chemical

Saracatinib

7189

50 mg

125 USD

7189

7189/50

Saracatinib

Potent and selective Src tyrosine kinase family inhibitor; anticancer; antiviral; orally bioavailable

Src Family Kinase Inhibitors

Small Molecules

50 mg

98%

542.03

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Potent and selective Src tyrosine kinase family inhibitor (IC50 = 4-10 nM). Inhibits Src, c-Yes, Fyn, Lyn, Blk, Fgr, and Lck. Exhibits selectivity over other tyrosine kinases (IC50 values are 30, 66 and 200 nM for v-Abl, EGFR and c-Kit, respectively). Suppresses invasion of HT1080 cells through a collagen matrix and inhibits metastasis in a murine model of bladder cancer. Inhibits the growth of prostate cancer cell lines. Also suppresses MERS-CoV replication at the early stage of replication (EC50 = 2.9 M) and displays broad-spectrum activity against other human coronaviruses. Also blocks dengue virus RNA replication. Reverses memory deficit in a mouse AD model and rescues synapse density. Inhibits osteoclast activity, resorption and formation. Induces autophagy. Orally bioavailable.

7189

AZD0530 AZD_0530 potent selective Src tyrosine kinase family inhibitors inhibits Src c-Yes Fyn Lyn Blk Fgr Lck MERS-cov Covid-19 antiviral dengue viruses AD Alzheimers disease osteoclast activity AZD 0530 Src Kinases COVID-19 Coronavirus 7189,

Potent and selective Src tyrosine kinase family inhibitor; anticancer; antiviral; orally bioavailable

N-(5-Chloro-1,3-benzodioxol-4-yl)-7-[2-(4-methyl-1-piperazinyl)ethoxy]-5-[(tetrahydro-2H-pyran-4-yl)oxy]-4-quinazolinamine

C 27 H 32 ClN 5 O 5

C27H32ClN5O5

379231-04-6

125

125 USD

AZD 0530

Store at -20°C