ChemicalBook--->CAS DataBase List--->13189-98-5

13189-98-5

13189-98-5 Structure

13189-98-5 Structure
IdentificationMore
[Name]

Fudosteine
[CAS]

13189-98-5
[Synonyms]

FUDOSTEINE
(r)-2-amino-3-(3-hydroxypropylthio)propionic acid
S-(3-HYDROXYPROPYL)CYSTEINE
3-((3-hydroxypropyl)thio)-alanin
s-(3-hydroxypropyl)-l-cystein
s-(3-hydroxypropyl)-l-cysteine
Fudosteine99%
FUDOSTEINE(SUBJECTTOPATENTFREE)
FUDESTEINE
Fudosteine (R)-2-Amino-3-(3-hydroxypropylthio)propionic acid
[EINECS(EC#)]

1592732-453-0
[Molecular Formula]

C6H13NO3S
[MDL Number]

MFCD00899873
[Molecular Weight]

179.24
[MOL File]

13189-98-5.mol
Chemical PropertiesBack Directory
[Appearance]

Off-White Powder
[Melting point ]

200-202°C (dec.)
[Boiling point ]

354.5±42.0 °C(Predicted)
[density ]

1.301±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[solubility ]

Water (Slightly)
[form ]

Solid
[pka]

2.09±0.10(Predicted)
[color ]

White to Light Brown
[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(O)(=O)[C@H](CSCCCO)N
[CAS DataBase Reference]

13189-98-5(CAS DataBase Reference)
Safety DataBack Directory
[RTECS ]

HA2350000
Hazard InformationBack Directory
[Hazard]

A reproductive hazard.
[Description]

Fudostein was launched in Japan as a new mucoactive agent for the treatment of bronchitis and respiratory congestion. This cysteine derivative was obtained from L-cysteine by condensation with either allylic alcohol in the presence of potassium persulfate or the corresponding bromoalcohol in the presence of a base. Fudostein was shown to significantly reduce mucus glycoprotein hypersecretion and inhibit infiltration of airway mucosa by lymphocytes and inflammatory cells in bronchitic rats. When given to bronchitic rabbits, an oral dose of 500 mg/kg daily potently decreased the fucose/ N-acetylneuraminic acid in sputa, so exhibiting mucoregulatory properties. In another study with SO2-exposed rabbits, fudostein suppressed blood flow of tracheal microvasculature increased by SO2, partly due to scavenging of superoxide anion.
[Chemical Properties]

Off-White Powder
[Originator]

SS Pharmaceutical/Mitsubishi Pharma (Japan)
[Uses]

A demonstrated antiinflammatory
[Uses]

An antiinflammatory expectorant MUC5 mucin obstructive pulmonary disease.
[Uses]

An antiinflammatory expectorant used in the treatment of MUC5 mucin obstructive pulmonary disease.
[Uses]

Fudosteine is a cysteine derivative that interferes with the increase in goblet cell number, expression of the mucin MUC5AC, and subsequent mucin secretion, in airways agonized with tobacco smoke, isoproterenol, lipopolysaccharide, TNF-α, or oxidants. Fudosteine, which is a thiol compound with antioxidant properties, limits NF-κB signaling and reduces inflammatory gene expression. It has greater bioavailability than N-acetyl-cysteine and increases cysteine levels in cells.
[Uses]

Fudosteine is a novel mucoactive agent and a MUC5AC mucin hypersecretion inhibitor. MUC5AC mucin synthesis and the expression of the MUC5AC gene were increased by LPS in rats or TNF-α in NCI-H292 cells; these effects were inhibited by fudosteine treatment
[Definition]

ChEBI: Fudosteine is an organic molecular entity.
[Brand name]

Cleanal
[Synthesis]

Fudosteine is synthesized by condensation of L-cysteine with 3-bromopropyl alcohol in aqueous NaOH, or by condensation of L-cysteine with allyl alcohol by means of aqueous potassium persulfate.
[storage]

Store at -20°C
[References]

[1] KOICHI TAKAHASHI . Effects of SS320A, a New Cysteine Derivative, on the Change in the Number of Goblet Cells Induced by Isoproterenol in Rat Tracheal Epithelium[J]. Japanese journal of pharmacology, 1998, 77 1: Pages 71-78. DOI: 10.1254/jjp.77.71
[2] C K RHEE. Effect of fudosteine on mucin production.[J]. European Respiratory Journal, 2008: 1195-1202. DOI: 10.1183/09031936.00018508
[3] RAHMAN I. Pharmacological antioxidant strategies as therapeutic interventions for COPD[J]. Biochimica et biophysica acta. Molecular basis of disease, 2012, 1822 5: Pages 714-728. DOI: 10.1016/j.bbadis.2011.11.004
Spectrum DetailBack Directory
[Spectrum Detail]

Fudosteine(13189-98-5)1HNMR
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