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TQ0210Savolitinibinhibit,Savolitinib,AZD 6094,Inhibitor,c-Met/HGFR,AZD6094,HMPL504,HMPL 504
Savolitinib (AZD-6094) is an effective, selective, and orally bioavailable c-Met inhibitor (IC50s: 5 nM/3 nM for c-Met/p-Met).
价 格：￥电议型 号：TQ0210产 地：中国大陆
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T7699AZD7325modulator,effect,inhibit,Cytochrome P450,Dravet,syndrome,Inhibitor,γ-Aminobutyric acid Recept
AZD-7325 is a GABA-Aα2,3 -selective receptor modulator.
价 格：￥电议型 号：T7699产 地：中国大陆
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T6772AZD3839 free baseAZD3839 free base,β-Secretase,BACE,AZD-3839 free base,inhibit,AZD 3839,AZD-3839,Bet
AZD3839 is a potent and selective BACE1 inhibitor with Ki of 26.1 nM, about 14-fold selectivity over BACE2. Phase 1.
价 格：￥电议型 号：T6772产 地：中国大陆
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T6400AZD3514selective,anti proliferation,LAPC4,Inhibitor,AZD3514,AZD-3514,oral,AZD 3514,rat,AR protein,pr
AZD3514 is a potent and oral androgen receptor downregulator with Ki of 2.2 μM and has ability of reducing AR protein expression.Phase 1.
价 格：￥电议型 号：T6400产 地：中国大陆
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T7681AZD-5069inhibit,CXCR,Inhibitor,AZD-5069,AZD5069,AZD 5069,CXC chemokine receptors
AZD-5069 is an chemokine receptor 2 antagonist (CXCR2; IC50 = 0.79 nM).
价 格：￥电议型 号：T7681产 地：中国大陆
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T6218SelumetinibARRY-142886；AZD6244；司美替尼
Selumetinib (AZD6244) is an effective, specific inhibitor of MEK1 and ERK1/2 phosphorylation (IC50: 14/10 nM).
价 格：￥电议型 号：T6218产 地：中国大陆
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T6093AZD-7762AZD7762
AZD7762, an effective and specific inhibitor of Chk1（IC50=5 nM）, is equally potent against Chk2 and less potent against CAM, Yes, Fyn, Lyn, Hck and Lck.
价 格：￥电议型 号：T6093产 地：中国大陆
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T6092SapitinibAZD-8931；沙普替尼
AZD8931, a reversible, ATP competitive inhibitor of EGFR(IC50=4 nM), ErbB2(IC50=3 nM) and ErbB3(IC50=4 nM), is more effective over Gefitinib or Lapatinib against NSCLC cell, 100-fold more specific for the ErbB family over MNK1 and Flt.
价 格：￥电议型 号：T6092产 地：中国大陆
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T6087AZD 6482KIN 193；AZD6482
AZD 6482 is a potent and selective p110β inhibitor with IC50 of 0.69 nM and a PI3Kβ inhibitor with IC50 of 10 nM.
价 格：￥电议型 号：T6087产 地：中国大陆
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T6083AZD8330ARRY-424704；ARRY-704
AZD8330 is a novel, selective, non-ATP competitive MEK 1/2 inhibitor with IC50 of 7 nM. Phase 1.
价 格：￥电议型 号：T6083产 地：中国大陆
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T6078SaracatinibAZD0530；塞卡替尼
Saracatinib (AZD0530) is an effective Src inhibitor (IC50: 2.7 nM), and effective to Lck, Fyn, Lyn, Blk, Fgr and c-Yes.
价 格：￥电议型 号：T6078产 地：中国大陆
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T5463VerdiperstatAZD3241；AZD 3241
Verdiperstat (AZD3241) is a selective, irreversible and orally active myeloperoxidase inhibitor, with an IC50 of 630 nM, and can be used in the research of neurodegenerative brain disorders.
价 格：￥电议型 号：T5463产 地：中国大陆
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T5409AZD3229
AZD3229 is a potent pan-KIT mutant inhibitor for the treatment of gastrointestinal stromal tumors. It demonstrates potent single-digit nM growth inhibition across a broad cell panel.
价 格：￥电议型 号：T5409产 地：中国大陆
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T5175azd1390
AZD1390 is an exceptionally potent inhibitor of ATM in cells (IC50: 0.78 nM) with >10,000-fold selectivity over closely related members of the PIKK family of enzymes.
价 格：￥电议型 号：T5175产 地：中国大陆
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T4489AKT-IN-16-[4-(1-氨基环丁基)苯基]-5-苯基-3-吡啶甲酰胺；AZD-26；AZD 26；AZD26
AZD-26 is an allosteric AKT inhibitor (IC50: 1.04 μM).
价 格：￥电议型 号：T4489产 地：中国大陆
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T4300AZD2098
AZD2098 is a potent CC-chemokine receptor 4 (CCR4) inhibitor used for asthma research.
价 格：￥电议型 号：T4300产 地：中国大陆
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T4265AZD4635HTL1071
AZD4635 is a new-type adenosine 2A receptor (A2AR) inhibitor(Ki=1.7 nM).
价 格：￥电议型 号：T4265产 地：中国大陆
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T4249AZD3759 hydrochloride
AZD3759 (hydrochloride) is an effective, orally active and central nervous system-penetrant EGFR inhibitor. At Km ATP concentrations, the IC50s are 0.2/0.3/0.2 nM for EGFR (L858R)/EGFR (wt)/EGFR (exon 19Del).
价 格：￥电议型 号：T4249产 地：中国大陆
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T3975AZD9496
AZD9496 is an orally available selective estrogen receptor(ERα) antagonist, with potential antineoplastic activity.
价 格：￥电议型 号：T3975产 地：中国大陆
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T3659ZorifertinibAZD3759
AZD3759 is an orally active, effective and central nervous system-penetrant EGFR inhibitor. The IC50 values were 0.2, 0.3 and 0.2 nM for EGFR L858R mutant, TK wild-type, and Exon 19Del enzymes, respectively.
价 格：￥电议型 号：T3659产 地：中国大陆
