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ChemicalBook--->CAS DataBase List--->488832-69-5

488832-69-5

488832-69-5 Structure

488832-69-5 Structure
IdentificationBack Directory
[Name]

Elesclomol
[CAS]

488832-69-5
[Synonyms]

CS-482
STA-4783
elesclomol
STA-4783;STA4783
Elesclomol USP/EP/BP
ElescloMol (STA-4783)
N1',N3'-dimethyl-N1',N3'-di(phenylcarbonothioyl)malonohydrazide
1,3-Bis[2-methyl-2-(phenylthioxomethyl)hydrazide]propanedioic acid
Propanedioic acid, 1,3-bis[2-methyl-2-(phenylthioxomethyl)hydrazide]
elescloMol, N'1,N'3-diMethyl-N'1,N'3-di(phenylcarbonothioyl)Malonohydrazide
[Molecular Formula]

C19H20N4O2S2
[MDL Number]

MFCD12911784
[MOL File]

488832-69-5.mol
[Molecular Weight]

400.52
Chemical PropertiesBack Directory
[density ]

1.313
[storage temp. ]

Store at -20°C
[solubility ]

insoluble in H2O; ≥20.15 mg/mL in DMSO; ≥5.68 mg/mL in EtOH with gentle warming and ultrasonic
[form ]

solid
[pka]

7.99±0.70(Predicted)
[color ]

Light yellow to yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard InformationBack Directory
[Definition]

ChEBI: A carbohydrazide obtained by formal condensation of the carboxy groups of malonic acid with the hydrino groups of two molar equivalents of N-methylbenzenecarbothiohydrazide
[Biological Activity]

elesclomol (also known as sta-4783), originally identified in a cell-based phenotypic screen for proapoptotic activity, is a novel small-molecule that potently induces apoptosis of cancer cells through the rapid generation of reactive oxygen species (ros) and the induction of unmanageable levels of oxidative stress. elesclomol exhibits autitumor activity against a broad spectrum of types of cancer cell in human tumor xengograft models due to its excessive ros production and elevated levels of oxidative stress leading to the death of cancer cells. elesclomol is currently being studies as a novel cancer therapeutic, in which it has demonstrated ability to prolong progression-free survival in study subjects.ronald k. blackman, kahlin cheung-ong, marinella gebbia, david a. proia, suqin he, jane kepros, aurelie jonneaux, philippe marchetti, jerome kluza, patricia e. rao, yumiko wada, guri giaever, corey nislow. mitochondrial electron transport is the cellular target of the oncology drug elesclomol. plos one 2012; 7(1): e29798jessica r. kirshner, suqin he, vishwasenani balasubramanyam, jane kepros, chin-yu yang, mei zhang, zhenjian du, james barsoum, and john bertin. elesclomol induces cancer cell apoptosis through oxidative stress. mol cancer ther 2008; 7:2319-2327
[target]

HSP70
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

Elesclomol(488832-69-5)1HNMR
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