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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items LM22A-4 - 10mM in DMSO , CAS No.37988-18-4
GRADE & PURITY 10mM in DMSO
Synonyms
LM 22A4 | LM22a4 | LM-22A4 | LM22A-4 | N1,N3,N5-Tris(2-hydroxyethyl)-1,3,5-benzenetricarboxamide | 5GCL3P6AF5 | N,N',N''-Tris(2-hydroxyethyl)-1,3,5-benzenetricarboxamide | N,N',N''Tris(2-hydroxyethyl)-1,3,5-benzenetricarboxamide | SCHEMBL3321012 | 1,3,5-B
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 Shipped at room temperature. Store at -20°C.
Application
LM22A-4 has been used as a component of dissociation medium for mouse embryonic stem cells (mESC) and human embryonic stem (hESC) aggregates.
Specifications Sinónimos
LM 22A4 | LM22a4 | LM-22A4 | LM22A-4 | N1, N3, N5-Tris(2-hydroxyethyl)-1, 3, 5-benzenetricarboxamide | 5GCL3P6AF5 | N, N', N''-Tris(2-hydroxyethyl)-1, 3, 5-benzenetricarboxamide | N, N', N''Tris(2-hydroxyethyl)-1, 3, 5-benzenetricarboxamide | SCHEMBL3321012 | 1, 3, 5-B
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Small molecule BDNF mimetic displaying neurotrophic activity. Partial agonist at TrkB, activating TrkB signaling. Displaces BDNF (IC 50 = 47 nM) in binding assays.\xa0Prevents neuronal degeneration with equal efficacy to that of BDNF in in vitro models of
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas C1=C(C=C(C=C1C(=O)NCCO)C(=O)NCCO)C(=O)NCCO IUPAC Name 1-N,3-N,5-N-tris(2-hydroxyethyl)benzene-1,3,5-tricarboxamide InChIKey RGWJKANXFYJKHN-UHFFFAOYSA-N INCHI 1S/C15H21N3O6/c19-4-1-16-13(22)10-7-11(14(23)17-2-5-20)9-12(8-10)15(24)18-3-6-21/h7-9,19-21H,1-6H2,(H,16,22)(H,17,23)(H,18,24) Isómeros SMILES C1=C(C=C(C=C1C(=O)NCCO)C(=O)NCCO)C(=O)NCCO Peso molecular 339.34 Reaxy-Rn 2398310 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2398310&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 Benzenoids Clase Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Benzamides Alternative Parents N-acylethanolamines Benzoyl derivatives Secondary carboxylic acid amides Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Benzamide - Benzoyl - N-acylethanolamine - Carboxamide group - Secondary carboxylic acid amide - Alkanolamine - Carboxylic acid derivative - Alcohol - Organooxygen compound - Organonitrogen compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as benzamides. These are organic compounds containing a carboxamido substituent attached 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 (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Peso molecular 339.340 g/mol XLogP3 -2.300 Hydrogen Bond Donor Count 6 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 9 Exact Mass 339.143 Da Monoisotopic Mass 339.143 Da Topological Polar Surface Area 148.000 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 358.000 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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