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Catalog No CAS NO Product name
CR3255
163769-88-8
YM-90709
YM-90709 is an interleukin-5 receptor antagonist. YM-90709 inhibits the binding of IL-5 to its receptor on peripheral human eosino..
CR1372
741713-40-6
R547
R547 is orally bioavailable diaminopyrimidine cyclin-dependent kinase inhibitor (CDKI) with potential antineoplastic activity. CDK..
CR1371
778270-11-4
GNF-2
GNF-2 is an allosteric inhibitor of Bcr-abl tyrosine kinase activity (IC50 = 267 nM); inhibits proliferation and induces apoptosis..
CR1370
931398-72-0
IOX2
IOX 2 is a potent inhibitor of HIF-1α prolyl hydroxylase-2 (PHD2) (IC50 = 21 nM). IOX 2 displays over 100-fold selectivity for PH..
CR1369
1260141-27-2
Vonoprazan Fumarate
Vonoprazan Fumarate, also known as TAK438, is a new medicine for treating acid-related diseases with a novel mechanism of action c..
CR1368
878739-06-1
AZ-628
AZ-628 is a selective, orally available Raf inhibitor with excellent pharmacokinetic properties and robust tumor growth inhibition..
CR1367
956104-40-8
Apalutamide
Apalutamide, also known as ARN-509 and JNJ-56021927 , is an androgen receptor antagonist with potential antineoplastic activity. A..
CR1366
211555-04-3
WHI-P154
WHI-P154 is a JAK3 inhibitor with IC50 = 1.8 microM. WHI-P154 displays no activity at JAK1 or JAK2. WHI-P154 also Inhibits STAT1 a..
CR1365
153436-54-5
PD153035
PD153035 is a ATP-competitive EGFR inhibitor with an IC50 and Ki of 25 and 6 pM. PD153035 effectively blocks the enhancement of mi..
CR1364
1050500-29-2
AST1306 tosilate
AST-1306 TsOH is a novel irreversible inhibitor of EGFR and ErbB2 with IC50 of 0.5 nM and 3 nM, also effective in mutation EGFR T7..
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Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.
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