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T10717InobrodibCBP-IN-1
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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T10098PGS-IN-1KME-4
PGS-IN-1 is a potent inhibitor of prostaglandin synthetase (PGS, IC50: 0.28 μM) and 5-lipoxygenase (IC50: 1.05 μM).
价 格：￥电议型 号：T10098产 地：中国大陆
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T10079MAO-IN-1MAO-IN-1
MAO-IN-1 is an inhibitor of monoamine oxidase B (MAO B; IC50: 20 nM).
价 格：￥电议型 号：T10079产 地：美洲
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T10098PGS-IN-1PGS-IN-1,KME-4,
PGS-IN-1 is a potent inhibitor of prostaglandin synthetase (PGS; IC50: 0.28 μM) and also inhibits 5-lipoxygenase (IC50: 1.05 μM).
价 格：￥电议型 号：T10098产 地：美洲
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T10303Aminoacyl tRNA synthetase-IN-1Aminoacyl tRNA synthetase-IN-1
Aminoacyl tRNA synthetase-IN-1 is an inhibitor of bacterial aminoacyl tRNA synthetase (aaRS).
价 格：￥电议型 号：T10303产 地：美洲
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T10519BET-IN-1BET-IN-1
BET-IN-1 is a bromodomain inhibitor extracted from patent WO/2013024104A1 (example 2, plC50: 6.0 - 7.0).
价 格：￥电议型 号：T10519产 地：美洲
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T10557BLM-IN-1BLM-IN-1
BLM-IN-1 is an effective Bloom syndrome protein (BLM) inhibitor (KD: 1.81 μM; IC50: 0.95 μM). It induces DNA damage response, apoptosis and proliferation arrest in cancer cells
价 格：￥电议型 号：T10557产 地：美洲
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T10643c-Fms-IN-1c-Fms-IN-1
c-Fms-IN-1 is an inhibitor of FMS kinase (IC50: 0.0008 μM).
价 格：￥电议型 号：T10643产 地：美洲
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T10682LCARM1-IN-1CARM1-IN-1
CARM1-IN-1 is a potent and specific CARM1(Coactivator-associated arginine methyltransferase 1) inhibitor (IC50: 8.6 uM). It shows very low activity against PRMT1 and SET7(IC50 > 600 uM).
价 格：￥电议型 号：T10682L产 地：美洲
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T10717CBP-IN-1CBP-IN-1
CBP-IN-1 is a potent inhibitor of p300/CBP bromodomain.
价 格：￥电议型 号：T10717产 地：美洲
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T10721CD73-IN-1CD73-IN-1
CD73-IN-1 is an inhibitor of CD73 with anticancer activity extracted from patent WO 2017153952 A1 (example 80).
价 格：￥电议型 号：T10721产 地：美洲
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T10723CDC25B-IN-1CDC25B-IN-1
CDC25B-IN-1 is a potent inhibitor of cell division cycle 25B (CDC25B) phosphatase (Ki: 8.5 μM). It potently inhibits cell proliferation and colony formation.
价 格：￥电议型 号：T10723产 地：美洲
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T10724Cdc7-IN-1Cdc7-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：美洲
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T10740CDK8-IN-1CDK8-IN-1
CDK8-IN-1 is a selective CDK8 inhibitor (IC50: 3 nM).
价 格：￥电议型 号：T10740产 地：美洲
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T10741CDK9-IN-1CDK9-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：美洲
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T10787Chitise-IN-1Chitise-IN-1,Chitinase-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：美洲
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T10836CLK1-IN-1CLK1-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：美洲
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T10863Complement C5-IN-1Complement C5-IN-1
Complement C5-IN-1 is a small-molecule inhibitor of complement component 5 protein (C5).
价 格：￥电议型 号：T10863产 地：美洲
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T10986DDX3-IN-1DDX3-IN-1
DDX3-IN-1 is a DEAD-box polypeptide 3 (DDX3) inhibitor with CC50 of 50 and 36 μM for HIV and HCV, respectively. Antiviral activity.
价 格：￥电议型 号：T10986产 地：美洲
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T11056DLK-IN-1DLK-IN-1
DLK-IN-1 is a selective oral active inhibitor of bisleucine zipper kinase (DLK, MAP3K12) with Ki of 3 nM. DLK-IN-1 is active in the Alzheimer´s disease model, retains excellent CNS permeability, and after multiple days of administration, its concentration
价 格：￥电议型 号：T11056产 地：美洲
