MB710
CAS No. 2230044-57-0
MB710( MB-710 )
Catalog No. M13571 CAS No. 2230044-57-0
MB710 is a small-molecule p53 mutant Y220C stabilizer, binds tightly to the Y220C pocket and stabilizes p53-Y220C in vitro.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | 1674 | Get Quote |
|
| 50MG | 2682 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameMB710
-
NoteResearch use only, not for human use.
-
Brief DescriptionMB710 is a small-molecule p53 mutant Y220C stabilizer, binds tightly to the Y220C pocket and stabilizes p53-Y220C in vitro.
-
DescriptionMB710 is a small-molecule p53 mutant Y220C stabilizer, binds tightly to the Y220C pocket and stabilizes p53-Y220C in vitro.
-
In VitroCell Viability Assay Cell Line:NUGC3 (mutant p53 Y220C), HUH-7 (mutant p53 Y220C), NUGC4 (p53 WT), HUH-6 cells (p53 WT)Concentration:0-200 μM Incubation Time:72 hours Result:Showed relatively low toxicity against all cell lines tested at concentrations up to 60?μM. NUGC3 was the most sensitive cell line.
-
In Vivo——
-
SynonymsMB-710
-
PathwayApoptosis
-
TargetMDM2-p53
-
RecptorMDM2-p53
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2230044-57-0
-
Formula Weight457.286
-
Molecular FormulaC16H16IN3O3S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 16.67 mg/mL (36.45 mM)
-
SMILESO=C(C1=C2N=C(N(CC)CC)SC2=C(N3C=CC=C3)C(I)=C1O)O
-
Chemical Name2-(diethylamino)-5-hydroxy-6-iodo-7-(1H-pyrrol-1-yl)benzo[d]thiazole-4-carboxylic acid
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Baud MGJ, et al. Eur J Med Chem. 2018 May 25;152:101-114.
molnova catalog
related products
-
Pifithrin-β
A cyclic analog of Pifithrin-α and a small molecule inhibitor of p53.
-
NSC-319726
NSC-319726 (NSC319726) is an allele-specific p53 mutant reactivator.
-
MMRi6
MMRi6 is a small molecule inhibitor that disrupts Mdm2-MdmX RING-RING interaction interactions in vitro and activates p53 in cancer cells.
Cart
sales@molnova.com