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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items CID-1067700 - ≥98% , CAS No.314042-01-8
Synonyms
AB00100899-01 | cid_1067700 | AKOS001627836 | CBMicro_017018 | CCG-13339 | KUC103669N-03 | KUC103669N-04 | 2-(benzoylcarbamothioylamino)-5,5-dimethyl-4,7-dihydrothieno[2,3-c]pyran-3-carboxylic acid | MFCD01557530 | HY-13452 | ML282 | Q27210667 | 2-(3-Benz
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.
Descripción general CID-1067700 is one of the first identified competitive inhibitors of nucleotide binding by Ras-related GTPases（Rab7 with a Ki of 13 nM).
Specifications Sinónimos
AB00100899-01 | cid_1067700 | AKOS001627836 | CBMicro_017018 | CCG-13339 | KUC103669N-03 | KUC103669N-04 | 2-(benzoylcarbamothioylamino)-5, 5-dimethyl-4, 7-dihydrothieno[2, 3-c]pyran-3-carboxylic acid | MFCD01557530 | HY-13452 | ML282 | Q27210667 | 2-(3-Benz
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
CID 1067700 is a potent and competitive inhibitor of Ras-related GTPase, which binds efficiently to the Rab7 nucleotide binding site.
CID 1067700 antagonizes the ras-related protein Rab-7 and reduces class-switch DNA recombination (CSR) in B cells and pla
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Pubchem Sid 504760372 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504760372 Sonrisas canónicas CC1(CC2=C(CO1)SC(=C2C(=O)O)NC(=S)NC(=O)C3=CC=CC=C3)C IUPAC Name 2-(benzoylcarbamothioylamino)-5,5-dimethyl-4,7-dihydrothieno[2,3-c]pyran-3-carboxylic acid InChIKey ATSWBWHRHAQVFM-UHFFFAOYSA-N INCHI 1S/C18H18N2O4S2/c1-18(2)8-11-12(9-24-18)26-15(13(11)16(22)23)20-17(25)19-14(21)10-6-4-3-5-7-10/h3-7H,8-9H2,1-2H3,(H,22,23)(H2,19,20,21,25) Isómeros SMILES CC1(CC2=C(CO1)SC(=C2C(=O)O)NC(=S)NC(=O)C3=CC=CC=C3)C WGK Alemania 3 Peso molecular 390.48 Reaxy-Rn 26955419 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=26955419&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 Clase Thienopyrans Subclass Not available Intermediate Tree Nodes Not available Direct Parent Thienopyrans Alternative Parents Benzoic acids and derivatives Thiophene carboxylic acids Benzoyl derivatives Pyrans Vinylogous amides Heteroaromatic compounds Thioureas Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carboxylic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Benzoic acid or derivatives - Thienopyran - Benzoyl - Thiophene carboxylic acid - Thiophene carboxylic acid or derivatives - Monocyclic benzene moiety - Pyran - Benzenoid - Heteroaromatic compound - Thiophene - Vinylogous amide - Thiourea - Oxacycle - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as thienopyrans. These are heterocyclic compounds containing a thiophene ring fused to a pyran ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad DMSO: 68 mg/mL(174mM), Need ultrasonic Peso molecular 390.500 g/mol XLogP3 3.400 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 3 Exact Mass 390.071 Da Monoisotopic Mass 390.071 Da Topological Polar Surface Area 148.000 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 578.000 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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