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T14152Akt1 and Akt2-IN-1Akt1 and Akt2-IN-1
Akt1 and Akt2-IN-1 is an allosteric inhibitor of Akt1 (IC50=3.5 nM) and Akt2 (IC50=42 nM). It has potent and balanced activity.
价 格：￥电议型 号：T14152产 地：美洲
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T14175Aldose reductase-IN-1Aldose reductase-IN-1
Aldose reductase-IN-1 is a aldose reductase inhibitor (IC50: 28.9 pM).
价 格：￥电议型 号：T14175产 地：美洲
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T14283amyloid P-IN-1amyloid P-IN-1
amyloid P-IN-1 is used research of diseases or disorders wherein depletion of serum amyloid P component (SAP). Which including Alzheimer´s disease, amyloidosis, osteoarthritis, and type 2 diabetes mellitus.
价 格：￥电议型 号：T14283产 地：美洲
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T14315AR-9281AR-9281,APAU,
AR9281 is a potent and selective inhibitor of soluble epoxide hydrolase (s-EH). It has potential for the treatment of hypertension and type 2 diabetes[1].
价 格：￥电议型 号：T14315产 地：美洲
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T14323ARQ 531ARQ 531
ARQ 531 is a reversible non-covalent inhibitor of Bruton’s Tyrosine Kinase (BTK). With IC50s of 0.85 nM and 0.39 nM for WT-BTK and C481S-BTK, respectively.
价 格：￥电议型 号：T14323产 地：美洲
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T1444LomefloxacinLomefloxacin,SC47111A,
Lomefloxacin is a synthetic broad-spectrum fluoroquinolone with antibacterial activity.
价 格：￥电议型 号：T1444产 地：美洲
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T14487AZM475271AZM475271,M475271,
AZM475271 is an inhibitor of Src kinase (IC50: 5 nM). Which has no inhibitory activity on Flt3, KDR, Tie-2.
价 格：￥电议型 号：T14487产 地：美洲
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T1758ABT-751ABT-751,ABT751,ABT 751
ABT-751 has been investigated for the treatment of Lung Cancer, Non-Small Cell Lung Cancer, and Non-Small-Cell Lung Cancer.
价 格：￥电议型 号：T1758产 地：美洲
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T18917ATP-Red 1ATP-Red 1
ATP-Red 1 is a multisite-binding switchable fluorescent probe. It can rapidly and selectively respond to intracellular concentrations of ATP in living cells.
价 格：￥电议型 号：T18917产 地：美洲
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T190901alpha, 24, 25-Trihydroxy VD21alpha, 24, 25-Trihydroxy VD2
1alpha, 24, 25-Trihydroxy VD2 is a vitamin D analog.
价 格：￥电议型 号：T19090产 地：美洲
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T2061APY0201APY0201
APY0201 is a effective, highly specific, ATP-competitive PIKfyve inhibitor (IC50: 5.2 nM). It can interrupt the conversion of phosphatidylinositol 3-phosphate (PtdIns3P) to PtdIns(3,5)P2.
价 格：￥电议型 号：T2061产 地：美洲
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T2098A77-01A77-01
A 77-01 is a potent inhibitor of TGF-(beta) type I receptor superfamily activin-like kinase ALK5 with IC50 of 25 nM.
价 格：￥电议型 号：T2098产 地：美洲
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T2120I-BET151I-BET151,GSK1210151A,
I-BET151 (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：美洲
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T2352AMI-1AMI-1,AMI1,AMI 1
AMI-1 is an effective and selective Histone Methyltransferase (HMT) inhibitor (IC50: 3.0/8.8 μM, for yeast Hmt1p, and human PRMT1).
价 格：￥电议型 号：T2352产 地：美洲
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T2662Alda-1Alda-1,Alda 1,
Alda-1 is an ALDH2 agonist, a cell-permeable activator of both the wild-type ALDH2*1 and the Asian E487K mutant ALDH2*2 forms of mitochondrial aldehyde dehydrogenase 2 (mtALDH2).
价 格：￥电议型 号：T2662产 地：美洲
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T2675AS 602801AS 602801,Bentamapimod,
AS 602801(Bentamapimod) is a novel, orally active inhibitor of JNK.
价 格：￥电议型 号：T2675产 地：美洲
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T4529ASP-9521ASP-9521,ASP9521,ASP 9521
ASP-9521 is an effective, specific and orally available AKR1C3 inhibitor (IC50: 11 nM, for human).
价 格：￥电议型 号：T4529产 地：美洲
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T5183AUT1AUT1
AUT1 (AUT-1) is a novel specific modulator of Kv3 channels (EC50: 4.7 and 4.9 uM for Kv3.1b and Kv3.2a).
价 格：￥电议型 号：T5183产 地：美洲
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T5353ABX-1431ABX-1431
ABX-1431 is a selective and orally available CNS-penetrant monoacylglycerol lipase (MAGL/MGLL) inhibitor (IC50: 14 nM).
价 格：￥电议型 号：T5353产 地：美洲
