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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items (R)-Selisistat - ≥98% , CAS No.848193-69-1
Synonyms
SCHEMBL1874310 | MS-23522 | Q27162493 | (1R)-6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide | AKOS025404919 | CHEBI:90370 | UNII-N4L745VB64 | (R)-selisistat | BDBM50425824 | (R)-EX-527 | Selisistat, (R)- | EX-527 (R)-enantiomer | N4L745VB64 | Seli
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 (R)-Selisistat ((R)-EX-527) is a R-enantiomer of Selisistat. Selisistat (EX-527) is a potent and selective SIRT1 inhibitor with IC 50 of 98 nM.
Form:Solid
IC50& Target:IC50: > 100 μM (SIRT1)
Specifications Sinónimos
SCHEMBL1874310 | MS-23522 | Q27162493 | (1R)-6-chloro-2, 3, 4, 9-tetrahydro-1H-carbazole-1-carboxamide | AKOS025404919 | CHEBI:90370 | UNII-N4L745VB64 | (R)-selisistat | BDBM50425824 | (R)-EX-527 | Selisistat, (R)- | EX-527 (R)-enantiomer | N4L745VB64 | Seli
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
(R)-Selisistat ((R)-EX-527) is a R-enantiomer of Selisistat. Selisistat (EX-527) is a potent and selective SIRT1 inhibitor with IC 50 of 98 nM.
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 Sonrisas canónicas C1CC(C2=C(C1)C3=C(N2)C=CC(=C3)Cl)C(=O)N IUPAC Name (1R)-6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide InChIKey FUZYTVDVLBBXDL-SECBINFHSA-N INCHI 1S/C13H13ClN2O/c14-7-4-5-11-10(6-7)8-2-1-3-9(13(15)17)12(8)16-11/h4-6,9,16H,1-3H2,(H2,15,17)/t9-/m1/s1 Isómeros SMILES C1C[C@H](C2=C(C1)C3=C(N2)C=CC(=C3)Cl)C(=O)N CAS alternativo 848193-69-1 Peso molecular 248.71 Reaxy-Rn 416178 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=416178&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 Indoles and derivatives Subclass Carbazoles Intermediate Tree Nodes Not available Direct Parent Carbazoles Alternative Parents 3-alkylindoles Benzenoids Aryl chlorides Pyrroles Heteroaromatic compounds Primary carboxylic acid amides Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Carbazole - 3-alkylindole - Indole - Aryl chloride - Aryl halide - Benzenoid - Heteroaromatic compound - Pyrrole - Carboxamide group - Primary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene 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.
Estructura 3D Objetivos asociados (humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad DMSO : 100 mg/mL (402.07 mM; Need ultrasonic) Peso molecular 248.710 g/mol XLogP3 2.500 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 1 Exact Mass 248.072 Da Monoisotopic Mass 248.072 Da Topological Polar Surface Area 58.900 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 323.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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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