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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items SDZ 220-581 - ≥98%(HPLC) , CAS No.174575-17-8
Synonyms
LMGP10010012 | alpha-Amino-2'-chloro-5-(phosphonomethyl)(1,1'-biphenyl)-3-propanoic acid | HMS3412C08 | Sdz 220-581 | SDZ220581 | Sdz-220-581 | SDZ220-581 | (alphaS)-alpha-Amino-2'-chloro-5-(phosphonomethyl)[1,1'-biphenyl]-3-propanoic acid | Abilene | (2S
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Why this grade ≥98%(HPLC) 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
LMGP10010012 | alpha-Amino-2'-chloro-5-(phosphonomethyl)(1, 1'-biphenyl)-3-propanoic acid | HMS3412C08 | Sdz 220-581 | SDZ220581 | Sdz-220-581 | SDZ220-581 | (alphaS)-alpha-Amino-2'-chloro-5-(phosphonomethyl)[1, 1'-biphenyl]-3-propanoic acid | Abilene | (2S
Especificaciones y pureza
≥98%(HPLC)
Mecanismos bioquímicos y fisiológicos
Competitive NMDA receptor antagonist (pKi= 7.7). Centrally active following oral administration (ED50< 3.2 mg/kg for protection against MES-induced seizures).
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Sonrisas canónicas C1=CC=C(C(=C1)C2=CC(=CC(=C2)CP(=O)(O)O)CC(C(=O)O)N)Cl IUPAC Name (2S)-2-amino-3-[3-(2-chlorophenyl)-5-(phosphonomethyl)phenyl]propanoic acid InChIKey VBRJFXSFCYEZMQ-HNNXBMFYSA-N INCHI 1S/C16H17ClNO5P/c17-14-4-2-1-3-13(14)12-6-10(8-15(18)16(19)20)5-11(7-12)9-24(21,22)23/h1-7,15H,8-9,18H2,(H,19,20)(H2,21,22,23)/t15-/m0/s1 Isómeros SMILES C1=CC=C(C(=C1)C2=CC(=CC(=C2)CP(=O)(O)O)C[C@@H](C(=O)O)N)Cl PubChem CID 128019 Peso molecular 369.74
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 Direct Parent Phenylalanine and derivatives Alternative Parents Chlorinated biphenyls Phenylpropanoic acids Amphetamines and derivatives L-alpha-amino acids Aralkylamines Chlorobenzenes Aryl chlorides Organic phosphonic acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Hydrocarbon derivatives Organic oxides Carbonyl compounds Organochlorides Organophosphorus compounds Organopnictogen compounds Monoalkylamines Molecular Framework Aromatic homomonocyclic compounds Substituents Phenylalanine or derivatives - Chlorinated biphenyl - Biphenyl - 3-phenylpropanoic-acid - Alpha-amino acid - Amphetamine or derivatives - L-alpha-amino acid - Aralkylamine - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Organophosphonic acid - Organophosphonic acid derivative - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organonitrogen compound - Organohalogen compound - Primary aliphatic amine - Organooxygen compound - Organophosphorus compound - Primary amine - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Amine - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organochloride - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as phenylalanine and derivatives. These are compounds containing phenylalanine or a derivative thereof resulting from reaction of phenylalanine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. 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 Solvent:DMSO, Max Conc. mg/mL: 9.24, Max Conc. mM: 25 with gentle warming; Solvent:1.1eq. NaOH, Max Conc. mg/mL: 36.97, Max Conc. mM: 100 Peso molecular 369.730 g/mol XLogP3 -1.200 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 6 Exact Mass 369.053 Da Monoisotopic Mass 369.053 Da Topological Polar Surface Area 121.000 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 485.000 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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