Tiopronin Chemical Properties

Melting point:

93-98 °C

Boiling point:

418.3±30.0 °C(Predicted)

Density 

1.249 (estimate)

refractive index 

1.5216 (estimate)

storage temp. 

Inert atmosphere,2-8°C

solubility 

DMSO (Slightly), Methanol (Slightly)

pka

3.36±0.10(Predicted)

form 

solid

color 

White

Merck 

14,9453

BRN 

1859822

CAS DataBase Reference

1953-02-2(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xn

Risk Statements 

22

Safety Statements 

36/37

WGK Germany 

3

RTECS 

MC0596500

HS Code 

2930.90.4950

Toxicity

LD50 i.v. in mice: 2.1 g/kg (Fujimura)

MSDS

• Language:English Provider:alpha-Mercaptopropionyl glycine
• Language:English Provider:SigmaAldrich

Tiopronin Usage And Synthesis

Description

Tiopronin is a sulfiydryl derivative of N-propylglycine useful in the treatment of cystine urolithiasis in children. It is also reportedly effective in the management of rheumatoid polyarthritis, possibly due to its inhibitory effect on the free oxygen radicals produced by inflammatory macrophages and granulocytes.

Description

Tiopronin is an antioxidant that has diverse biological activities. It reduces free radical production by murine macrophages and granulocytes in vitro in a dose-dependent manner. Tiopronin induces expression of hypoxia-inducible factor 1α (HIF-1α) and increases VEGF secretion in human colon carcinoma cells. Rectal administration (500 μL of a 10 mM solution) reduces myeloperoxidase activity and reduces pro-inflammatory cytokine production in the colon in a rat model of colitis. Tiopronin (80-320 mg/kg per day) reduces the incidence of cleft palate in fetuses born to female mice orally exposed to teratogenic methylmercury chloride. Tiopronin (100 mg/kg) reduces heme oxygenase 1 mRNA expression, lipid peroxidation, and transverse aortic constriction in a mouse model of cardiac hypertrophy. Tiopronin (20 mg/kg) is hepatoprotective, increasing activity of the antioxidant enzymes superoxide dismutase and glutathione peroxidase and reversing hepatocyte degeneration in a rat model of high-fat diet-induced non-alcoholic steatohepatitis.

Chemical Properties

White Solid

Originator

Roussel-Uclaf (Japan)

Uses

N-(2-Mercaptopropionyl)glycine or Tiopronin has been used:

• in the preparation of polyethylenimine (PEI)-coated gold microparticles (PEI-gold) for biolistic delivery of nucleic acids
• to study the role of reactive oxygen species (ROS) at the reperfusion stage in in vivo isoflurane preconditioning-induced neuroprotection
• as a ROS inhibitor to study its effect on lysophosphatidylcholine (LPC)-induced inflammasome activation

Uses

It is used as antidote against heavy metal poisoning; hepatoprotectant; mucolytic.

Definition

ChEBI: Tiopronin is a N-acyl-amino acid.

Manufacturing Process

α-Benzylmercaptopropionic acid (melting point 76°C to 78°C; 100 g) prepared by condensation of α-mercaptopropionic acid with benzyl chloride is allowed to stand overnight with 80 g of thionyl chloride. After removal of excess thionyl chloride distillation in vacuo gives 70 g of α-benzylmercaptopropionic acid chloride of boiling point 138°C to 139°C/7 to 8 mm Hg.
Then, 25 g of glycine is dissolved in 165 ml of 2 N sodium hydroxide solution and 70 g of α-benzylmercaptopropionic acid chloride and 100 ml of 2 N sodium hydroxide solution are dropped thereinto simultaneously at 3°C to 5°C. The solution is then stirred at room temperature for 3 to 4 hours to complete the reaction, the reaction solution is washed with ether, the aqueous layer is acidified with hydrochloric acid, and the resulting crystals are collected by filtration. These are recrystallized from a mixture of methanol and ethyl acetate to give 60 g of α-benzylmercaptopropionylglycine of melting point 133°C to 134°C.
This α-benzylmercaptopropionylglycine (60 g) is dissolved in 400 ml of liquid ammonia, kept at about -50°C, and 12 g of sodium metal is gradually added thereto. After the reaction, excess ammonia is removed therefrom, the residue is dissolved in water, washed with ether and the residual aqueous layer is adjusted to pH 1 with hydrochloric acid and concentrated in vacuo in a stream of hydrogen sulfide. The crystalline residue is dried and recrystallized from ethyl acetate to give 25 g of α-mercaptopropionylglycine of melting point 95°C to 97°C.

brand name

Thiola

Therapeutic Function

Antidote (heavy metal)

Biochem/physiol Actions

N-(2-Mercaptopropionyl)glycine (NMPG) is a thiol compound associated with autoimmune hypoglycemia. It is a diffusible antioxidant and reduces the severity of colonic injury. NMPG also relieves myeloperoxidase activity and stimulates hypoxia-inducible factor-1 (HIF-1) - vascular endothelial growth factor (VEGF) pathway for ulcer healing.

Veterinary Drugs and Treatments

Tiopronin is indicated for the prevention of cystine urolithiasis in patients where dietary therapy combined with urinary alkalinization is not completely effective. It may also be useful in combination with urine alkalinization to dissolve stones.

Tiopronin(1953-02-2)Related Product Information

• Sodium thioglycolate
• Mercaptoacetic acid
• POTASSIUM THIOGLYCOLATE
• Calcium thioglycolate
• 2-Ethylhexyl mercaptoacetate
• L-Cysteine
• Glycine
• Diethylstilbestrol
• Betaine
• 3-Mercaptopropionic acid
• TIOPRONIN SODIUM
• BUCILLAMINE
• Stepronin
• 2-Mercaptoethanol
• Glycine, N-(1-oxo-2-((2-thienylcarbonyl)thio)propyl)-, 4-(acetylamino) phenyl ester
• ICI 154,129
• Glycine, N-(1-oxo-2-((2-thienylcarbonyl)thio)propyl)-, 2-(butoxycarbon yl)phenyl ester
• Glycine, N-(1-oxo-2-((2-thienylcarbonyl)thio)propyl)-, 2-(ethoxycarbon yl)phenyl ester