Tranilast

Tranilast
Clinical data

AHFS/Drugs.com	International Drug Names
Routes of administration	Oral
ATC code	none
Legal status
Legal status	℞ (Prescription only)
Identifiers
IUPAC name 2-{[(2E)-3-(3,4-dimethoxyphenyl)prop-2- enoyl]amino}benzoic acid
CAS Number	53902-12-8
PubChem (CID)	5282230
IUPHAR/BPS	6326
UNII	HVF50SMY6E^Y
ChEBI	CHEBI:77572
ChEMBL	CHEMBL415324
ECHA InfoCard	100.150.125
Chemical and physical data
Formula	C₁₈H₁₇NO₅
Molar mass	327.33 g/mol
3D model (Jmol)	Interactive image
SMILES COC1=C(C=C(C=C1)C=CC(=O)NC2=CC=CC=C2C(=O)O)OC
InChI InChI=1S/C18H17NO5/c1-23-15-9-7-12(11-16(15)24-2)8-10-17(20)19-14-6-4-3-5-13(14)18(21)22/h3-11H,1-2H3,(H,19,20)(H,21,22)/b10-8+ Key:NZHGWWWHIYHZNX-CSKARUKUSA-N

Tranilast (INN, brand name Rizaben) is an antiallergic drug. It was developed by Kissei Pharmaceuticals and was approved in 1982 for use in Japan and South Korea for bronchial asthma. Indications for keloid and hypertrophic scar were added in 1993.^[1] It has been used for the treatment of allergic disorders such as asthma, allergic rhinitis and atopic dermatitis.

In-vitro it reduces collagen synthesis in fibroblasts,^[2] and inhibits growth of neurofibroma cells.^[3]

In-vitro it inhibits the production of interleukin-6 in endothelial cells.^[4]

It is relatively safe and well tolerated by most patients at doses of up to 600 mg/day for months.

After promising results in three small trial Tranilast was studied in a major clinical trial (the PRESTO trial) for prevention of restenosis after percutaneous transluminal coronary revascularization, but was not found effective for that application.^[5]

It has also been investigated for use as an antiproliferative drug on drug-eluting stents.

A phase II trial is recruiting rheumatoid arthritis patients.^[6]

A phase III trial is evaluating tranilast for Pterygium.^[7]

References

↑ http://www.fiercebiotech.com/story/press-release-nuon-therapeutics-completes-agreement-tranilast-kissei-pharmaceutical/2007-07-23
↑ http://jb.oxfordjournals.org/cgi/content/abstract/116/4/892
↑ http://www.jstage.jst.go.jp/article/tjem/217/3/217_193/_article "Tranilast, an Anti-Allergic Drug, Down-Regulates the Growth of Cultured Neurofibroma Cells Derived from Neurofibromatosis Type 1" 2009
↑ http://molpharm.aspetjournals.org/content/62/4/856.full "Tranilast Inhibits Cytokine-Induced Nuclear Factor κB Activation in Vascular Endothelial Cells" 2002
↑ http://www.circ.ahajournals.org/cgi/content/full/106/10/1243 "Results of Prevention of REStenosis with Tranilast and its Outcomes (PRESTO) Trial" 2002
↑ http://clinicaltrials.gov/ct2/show/NCT00882024
↑ http://clinicaltrials.gov/ct2/show/NCT01003613

External links

ChemSpider entry

This article is issued from Wikipedia - version of the 9/1/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.