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Tranilast

Catalog No. T0318 Name Sigma Aldrich
CAS Number 53902-12-8 Website http://www.sigmaaldrich.com
M. F. C18H17NO5 Telephone 1-800-521-8956
M. W. 327.33128 Fax
Purity ≥98% (HPLC) Email
Storage Chembase ID: 5256

SYNONYMS

IUPAC name
2-[3-(3,4-dimethoxyphenyl)prop-2-enamido]benzoic acid
IUPAC Traditional name
tranilast
Synonyms
Rizaben
N-(3,4-Dimethoxycinnamoyl)anthranilic acid
SB-252218
3,4-DAA
2-[[3-(3,4-Dimethoxyphenyl)-1-oxo-2-propenyl]amino] benzoic acid

DATABASE IDS

CAS Number 53902-12-8
PubChem SID 24278719
MDL Number MFCD00864787

PROPERTIES

Empirical Formula (Hill Notation) C18H17NO5
Purity ≥98% (HPLC)
Gene Information human ... VEGFA(7422), VEGFB(7423), VEGFC(7424)
Apperance white to beige powder
Melting Point 166.2-168.2 °C(lit.)
Solubility DMSO: >10 mg/mL
Solubility H2O: insoluble
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
Risk Statements 22
RTECS DG8731000
Safety Statements 26-36
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Tranilast is an anti-asthma drug, which inhibits LTC4 and PGE2 formation in stimulated monocytes, but does not inhibit cyclooxygenase or lipoxygenase activity; inhibits mast cell degranulation; inhibits VEGF-induced angiogenesis in vivo and also inhibits proliferation and tube formation of human endothelial cells in vitro. Tranilast may represent a new class of drugs for therapy to treat ongoing TH1-mediated autoimmune diseases.
Description (简体中文)
Biochem/physiol Actions
Tranilast is an anti-asthma drug, which inhibits LTC4 and PGE2 formation in stimulated monocytes, but does not inhibit cyclooxygenase or lipoxygenase activity; inhibits mast cell degranulation; inhibits VEGF-induced angiogenesis in vivo and also inhibits proliferation and tube formation of human endothelial cells in vitro. Tranilast may represent a new class of drugs for therapy to treat ongoing TH1-mediated autoimmune diseases.

REFERENCES