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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 1-benzyl-APDC - Moligand™ , Agonist of mGlu 6 receptor, CAS No.171336-76-8, Agonist of mGlu 6 receptor
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
DTXSID60573467 | 4-amino-1-(phenylmethyl)pyrrolidine-2,4-dicarboxylic acid | 4-Amino-1-benzyl-pyrrolidine-2,4-dicarboxylic acid(1-benzyl-APDC) | Q27070803 | (2R,4R)-4-Amino-1-benzyl-pyrrolidine-2,4-dicarboxylic acid | (2R,4R)-4-amino-1-benzylpyrrolidine-2
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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 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
DTXSID60573467 | 4-amino-1-(phenylmethyl)pyrrolidine-2, 4-dicarboxylic acid | 4-Amino-1-benzyl-pyrrolidine-2, 4-dicarboxylic acid(1-benzyl-APDC) | Q27070803 | (2R, 4R)-4-Amino-1-benzyl-pyrrolidine-2, 4-dicarboxylic acid | (2R, 4R)-4-amino-1-benzylpyrrolidine-2
Especificaciones y pureza
Moligand™
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Agonist of mGlu 6 receptor
Nombres e identificadores Sonrisas canónicas OC(=O)[C@H]1C[C@](CN1Cc1ccccc1)(N)C(=O)O IUPAC Name 4-amino-1-(phenylmethyl)pyrrolidine-2,4-dicarboxylic acid InChIKey LYCSUAGKQMUTBR-ZWNOBZJWSA-N INCHI 1S/C13H16N2O4/c14-13(12(18)19)6-10(11(16)17)15(8-13)7-9-4-2-1-3-5-9/h1-5,10H,6-8,14H2,(H,16,17)(H,18,19)/t10-,13-/m1/s1 Isómeros SMILES C1[C@@H](N(C[C@]1(C(=O)O)N)CC2=CC=CC=C2)C(=O)O PubChem CID 15508178
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 Proline and derivatives Alternative Parents L-alpha-amino acids D-alpha-amino acids Pyrrolidine carboxylic acids Phenylmethylamines Benzylamines Aralkylamines N-alkylpyrrolidines Dicarboxylic acids and derivatives Trialkylamines Amino acids Azacyclic compounds Carboxylic acids Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides Molecular Framework Aromatic heteromonocyclic compounds Substituents Proline or derivatives - Alpha-amino acid - L-alpha-amino acid - D-alpha-amino acid - Benzylamine - Phenylmethylamine - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Aralkylamine - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Benzenoid - N-alkylpyrrolidine - Pyrrolidine - Tertiary amine - Tertiary aliphatic amine - Amino acid - Organoheterocyclic compound - Azacycle - Carboxylic acid - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Hydrocarbon derivative - Primary amine - Carbonyl group - Organic oxide - Organic oxygen compound - Amine - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as proline and derivatives. These are compounds containing proline or a derivative thereof resulting from reaction of proline 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 Peso molecular 264.280 g/mol XLogP3 -4.500 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 4 Exact Mass 264.111 Da Monoisotopic Mass 264.111 Da Topological Polar Surface Area 104.000 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 368.000 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.
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