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Details

Stereochemistry ACHIRAL
Molecular Formula C7H4N2OS2
Molecular Weight 196.249
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACIBENZOLAR

SMILES

SC(=O)C1=CC=CC2=C1SN=N2

InChI

InChIKey=CGIHPACLZJDCBQ-UHFFFAOYSA-N
InChI=1S/C7H4N2OS2/c10-7(11)4-2-1-3-5-6(4)12-9-8-5/h1-3H,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C7H4N2OS2
Molecular Weight 196.249
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The glabra1 mutation affects cuticle formation and plant responses to microbes.
2010-10
SABP2, a methyl salicylate esterase is required for the systemic acquired resistance induced by acibenzolar-S-methyl in plants.
2010-08-04
AtNUDX6, an ADP-ribose/NADH pyrophosphohydrolase in Arabidopsis, positively regulates NPR1-dependent salicylic acid signaling.
2010-04
Managing phenol contents in crop plants by phytochemical farming and breeding-visions and constraints.
2010-03-02
Strategic distribution of protective proteins within bran layers of wheat protects the nutrient-rich endosperm.
2010-03
Enhanced disease susceptibility 1 and salicylic acid act redundantly to regulate resistance gene-mediated signaling.
2009-07
Salicylic acid and systemic acquired resistance play a role in attenuating crown gall disease caused by Agrobacterium tumefaciens.
2008-02
Effects of Inducers of Systemic Acquired Resistance on Reproduction of Meloidogyne javanica and Rotylenchulus reniformis in Pineapple.
2006-09
Signaling requirements and role of salicylic acid in HRT- and rrt-mediated resistance to turnip crinkle virus in Arabidopsis.
2004-12
Effects of Acibenzolar-S-Methyl Application to Rotylenchulus reniformis and Meloidogyne javanica.
2003-03
Abscisic acid determines basal susceptibility of tomato to Botrytis cinerea and suppresses salicylic acid-dependent signaling mechanisms.
2002-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:14:38 GMT 2025
Edited
by admin
on Mon Mar 31 19:14:38 GMT 2025
Record UNII
TR536JBP4L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,2,3-BENZOTHIADIAZOLE-7-CARBOTHIOIC S-ACID
Preferred Name English
ACIBENZOLAR
ISO  
Common Name English
ACIBENZOLAR [ISO]
Common Name English
BENZO(1,2,3)THIADIAZOLE-7-CARBOTHIOIC S-ACID
Common Name English
Code System Code Type Description
FDA UNII
TR536JBP4L
Created by admin on Mon Mar 31 19:14:38 GMT 2025 , Edited by admin on Mon Mar 31 19:14:38 GMT 2025
PRIMARY
EPA CompTox
DTXSID20155187
Created by admin on Mon Mar 31 19:14:38 GMT 2025 , Edited by admin on Mon Mar 31 19:14:38 GMT 2025
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WIKIPEDIA
ACIBENZOLAR
Created by admin on Mon Mar 31 19:14:38 GMT 2025 , Edited by admin on Mon Mar 31 19:14:38 GMT 2025
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CHEBI
73185
Created by admin on Mon Mar 31 19:14:38 GMT 2025 , Edited by admin on Mon Mar 31 19:14:38 GMT 2025
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CAS
126448-41-7
Created by admin on Mon Mar 31 19:14:38 GMT 2025 , Edited by admin on Mon Mar 31 19:14:38 GMT 2025
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PUBCHEM
10171321
Created by admin on Mon Mar 31 19:14:38 GMT 2025 , Edited by admin on Mon Mar 31 19:14:38 GMT 2025
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ALANWOOD
acibenzolar
Created by admin on Mon Mar 31 19:14:38 GMT 2025 , Edited by admin on Mon Mar 31 19:14:38 GMT 2025
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