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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items CGS 19755 - Moligand™ , Antagonist of GluN2A;Antagonist of GluN2B;Antagonist of GluN2C;Antagonist of GluN2D, CAS No.110347-85-8, Antagonist of GluN2A;Antagonist of GluN2B;Antagonist of GluN2C;Antagonist of GluN2D
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. Synonyms
AKOS015914119 | 2-Piperidinecarboxylic acid, 4-(phosphonomethyl)-, (2R,4S)- | 4VGJ4A41L2 | CAS-110347-85-8 | N0905W44Y3 | SCHEMBL120234 | 4-Phosphonomethyl-piperidine-2-carboxylic acid | CGS19755 | CGS-19755 | 4-Phosphonomethyl-piperidine-2-carboxylic aci
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Why this grade Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal 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 Sinónimos
AKOS015914119 | 2-Piperidinecarboxylic acid, 4-(phosphonomethyl)-, (2R, 4S)- | 4VGJ4A41L2 | CAS-110347-85-8 | N0905W44Y3 | SCHEMBL120234 | 4-Phosphonomethyl-piperidine-2-carboxylic acid | CGS19755 | CGS-19755 | 4-Phosphonomethyl-piperidine-2-carboxylic aci
Especificaciones y pureza
Moligand™
Mecanismos bioquímicos y fisiológicos
Potent, competitive NMDA receptor antagonist. Anticonvulsant and neuroprotective.
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Antagonist of GluN2A;Antagonist of GluN2B;Antagonist of GluN2C;Antagonist of GluN2D
Nombres e identificadores Sonrisas canónicas C1CNC(CC1CP(=O)(O)O)C(=O)O IUPAC Name (2S,4R)-4-(phosphonomethyl)piperidine-2-carboxylic acid InChIKey LPMRCCNDNGONCD-RITPCOANSA-N INCHI 1S/C7H14NO5P/c9-7(10)6-3-5(1-2-8-6)4-14(11,12)13/h5-6,8H,1-4H2,(H,9,10)(H2,11,12,13)/t5-,6+/m1/s1 Isómeros SMILES C1CN[C@@H](C[C@@H]1CP(=O)(O)O)C(=O)O Peso molecular 223.17 Reaxy-Rn 4253562 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4253562&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 acids and derivatives Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids Direct Parent L-alpha-amino acids Alternative Parents Piperidinecarboxylic acids Organic phosphonic acids Amino acids Monocarboxylic acids and derivatives Dialkylamines Carboxylic acids Azacyclic compounds Organopnictogen compounds Organophosphorus compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic heteromonocyclic compounds Substituents L-alpha-amino acid - Piperidinecarboxylic acid - Piperidine - Organophosphonic acid - Organophosphonic acid derivative - Amino acid - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Secondary amine - Organoheterocyclic compound - Azacycle - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Hydrocarbon derivative - Organic oxygen compound - Amine - Carbonyl group - Organic nitrogen compound - Aliphatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. External Descriptors non-proteinogenic alpha-amino acid 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 Solvent:water, Max Conc. mg/mL: 5.58, Max Conc. mM: 25 Peso molecular 223.160 g/mol XLogP3 -3.900 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 3 Exact Mass 223.061 Da Monoisotopic Mass 223.061 Da Topological Polar Surface Area 107.000 Ų Heavy Atom Count 14 Formal Charge 0 Complexity 263.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 2 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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Reconstitution Calculator Reseñas Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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