ChemicalBook--->CAS DataBase List--->1523437-16-2

1523437-16-2

1523437-16-2 Structure

1523437-16-2 Structure
IdentificationBack Directory
[Name]

ML291
[CAS]

1523437-16-2
[Synonyms]

ML291
ML291 >=98% (HPLC)
[EINECS(EC#)]

808-922-2
[Molecular Formula]

C16H16ClN3O6S
[MDL Number]

MFCD28016591
[MOL File]

1523437-16-2.mol
[Molecular Weight]

413.83
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

≤1mg/ml in DMSO;10mg/ml in dimethyl formamide
[form ]

crystalline solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H315-H335
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Hazard InformationBack Directory
[Biological Activity]

ml-291 is an apoptosis inducer.apoptosis, a process of programmed cell death, occurs in multi-cellular organisms. biochemical events result in characteristic cell changes (morphology) and death. these changes include cell shrinkage, nuclear fragmentation, blebbing, chromatin condensation, chromosomal dna fragmentation, as well as global mrna decay.
[in vitro]

ml-291 was identified as a novel activator of the apoptotic arm of the unfolded protein response (upr), but not the adaptive arm. specifically, ml-291 could activate signaling via perk/eif2α/chop with ec50 value of 762 nm but not through ire1/xbp1. moreover, ml-291 induced apoptosis in mouse embryonic fibroblasts overexpressing chop, but not in wild-type or chop knockout cells. ml-291 showed minimal activity against a panel of 67 receptors, ion channels, as well as transporters, with the exception of the dopamine transporter with 68% inhibition. in addition, ml-291 showed greater cytotoxicity than average antitumor cell cytotoxicity against colon, melanoma, and renal cancer cell lines in an nci-60 panel [1].
[References]

[1] flaherty, d. p.,golden, j.e.,liu, c., et al. selective small molecule activator of the apoptotic arm of the upr. probe reports from the nih molecular libraries program (2012).
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