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Fudosteine

CAS No.
13189-98-5
Chemical Name:
Fudosteine
Synonyms
Fudostin;Fudostan;FUDESTEINE;FUDOSTEINE;fodosteine;Fu si temple;Fudosteine99%;D6-Fudosteine HCl;Fudosteine USP/EP/BP;Fulvestrant 9 sulfone D5
CBNumber:
CB1128341
Molecular Formula:
C6H13NO3S
Molecular Weight:
179.24
MDL Number:
MFCD00899873
MOL File:
13189-98-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-15 20:54:36

Fudosteine Properties

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)
FDA UNII UR9VPI71PT

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
RTECS  HA2350000
NFPA 704
0
2 0

Fudosteine price More Price(62)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 16722 Fudosteine ≥95% 13189-98-5 10mg $36 2026-04-30 Buy
Cayman Chemical 16722 Fudosteine ≥95% 13189-98-5 25mg $70 2026-04-30 Buy
Cayman Chemical 16722 Fudosteine ≥95% 13189-98-5 50mg $120 2026-04-30 Buy
Cayman Chemical 16722 Fudosteine ≥95% 13189-98-5 100mg $219 2026-04-30 Buy
Usbiological H9111-47 S-(3-Hydroxypropyl)cysteine 100mg $418 2026-06-03 Buy
Product number Packaging Price Buy
16722 10mg $36 Buy
16722 25mg $70 Buy
16722 50mg $120 Buy
16722 100mg $219 Buy
H9111-47 100mg $418 Buy

Fudosteine Chemical Properties,Uses,Production

Description

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.

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

An antiinflammatory expectorant MUC5 mucin obstructive pulmonary disease.

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

Uses

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

Uses

A demonstrated antiinflammatory

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.

Definition

ChEBI: Fudosteine is an organic molecular entity.

brand name

Cleanal, Spelear (Mitsubishi Pharma)

Hazard

A reproductive hazard.

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.

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

Fudosteine Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 352)Suppliers
Supplier Tel Email Country ProdList Advantage
Jiangsu Chia Tai Feng Hai Pharmaceutical Co.,Ltd 025-57033246-8069 17305112672 kiderer@163.com China 20 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
Pure Chemistry Scientific Inc. 001-857-928-2050 or 1-888-588-9418 sales@chemreagents.com United States 10174 62
Adamas Reagent, Ltd. 400-6009262 15618770481 yhx@titansci.com China 14098 59
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2110 70
Shanghai Longsheng chemical Co.,Ltd. 58099637 13585536065 sales@shlschem.com China 9880 59
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696 info@hanhongsci.com China 42917 64
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
XiaoGan ShenYuan ChemPharm co,ltd 15527621225; 15527621225 1791901229@qq.com China 6746 52

View Lastest Price from Fudosteine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fudosteine pictures 2026-09-11 Fudosteine
13189-98-5
10g 99%~101% 10kg/month WUHAN FORTUNA CHEMICAL CO., LTD
Fudosteine pictures 2026-07-15 Fudosteine
13189-98-5
1kg 98% 1000kgs Shaanxi Dideu New Materials Co. Ltd
Fudosteine pictures 2026-06-13 Fudosteine
13189-98-5
$34.00 99.81% 10g TargetMol Chemicals Inc.
  • Fudosteine pictures
  • Fudosteine
    13189-98-5
  • $0.00
  • 99%~101%
  • WUHAN FORTUNA CHEMICAL CO., LTD
  • Fudosteine pictures
  • Fudosteine
    13189-98-5
  • $0.00
  • 98%
  • Shaanxi Dideu New Materials Co. Ltd
  • Fudosteine pictures
  • Fudosteine
    13189-98-5
  • $34.00
  • 99.81%
  • TargetMol Chemicals Inc.

Fudosteine Spectrum

FUDESTEINE Fudosteine (R)-2-Amino-3-(3-hydroxypropylthio)propionic acid (2R)-2-amino-3-(3-hydroxypropylsulfanyl)propanoic acid (2R)-2-amino-3-(3-hydroxypropylthio)propionic acid (2R)-2-azanyl-3-(3-hydroxypropylsulfanyl)propanoic acid 3-[(3-Hydroxypropyl)thio]alanine (r)-2-amino-3-(3-hydroxypropylthio)propionic acid S-(3-HYDROXYPROPYL)CYSTEINE FUDOSTEINE 2-amino-3-(3-hydroxypropylthio)propanoic acid 3-((3-hydroxypropyl)thio)-alanin s-(3-hydroxypropyl)-l-cystein s-(3-hydroxypropyl)-l-cysteine Fudosteine99% FUDOSTEINE(SUBJECTTOPATENTFREE) (R)-2-amino-3-((3-hydroxypropyl)thio)propanoic acid L-Cysteine, S-(3-hydroxypropyl)- Fudosteine,S-(3-Hydroxypropyl)cysteine,3-[(3-Hydroxypropyl)thio]alanine Fudosteine USP/EP/BP Fudosteine Impurities1413 fodosteine Fudosteine D6Q: What is Fudosteine D6 Q: What is the CAS Number of Fudosteine D6 Q: What is the storage condition of Fudosteine D6 Q: What are the applications of Fudosteine D6 FudosteineQ: What is Fudosteine Q: What is the CAS Number of Fudosteine Q: What is the storage condition of Fudosteine Q: What are the applications of Fudosteine Fu si temple Fulvestrant 9 sulfone D5 Fudostin Fudostan D6-Fudosteine HCl 13189-98-5 C6H13O2S Amino Acids 13C, 2H, 15N Amino Acids & Derivatives Other APIs Sulfur & Selenium Compounds