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Details

Stereochemistry ACHIRAL
Molecular Formula C5H12N4O.ClH
Molecular Weight 180.636
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TIFORMIN HYDROCHLORIDE

SMILES

Cl.NC(=N)NCCCC(N)=O

InChI

InChIKey=QHQKFKHTHUDEQS-UHFFFAOYSA-N
InChI=1S/C5H12N4O.ClH/c6-4(10)2-1-3-9-5(7)8;/h1-3H2,(H2,6,10)(H4,7,8,9);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C5H12N4O
Molecular Weight 144.175
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Tiformin (also known as γ-Guanidinobutyramide) is a butyramide derivate with antidiabetic activity. Tiformin was isolated for the first time from a medium containing arginine which had been transformed by washed cells of Streptomyces griseus. In preclinical models, oral administration of Tiformin depresses blood glucose in rats and rabbits. Tiformin given i.v. produced hyperglycemia and sometimes death of experimental animals. Tiformin is not significantly metabolized in the rat or dog.

Originator

Sources: Biochimica et Biophysica Acta (1955), 18, 589.

Approval Year

PubMed

PubMed

TitleDatePubMed
Development of an in vitro cleavage assay system to examine vaccinia virus I7L cysteine proteinase activity.
2005 Aug 16
Falstatin, a cysteine protease inhibitor of Plasmodium falciparum, facilitates erythrocyte invasion.
2006 Nov
Stage- and gender-specific proteomic analysis of Brugia malayi excretory-secretory products.
2008
Patents

Sample Use Guides

rat: 1400 mg​/kg rabbit: 800 mg​/kg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 19:07:30 GMT 2023
Edited
by admin
on Sat Dec 16 19:07:30 GMT 2023
Record UNII
6T8E9HET7P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TIFORMIN HYDROCHLORIDE
Common Name English
.GAMMA.-GUANIDINOBUTYRAMIDE HYDROCHLORIDE
Systematic Name English
BUTANAMIDE, 4-((AMINOIMINOMETHYL)AMINO)-, MONOHYDROCHLORIDE
Systematic Name English
4-GUANIDINOBUTYRAMIDE HYDROCHLORIDE
Systematic Name English
HL-523
Code English
BUTANAMIDE, 4-((AMINOIMINOMETHYL)AMINO)-, HYDROCHLORIDE (1:1)
Systematic Name English
HL523
Code English
Code System Code Type Description
FDA UNII
6T8E9HET7P
Created by admin on Sat Dec 16 19:07:30 GMT 2023 , Edited by admin on Sat Dec 16 19:07:30 GMT 2023
PRIMARY
CAS
23256-39-5
Created by admin on Sat Dec 16 19:07:30 GMT 2023 , Edited by admin on Sat Dec 16 19:07:30 GMT 2023
PRIMARY
PUBCHEM
3032789
Created by admin on Sat Dec 16 19:07:30 GMT 2023 , Edited by admin on Sat Dec 16 19:07:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID50177832
Created by admin on Sat Dec 16 19:07:30 GMT 2023 , Edited by admin on Sat Dec 16 19:07:30 GMT 2023
PRIMARY
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