MS170

MS170 Suppliers list
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Company Name: Nantong QuanYi Biotechnology Co., Ltd  
Tel: 0513-66337626 18051384581
Email: sales@chemhifuture.com
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Company Name: Aladdin Scientific  
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Email: tp@aladdinsci.com
MS170 Basic information
Product Name:MS170
Synonyms:MS170
CAS:2376136-61-5
MF:C45H56ClN9O7
MW:870.44
EINECS:
Product Categories:
Mol File:2376136-61-5.mol
MS170 Structure
MS170 Chemical Properties
Boiling point 1114.1±65.0 °C(Predicted)
density 1.341±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
form Solid
pka10.75±0.40(Predicted)
color Light yellow to yellow
Safety Information
MSDS Information
MS170 Usage And Synthesis
UsesMS170 is a potent and selective PROTAC AKT degrader. MS170 depletes cellular total AKT (T-AKT) with the DC50 value of 32 nM. MS170 binds to AKT1, AKT2, and AKT3 with Kds of 1.3 nM, 77 nM, and 6.5 nM, respectively[1].
Biological ActivityMS170 is a potent and selective PROTAC AKT degrader. MS170 depletes cellular total AKT (T-AKT) with the DC50 value of 32 nM. MS170 binds to AKT1, AKT2, and AKT3 with Kds of 1.3 nM, 77 nM, and 6.5 nM, respectively[1]. Cereblon (CRBN)-recruiting degrader MS170 is an effective AKT degrader without a ″hook effect″. MS170 selectively induces robust AKT protein degradation, inhibits downstream signaling, and suppresses cancer cell proliferation. MS170 concentration- and time-dependently induces AKT degradation through the ubiquitin-proteasome system (UPS)[1]. MS170 (10 nM-10 μM) effectively inhibits the proliferation in multiple cancer cell lines[1]. MS170 (1 nM-10 μM) concentration-dependently depletes cellular total AKT (T-AKT) with the DC50 value of 32±18 nM[1]. MS170 (a single intraperitoneal injection at a dose of 50 mg/kg) is bioavailable in mice via IP injection[1].
in vivo

MS170 (a single intraperitoneal injection at a dose of 50 mg/kg) is bioavailable in mice via IP injection[1].

Animal Model:Male Swiss albino mice[1]
Dosage:Single 50 mg/kg(Pharmacokinetic Analysis)
Administration:IP injection over 8 h
Result:Bioavailable in mouse PK studies. The Cmax is1.4 μM at 2 h.
IC 50Akt1: 1.3 nM (Kd); Akt2: 77 nM (Kd); Akt3: 6.5 nM (Kd); CRBN-DDB1
References[1]. Yu X, et al. Design, Synthesis, and Evaluation of Potent, Selective, and Bioavailable AKT Kinase Degraders. J Med Chem. 2021;64(24):18054-18081.
MS170 Preparation Products And Raw materials
Tag:MS170(2376136-61-5) Related Product Information
dTAGV-1 GlyT2-IN-1 Y-27632 DT2216 AU-15330 AKT2 Protein, HUMAN (ACTIVE, SF9, GST)