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Fudosteine - 10mM in Water, high purity , CAS No.13189-98-5
MUC5AC mucin hypersecretion inhibitor
Basic Description
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
Specifications & Purity
10mM in Water
Biochemical and Physiological Mechanisms
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.
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic acids and derivatives
Class
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
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
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.
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
(2R)-2-amino-3-(3-hydroxypropylsulfanyl)propanoic acid
INCHI
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
InChIKey
KINWYTAUPKOPCQ-YFKPBYRVSA-N
Smiles
C(CO)CSCC(C(=O)O)N
Isomeric SMILES
C(CO)CSC[C@@H](C(=O)O)N
Molecular Weight
179.24
Reaxy-Rn
42863514
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=42863514&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Molecular Weight
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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