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K-756

CAS No.
130017-40-2
Chemical Name:
K-756
Synonyms
K-756;K-756 >=98% (HPLC);K-756,PARP,Inhibitor,poly ADP ribose polymerase,K756,K 756,inhibit;2(1H)-Quinazolinone, 3-[[1-(6,7-dimethoxy-4-quinazolinyl)-4-piperidinyl]methyl]-3,4-dihydro-
CBNumber:
CB03384776
Molecular Formula:
C24H27N5O3
Molecular Weight:
433.5
MDL Number:
MOL File:
130017-40-2.mol
Last updated:2024-07-02 08:54:58

K-756 Properties

Melting point 216-218 °C
Boiling point 680.0±55.0 °C(Predicted)
Density 1.261±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO:4.55(Max Conc. mg/mL);10.5(Max Conc. mM)
pka 14.92±0.20(Predicted)
form Solid
color White to off-white

K-756 price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0035125 K-756 >99.0% 130017-40-2 5mg $180 2021-12-16 Buy
ChemScene CS-0035125 K-756 >99.0% 130017-40-2 10mg $320 2021-12-16 Buy
ChemScene CS-0035125 K-756 >99.0% 130017-40-2 25mg $680 2021-12-16 Buy
Product number Packaging Price Buy
CS-0035125 5mg $180 Buy
CS-0035125 10mg $320 Buy
CS-0035125 25mg $680 Buy

K-756 Chemical Properties,Uses,Production

Description

K-756 is a a selective Wnt/β-catenin pathway inhibitor. K-756 is also a tankyrase (TNKS) inhibitor. K-756 binds to the induced pocket of TNKS and inhibits its enzyme activity. could be a leading compound in the development of anticancer agents.

in vitro

K-756 binds to the induced pocket of TNKS and inhibits its enzyme activity. Moreover, PARP family enzyme assays showed that K-756 is a selective TNKS inhibitor. K-756 inhibited the cell growth of APC-mutant colorectal cancer COLO 320DM and SW403 cells by inhibiting the Wnt/β-catenin pathway. _x000D_ _x000D_ Reference: Mol Cancer Ther. 2016 Jul;15(7):1525-34. https://pubmed.ncbi.nlm.nih.gov/27196752/

in vivo

An in vivo study showed that the oral administration of K-756 inhibited the Wnt/β-catenin pathway in colon cancer xenografts in mice._x000D_ _x000D_ Reference: Mol Cancer Ther. 2016 Jul;15(7):1525-34. https://pubmed.ncbi.nlm.nih.gov/27196752/

target

K-756 is a direct and selective tankyrase (TNKS) inhibitor, which inhibits the ADP-ribosylation activity of TMS1 amd TMLS2 with IC50s of 31 and 36 nM, respectively.

104260-24-4
13790-39-1
130017-40-2
Synthesis of K-756 from 3-(piperidin-4-ylmethyl)-3,4-dihydroquinazolin-2(1H)-one and 4-Chloro-6,7-dimethoxyquinazoline

K-756 Preparation Products And Raw materials

Global( 16)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32760 60
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Aladdin Scientific
+1-+1(833)-552-7181 sales@aladdinsci.com United States 52927 58
Shanghai Chaolan Chemical Technology Center QQ:65489617 15618227136 info@SuperLan-chem.com China 9882 58
Angel Pharmatech, Ltd. 17317130613 3358272972@qq.com China 3248 58
Fan De(Beijing) Biotechnology Co., Ltd. 15911056312 liming@bio-fount.com China 9730 58
Shanghai Dongyang Biotechnology Co., Ltd. 0512-0512-13601744364 13601744364 chemsharker@126.com China 890 58
Chengdu Peter-like Biotechnology Co., Ltd. 028-81700200 18108052721 2850505130@qq.com China 5182 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
Energy Chemical 021-58432009 400-005-6266 marketing1@energy-chemical.com China 44843 58

K-756 Spectrum

K-756 2(1H)-Quinazolinone, 3-[[1-(6,7-dimethoxy-4-quinazolinyl)-4-piperidinyl]methyl]-3,4-dihydro- K-756 >=98% (HPLC) K-756,PARP,Inhibitor,poly ADP ribose polymerase,K756,K 756,inhibit 130017-40-2