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T7021ZM241385P1 receptor,Inhibitor,ZM241385,inhibit,ZM 241385,ZM-241385,Adenosine Receptor
ZM-241385 is a high-affinity antagonist ligand selective for the adenosine A2A receptor.
价 格:¥电议型 号:T7021产 地:中国大陆
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T24076FzM1
FzM1 is a negative allosteric modulator (NAM) of Frizzled receptor FZD4. FzM1 reduces WNT5A-dependent WNT responsive element (WRE) activity (log EC50inh=?6.2). FzM1 binds to an allosteric binding site located in intracellular loop 3 (ICL3) of FZD4 and alters the conformation of the receptor, ultimately inhibiting the WNT/β-catenin cascade
价 格:¥电议型 号:T24076产 地:中国大陆
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T9969EZM0414EZM0414
EZM0414 is a potent, selective, orally bioavailable inhibitor of SETD2 with IC50 of 18 nM in SETD2 biochemical assay and IC50 of 34 nM in a cellular assay. EZM0414 can be used for the research of relapsed or refractory multiple myeloma and diffuse large B-cell lymphoma [1].
价 格:¥电议型 号:T9969产 地:中国大陆
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T15363FzM1.8FzM-1.8,FzM1.8
FzM1.8 is an allosteric FZD4 agonist with a pEC50 of 6.4. FzM1.8 binds to FZD4, promotes TCF/LEF transcriptional activity in the absence of any WNT ligand, and activates the WNT/β-catenin pathway.
价 格:¥电议型 号:T15363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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T6077ZM-447439ZM 447439
ZM 447439 is a selective and ATP-competitive inhibitor for Aurora A and Aurora B with IC50 of 110 nM and 130 nM, respectively. It is more than 8-fold selective for Aurora A/B than MEK1, Src, Lck and has little effect against CDK1/2/4, Plk1, Chk1, etc.
价 格:¥电议型 号:T6077产 地:中国大陆
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T5605EZM 2302GSK3359088
EZM2302 is a selective, and orally available arginine methyltransferase CARM1 inhibitor (IC50: 6 nM).
价 格:¥电议型 号:T5605产 地:中国大陆
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T4386PZM21
PZM21 is an effective and selective μ opioid receptor agonist (EC50: 1.8 nM).
价 格:¥电议型 号:T4386产 地:中国大陆
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T3259FPS-ZM1
FPS-ZM1 is a high-affinity RAGE specific inhibitor that blocks Aβ binding to the V domain of RAGE.
价 格:¥电议型 号:T3259产 地:中国大陆
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T2464NSC319726ZMC1
NSC319726, a mutant p53R175 reactivator, suppresses growth of fibroblasts that expresses the p53R175 mutation (IC50 = 8 nM).
价 格:¥电议型 号:T2464产 地:中国大陆
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T2146FulvestrantZM 182780;ZD 9238;ICI 182780;氟维司群
Fulvestrant is a potent Estrogen Receptor antagonist (IC50: 9.4 nM).
价 格:¥电议型 号:T2146产 地:中国大陆
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T2041PD153035SU-5271;AG1517;NSC 669364;ZM 252868
PD153035 hydrochloride is an effective and selective inhibitor of EGFR (Ki/IC50: 5.2/29 pM, in cell-free assays); little inhibitory against FGFR, PGDFR, InsR, CSF-1 and Src.
价 格:¥电议型 号:T2041产 地:中国大陆
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T1851ZM 336372Zinc00581684
ZM 336372 is a potent and selective c-Raf inhibitor.
价 格:¥电议型 号:T1851产 地:中国大陆
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T1764Adezmapimod4-(4-氟苯基)-2-(4-甲基亚磺酰基苯基)-5-(4-吡啶基)-1H-咪唑;PB 203580;RWJ 64809;SB203580
SB 203580 is a p38 MAPK inhibitor (IC50: 0.3-0.5 μM). It shows more than 100-fold selectivity over PKB, LCK, and GSK-3β.
价 格:¥电议型 号:T1764产 地:中国大陆
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T1761PD153035 hydrochlorideTyrphostin AG 1517;SU 5271;ZM 252868 HCl;PD153035 HCl;ZM 252868;AG 1517
PD153035 hydrochloride (ZM 252868; AG 1517) is a effective and selective inhibitor of EGFR (Ki: 5.2 pM, IC50: 29 pM); few influence against FGFR, PGDFR, InsR, CSF-1, and Src.
价 格:¥电议型 号:T1761产 地:中国大陆
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T1754ZM 306416CB 676475
ZM 306416, a VEGFR1 inhibitor (IC50: 0.33 μM), can also inhibit EGFR (IC50<10 nM).
价 格:¥电议型 号:T1754产 地:中国大陆
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T14955Chlorthenoxazine氯西诺嗪;Chlorethylbenzmethoxazone
Chlorthenoxazine has anti-inflammatory activity.
价 格:¥电议型 号:T14955产 地:中国大陆
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T1178TemozolomideNSC 362856;TMZ;TZM;CCRG 81045;替莫唑胺
Temozolomide is a DNA alkylating agent interfering with DNA replication.
价 格:¥电议型 号:T1178产 地:中国大陆
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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