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· · COA & SDS available for every product · Same-day shipping on in-stock items AZD-6280 - ≥98% , GABA receptor alpha-3 subunit positive allosteric modulator, CAS No.942436-93-3, GABA receptor alpha-3 subunit positive allosteric modulator
Synonyms
B9Z1OEH19D | 4-amino-8-(2,5-dimethoxyphenyl)-N-propylcinnoline-3-carboxamide | AZD6280 | SCHEMBL1962946 | AZD 6280 | UNII-B9Z1OEH19D | 3-Cinnolinecarboxamide, 4-amino-8-(2,5-dimethoxyphenyl)-N-propyl- | NVWCZRPXYVDQEE-UHFFFAOYSA-N | CHEMBL1783256
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview
AZD6280 is a novel, subtype-selective GABAAα2/3 receptor positive modulators, used for treatment of generalized anxiety disorder.
Specifications Synonyms
B9Z1OEH19D | 4-amino-8-(2,5-dimethoxyphenyl)-N-propylcinnoline-3-carboxamide | AZD6280 | SCHEMBL1962946 | AZD 6280 | UNII-B9Z1OEH19D | 3-Cinnolinecarboxamide, 4-amino-8-(2,5-dimethoxyphenyl)-N-propyl- | NVWCZRPXYVDQEE-UHFFFAOYSA-N | CHEMBL1783256
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
AZD-6280 is a selective GABAA(α2/3) receptor modulator, used for treatment of generalized anxiety disorder.
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
POSITIVE ALLOSTERIC MODULATOR
Mechanism of action
GABA receptor alpha-3 subunit positive allosteric modulator
Product Properties Names and Identifiers Pubchem Sid 528763204 Canonical Smiles CCCNC(=O)C1=NN=C2C(=C1N)C=CC=C2C3=C(C=CC(=C3)OC)OC IUPAC Name 4-amino-8-(2,5-dimethoxyphenyl)-N-propylcinnoline-3-carboxamide InChIKey NVWCZRPXYVDQEE-UHFFFAOYSA-N INCHI 1S/C20H22N4O3/c1-4-10-22-20(25)19-17(21)14-7-5-6-13(18(14)23-24-19)15-11-12(26-2)8-9-16(15)27-3/h5-9,11H,4,10H2,1-3H3,(H2,21,23)(H,22,25) Isomeric SMILES CCCNC(=O)C1=NN=C2C(=C1N)C=CC=C2C3=C(C=CC(=C3)OC)OC PubChem CID 23630026 Molecular Weight 366.41
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Diazanaphthalenes Subclass Benzodiazines Intermediate Tree Nodes Not available Direct Parent Cinnolines Alternative Parents Dimethoxybenzenes Phenoxy compounds Anisoles 2-heteroaryl carboxamides Aminopyridazines Alkyl aryl ethers Vinylogous amides Heteroaromatic compounds Secondary carboxylic acid amides Amino acids and derivatives Azacyclic compounds Primary amines Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Cinnoline - P-dimethoxybenzene - Dimethoxybenzene - 2-heteroaryl carboxamide - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Aminopyridazine - Monocyclic benzene moiety - Benzenoid - Pyridazine - Heteroaromatic compound - Vinylogous amide - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Ether - Azacycle - Carboxylic acid derivative - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Primary amine - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as cinnolines. These are organic aromatic compounds containing a benzene fused to a pyridazine ring. External Descriptors Not available Data sources 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.
3D Structure Associated Targets(Human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility DMSO : 62.5 mg/mL (170.57 mM; Need ultrasonic) Molecular Weight 366.400 g/mol XLogP3 3.100 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 6 Exact Mass 366.169 Da Monoisotopic Mass 366.169 Da Topological Polar Surface Area 99.400 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 492.000 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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