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T24741RS1-PDK1 inhibitor；RS1-PDK1抑制剂RS-1|||RS1|||RS 1；RS-1|||RS1|||RS 1
RS1-PDK1 inhibitor (RS 1) is a selective inhibitor of the protein kinase PDK1 that can be used to treat and prevent disease or disorders.
价 格：￥电议型 号：T24741产 地：中国大陆
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T24708Remogliflozin；化合物 T24708GSK189074|||Remogliflozin A|||GSK-189074|||GSK 189074；GSK189074|||Remogliflo
Remogliflozin is an effective sodium-glucose transporter 2 inhibitor (Kis = 12.4 and 26 nM for human and rat SGLT2, respectively).
价 格：￥电议型 号：T24708产 地：中国大陆
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T2455PFK-015；化合物PFK-015PFK15|||PFK 015；PFK15|||PFK 015
PFK-015 (PFK15) is an effective inhibitor of PFKFB3 (IC50: 110 nM) and inhibits PFKFB3 activity in Y cells (IC50: 20 nM).
价 格：￥电议型 号：T2455产 地：中国大陆
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T24504MSK-195；化合物 T24504MSK 195|||MSK195；MSK 195|||MSK195
MSK-195 is an effective TRPV1 agonist.
价 格：￥电议型 号：T24504产 地：中国大陆
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T24439MDK6204；化合物 T24439CLK1/2 IN 2|||CLK1/2IN2|||CLK1/2-inhibitor-2|||CLK1/2-IN-2|||CLK1/2 inhibitor 2；CL
MDK6204 is a selective inhibitor of CLK1 and CLK2.
价 格：￥电议型 号：T24439产 地：中国大陆
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T24104GSK106；化合物 T24104GSK-106|||GSK 106；GSK-106|||GSK 106
GSK106 is a negative control used in binding and functional assays for PAD4 inhibitors.
价 格：￥电议型 号：T24104产 地：中国大陆
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T23897CLK1/2-IN-3；CLK1/2抑制剂3CLK1/2 inhibitor 3|||CLK1/2-inhibitor-3|||CLK1/2 IN 3|||CLK1/2IN3；CLK1/2 inhib
CLK1/2-IN-3 (Cpd-3) is a potent and selective CLK1 and CLK2 inhibitor with antiproliferative activity and inhibits the activities of CLK1, CLK2, SRPK1, SRPK2, and SRPK3.CLK1/2-IN-3 induces nuclear speckle enlargement, which induces S6K pre-mRNA-selective splicing and subsequent inhibition of cell growth of multiple cancer cell types. cancer cell types cell growth.
价 格：￥电议型 号：T23897产 地：中国大陆
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T23896CLK1/2-IN-1；化合物 T23896CLK1/2 inhibitor 1|||CLK1/2IN1|||CLK1/2-inhibitor-1；CLK1/2 inhibitor 1|||CLK1/
CLK1/2-IN-1 is a CLK1 and CLK2 inhibitor and it also inhibits SRPK1 and SRPK2.
价 格：￥电议型 号：T23896产 地：中国大陆
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T2357GSK1059615；化合物GSK-1059615GSK 1059615|||GSK-1059615；GSK 1059615|||GSK-1059615
GSK1059615 has been used in trials studying the treatment of Lymphoma, Solid Tumours, Endometrial Cancer, Solid Tumor Cancer, and Metastatic Breast Cancer.
价 格：￥电议型 号：T2357产 地：中国大陆
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T2329Dolutegravir sodium；度鲁特韦钠盐GSK1349572|||GSK-1349572A；度鲁特韦钠|||GSK1349572|||度鲁特韦钠盐|||GSK-1349572A
Dolutegravir sodium (GSK-1349572A) salt(DTG; GSK1349572) is an HIV integrase inhibitor(IC50: 2.7 nM), modest activity against raltegravir-resistant signature mutants Y143R, Q148K, N155H, and G140S/Q148H.
价 格：￥电议型 号：T2329产 地：中国大陆
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T22986MK 1903；化合物MK 1903MK-1903|||MK 1903|||MK 1903|||MK1903；0
MK 1903 is a potent and selective complete agonist for the hydroxy-carboxylic acid receptor 2 (HCA2). HCA2 is also known as G protein-coupled receptor 109A(GPR109A). MK 1903 reduced Foschlin-induced cAMP production in uniform time-resolved fluorescence (htf) measurements using CHO cells expressing the human receptor (ECso-12.9 nM).
价 格：￥电议型 号：T22986产 地：中国大陆
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T22776Ezatiostat hydrochloride；Ezatiostat盐酸盐TLK199 HCl|||TER199；TLK199 HCl|||Ezatiostat盐酸盐|||TER199
Ezatiostat hydrochloride (TLK199 HCl) is an effective inhibitor of glutathione S-transferase. Ezatiostat hydrochloride is a novel glutathione analog and the potential treatment of cytopenias. In addition, Ezatiostat hydrochloride has been revealed to selectively bind to and thus inhibit GSTP1-1.
价 格：￥电议型 号：T22776产 地：中国大陆
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T22254Alflutinib；化合物AlflutinibAST2818|||ASK120067；AST2818|||ASK120067
Alflutinib (ASK120067) is an inhibitor of EGFR, and its targets including EGFR activating mutations and T790M, thus leading to tumor growth inhibition.
价 格：￥电议型 号：T22254产 地：中国大陆
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T2125Trametinib曲美替尼GSK1120212|||曲美替尼|||JTP-74057
Trametinib (GSK1120212) is a MEK inhibitor that inhibits MEK1 and MEK2 (IC50=0.7/0.9 nM) with ATP non-competitive and oral activity. Trametinib activates autophagy and induces apoptosis.
价 格：￥电议型 号：T2125产 地：中国大陆
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T2120I-BET151；化合物I-BET151GSK1210151A；GSK1210151A
I-BET151 (GSK1210151A) (GSK1210151A) is a specific BET inhibitor for BRD2/3/4 (IC50: 0.5/0.25/0.79 μM, in cell-free assays).
价 格：￥电议型 号：T2120产 地：中国大陆
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T2079GSK126；化合物GSK126GSK2816126A|||EZH2 inhibitor；GSK2816126A|||EZH2 inhibitor
GSK126 (GSK2816126A) is an EZH2 methyltransferase inhibitor (IC50=9.9 nM) that is potent and selective. GSK126 has antitumor activity, inhibiting tumor cell proliferation and suppressing angiogenesis.
价 格：￥电议型 号：T2079产 地：中国大陆
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T20219Bioresmethrin；化合物 T20219Penick-1390|||Bioresmetrina|||Penick 1390|||Penick1390；Penick-1390|||Bioresm
Bioresmethrin is a pesticide of synthetic pyrethroid.
价 格：￥电议型 号：T20219产 地：中国大陆
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T1988Duvelisib；度维利塞INK1197|||IPI-145；INK1197|||IPI-145|||度维利塞
Duvelisib (INK1197) is an orally bioavailable, highly selective and potent small molecule inhibitor of the delta and gamma isoforms of phosphoinositide-3 kinase (PI3K) with potential immunomodulating and antineoplastic activities.
价 格：￥电议型 号：T1988产 地：中国大陆
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T19628GSK 189254 HCl；化合物 T19628GSK-189254A|||GSK 189254A|||GSK 189254 hydrochloride|||GSK189254A；GSK-18925
GSK 189254A is a histamine H3 receptor antagonist for the treatment of narcolepsy. Histamine H3 receptor antagonists have been shown to increase the release of neurotransmitters in the brain and to enhance cognition in vivo. The compound may also be useful in the treatment of dementia and neuropathic pain.
价 格：￥电议型 号：T19628产 地：中国大陆
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T19603Vitamin K；维生素KKephton|||Vitamin K1(20)；Kephton|||维生素K|||Vitamin K1(20)
Vitamin K (Kephton) has blood coagulation action and is important for coagulation factors, matrix-Gla protein, and osteocalcin.
价 格：￥电议型 号：T19603产 地：中国大陆
