ML291

ML291 Suppliers list
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Products Intro: Product Name:ML291
CAS:1523437-16-2
Purity:98% Package:1mg;5mg;10mg
Company Name: Tianjin Kailiqi Biotechnology Co., Ltd.  
Tel: 15076683720
Email: klq@cw-bio.com
Products Intro: Product Name:ML-291
CAS:1523437-16-2
Purity:大于98% Package:1g,5g,10g,25g根据客户需要分装 Remarks:Not For Human Use, Lab Use Only.
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:ML-291
CAS:1523437-16-2
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
Company Name: MedBioPharmaceutical Technology Inc  
Tel: 021-69568360 18916172912
Email: order@med-bio.cn
Products Intro: Product Name:ML291
CAS:1523437-16-2
Purity:98% Package:5mg; 10mg; 25mg Remarks:Medbio
Company Name: Energy Chemical  
Tel: 021-58432009 400-005-6266
Email: marketing@energy-chemical.com
Products Intro: Product Name:ML291 >=98% (HPLC)
CAS:1523437-16-2
Purity:NULL Package:25mg;5mg Remarks:NULL
ML291 Basic information
Product Name:ML291
Synonyms:ML291;ML291 >=98% (HPLC);2-Furancarboxamide, N-[4-[(4-chloro-1-piperidinyl)sulfonyl]phenyl]-5-nitro-
CAS:1523437-16-2
MF:C16H16ClN3O6S
MW:413.83
EINECS:808-922-2
Product Categories:
Mol File:1523437-16-2.mol
ML291 Structure
ML291 Chemical Properties
density 1.56±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility ≤1mg/ml in DMSO;10mg/ml in dimethyl formamide
form crystalline solid
pka11.24±0.70(Predicted)
color Off-white to light yellow
Safety Information
MSDS Information
ML291 Usage And Synthesis
Biological Activityml-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 vitroml-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).
ML291 Preparation Products And Raw materials
Tag:ML291(1523437-16-2) Related Product Information
5-(1,3-Benzodioxol-5-yl)-N-[(3,5-dichlorophenyl)methyl]-4-pyrimidinamine hydrochloride ML115 ML246 5-[6-(4-Methoxyphenyl)pyrazolo[1,5-a] ML318 ML349 ML355 ML198 ML402 1-(4-(4-(benzo[d][1,3]dioxole-5-carbonyl)piperazin-1-yl)phenyl)ethan-1-one 2-(3,4-dichlorophenyl)-N-[4-(1,2-oxazol-3-ylsulfamoyl)phenyl]acetamide ML-228 ML-098 [(3R)-3-(Hydroxymethyl)-1-piperidinyl][4-[2-(4-methoxyphenyl)ethynyl]phenyl]-methanone Nodinitib-1 9-Azabicyclo[3.3.1]nonane-9-acetamide, N-(2-chlorophenyl)-3-[(3,4,5-trimethoxybenzoyl)amino]-, (3-exo)-