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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Fudosteine - 10mM in Water , CAS No.13189-98-5
GRADE & PURITY 10mM in Water
Synonyms
DS-2359 | Oprea1_041651 | Cleanal (TN) | S-(3-Hydroxypropyl)-L-cysteine | BIDD:GT0580 | CHEBI:31637 | (2R)-2-amino-3-[(3-hydroxypropyl)sulfanyl]propanoic acid | AKOS010386681 | NCGC00164556-01 | S-3-hydroxypropylcysteine | DTXCID2026440 | Astrocar | DTXSI
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in Water 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.
Specifications Sinónimos
DS-2359 | Oprea1_041651 | Cleanal (TN) | S-(3-Hydroxypropyl)-L-cysteine | BIDD:GT0580 | CHEBI:31637 | (2R)-2-amino-3-[(3-hydroxypropyl)sulfanyl]propanoic acid | AKOS010386681 | NCGC00164556-01 | S-3-hydroxypropylcysteine | DTXCID2026440 | Astrocar | DTXSI
Especificaciones y pureza
10mM in Water
Mecanismos bioquímicos y fisiológicos
MUC5AC mucin hypersecretion inhibitor. Reduces MUC5AC gene expression. Reduces p-p38 MAPK and p-ERK expression. Decreases the number of goblet cells. Reduces airway hyper-responsiveness and airway inflammation in vivo. Orally active.
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
C(CO)CSCC(C(=O)O)N
IUPAC Name
(2R)-2-amino-3-(3-hydroxypropylsulfanyl)propanoic acid
InChIKey
KINWYTAUPKOPCQ-YFKPBYRVSA-N
INCHI
1S/C6H13NO3S/c7-5(6(9)10)4-11-3-1-2-8/h5,8H,1-4,7H2,(H,9,10)/t5-/m0/s1
Isómeros SMILES
C(CO)CSC[C@@H](C(=O)O)N
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=42863514&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 - Cysteine and derivatives Direct Parent L-cysteine-S-conjugates Alternative Parents L-alpha-amino acids Amino acids Sulfenyl compounds Monocarboxylic acids and derivatives Dialkylthioethers Carboxylic acids Primary alcohols Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents L-cysteine-s-conjugate - Alpha-amino acid - L-alpha-amino acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Thioether - Sulfenyl compound - Dialkylthioether - Alcohol - Hydrocarbon derivative - Organic oxide - Primary amine - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Organic nitrogen compound - Aliphatic acyclic compound Descripción 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 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 179.240 g/mol XLogP3 -3.000 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 6 Exact Mass 179.062 Da Monoisotopic Mass 179.062 Da Topological Polar Surface Area 109.000 Ų Heavy Atom Count 11 Formal Charge 0 Complexity 120.000 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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