|
V0390
|
EPZ-015666 |
1616391-65-1 |
EPZ015666 (GSK-3235025), an analog ofEPZ-015866, is a potent, selective and orally bioavailable inhibitor of PRMT5 (protein arginine methyltransferase) with antineoplastic activity. |
|
V2967
|
PF-05089771 |
1235403-62-9 |
PF-05089771 (PF05089771) is a potent and subtype selective NaV1.7 inhibitor (IC50 = 11 nM) and Nav1.8voltage-gated sodium channelblocker with the potential to be used in the treatment of chronic neuropathic pain. |
|
V0001
|
维奈妥拉 |
1257044-40-8 |
Venetoclax (formerly known as ABT-199 or GDC-0199; Venclexta) is a potent, selective andorally bioavailablesmall molecule inhibitor of theanti-apoptotic protein BCL-2 (B-cell lymphoma-2) with Ki of<0.01 nM. |
|
V0611
|
AZD3463 |
1356962-20-3 |
AZD-3463 (AZD3463) is a novel, potent and selective ALK/IGF1R inhibitor with potential anticancer activity. |
|
V0245
|
阿卡地新 |
2627-69-2 |
Acadesine (also known as NSC105823,AICA-riboside, and AICAR) is a novel and potent AMPK (AMP-activated protein kinase) activatorwith potential antitumor and antidiabetic activity. |
|
V39377
|
DBCO-PEG3-TCO |
|
DBCO-PEG3-TCO is a non-cleavable (non-degradable) ADC linker containing 3 Polyethylene glycol (PEG) units, which may be utilized to prepare Antibody-drug conjugates (ADC). |
|
V0633
|
GW2580 (SC203877) |
870483-87-7 |
GW2580 (also known as SC-203877)is a novel, potent, selective, and orally bioavailable c-Fms kinaseCSF-1R inhibitor with potential antineoplastic activity. |
|
V47750
|
15-去甲-14-氧代赖百当-8(17),12-二烯-18-酸 |
1039673-32-9 |
15-Nor-14-oxolabda-8(17),12E-Diene-18-oic acid (compound 9) is a compound extracted from Chloranthus spicatus. |
|
V20571
|
延命草醇 |
28957-06-4 |
Enmenol is a novel and potent bioactive compound |
|
V0075
|
AZD-1390 |
2089288-03-7 |
AZD1390 (AZD-1390) is a novel, potent, selective, first-in-class orally bioavailable and CNS penetrant inhibitor of Ataxia-telangiectasia mutated (ATM) kinase with potential anticancer activity. |
|
V35046
|
Ditiocarb (Diethyldithiocarbamic acid) |
147-84-2 |
Ditiocarb (Diethyldithiocarbamic acid) is a copper reagent that reacts with Cu2+ solution to form a complex, which increases the copper replacement precipitation rate. |