Tempostatin

Tempostatin Uses, Dosage, Side Effects, Food Interaction and all others data.

Tempostatin is a low molecular weight quinazolinone alkaloid, and a potent inhibitor of collagen alpha1(I) and matrix metalloproteinase 2 (MMP-2) gene expression. Tempostatin also effectively suppresses tumor progression and metastasis in mice. Collgard Biopharmaceuticals is developing halofuginone for the treatment of scleroderma and received orphan drug designation from the U.S. Food and Drug Administration in March, 2000.

Tempostatin, a fully synthetic small molecule, is a potent and selective regulator of stromal cell activation, cell migration and Collagen type I synthesis, a process that has been identified as a 'master switch' in the body's tissue repair process.

Table Of contents

• Tempostatin
• Uses
• Dosage
• Side Effect
• Precautions
• Interactions
• Uses during Pregnancy
• Uses during Breastfeeding
• Accute Overdose
• Food Interaction
• Half Life
• Volume of Distribution
• Clearance
• Interaction With other Medicine
• Contradiction
• Storage

Trade Name	Tempostatin
Generic	Halofuginone
Halofuginone Other Names	Halofuginone
Type
Formula	C16H17BrClN3O3
Weight	Average: 414.681 Monoisotopic: 413.014181779
Groups	Investigational, Vet approved
Therapeutic Class
Manufacturer
Available Country
Last Updated:	September 19, 2023 at 7:00 am

Uses

For the treatment of scleroderma, cancer, and restenosis.

How Tempostatin works

Tempostatin is a potent inhibitor of collagen a1(I) and matrix metalloproteinase 2 (MMP-2) gene expression. Tempostatin also suppresses extracellular matrix deposition and cell proliferation. The profound antitumoral effect of halofuginone is attributed to its combined inhibition of the tumor stromal support, vascularization, invasiveness, and cell proliferation.

Elimination Route

Readily bioavailable and rapidly absorbed following oral administration.

Half Life

23.8 to 72.1 hours

Innovators Monograph

You find simplified version here Tempostatin