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G650117-100mgGSK163090 is a potent, selective and orally active 5-HT 1A/1B/1D receptor antagonist with pK i values of 9.4/8.5/9.7, respectively. GSK163090 inhibits the functional activity of serotonin reuptake transporter (SerT) with a pK i value of 6.1.
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G650117-10mgGSK163090 is a potent, selective and orally active 5-HT 1A/1B/1D receptor antagonist with pK i values of 9.4/8.5/9.7, respectively. GSK163090 inhibits the functional activity of serotonin reuptake transporter (SerT) with a pK i value of 6.1.
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G650117-50mgGSK163090 is a potent, selective and orally active 5-HT 1A/1B/1D receptor antagonist with pK i values of 9.4/8.5/9.7, respectively. GSK163090 inhibits the functional activity of serotonin reuptake transporter (SerT) with a pK i value of 6.1.
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G650117-5mgGSK163090 is a potent, selective and orally active 5-HT 1A/1B/1D receptor antagonist with pK i values of 9.4/8.5/9.7, respectively. GSK163090 inhibits the functional activity of serotonin reuptake transporter (SerT) with a pK i value of 6.1.
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G656138-1mlGSK163090 is a potent, selective and orally active 5-HT 1A/1B/1D receptor antagonist with pK i values of 9.4/8.5/9.7, respectively. GSK163090 inhibits the functional activity of serotonin reuptake transporter (SerT) with a pK i value of 6.1.
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G649831-10mgGSK1790627 is the N-deacetylated metabolite of Trametinib ( HY-10999 ). Trametinib is an orally active MEK inhibitor, and activates autophagy and induces apoptosis.In VitroGSK1790627 (1, 10 and 50 μM, 60 min) is stable in the presence of recombinant
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G649831-25mgGSK1790627 is the N-deacetylated metabolite of Trametinib ( HY-10999 ). Trametinib is an orally active MEK inhibitor, and activates autophagy and induces apoptosis.In VitroGSK1790627 (1, 10 and 50 μM, 60 min) is stable in the presence of recombinant
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G649831-50mgGSK1790627 is the N-deacetylated metabolite of Trametinib ( HY-10999 ). Trametinib is an orally active MEK inhibitor, and activates autophagy and induces apoptosis.In VitroGSK1790627 (1, 10 and 50 μM, 60 min) is stable in the presence of recombinant
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G649831-5mgGSK1790627 is the N-deacetylated metabolite of Trametinib ( HY-10999 ). Trametinib is an orally active MEK inhibitor, and activates autophagy and induces apoptosis.In VitroGSK1790627 (1, 10 and 50 μM, 60 min) is stable in the presence of recombinant
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G646442-10mgGSK1940029 (SCD inhibitor 1) is a stearoyl-coa desaturase ( SCD ) inhibitor extracted from patent WO/2009060053 A1, compound example 16.In VitroGSK1940029 (SCD inhibitor 1) is a stearoyl-coa desaturase (SCD), which can be used to treat and/or
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G646442-1mgGSK1940029 (SCD inhibitor 1) is a stearoyl-coa desaturase ( SCD ) inhibitor extracted from patent WO/2009060053 A1, compound example 16.In VitroGSK1940029 (SCD inhibitor 1) is a stearoyl-coa desaturase (SCD), which can be used to treat and/or
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G646442-50mgGSK1940029 (SCD inhibitor 1) is a stearoyl-coa desaturase ( SCD ) inhibitor extracted from patent WO/2009060053 A1, compound example 16.In VitroGSK1940029 (SCD inhibitor 1) is a stearoyl-coa desaturase (SCD), which can be used to treat and/or