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产品数：86095
参观次数：4040065
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T6168ZSTK474
PI3K Inhibitor ZSTK474 is an orally available, s-triazine derivative, ATP-competitive phosphatidylinositol 3-kinase (PI3K) inhibitor with potential antineoplastic activity.
价 格：￥电议型 号：T6168产 地：中国大陆
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T6167SU9516
SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also has inhibitory effects on CDK1 and CDK4, with IC50s of 40 nM and 200 nM, respectively.
价 格：￥电议型 号：T6167产 地：中国大陆
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T6166TelatinibBay 57-9352；替拉替尼
Telatinib is an effective inhibitor of VEGFR2/3, c-Kit, and PDGFRα. The IC50s of Telatinib forVEGFR2/3, c-Kit and PDGFRα are 6 nM/4 nM, 1 nM, and 15 nM, respectively.
价 格：￥电议型 号：T6166产 地：中国大陆
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T6165Bardoxolone MethylTP-155；NSC 713200；甲基巴多索隆；CDDO Methyl ester；RTA 402
Bardoxolone Methyl, an IKK inhibitor, exhibits effective proapoptotic and anti-inflammatory activities.
价 格：￥电议型 号：T6165产 地：中国大陆
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T6163Salirasib沙利雷塞；法尼基硫代水杨酸；FTS；Farnesyl Thiosalicylic Acid；S-Farnesylthiosalicylic acid
Salirasib(Ki=2.6 μM), an effective competitive prenylated protein methyltransferase (PPMTase) inhibitor, inhibits Ras methylation with potential antineoplastic activity.
价 格：￥电议型 号：T6163产 地：中国大陆
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T6162BS-181 hydrochlorideBS-181 HCl
BS-181 HCl is a highly selective CDK7 inhibitor with IC50 of 21 nM. It is more than 40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.
价 格：￥电议型 号：T6162产 地：中国大陆
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T6161Tubastatin A HydrochlorideTubastatin A HCl；TSA HCl
Tubastatin A HCl is an effective and specific HDAC6 inhibitor (IC50: 15 nM). It has selectivity (>1000-fold) against all other isozymes except HDAC8 (>57-fold).
价 格：￥电议型 号：T6161产 地：中国大陆
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T6160VU 0364439
VU 0364439 is a mGlu4 positive allosteric modulator (C50: 19.8 nM).
价 格：￥电议型 号：T6160产 地：中国大陆
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T6159LY-2584702 free base
LY2584702 is a selective, ATP-competitive p70S6K inhibitor(IC50: 4 nM).
价 格：￥电议型 号：T6159产 地：中国大陆
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T6158LDN-193189 HClLDN193189 Hydrochloride
LDN193189 hydrochloride is a selective BMP type I receptor kinases inhibitor.
价 格：￥电议型 号：T6158产 地：中国大陆
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T6157Devimistat辛酸；6,8-Bis(benzylthio)octanoic acid；CPI613；CPI-613；CPI 613
CPI-613, a lipoate analog, inhibits mitochondrial enzymes pyruvate dehydrogenase (PDH) and α-ketoglutarate dehydrogenase, disrupts tumor cell mitochondrial metabolism. It has potential chemopreventive and antineoplastic activities, and has been used in tr
价 格：￥电议型 号：T6157产 地：中国大陆
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T6156Ruxolitinib (S enantiomer)S-Ruxolitinib；INCB018424；INCB18424；Ruxolitinib S enantiomer；环丙基[4-[3-(1H-咪
Ruxolitinib S enantiomer is the S-enantiomer of Ruxolitinib. Ruxolitinib is the first potent, selective JAK1/2 inhibitor.
价 格：￥电议型 号：T6156产 地：中国大陆
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T6152PD318088
PD318088 is a non-ATP competitive allosteric MEK1/2 inhibitor, binding simultaneously with ATP in a region of the MEK1 active site that is adjacent to the ATP-binding site.
价 格：￥电议型 号：T6152产 地：中国大陆
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T6149YH239-EE
YH239-EE, the ethyl ester of YH239, is a potent p53-MDM2 antagonist and an apoptosis inducer.
价 格：￥电议型 号：T6149产 地：中国大陆
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T6147NortadalafilDemethyl Tadalafil；去甲基他达那非
Nortadalafil is demethyl Tadalafil, which is a PDE5 inhibitor, treating erectile dysfunction (ED) ; and under the name Adcirca for the treatment of pulmonary arterial hypertensio.
价 格：￥电议型 号：T6147产 地：中国大陆
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T6146Dorsomorphin dihydrochloride6-[4-[2-(1-哌啶基)乙氧基]苯基]-3-(4-吡啶基)吡唑并[1,5-A]嘧啶；Dorsomorphin (Compound C) 2
Dorsomorphin is a potent, selective and ATP-competitive AMPK inhibitor (Ki: 109 nM) and does not exhibit significant activity on structurally related kinases.
价 格：￥电议型 号：T6146产 地：中国大陆
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T6145ZM39923 hydrochlorideZM 39923 HCl；JAK3 Inhibitor IV
ZM 39923 HCl is an JAK1/3 inhibitor with pIC50 of 4.4/7.1, almost no activity to JAK2 and modestly potent to EGFR; also found to be sensitive to transglutaminase.
价 格：￥电议型 号：T6145产 地：中国大陆
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T6144KB-R7943 mesylateKB-R7943
KB-R7943 mesylate is a widely used inhibitor of the reverse Na+/Ca2+ exchanger (NCXrev) with IC50 of 5.7±2.1 μM.
价 格：￥电议型 号：T6144产 地：中国大陆
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T6143PI-103PI103；PI 103
PI-103 is a potent, cell-permeable, ATP-competitive inhibitor of PI3K family members (IC50s: 2/3/3/15/30/23 nM for p110α/β/δ/γ, mTOR, and DNA-PK).
价 格：￥电议型 号：T6143产 地：中国大陆
