 GMT 2023
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CHEBI
17637
Created by admin on Fri Dec 15 18:17:27 GMT 2023 , Edited by admin on Fri Dec 15 18:17:27 GMT 2023
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NSC
403256
Created by admin on Fri Dec 15 18:17:27 GMT 2023 , Edited by admin on Fri Dec 15 18:17:27 GMT 2023
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PUBCHEM
11279
Created by admin on Fri Dec 15 18:17:27 GMT 2023 , Edited by admin on Fri Dec 15 18:17:27 GMT 2023
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MESH
C005236
Created by admin on Fri Dec 15 18:17:27 GMT 2023 , Edited by admin on Fri Dec 15 18:17:27 GMT 2023
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CAS
567-61-3
Created by admin on Fri Dec 15 18:17:27 GMT 2023 , Edited by admin on Fri Dec 15 18:17:27 GMT 2023
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EPA CompTox
DTXSID20205257
Created by admin on Fri Dec 15 18:17:27 GMT 2023 , Edited by admin on Fri Dec 15 18:17:27 GMT 2023
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