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T68304AZD-2066 hydrochloride；化合物 AZD-2066 hydrochlorideAZD-2066 hydrochloride
AZD-2066 hydrochloride is an mGlu5 antagonist.
价 格：￥电议型 号：T68304产 地：中国大陆
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T68281AZD-1386；化合物 AZD-1386AZD-1386
AZD1386 is an orally available antagonist of the transient receptor potential channel TRPV1. Note: Structure of this product was from NIH/NCATS web page: https://drugs.ncats.io/drug/210323T9CP and drugbank web page: https://go.drugbank.com/drugs/DB15333.
价 格：￥电议型 号：T68281产 地：中国大陆
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T68271AZD1386；化合物 AZD1386AZD1386
AZD1386 is a TRPV1 antagonist. AZD1386 acts as a competitive antagonist at the channel´s capsaicin binding site.
价 格：￥电议型 号：T68271产 地：中国大陆
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T68240AZD-9819；化合物 AZD-9819AZD-9819
AZD-9819 is an inhibitor of human neutrophil elastase for potential treatment of chronic obstructive pulmonary disease (COPD).
价 格：￥电议型 号：T68240产 地：中国大陆
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T6774AZD-8835；化合物AZD8835AZD8835；AZD8835
AZD-8835 is a mixed inhibitor of PI3Kα/δ (IC50: 6.2/5.7 nM), also with selectivity against PI3Kβ/γ (IC50: 431/90 nM).
价 格：￥电议型 号：T6774产 地：中国大陆
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T6773AZD8186；化合物AZD8186AZD8186
AZD8186 is an effective and specific PI3Kβ/δ inhibitor (IC50: 4/12 nM).
价 格：￥电议型 号：T6773产 地：中国大陆
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T6772AZD3839 free base；化合物AZD3839AZD3839；AZD3839
AZD3839 free base 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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T6770AZD0156；化合物AZD0156AZD0156
AZD0156 , an effective and specific inhibitors of ATM kinase, is potential antineoplastic activities and chemo-/radio-sensitizing.
价 格：￥电议型 号：T6770产 地：中国大陆
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T64378AZD0095；化合物AZD0095AZD0095
AZD0095 is a selective inhibitor of MCT4?with an IC50 of 1.3 nM.
价 格：￥电议型 号：T64378产 地：中国大陆
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T64362AZD0780；化合物AZD0780PCSK9-IN-12|||EX-A6975；PCSK9-IN-12|||EX-A6975
AZD0780 (EX-A6975) exhibits bind affinity for PCSK9 ( Kd ＜200 nM). AZD0780 has research value in cholesterol metabolism.
价 格：￥电议型 号：T64362产 地：中国大陆
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T6400AZD3514；化合物AZD3514AZD3514
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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T6399AZD1981；化合物AZD1981Prostaglandin Receptor|||AZD 1981|||AZD1981|||Inhibitor|||AZD 1981|||AZD-1981|||AZ
AZD1981 is an effective and specific CRTh2 (DP2) receptor antagonist (IC50: 4 nM), showing >1000-fold selectivity over more than 340 other enzymes and receptors, including DP1. AZD1981 has been used in trials studying the treatment and basic science of Asthma, Postmenopausal, Pharmakokinetic, Asthma Patients, and Drug Interaction, among others.
价 格：￥电议型 号：T6399产 地：中国大陆
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T63838AZD5462；化合物AZD5462AZD5462
AZD5462 is a potent orally available relaxin receptor RXFP1 agonist for the study of heart failure and cancer.
价 格：￥电议型 号：T63838产 地：中国大陆
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T63236AZD4625；化合物 AZD4625AZD4625
AZD4625 (Compound 21) is a selective, potent, orally active, covalent and mutagenic mutant GTPaseKRASG12C inhibitor.
价 格：￥电议型 号：T63236产 地：中国大陆
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T6218Selumetinib；司美替尼ARRY-142886|||AZD6244；ARRY-142886|||司美替尼|||AZD6244
Selumetinib (AZD6244) (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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T62154AZD1208 hydrochloride；化合物 AZD1208 hydrochlorideAZD1208 hydrochloride
AZD1208 hydrochloride is a highly selective, potent and orally active PIM inhibitor.
价 格：￥电议型 号：T62154产 地：中国大陆
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T61895AZD7254；化合物 AZD7254AZD7254
AZD7254 is an oral effective Smoothened (SMO) inhibitor, and the EC50 of sonic Hh protein (shh) is 1.0 nM.
价 格：￥电议型 号：T61895产 地：中国大陆
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T61708AZD 2066 hydrate；化合物 AZD 2066 hydrateAZD 2066 hydrate
AZD 2066 hydrate is a selective, orally active, and brain-penetrant antagonist of mGluR5. It exhibits antinociceptive effects [1].
价 格：￥电议型 号：T61708产 地：中国大陆
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T61028Mitiperstat；化合物MitiperstatAZD4831；AZD4831
Mitiperstat is a potent myeloperoxidase (MPO) inhibitor that is effective in preventing cardiovascular diseases such as heart failure and coronary artery disease.
价 格：￥电议型 号：T61028产 地：中国大陆
