Fudosteine - ≥99% , CAS No.13189-98-5

CAS: 13189-98-5 Cat. No.: F129236 Peso molecular: 179.24

GRADE & PURITY ≥99%

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

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

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

≥99%

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 -20°C

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 504757032
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757032
• 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
• Peso molecular: 179.24
• Reaxy-Rn: 42863514
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=42863514&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Cysteine and derivatives
              • Level8 L-cysteine-S-conjugates

• 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.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (no humanos)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in DMSO and Water
• 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