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Cavosonstat - 99%, high purity , Alcohol dehydrogenase class III inhibitor, CAS No.1371587-51-7, Alcohol dehydrogenase class III inhibitor

COA

Grade & Purity:

≥98%

Cas Number: 1371587-51-7
Molecular Weight: 299.71
PubChem CID: 56960912

In stock

Item Number

C650768

Grouped product items
SKU	Size	Availability	Price
C650768-1mg	1mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$69.90
C650768-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$168.90
C650768-10mg	10mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$274.90
C650768-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$549.90

View related series

Amino Acid/Protein Metabolism (1836) CFTR (52) GSNOR (4) Membrane Transporter (607) Membrane Transporter/Ion Channel (1822) Metabolic Enzyme/Protease (4860)

Basic Description

Synonyms	Cavosonstat \| SCHEMBL1289569 \| N-91115 \| 3-Chloro-4-(6-hydroxy-2-quinolinyl)benzoic acid \| DB14775 \| UNII-O2Z8Q22ZE4 \| 3-chloro-4-(6-hydroxyquinolin-2-yl)benzoic acid \| BXSZILNGNMDGSL-UHFFFAOYSA-N \| Benzoic acid, 3-chloro-4-(6-hydroxy-2-quinolinyl)- \| Q27
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	Cavosonstat (N91115) is an orally active S-nitrosoglutathione reductase (GSNOR) inhibitor. Cavosonstat is a CFTR stabilizer, and can be used for cystic fibrosis research.
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Action Type	INHIBITOR
Mechanism of action	Alcohol dehydrogenase class III inhibitor
Product Description	Cavosonstat (N91115) is an orally active S-nitrosoglutathione reductase (GSNOR) inhibitor. Cavosonstat is a CFTR stabilizer, and can be used for cystic fibrosis research.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Quinolines and derivatives
    - Subclass Phenylquinolines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Quinolines and derivatives
Subclass	Phenylquinolines
Intermediate Tree Nodes	Not available
Direct Parent	Phenylquinolines
Alternative Parents	Phenylpyridines Hydroxyquinolines 3-halobenzoic acids Halobenzoic acids Benzoic acids Benzoyl derivatives Chlorobenzenes 1-hydroxy-2-unsubstituted benzenoids Aryl chlorides Heteroaromatic compounds Carboxylic acids Azacyclic compounds Organochlorides Hydrocarbon derivatives Organonitrogen compounds Organooxygen compounds Organic oxides
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Phenylquinoline - 2-phenylpyridine - Hydroxyquinoline - Halobenzoic acid - 3-halobenzoic acid - Halobenzoic acid or derivatives - 3-halobenzoic acid or derivatives - Benzoic acid or derivatives - Benzoic acid - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Chlorobenzene - Halobenzene - Phenol - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyridine - Heteroaromatic compound - Azacycle - Carboxylic acid - Carboxylic acid derivative - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	3-chloro-4-(6-hydroxyquinolin-2-yl)benzoic acid
INCHI	InChI=1S/C16H10ClNO3/c17-13-8-10(16(20)21)1-4-12(13)15-5-2-9-7-11(19)3-6-14(9)18-15/h1-8,19H,(H,20,21)
InChIKey	BXSZILNGNMDGSL-UHFFFAOYSA-N
Smiles	C1=CC(=C(C=C1C(=O)O)Cl)C2=NC3=C(C=C2)C=C(C=C3)O
Isomeric SMILES	C1=CC(=C(C=C1C(=O)O)Cl)C2=NC3=C(C=C2)C=C(C=C3)O
PubChem CID	56960912
Molecular Weight	299.71

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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8 results found

Lot Number	Certificate Type	Date	Item
J2423607	Certificate of Analysis	Jul 01, 2024	C650768
J2423616	Certificate of Analysis	Jul 01, 2024	C650768
J2423618	Certificate of Analysis	Jul 01, 2024	C650768
J2423620	Certificate of Analysis	Jul 01, 2024	C650768
J2423622	Certificate of Analysis	Jul 01, 2024	C650768
J2423623	Certificate of Analysis	Jul 01, 2024	C650768
J2423627	Certificate of Analysis	Jul 01, 2024	C650768
J2423629	Certificate of Analysis	Jul 01, 2024	C650768

Chemical and Physical Properties

Solubility	DMSO : 50 mg/mL (166.83 mM; Need ultrasonic)
Molecular Weight	299.710 g/mol
XLogP3	3.700
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	2
Exact Mass	299.035 Da
Monoisotopic Mass	299.035 Da
Topological Polar Surface Area	70.400 Å²
Heavy Atom Count	21
Formal Charge	0
Complexity	392.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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