Indoluidin E is an indoluidin D derivative, and potent selective dihydroorotate dehydrogen..
Vamotinib (PF-114) is a potent, selective and orally available inhibitor of native (IC50=0..
Lirafugratinib (RLY-4008, RYL4008) is a potent, highly selective and irreversible FGFR2 in..
MTK458 (MTK-458) is a potent, selective and brain penetrant PINK1 activator, MTK-458 promo..
SW222746 (SW 222746) is a potent selective, orally active inhibitor of 15-Prostaglandin de..
TBA-7371 (TBA7371, AZ 7371) is a potent, non-covalent inhibitor of decaprenylphosphoryl-&b..
MR120 (CCR6 antagonist 1b) is a potent, selective CCR6 antagonist, disrupts the CCL20-indu..
FHP01 (BA103) is a potent, small molecule inhibitor of DDX3X helicase activity with IC50 o..
GLPG2451 (GLPG 2451) is a potent potentiator of cystic fibrosis transmembrane conductance ..
BDM44768 (BDM 44768) is a potent, selective catalytic site inhibitor of insulin-degrading ..
BDM88951 (BDM 88951) is a highly potent, selective inhibitor of endoplasmic reticulum amin..
Vidofludimus (IMU-838) is a selective and potent second-generation dihydroorotate dehydrog..
H3B-6545 is a potent, covalent antagonist of both wild-type and mutant estrogen receptor a..
MPT0B390 (B390) is a selective HDAC1/2 inhibitor and an effective inducer of metalloprotei..
Z0933M is a potent S phase kinase-associated protein 1 (Skp1) inhibitor with Kd of 54 nM, ..
cjoc42 is a specific small molecule that is capable of binding to gankyrin (ITC Kd=580 nM)..
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