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T12432PF-06928215
PF-06928215 is an inhibitor of cGAS (cyclic GMP-AMP Synthase) (IC50 of 4.9 μΜ).
价 格：￥电议型 号：T12432产 地：中国大陆
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T12431PF-06882961
PF-06882961 is an orally bioavailable glucagon-like peptide-1 receptor (GLP-1R) agonist.
价 格：￥电议型 号：T12431产 地：中国大陆
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T12430PF-06821497
PF-06821497 is a selective and orally active Enhancer of Zeste Homolog 2 (EZH2) inhibitor, with robust tumor growth inhibition.
价 格：￥电议型 号：T12430产 地：中国大陆
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T12428LPF-06726304
PF-06726304 shows robust antitumor growth activity. PF-06726304 is an effective and selective EZH2 inhibitor. PF-06726304 inhibits wild-type and Y641N mutant EZH2 (Kis: 0.7 and 3.0 nM, respectively).
价 格：￥电议型 号：T12428L产 地：中国大陆
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T12427Brepocitinib P-TosylatePF-06700841 P-Tosylate
PF-06700841 P-Tosylate is a potent dual inhibitor of Janus kinase 1 (JAK1) and TYK2 (IC50s of 17 nM and 23 nM, respectively).
价 格：￥电议型 号：T12427产 地：中国大陆
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T12425PF-06424439 methanesulfonate
PF-06424439 methanesulfonate is an oral, potent and selective imidazopyridine diacylglycerol acyltransferase 2 (DGAT2) inhibitor(IC50 of 14 nM)[1]. PF-06424439 methanesulfonate is slowly reversible, time-dependent inhibitor, which inhibits DGAT2 in a nonc
价 格：￥电议型 号：T12425产 地：中国大陆
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T12421PF-04885614
PF-04885614 is a potent inhibitor of NaV1.8, has potential for neurological and neurodevelopmental diseases treatment.
价 格：￥电议型 号：T12421产 地：中国大陆
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T11826LCH-7749944GNF-PF-2356
LCH-7749944 effectively suppresses the proliferation of human gastric cancer cells through downregulation of PAK4/c-Src/EGFR/cyclin D1 pathway and induces apoptosis. LCH-7749944 is a potent PAK4 inhibitor with an IC50 of 14.93 μM.
价 格：￥电议型 号：T11826产 地：中国大陆
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T10199GNF-PF-37778-Nitrotryptanthrin
GNF-PF-3777 (8-Nitrotryptanthrin) is a potent inhibitor of human indoleamine 2,3-dioxygenase 2 (hIDO2; Ki: 0.97 μM).
价 格：￥电议型 号：T10199产 地：中国大陆
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T0108Bumetanide布美他尼；PF 1593；Ro 10-6338
Bumetanide is a potent sulfamoylanthranilic acid derivative belonging to the class of loop diuretics. In the brain, bumetanide may prevent seizures in neonates by blocking the bumetanide-sensitive sodium-potassium-chloride cotransporter (NKCC1), thereby i
价 格：￥电议型 号：T0108产 地：中国大陆
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T001-00000003PF-04745637PF 4745637；PF-4745637；PF 04745637；PF4745637；PF04745637
PF-04745637 is a potent and selective TRPA1 antagonist with an IC50 of 17 nM[1].
价 格：￥电议型 号：T001-00000003产 地：中国大陆
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T0108BumetanideBumetanide,PF 1593,Ro 10-6338
Bumetanide is a potent sulfamoylanthranilic acid derivative belonging to the class of loop diuretics. In the brain, bumetanide may prevent seizures in neonates by blocking the bumetanide-sensitive sodium-potassium-chloride cotransporter (NKCC1), thereby i
价 格：￥电议型 号：T0108产 地：美洲
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T10199GNF-PF-3777GNF-PF-3777,8-Nitrotryptanthrin,
GNF-PF-3777 (8-Nitrotryptanthrin) is a potent inhibitor of human indoleamine 2,3-dioxygenase 2 (hIDO2; Ki: 0.97 μM).
价 格：￥电议型 号：T10199产 地：美洲
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T11450GosogliptinGosogliptin,PF-00734200,PF-734200
Gosogliptin is a potent and selective inhibitor of dipeptidyl peptidase-IV (DPP-IV).?
价 格：￥电议型 号：T11450产 地：美洲
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T11826LCH-7749944LCH-7749944,GNF-PF-2356,
LCH-7749944 effectively suppresses the proliferation of human gastric cancer cells through downregulation of PAK4/c-Src/EGFR/cyclin D1 pathway and induces apoptosis.?LCH-7749944 is a potent PAK4 inhibitor with an IC50 of 14.93 μM.?
价 格：￥电议型 号：T11826产 地：美洲
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T12414PF-00356231 hydrochloridePF-00356231 hydrochloride
PF-00356231 hydrochloride is an inhibitor of matrix metalloproteinase MMP-12 with IC50 of 1.4 μM.
价 格：￥电议型 号：T12414产 地：美洲
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T12415PF-00446687PF-00446687
PF-00446687 is a selective agonist of melanocortin-4 receptor (MC4R) (EC50 of 12?±?1 nM).
价 格：￥电议型 号：T12415产 地：美洲
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T12416PF-03654746 TosylatePF-03654746 Tosylate
PF-03654746 Tosylate is selective antagonist of histamine H3 receptor with high brain penetration.
价 格：￥电议型 号：T12416产 地：美洲
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T12417PF-04217903 methanesulfonatePF-04217903 methanesulfonate
PF-04217903 methanesulfonate is a potent ATP-competitive inhibitor of c-Met kinase (Ki of 4.8 nM for human c-Met).
价 格：￥电议型 号：T12417产 地：美洲
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T12419PF-04634817 succinatePF-04634817 succinate
PF-0463481 succinate is a potent and orally active dual antagonist of CCR2/CCR5 with comparable human and rodent CCR2 potency with IC50 of 20.8 nM.
价 格：￥电议型 号：T12419产 地：美洲
