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· · COA & SDS available for every product · Same-day shipping on in-stock items GPi 688 - ≥99%(HPLC) , CAS No.918902-32-6
Synonyms
2-Chloro-N-[1-[(2R)-2,3-dihydroxypropyl]-1,2,3,4-tetrahydro-2-oxo-3-quinolinyl]-6H-thieno[2,3-b]pyrrole-5-carboxamide
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Why this grade ≥99%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C Ships Wet ice 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.
Specifications Synonyms
2-Chloro-N-[1-[(2R)-2, 3-dihydroxypropyl]-1, 2, 3, 4-tetrahydro-2-oxo-3-quinolinyl]-6H-thieno[2, 3-b]pyrrole-5-carboxamide
Specifications & Purity
≥99%(HPLC)
Biochemical and Physiological Mechanisms
Allosteric glycogen phosphorylase inhibitor; acts at the indole site of glycogen phosphorylase. Inhibits Glukagon-mediated hyperglycemiain vivoin the rat.
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles C1C(C(=O)N(C2=CC=CC=C21)CC(CO)O)NC(=O)C3=CC4=C(N3)SC(=C4)Cl IUPAC Name 2-chloro-N-[1-[(2R)-2,3-dihydroxypropyl]-2-oxo-3,4-dihydroquinolin-3-yl]-6H-thieno[2,3-b]pyrrole-5-carboxamide InChIKey UICNBXVDHCBKCE-PUODRLBUSA-N INCHI 1S/C19H18ClN3O4S/c20-16-7-11-6-13(22-18(11)28-16)17(26)21-14-5-10-3-1-2-4-15(10)23(19(14)27)8-12(25)9-24/h1-4,6-7,12,14,22,24-25H,5,8-9H2,(H,21,26)/t12-,14?/m1/s1 Isomeric SMILES C1C(C(=O)N(C2=CC=CC=C21)C[C@H](CO)O)NC(=O)C3=CC4=C(N3)SC(=C4)Cl Molecular Weight 419.88 Reaxy-Rn 12231679 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=12231679&ln=
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 Organic acids and derivatives Class Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent N-acyl-alpha amino acids and derivatives Alternative Parents Hydroquinolones Hydroquinolines Thienopyrroles 2,3,5-trisubstituted thiophenes 2-heteroaryl carboxamides Pyrrole carboxamides Substituted pyrroles Aryl chlorides Benzenoids Tertiary carboxylic acid amides Azoles Heteroaromatic compounds Secondary carboxylic acid amides 1,2-diols Secondary alcohols Lactams Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives Carbonyl compounds Primary alcohols Organochlorides Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents N-acyl-alpha amino acid or derivatives - Tetrahydroquinolone - Quinolone - Tetrahydroquinoline - 2-heteroaryl carboxamide - Pyrrole-2-carboxamide - Pyrrole-2-carboxylic acid or derivatives - Thienopyrrole - 2,3,5-trisubstituted thiophene - Aryl halide - Aryl chloride - Substituted pyrrole - Benzenoid - Thiophene - Tertiary carboxylic acid amide - Heteroaromatic compound - Azole - Pyrrole - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - 1,2-diol - Lactam - Organoheterocyclic compound - Azacycle - Organochloride - Organohalogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - Organooxygen compound - Primary alcohol - Alcohol - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. 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) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 41.99, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 10.5, Max Conc. mM: 25 Molecular Weight 419.900 g/mol XLogP3 2.500 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 5 Exact Mass 419.071 Da Monoisotopic Mass 419.071 Da Topological Polar Surface Area 134.000 Ų Heavy Atom Count 28 Formal Charge 0 Complexity 612.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 Undefined Atom Stereocenter Count 1 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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