<Suppliers Price>

NSC 319726

Names

[ CAS No. ]:
71555-25-4

[ Name ]:
NSC 319726

[Synonym ]:
N'-[(1E)-1-(2-Pyridinyl)ethylidene]-1-azetidinecarbothiohydrazide
Azetidine-1-thiocarboxylic acid 2-[1-(2-pyridyl)ethylidene]hydrazide
1-Azetidinecarbothioic acid, 2-[(1E)-1-(2-pyridinyl)ethylidene]hydrazide
Azetidine-1-thiocarboxylic acid 2-[1-(2-pyridinyl)ethylidene]hydrazide
1-AZETIDINESULFONAMIDE
azetidine-1-sulphonamide
NSC319726
1-Azetidinecarbothioic acid [1-(2-pyridinyl)ethylidene]hydrazide

Biological Activity

[Description]:

NSC319726 is a mutant p53R175 reactivator; inhibits growth of fibroblasts expressing the p53R175 mutation (IC50 = 8 nM); shows no inhibition for p53 wild-type cells.IC50 value: 8 nM [1]Target: mutant p53R175 reactivatorin vitro: For NSC319726, the effect was even greater as the IC50for the 175 mutant was 8 nM while the IC50 of the WT was not reached. NSC319726 did not induce WT p53 protein levels or transcriptional activity as common cytotoxic agents such as etoposide do in vitro. NSC319726 exhibited a much higher sensitivity for the MEF-p53R172H/R172H cell line as compared to the p53+/+ and p53-/- controls. NSC319726 treatment of a MEF cell line derived from p53R172H/R172H mice resulted in aloss of PAB240 immunoflouresence staining. in vivo: At a dose of 1mg/kg, tumor growth of the H460 (p53+/+) and MDAMB468 (p53R273W) xenografts was not inhibited relative to the vehicle control whereas tumor growth was significantly inhibited in the TOV112D (p53R175H) xenografts. When we lowered the dose ten-fold to 0.1 mg/kg in the TOV112D mice, we observed only a small difference in tumor growth inhibition demonstrating both a dosage effect of the drug and a larger therapeutic window.Taken together, these findings provide in vivo evidence for allele specific p53 mutant reactivation.

[Related Catalog]:

Signaling Pathways >> Apoptosis >> MDM-2/p53
Research Areas >> Cancer

[References]

[1]. Yu X, et al. Allele-specific p53 mutant reactivation. Cancer Cell. 2012 May 15;21(5):614-25.


[Related Small Molecules]

Pifithrin-α hydrobromide | RG7388 | Nutlin-3a | AMG232 | Pifithrin-β (hydrobromide) | Stylomycin aminonucleoside | RG7112 | APR-246 | NVP-HDM201 | SAR 405838 | RITA (NSC 652287) | NVP-CGM097 | Tenovin-1 | SJ 172550

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
367.7±34.0 °C at 760 mmHg

[ Molecular Formula ]:
C11H14N4S

[ Molecular Weight ]:
234.321

[ Flash Point ]:
176.2±25.7 °C

[ Exact Mass ]:
234.093918

[ PSA ]:
72.61000

[ LogP ]:
0.17

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.659

[ Storage condition ]:
-20°C

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CM4387000
CHEMICAL NAME :
1-Azetidinethiocarboxylic acid, (1-(2-pyridyl)ethylidene)hydrazide
CAS REGISTRY NUMBER :
71555-25-4
LAST UPDATED :
199612
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C11-H14-N4-S
MOLECULAR WEIGHT :
234.35
WISWESSER LINE NOTATION :
T6NJ BY1&UNMYUS&- AT4NTJ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
DNA inhibition
TEST SYSTEM :
Microorganism - not otherwise specified
DOSE/DURATION :
2460 ug/L
REFERENCE :
AMACCQ Antimicrobial Agents and Chemotherapy. (American Soc. for Microbiology, 1913 I St., NW, Washington, DC 20006) V.1- 1972- Volume(issue)/page/year: 18,317,1980

Precursor & DownStream


Related Compounds