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Details

Stereochemistry ACHIRAL
Molecular Formula C17H11ClN2O2S
Molecular Weight 342.799
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TILOMISOLE

SMILES

OC(=O)CC1=C(N2C(S1)=NC3=C2C=CC=C3)C4=CC=C(Cl)C=C4

InChI

InChIKey=PUYFLGQZLHVTHX-UHFFFAOYSA-N
InChI=1S/C17H11ClN2O2S/c18-11-7-5-10(6-8-11)16-14(9-15(21)22)23-17-19-12-3-1-2-4-13(12)20(16)17/h1-8H,9H2,(H,21,22)

HIDE SMILES / InChI

Molecular Formula C17H11ClN2O2S
Molecular Weight 342.799
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

Tilomisole (also known as Wy-18,251) is a benzimidazole derivative patented by American Home Products Corp. as an antineoplastic agent with immunomodulating and antimetastatic activity. Tilomisole significantly enhanced the blastogenic response of cancer patients' lymphocytes in vitro. Tilomisole significantly increases macrophage phagocytosis against 51chromium labeled opsonized chicken red blood cells. In preclinical models, Tilomisole administration significantly increases peripheral blood lymphocytes in rats and demonstrates marked anti-inflammatory activity. The acute anti-inflammatory of Tilomisole.) was similar to aspirin, but in contrast to aspirin, Tilomisole failed to demonstrate antipyretic activity. Tilomisole also inhibited chronic inflammatory responses in the adjuvant- and collagen-induced arthritis models. Unfortunately, in clinical trials, Tilomisole failed to demonstrate significant antitumor responses.

Originator

Approval Year

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
60 mg/m2 orally (p.o.) weekly, and 60, 300, or 960 mg/m2 p.o. daily for 1 month.
Route of Administration: Oral
Substance Class Chemical
Record UNII
651G60U372
Record Status Validated (UNII)
Record Version