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Details

Stereochemistry ACHIRAL
Molecular Formula C5H9N3S.ClH
Molecular Weight 179.671
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-ISOTHIOUREIDOBUTYRONITRILE HYDROCHLORIDE

SMILES

Cl.NC(=N)SCCCC#N

InChI

InChIKey=NCXJZJFDQMKRKM-UHFFFAOYSA-N
InChI=1S/C5H9N3S.ClH/c6-3-1-2-4-9-5(7)8;/h1-2,4H2,(H3,7,8);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 C5H9N3S
Molecular Weight 143.21
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

4-Isothioureidobutyronitrile (Kevetrin) is a small molecule that has demonstrated the potential of becoming a breakthrough cancer treatment by inducing activation of p53. It is a water-soluble, small molecule and activator of the tumor suppressor protein p53, with potential antineoplastic activity. Upon intravenous administration, 4-thioureidobutyronitrile activates p53 which in turn induces the expressions of p21 and PUMA (p53 up-regulated modulator of apoptosis), thereby inhibiting cancer cell growth and causing tumor cell apoptosis. 4-Thioureidobutyronitrile may be effective in drug-resistant cancers with mutated p53. p53 tumor suppressor, a transcription factor regulating the expression of many stress response genes and mediating various anti-proliferative processes, is often mutated in cancer cells. Cellceutix continues to build upon the successful Phase 1 trial evaluating Kevetrin in treating advanced solid tumors conducted at Dana-Farber Cancer Institute and Beth Israel Deaconess Medical Center. Kevetrin, in IV form, was shown to safely modulate, in a non-genotoxic manner, the key tumor suppressor protein p53 as measured through increased expression of p21, a key downstream biomarker of p53. Cellceutix is advancing Kevetrin under an Orphan Drug designation from the Food and Drug Administration (FDA) for the treatment of ovarian cancer, pancreatic cancer and childhood retinoblastoma.

Approval Year

Patents

Sample Use Guides

Ovarian Cancer: Kevetrin 250 mg/m2 IV per dose every other day (q.o.d.)/ 3 doses per week (750 mg/m2 per week), for 3 weeks (single cycle; total 9 doses) Follow-up For 3 weeks after Kevetrin treatment ends; Kevetrin 350 mg/m2 IV per dose every other day (q.o.d.)/ 3 doses per week (1050 mg/m2 per week), for 3 weeks (single cycle; total 9 doses) Follow-up For 3 weeks after Kevetrin treatment ends
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:42:22 GMT 2023
Edited
by admin
on Sat Dec 16 09:42:22 GMT 2023
Record UNII
NL6L2371DP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-ISOTHIOUREIDOBUTYRONITRILE HYDROCHLORIDE
Common Name English
KEVETRIN HYDROCHLORIDE
Common Name English
CARBAMIMIDOTHIOIC ACID, 3-CYANOPROPYL ESTER, MONOHYDROCHLORIDE
Common Name English
Code System Code Type Description
FDA UNII
NL6L2371DP
Created by admin on Sat Dec 16 09:42:22 GMT 2023 , Edited by admin on Sat Dec 16 09:42:22 GMT 2023
PRIMARY
PUBCHEM
49778916
Created by admin on Sat Dec 16 09:42:22 GMT 2023 , Edited by admin on Sat Dec 16 09:42:22 GMT 2023
PRIMARY
CAS
66592-89-0
Created by admin on Sat Dec 16 09:42:22 GMT 2023 , Edited by admin on Sat Dec 16 09:42:22 GMT 2023
PRIMARY
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