The store will not work correctly when cookies are disabled.
Javascript est désactivé dans votre navigateur. Pour une meilleure expérience sur notre site, assurez-vous d’activer JavaScript dans votre navigateur.
· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock benzylcysteine - Moligand™ , Inhibitor of Alanine/serine/cysteine transporter 2, CAS No.B607997, Inhibitor of Alanine/serine/cysteine transporter 2
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
S-Benzyl-L-cysteine, 97% | NCGC00013519-02 | L-S-Benzylcysteine | NCGC00013519 | NCGC00096633-01 | Felixene | Benzylcysteine | FD21339 | HY-103025 | B0865 | AS-15564 | EINECS 221-273-4 | GTPL4501 | Q27075094 | Q5807233 | CCG-37910 | DTXSID60180650 | DB045
🧪
Why this grade Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping Room temperature Ships Check lot-specific COA for exact specifications.
📋
Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
📚
Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonymes
S-Benzyl-L-cysteine, 97% | NCGC00013519-02 | L-S-Benzylcysteine | NCGC00013519 | NCGC00096633-01 | Felixene | Benzylcysteine | FD21339 | HY-103025 | B0865 | AS-15564 | EINECS 221-273-4 | GTPL4501 | Q27075094 | Q5807233 | CCG-37910 | DTXSID60180650 | DB045
Spécifications et pureté
Moligand™
Conditions de stockage de stockage
Room temperature
Mécanisme d'action
Inhibitor of Alanine/serine/cysteine transporter 2
Noms et identifiants Sourires canoniques
N[C@H](C(=O)O)CSCc1ccccc1
IUPAC Name
(2R)-2-amino-3-(benzylsulfanyl)propanoic acid
InChIKey
GHBAYRBVXCRIHT-VIFPVBQESA-N
INCHI
1S/C10H13NO2S/c11-9(10(12)13)7-14-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13)/t9-/m0/s1
Isomères SMILES
C1=CC=C(C=C1)CSC[C@@H](C(=O)O)N
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 Classe Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Cysteine and derivatives Direct Parent L-cysteine-S-conjugates Alternative Parents L-alpha-amino acids Benzene and substituted derivatives Amino acids Sulfenyl compounds Monocarboxylic acids and derivatives Dialkylthioethers Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents L-cysteine-s-conjugate - Alpha-amino acid - L-alpha-amino acid - Monocyclic benzene moiety - Benzenoid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Thioether - Sulfenyl compound - Dialkylthioether - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as l-cysteine-s-conjugates. These are compounds containing L-cysteine where the thio-group is conjugated. External Descriptors S-hydrocarbyl-L-cysteine 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Poids moléculaire 211.280 g/mol XLogP3 -1.200 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 5 Exact Mass 211.067 Da Monoisotopic Mass 211.067 Da Topological Polar Surface Area 88.600 Ų Heavy Atom Count 14 Formal Charge 0 Complexity 181.000 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
Calculateurs de solution Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Avis 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 →
We use cookies to ensure the website functions properly and, where permitted, to improve your experience. You can manage your preferences at any time in Settings. Learn more in our
Cookie Policy. Paramètres Accepter tout Refuser
Shall we send you a message when we have discounts available?
Remind me later Autoriser
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
Copyright © 2023–present Aladdin Scientific Corp. All rights reserved.
