CAS NO. |
Products Name |
148081-72-5 |
HTHQ |
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HTHQ, which is a hydroquinone monoalkyl ether, is a potent anti-oxidative agent, even at low dose levels. |
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1219810-16-8 |
RSL3 (1S,3R-) |
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RSL3 (1S,3R-) is the inhibitor of the glutathione (GSH) peroxidase 4, which can inhibit the cysteine/glutamate amino acid transporter system xc- that blocks GSH synthesis with an IC 50 of 100 nM.[1] [2] |
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180977-44-0 |
GGTI298 |
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GGTI298 is a CAAZ peptidomimetic geranylgeranyltransferase I (GGTase I) inhibitor, strongly inhibiting the processing of geranylgeranylated Rap1A with little effect on processing of farnesylated Ha-Ras, with IC50 values of 3 and > 10 μM, respectively. |
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1210416-52-6 |
LGH447 |
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PIM447 is novel pan-PIM kinase inhibitor, including Moloney Murine Leukemia (PIM) 1, 2, and 3 Kinase. |
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923978-27-2 |
Elafibranor (GFT505) |
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Elafibranor (GFT505) is an agonist of the peroxisome proliferator-activated receptor(PPAR)-α and -δ, induces resolution of nonalcoholic steatohepatitis without fibrosis worsening. |
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890128-81-1 |
BFH-772 |
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BFH772 is a potent oral VEGFR2 inhibitor, which is highly effective at targeting VEGFR2 kinase with an IC50 value of 3 nM. |
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133052-90-1 |
GF109203X |
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Bisindolylmaleimide I (GF109203X) is a highly selective, cell-permeable, and reversible protein kinase C (PKC) inhibitor with a Ki value of 14 nM. |
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1173097-76-1 |
U0126-EtOH |
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U0126-EtOH(U-0126) is a highly selective inhibitor of MEK1/2 with IC50 of 0.07 μM/0.06 μM, 100-fold higher affinity for ΔN3-S218E/S222D MEK than PD098059. |
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1675203-84-5 |
PD-L1 inhibitor 1 |
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BMS-202 is a inhibitor of the PD-1 (Programmed death- 1) /PD-Ll (Programmed death-ligand 1) protein/protein interaction, extracted from patent WO/2015034820 A1, compound example 202. |
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