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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Bikinin - 10mM in DMSO , CAS No.188011-69-0
GRADE & PURITY 10mM in DMSO
Synonyms
STK005425 | BCP15563 | Bikinin | Bikinin; Abrasin | Abrasin | HMS2304N16 | DB08578 | IFLab1_000935 | HY-12524 | SX2 | 4-((5-Bromopyridin-2-yl)amino)-4-oxobutanoic acid | S7722 | F0216-0029 | 3-[(5-bromopyridin-2-yl)carbamoyl]propanoic acid | 4-[(5-bromopy
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 Bikinin is an ATP-competitive Arabidopsis GSK-3 inhibitor, and acts as a strong activator of brassinosteroid (BR) signaling.
Specifications Sinónimos
STK005425 | BCP15563 | Bikinin | Bikinin; Abrasin | Abrasin | HMS2304N16 | DB08578 | IFLab1_000935 | HY-12524 | SX2 | 4-((5-Bromopyridin-2-yl)amino)-4-oxobutanoic acid | S7722 | F0216-0029 | 3-[(5-bromopyridin-2-yl)carbamoyl]propanoic acid | 4-[(5-bromopy
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Cell-permeable, ATP-competitive GSK-3 inhibitor. Highly selective for 7 Arabidopsis. Strongly activates brassinosteroid signalling .
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
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Nombres e identificadores Sonrisas canónicas C1=CC(=NC=C1Br)NC(=O)CCC(=O)O IUPAC Name 4-[(5-bromopyridin-2-yl)amino]-4-oxobutanoic acid InChIKey XFYYQDHEDOXWGA-UHFFFAOYSA-N INCHI 1S/C9H9BrN2O3/c10-6-1-2-7(11-5-6)12-8(13)3-4-9(14)15/h1-2,5H,3-4H2,(H,14,15)(H,11,12,13) Isómeros SMILES C1=CC(=NC=C1Br)NC(=O)CCC(=O)O WGK Alemania 3 Peso molecular 273.09 Reaxy-Rn 8144877 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8144877&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 nitrogen compounds Clase Organonitrogen compounds Subclass N-arylamides Intermediate Tree Nodes Not available Direct Parent N-arylamides Alternative Parents Pyridines and derivatives Imidolactams Fatty amides Aryl bromides Heteroaromatic compounds Secondary carboxylic acid amides Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteromonocyclic compounds Substituents N-arylamide - Aryl bromide - Aryl halide - Fatty amide - Pyridine - Fatty acyl - Imidolactam - Heteroaromatic compound - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organoheterocyclic compound - Organopnictogen compound - Hydrocarbon derivative - Organic oxygen compound - Organohalogen compound - Organobromide - Organooxygen compound - Carbonyl group - Organic oxide - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as n-arylamides. These are organic compounds that contain a carboxamide group that is N-linked to a aryl group. They have the generic structure RC(=O)N(R')H, R = organyl group and R'= aryl group. 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 Sensibilidad Heat Sensitive Punto de fusión (°C) 144 °C Peso molecular 273.080 g/mol XLogP3 0.500 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 4 Exact Mass 271.98 Da Monoisotopic Mass 271.98 Da Topological Polar Surface Area 79.300 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 248.000 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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