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T10937D-JNKI-1；化合物 T10937XG-102|||AM-111；XG-102|||AM-111
D-JNKI-1 (AM-111) is a highly effective and cell-permeable peptide inhibitor.
价 格：￥电议型 号：T10937产 地：中国大陆
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T10836CLK1-IN-1化合物 T10836CLK1 IN 1|||CLK1IN1|||CLK-1-IN-1
CLK1-IN-1 is a potent and selective inhibitor of the Cdc2-like kinase 1 (CLK1; IC50: 2 nM).
价 格：￥电议型 号：T10836产 地：中国大陆
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T10829CKI-7 free base；化合物 T10829CKI-7；CKI-7
CKI-7 free base is a potent and ATP-competitive inhibitor of casein kinase 1 (CK1; IC50: 6 μM; Ki: 8.5 μM) and a selective Cdc7 kinase inhibitor. CKI-7 free base also inhibits SGK, ribosomal S6 kinase-1 (S6K1), and MSK1.
价 格：￥电议型 号：T10829产 地：中国大陆
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T10828CK2/PIM1-IN-1；化合物 T10828CK2/PIM1-IN-1
CK2/PIM1-IN-1 is an inhibitor of CK2 and PIM1 (IC50s: 3.787 μM and 4.327 μM). It is developed for the research of proliferative disorders such as cancer, as well as other kinase-associated conditions.
价 格：￥电议型 号：T10828产 地：中国大陆
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T10827CK2/ERK8-IN-1；化合物CK2/ERK8-IN-1TMCB；TMCB
CK2/ERK8-IN-1 (TMCB) is a dual inhibitor of casein kinase 2 (CK2) (Ki: 0.25 ?M) and ERK8 (IC50s: 0.50 μM) with pro-apoptotic efficacy. CK2/ERK8-IN-1 also binds to PIM1, DYRK1A, and HIPK2 (Kis: 8.65 ?M, 11.9 ?M, and 15.25 ?M).
价 格：￥电议型 号：T10827产 地：中国大陆
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T10826CK-666；化合物CK-666CK-666
CK-666 is a cell-permeable inhibitor of actin-related protein Arp2/3 complex. It binds to the Arp2/3 complex, stabilizes the inactive state of the complex, blocking the movement of the Arp2 and Arp3 subunits into the activated filament-like (short pitch) conformation.
价 格：￥电议型 号：T10826产 地：中国大陆
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T10822Cirsimarin；滨蓟黄甙Cirsitakaoside；Cirsitakaoside
Cirsimarin (Cirsitakaoside) is a flavonoid isolated from Microtea debilis. It shows a potent antilipogenic effect and decreases adipose tissue deposition in mice. Cirsimarin has antagonist activity on the adenosine A1 receptor and inhibitory effect on phosphodiesterase.
价 格：￥电议型 号：T10822产 地：中国大陆
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T10813Cilobradine hydrochloride；西洛雷定盐酸盐DK-AH 269；DK-AH 269
Cilobradine hydrochloride (DK-AH 269) is an HCN Channel blocker and an open channel blocker of neuronal Ih and related cardiac If channels.
价 格：￥电议型 号：T10813产 地：中国大陆
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T10804CHMFL-PI3KD-317；化合物CHMFL-PI3KD-317CHMFL-PI3KD-317
CHMFL-PI3KD-317 is a highly potent, selective and orally active PI3Kδ inhibitor, with an IC50 of 6 nM, and exhibits over 10-1500 fold selectivity over other class I, II and III PIKK family isoforms, such as PI3Kα (IC50, 62.6 nM), PI3Kβ (IC50, 284 nM), PI3Kγ (IC50, 202.7 nM), PIK3C2A (IC50, >10000 nM), PIK3C2B (IC50, 882.3 nM), VPS34 (IC50, 1801.7 nM), PI4KIIIA (IC50, 574.1 nM) and PI4KIIIB (IC50, 300.2 nM). CHMFL-PI3KD-317 inhibits PI3Kδ-mediated Akt T308 phosphorylation in Raji cells, with an E
价 格：￥电议型 号：T10804产 地：中国大陆
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T10801CHMFL-ABL/KIT-155；化合物 T10801CHMFL-ABL-KIT-155；CHMFL-ABL-KIT-155
CHMFL-ABL/KIT-155 is a highly potent and orally active type II ABL/c-KIT dual kinase inhibitor (IC50s: 46 nM/75 nM). It arrests cell cycle progression and induces apoptosis.
价 格：￥电议型 号：T10801产 地：中国大陆
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T10793CHK1 inhibitor；化合物 T10793GDC-0575 analog；GDC-0575 analog
CHK1 inhibitor (GDC-0575 analog) is a CHK1 inhibitor.
价 格：￥电议型 号：T10793产 地：中国大陆
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T10792LCHK1-IN-4 hydrochloride；化合物CHK1-IN-4盐酸盐CHK1-IN-4 hydrochloride（2120398-41-4 Free base）；CHK1-IN-4 hyd
CHK1-IN-4 hydrochloride is a potent inhibitor of checkpoint kinase 1 (chk1). CHK1-IN-4 hydrochloride potently inhibits chk1 phosphorylation in the tumor cells. CHK1-IN-4 hydrochloride has anti-tumor activity.
价 格：￥电议型 号：T10792L产 地：中国大陆
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T10792CHK1-IN-4；化合物 T10792CHK1-IN-4
CHK1-IN-4 is a potent inhibitor of checkpoint kinase 1 (chk1) and potently inhibits chk1 phosphorylation in the tumor cells with anti-tumor activity.
价 格：￥电议型 号：T10792产 地：中国大陆
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T10791CHK1-IN-3；化合物CHK1-IN-3CHK1-IN-3
CHK1-IN-3 is an inhibitor of checkpoint kinase 1 (CHK1; IC50: 0.4 nM).
价 格：￥电议型 号：T10791产 地：中国大陆
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T10790CHK1-IN-2；化合物 T10790CHK1-IN-2
CHK1-IN-2 is an inhibitor of checkpoint kinase 1 (CHK1; IC50: 6 nM).
价 格：￥电议型 号：T10790产 地：中国大陆
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T1077Fluvoxamine maleate；氟伏沙明马来酸盐MK-264|||DU-23000 (maleate)；氟伏沙明马来酸盐|||马来酸氟伏沙明|||MK-264|||DU-23000 (male
Fluvoxamine maleate (DU-23000 (maleate)) is a selective serotonin reuptake inhibitor that is used in the treatment of depression and a variety of anxiety disorders.
价 格：￥电议型 号：T1077产 地：中国大陆
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T10766Ceritinib D7；化合物 T10766LDK378 D7；LDK378 D7
Ceritinib D7 (LDK378 D7) is a deuterium-labeled Ceritinib. Ceritinib is an ATP-competitive inhibitor of ALK tyrosine kinase.
价 格：￥电议型 号：T10766产 地：中国大陆
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T10756Cenicriviroc Mesylate；化合物 T10756TBR-652 Mesylate|||TAK-652 Mesylate；TBR-652 Mesylate|||TAK-652 Mesyl
Cenicriviroc Mesylate is a dual CCR2/CCR5 antagonist, also inhibits both HIV-1 and HIV-2 with anti-inflammatory and antiinfective activity.
价 格：￥电议型 号：T10756产 地：中国大陆
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T1075Vitamin K1；叶绿醌Phylloquinone|||Phytomenadione|||Phytonadione|||Phyllohydroquinone；Phylloquinone|||维生素
Vitamin K1 (Phylloquinone) a fat-soluble, naturally occurring vitamin with antihemorrhagic and prothrombogenic activity.
价 格：￥电议型 号：T1075产 地：中国大陆
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T10747CDK9-IN-9；化合物 T10747CDK9-IN-9
CDK9-IN-9 is a potent and selective CDK9 inhibitor (IC50: 1.8 nM) with anti-cancer activity. It inhibits CDK2 (IC50: 155 nM).
价 格：￥电议型 号：T10747产 地：中国大陆
