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Catalog No CAS NO Product name
CR3212
315183-21-2
PAC-1
PAC-1 is known as VO-100 and procaspase activating compound-1; which selectively induces apoptosis, or cell suicide, in cancerous ..
CR3211
883986-34-3
AZD2932
AZD2932 effectively inhibits the activities of VEGFR-2 (IC50, 8 nM), PDGFRβ (IC50,4 nM), Flt-3 (IC50, 7 nM), and c-Kit (IC50, 9 n..
CR3210
38275-34-2
PK11000
PK11000 is a mild thiol alkylator with anticancer activity in several cell lines, especially those with mutationally compromised p..
CR3209
188968-51-6
Cilengitide
Cilengitide (EMD 121974) is the αvβ3 and αvβ5 integrin receptor antagonist. In cell adhesion studies assessing the human m..
CR3208
445295-04-5
CP671305
CP-671305 is a potent, selective and orally active inhibitor of phosphodiesterase-4-D (PDE4-D) with IC50 of 3 nM. In Vitro: CP-671..
CR3207
1572510-42-9
JNJ-632
JNJ-632 is a potent HVV capsid assembly modulator and HBV replication inhibitor with EC50 of 100-200 nM for genotypes A-D. Adminis..
CR3206
68099-86-5
Bepridil hydrochloride
Bepridil Hydrochloride is the hydrochloride salt form of bepridil, a calcium antagonist and class IV anti-arrhythmic agent. Beprid..
CR3205
18228-17-6
KG-501
KG-501 (2-naphthol-AS-E-phosphate) is a cAMP response element-binding protein (CREB) inhibitor that disrupts CREB-dependent transc..
CR3251
154039-60-8
Marimastat
Marimastat, aslo known as BB-2516 and TA-2516, is an orally-active synthetic hydroxamate and inhibitor of matrix metalloproteinase..
CR3204
1169562-71-3
BMS-863233 HCl
BMS-863233, also known as XL-413, is an orally bioavailable cell division cycle 7 homolog (CDC7) kinase inhibitor with potential a..
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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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