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· · COA & SDS available for every product · Same-day shipping on in-stock items O8 OGG1 Inhibitor - ≥98%(HPLC) , CAS No.350997-39-6
Synonyms
AB00102917-01 | AKOS003956278 | BBL037375 | Cambridge id 6132595 | 3,4-dichlorobenzo[b]thiophene-2-carbohydrazide | HY-112902 | MFCD01993639 | OGG1-IN-O8 | 3,4-dichloro-1-benzothiophene-2-carbohydrazide | O8 OGG1 Inhibitor- Bio-X | OGG1-IN-08 | OGG1 inhib
Shipped In
Ice chest + Ice pads
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Why this grade ≥98%(HPLC) 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.
Specifications Synonyms
AB00102917-01 | AKOS003956278 | BBL037375 | Cambridge id 6132595 | 3, 4-dichlorobenzo[b]thiophene-2-carbohydrazide | HY-112902 | MFCD01993639 | OGG1-IN-O8 | 3, 4-dichloro-1-benzothiophene-2-carbohydrazide | O8 OGG1 Inhibitor- Bio-X | OGG1-IN-08 | OGG1 inhib
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
Potent and selective 8-oxoguanine DNA glycosylase 1 (OGG1) inhibitor (IC50= 0.2 μM in a gel based assay). Exhibits > 200-fold selectivity for OGG1 over other DNA glycosylases, NEIL1 and NTH1.
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 488191657 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488191657 Canonical Smiles C1=CC2=C(C(=C1)Cl)C(=C(S2)C(=O)NN)Cl IUPAC Name 3,4-dichloro-1-benzothiophene-2-carbohydrazide InChIKey HSSHUDKWJRJKPV-UHFFFAOYSA-N INCHI 1S/C9H6Cl2N2OS/c10-4-2-1-3-5-6(4)7(11)8(15-5)9(14)13-12/h1-3H,12H2,(H,13,14) Isomeric SMILES C1=CC2=C(C(=C1)Cl)C(=C(S2)C(=O)NN)Cl Molecular Weight 261.13 Reaxy-Rn 28962077 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=28962077&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 Organoheterocyclic compounds Class Benzothiophenes Subclass 1-benzothiophenes Intermediate Tree Nodes Not available Direct Parent 1-benzothiophenes Alternative Parents Thiophene carboxamides Benzenoids Aryl chlorides Vinylogous halides Heteroaromatic compounds Carboxylic acid hydrazides Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 1-benzothiophene - Thiophene carboxamide - Thiophene carboxylic acid or derivatives - Aryl chloride - Aryl halide - Benzenoid - Heteroaromatic compound - Vinylogous halide - Thiophene - Carboxylic acid hydrazide - Carboxylic acid derivative - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as 1-benzothiophenes. These are aromatic heterocyclic compound containing the Benzo[b]thiophene ring system. 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: 26.11, Max Conc. mM: 100 Molecular Weight 261.130 g/mol XLogP3 3.100 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 1 Exact Mass 259.958 Da Monoisotopic Mass 259.958 Da Topological Polar Surface Area 83.400 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 266.000 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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