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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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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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T10787Chitinase-IN-1；化合物 T10787Chitinase-IN-1
Chitinase-IN-1 is an insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide.
价 格：￥电议型 号：T10787产 地：中国大陆
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T10743CDK9-IN-11；化合物 T10743CDK9-IN-11
CDK9-IN-11 is a potent CDK9 inhibitor that is the ligand for the PROTAC CDK9 Degrader-1 [1].
价 格：￥电议型 号：T10743产 地：中国大陆
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T10742CDK9-IN-10；化合物CDK9-IN-10CDK9-IN-10
CDK9-IN-10 is a potent CDK9 inhibitor and the ligand for the PROTAC CDK9 degrader-2.
价 格：￥电议型 号：T10742产 地：中国大陆
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T10741CDK9-IN-1；化合物 T10741CDK9-IN-1
CDK9-IN-1 is a novel, selective CDK9 inhibitor for the treatment of HIV infection (IC50: 39 nM for CDK9/CycT1).
价 格：￥电议型 号：T10741产 地：中国大陆
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T10740CDK8-IN-1；化合物CDK8-IN-1CDK8-IN-1
CDK8-IN-1 is a selective CDK8 inhibitor (IC50: 3 nM).
价 格：￥电议型 号：T10740产 地：中国大陆
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T10739CDK8/19-IN-1；化合物 T10739CDK8/19-IN-1
CDK8/19-IN-1 is a selective and oral bioavailable CDK8/19 dual inhibitor (IC50s: 0.46 nM, 0.99 nM, and 270 nM for CDK8, CDK19, and CDK9).
价 格：￥电议型 号：T10739产 地：中国大陆
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T10724Cdc7-IN-1；化合物 T10724Cdc7-IN-1
Cdc7-IN-1 is a highly selective and ATP competitive inhibitor of Cdc7 kinase (IC50: 0.6 nM at 1 mM ATP). It potently inhibits Cdc7 activity in cancer cells and effectively induces cell death.
价 格：￥电议型 号：T10724产 地：中国大陆
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T10723CDC25B-IN-1；化合物CDC25B-IN-1ethyl 3-[(3-methoxynaphthalen-1-yl)amino]benzoate；ethyl 3-[(3-methoxynapht
CDC25B-IN-1 is an inhibitor of CDC25B with a Ki of 8.5 μM. CDC25B-IN-1 increases the G2/M phase by inhibiting cell proliferation and colony formation.
价 格：￥电议型 号：T10723产 地：中国大陆
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T10721CD73-IN-1；CD73 抑制剂1CD73-IN-1
CD73-IN-1 is a CD73 inhibitor with anticancer activity.
价 格：￥电议型 号：T10721产 地：中国大陆
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T10717Inobrodib；化合物CBP-IN-1CBP-IN-1；CBP-IN-1
Inobrodib (CBP-IN-1) is a potent inhibitor of p300/CBP bromodomain.
价 格：￥电议型 号：T10717产 地：中国大陆
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T10697CB2R-IN-1；化合物 T10697CB2R-IN-1
CB2R-IN-1 is a potent inverse agonist of the cannabinoid CB2 receptor (Ki: 0.9 nM).
价 格：￥电议型 号：T10697产 地：中国大陆
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T10682LCARM1-IN-1；化合物CARM1-IN-1CARM1-IN-7G；CARM1-IN-7G
CARM1-IN-1 (CARM1-IN-7G) is a selective inhibitor of CARM1 with IC50 of 8.6 μM. CARM1-IN-1 shows weak activity against PRMT1 and SET7 with IC50 > 600 μM.
价 格：￥电议型 号：T10682L产 地：中国大陆
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T10653c-met-IN-1；化合物 T10653c-met-IN-1
c-met-IN-1 is a potent and selective c-Met inhibitor (IC50: 1.1 nM) with antitumor activity.
价 格：￥电议型 号：T10653产 地：中国大陆
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T10644c-Fms-IN-10；化合物 T10644c-Fms-IN-10
c-Fms-IN-10 is the derivative of thieno [3,2-d] pyrimidine, a kinase inhibitor of FMS (Colony-stimulating factor-1 receptor, CSF-1R; IC50: 2 nM) with anti-tumor activity.
价 格：￥电议型 号：T10644产 地：中国大陆
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T10643c-Fms-IN-1；化合物c-Fms-IN-1c-Fms-IN-1
c-Fms-IN-1 is an inhibitor of c-FMS kinase (IC50 = 0.8 nM).
价 格：￥电议型 号：T10643产 地：中国大陆
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T106365α-reductase-IN-1；化合物 T106365α-reductase-IN-1
5α-reductase-IN-1 is a potent inhibitor of the enzyme 5α-reductase. This compound is primarily employed in research studies to investigate its potential efficacy in treating patterned alopecia. It is commonly used in combination with minoxidil, a well-known treatment for hair loss.
价 格：￥电议型 号：T10636产 地：中国大陆
