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I649092-50mgIDO1/TDO-IN-4 is a potent IDO1/TDO dual inhibitor, with IC 50 values of 3.53 μM (IDO1) and 1.15 μM (TDO). IDO1/TDO-IN-4 forms hydrogen bond with IDO1 , and π−π stacking interaction with TDO. IDO1/TDO-IN-4 can be used in the research of depression,
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I649092-5mgIDO1/TDO-IN-4 is a potent IDO1/TDO dual inhibitor, with IC 50 values of 3.53 μM (IDO1) and 1.15 μM (TDO). IDO1/TDO-IN-4 forms hydrogen bond with IDO1 , and π−π stacking interaction with TDO. IDO1/TDO-IN-4 can be used in the research of depression,
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I651200-10mgIDO2-IN-1 is an orally active and potent Indoleamine 2,3-dioxygenase 2 ( IDO2 ) inhibitor with an IC 50 value of 112 nM. IDO2-IN-1 can be used for inflammatory autoimmunity researchIn VitroIDO2-IN-1 (compound 22) shows stronger inhibition on IDO2
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I651200-5mgIDO2-IN-1 is an orally active and potent Indoleamine 2,3-dioxygenase 2 ( IDO2 ) inhibitor with an IC 50 value of 112 nM. IDO2-IN-1 can be used for inflammatory autoimmunity researchIn VitroIDO2-IN-1 (compound 22) shows stronger inhibition on IDO2
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I650755-10mgIfetroban (BMS-180291) sodium is an orally active antagonist of thromboxane A2 ( TXA2 ) or prostaglandin H2 ( PGH2 ) receptor. Ifetroban sodium shows antiplatelet activity, and inhibits tumor cell migration without affecting cell proliferation.
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I650755-1mgIfetroban (BMS-180291) sodium is an orally active antagonist of thromboxane A2 ( TXA2 ) or prostaglandin H2 ( PGH2 ) receptor. Ifetroban sodium shows antiplatelet activity, and inhibits tumor cell migration without affecting cell proliferation.
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I650755-5mgIfetroban (BMS-180291) sodium is an orally active antagonist of thromboxane A2 ( TXA2 ) or prostaglandin H2 ( PGH2 ) receptor. Ifetroban sodium shows antiplatelet activity, and inhibits tumor cell migration without affecting cell proliferation.
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I649678-10mgIGUANA-1 is a potent inhibitor of ALDH1B1 , which is a mitochondrial enzyme that promotes colorectal and pancreatic cancer . IGUANA-1 has significant inhibition against cancer cellsForm:SolidIC50&: Target:ALDH1.
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I649678-25mgIGUANA-1 is a potent inhibitor of ALDH1B1 , which is a mitochondrial enzyme that promotes colorectal and pancreatic cancer . IGUANA-1 has significant inhibition against cancer cellsForm:SolidIC50&: Target:ALDH1.
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I649678-50mgIGUANA-1 is a potent inhibitor of ALDH1B1 , which is a mitochondrial enzyme that promotes colorectal and pancreatic cancer . IGUANA-1 has significant inhibition against cancer cellsForm:SolidIC50&: Target:ALDH1.
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I649678-5mgIGUANA-1 is a potent inhibitor of ALDH1B1 , which is a mitochondrial enzyme that promotes colorectal and pancreatic cancer . IGUANA-1 has significant inhibition against cancer cellsForm:SolidIC50&: Target:ALDH1.
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I646982-10mgIHMT-PI3Kδ-372 is a potent and selective PI3Kδ inhibitor with an IC 50 of 14 nM. IHMT-PI3Kδ-372 shows high selectivity over other class I PI3Ks (56∼83 fold) and other protein kinases. IHMT-PI3Kδ-372 can be uesd for chronic obstructive pulmonary