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T6733WZ-3146EGFR,HER1,WZ-3146,Epidermal growth factor receptor,WZ 3146,ErbB-1,WZ3146,inhibit,Inhibitor
WZ3146 is a mutant-selective irreversible inhibitor of EGFR(L858R) and EGFR(E746_A750) with IC50 of 2 nM and 2 nM; does not inhibit ERBB2 phosphorylation (T798I).
价 格：￥电议型 号：T6733产 地：中国大陆
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TQ0012AZ3451AZ 3451,inhibit,Protease Activated Receptor (PAR),AZ-3451,AZ3451,Thrombin receptors,Inhibitor
AZ3451 is an allosteric antagonist of protease-activated receptor-2 (PAR2, IC50: 23 nM).
价 格：￥电议型 号：TQ0012产 地：中国大陆
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T3175LDHA-IN-4AZ33；AZ 33；LDHA Inhibitor；AZ-33
AZ-33 is an LDHA inhibitor. Binding affinity to 6-His-tagged human LDHA (2 to 322 amino acid residue) expressed in Escherichia coli BL21 (DE3) cells by SPR analysis with an active value of 0.093 μM.
价 格：￥电议型 号：T3175产 地：中国大陆
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T2319Acotiamide monohydrochloride trihydrateYM-443 HCl；Z-338 HCl；Acotiamide hydrochloride；盐酸阿考替胺
Acotiamide Hydrochloride is the hydrochloride salt form of acotiamide, a prokinetic agent with gastrointestinal (GI) motility-enhancing activity. Although the exact mechanism by which acotiamide exerts its effect has yet to be fully elucidated, this agent
价 格：￥电议型 号：T2319产 地：中国大陆
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T21343PTZ-343吩噻嗪-10-基-丙基磺酸钠盐；PTZ 343；PTZ-343 sodium；PTZ343
PTZ-343 is a potent enhancer of Luminol, acts as an electron transfer mediator, reacting with HRP-II to release HRP and a PTZ-343 radical, which oxidizes luminol anions to induce light emission.
价 格：￥电议型 号：T21343产 地：中国大陆
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T0499Oxybenzone二苯酮-3；紫外线吸收剂UV-9；Escalol 567；KAHSCREEN BZ-3；Eusolex 4360；Benzophenone 3
Oxybenzone is an organic compound used in sunscreens. It is a derivative of benzophenone.
价 格：￥电议型 号：T0499产 地：中国大陆
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T2319Acotiamide hydrochlorideAcotiamide hydrochloride,YM-443 HCl,Z-338 HCl
Acotiamide Hydrochloride is the hydrochloride salt form of acotiamide, a prokinetic agent with gastrointestinal (GI) motility-enhancing activity. Although the exact mechanism by which acotiamide exerts its effect has yet to be fully elucidated, this agent
价 格：￥电议型 号：T2319产 地：美洲
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T74539DIZ-3；化合物 DIZ-3DIZ-3
DIZ-3, a selective multimeric G-quadruplex (G4) ligand, employs a G4-ligand-dimerizing approach to intercalate into the G4-G4 interface, thereby stabilizing its higher-order structure. This compound effectively induces cell cycle arrest and apoptosis, inhibiting cell proliferation in cancer cells characterized by alternative lengthening of telomeres (ALT) [1].
价 格：￥电议型 号：T74539产 地：中国大陆
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T6733WZ-3146；化合物WZ3146WZ-3146
WZ3146 is a mutant-selective irreversible inhibitor of EGFR(L858R) and EGFR(E746_A750) with IC50 of 2 nM and 2 nM; does not inhibit ERBB2 phosphorylation (T798I).
价 格：￥电议型 号：T6733产 地：中国大陆
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T665021-Cbz-3-Hydroxyazetidine；化合物 1-Cbz-3-Hydroxyazetidine1-Cbz-3-Hydroxyazetidine
1-Cbz-3-Hydroxyazetidine is a useful organic compound for research related to life sciences. The catalog number is T66502 and the CAS number is 128117-22-6.
价 格：￥电议型 号：T66502产 地：中国大陆
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T5182AMZ30；化合物AMZ30AMZ-30|||inhibit|||Inhibitor|||AMZ30|||AMZ 30|||AMZ 30|||AMZ-30|||AMZ30；AMZ-30|||inhib
AMZ30 is a selective inhibitor of PME-1 (IC50: 600 nM). It also reduces the demethylated form of PP2A in living cells.
价 格：￥电议型 号：T5182产 地：中国大陆
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T35288Z 300；化合物 T35288Z-300|||Z300；Z-300|||Z300
Z 300 is a histamine H2-receptor antagonist. Z 300 inhibits acid secretion and promotes gastric mucus metabolism in the corpus region.
价 格：￥电议型 号：T35288产 地：中国大陆
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T3175LDHA-IN-4；化合物AZ33AZ 33|||AZ-33|||LDHA Inhibitor|||AZ33；AZ 33|||AZ-33|||LDHA Inhibitor|||AZ33
LDHA-IN-4 (AZ33) is an LDHA inhibitor. Binding affinity to 6-His-tagged human LDHA (2 to 322 amino acid residue) expressed in Escherichia coli BL21 (DE3) cells by SPR analysis with an active value of 0.093 μM.
价 格：￥电议型 号：T3175产 地：中国大陆
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T29200Z-335 sodium；化合物 T29200Z 335|||Z335|||Z-335；Z 335|||Z335|||Z-335
Z-335 Salt, a thromboxane A2 receptor antagonist, is used potentially for the treatment of arterial occlusive disease.
价 格：￥电议型 号：T29200产 地：中国大陆
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T27522GZ389988；化合物 T27522GZ-389988|||GZ 389988；GZ-389988|||GZ 389988
GZ389988 is a potent Trk inhibitor.
价 格：￥电议型 号：T27522产 地：中国大陆
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T23764AZ3976；化合物AZ3976AZ 3976|||AZ-3976；AZ 3976|||AZ-3976
AZ3976 is an inhibitor of PAI-1 with an IC50 of 16 μM in a plasma clot lysis assay. AZ3976 displays profibrinolytic activities.
价 格：￥电议型 号：T23764产 地：中国大陆
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T2319Acotiamide monohydrochloride trihydrate盐酸阿考替胺Acotiamide hydrochloride|||YM-443 HCl|||盐酸阿考替胺|||Z-338
Acotiamide monohydrochloride trihydrate (Z-338 HCl) is the hydrochloride salt form of acotiamide, a prokinetic agent with gastrointestinal (GI) motility-enhancing activity. Although the exact mechanism by which acotiamide exerts its effect has yet to be fully elucidated, this agent appears to inhibit acetylcholinesterase (AchE), an enzyme responsible for the breakdown of acetylcholine (Ach). Increased Ach concentrations lead to an improvement of gastric emptying and GI motility and eventually to
价 格：￥电议型 号：T2319产 地：中国大陆
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T21343PTZ-343；吩噻嗪-10-基-丙基磺酸钠盐PTZ-343 sodium|||PTZ 343；PTZ-343 sodium|||PTZ 343|||吩噻嗪-10-基-丙基磺酸钠盐
PTZ-343 is a potent enhancer of Luminol, acts as an electron transfer mediator, reacting with HRP-II to release HRP and a PTZ-343 radical, which oxidizes luminol anions to induce light emission.
价 格：￥电议型 号：T21343产 地：中国大陆
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T19671AZ31；化合物AZ31AZ 31|||AZ-31；AZ 31|||AZ-31
AZ31 is an ATM inhibitor with potency, high selectivity, and oral activity.AZ31 inhibits ATM enzymes, intracellular ATM, with IC50 values of <1.2 nM and 46 nM, respectively.AZ31 exhibits excellent ATR selectivity, PIKK family selectivity, and pan-kinase selectivity.AZ31 is a potent in vitro radiosensitizer that can be used for cancer research.
价 格：￥电议型 号：T19671产 地：中国大陆
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T17279Z-321；化合物 T17279Z-321
Z-321 is an inhibitor of prolyl endopeptidase.
价 格：￥电议型 号：T17279产 地：中国大陆
