Ifflaiamine is a natural product isolated and purified from the wood of Flindersia ifflaiana F. Muell.

iGOT1-01 is a potent aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1; GOT1) inhibitor. iGOT1-01 has IC50s of 85 μM and 11.3 μM in MDH coupled GOT1 enzymatic assay and GOT1/GLOX/HRP assay, respectively. iGOT1-01 has anti-cancer activity.

iGOT1-01 is a potent aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1; GOT1) inhibitor. iGOT1-01 has IC50s of 85 μM and 11.3 μM in MDH coupled GOT1 enzymatic assay and GOT1/GLOX/HRP assay, respectively. iGOT1-01 has anti-cancer activity.

iGOT1-01 is a potent aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1; GOT1) inhibitor. iGOT1-01 has IC50s of 85 μM and 11.3 μM in MDH coupled GOT1 enzymatic assay and GOT1/GLOX/HRP assay, respectively. iGOT1-01 has anti-cancer activity.

iGOT1-01 is a potent aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1; GOT1) inhibitor. iGOT1-01 has IC50s of 85 μM and 11.3 μM in MDH coupled GOT1 enzymatic assay and GOT1/GLOX/HRP assay, respectively. iGOT1-01 has anti-cancer activity.

iGOT1-01 is a potent aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1; GOT1) inhibitor. iGOT1-01 has IC50s of 85 μM and 11.3 μM in MDH coupled GOT1 enzymatic assay and GOT1/GLOX/HRP assay, respectively. iGOT1-01 has anti-cancer activity.

IHR 1 is a potent Smo antagonist with IC50 of 7.6 nM.

IHR 1 is a potent Smo antagonist with IC50 of 7.6 nM.

IHR 1 is a potent Smo antagonist with IC50 of 7.6 nM.

IHR 1 is a potent Smo antagonist with IC50 of 7.6 nM.

IITZ-01 is an inhibitor of lysosomotropic autophagy. It can enhance autophagosome accumulation and inhibit autophagosomal degradation that finally resulting in the inhibition of autophagy.

IKK 16 HCl is a selective inhibitor of IκB kinase (IKK) with IC50s of 40, 70 and 200 nM for IKKβ, IKK complex and IKKα respectively.

IKK 16 HCl is a selective inhibitor of IκB kinase (IKK) with IC50s of 40, 70 and 200 nM for IKKβ, IKK complex and IKKα respectively.

IKK 16 HCl is a selective inhibitor of IκB kinase (IKK) with IC50s of 40, 70 and 200 nM for IKKβ, IKK complex and IKKα respectively.

IKK 16 HCl is a selective inhibitor of IκB kinase (IKK) with IC50s of 40, 70 and 200 nM for IKKβ, IKK complex and IKKα respectively.

Ikshusterol is a natural product isolated and purified from the herbs of Lycopodium obscurum Linn..

Ikshusterol is a natural product isolated and purified from the herbs of Lycopodium obscurum Linn..

Ilaprazole inhibited TOPK activities with high affinity and selectivity.

Ilaprazole inhibited TOPK activities with high affinity and selectivity.

Ilaprazole inhibited TOPK activities with high affinity and selectivity.

Ilaprazole inhibited TOPK activities with high affinity and selectivity.

Ilaprazole inhibited TOPK activities with high affinity and selectivity.

Ilicic acid is a natural product isolated and purified from the bark of Laggera pterodonta with anti-hyperglycemic and anti-inflammatory activities.

Ilicic acid is a natural product isolated and purified from the bark of Laggera pterodonta with anti-hyperglycemic and anti-inflammatory activities.

ILK-IN-2 is a ILK inhibitor.

ILK-IN-2 is a ILK inhibitor.

ILK-IN-2 is a ILK inhibitor.

ILK-IN-3 is an integrin linked kinase inhibitor.

ILK-IN-3 is an integrin linked kinase inhibitor.

ILK-IN-3 is an integrin linked kinase inhibitor.

ILK-IN-3 is an integrin linked kinase inhibitor.

ILK-IN-3 is an integrin linked kinase inhibitor.

Iloprost is a synthetic analogue of prostacyclin PGI2.

Iloprost is a synthetic analogue of prostacyclin PGI2.

Iloprost is a synthetic analogue of prostacyclin PGI2.

Iloprost is a synthetic analogue of prostacyclin PGI2.

Iloprost is a synthetic analogue of prostacyclin PGI2.

Iloprost is a synthetic analogue of prostacyclin PGI2.