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R2101012 Dafadine-A Dafadine-A是dafadine类似物,是C. elegans DAF-9 细胞色素P450抑制剂,还能抑制哺乳动物的CYP27A1。
R2101013 Fluxapyroxad Fluxapyroxad is a broad-spectrum fungicide that inhibits the succinate dehydroge
R2101014 WIKI4 WIKI4是Wnt/_beta_-catenin信号转到抑制剂,EC50值约75nM。
R2101015 PCNA-I 1 PCNA-I1 is a proliferating cell nuclear antigen (PCNA) inhibitor. It inhibits gr
R2101016 CYM50308 CYM50308 是一种有效的,选择性和高亲和力的鞘氨醇-1-磷酸受体 4 (S1P4-R) 激动剂,EC50 为 56 nM。CYM50308 对 S1P4-
R2101017 BC-1215 BC-1215 是 F-box protein 3 (FBXO3) 的抑制剂,IL-1β 释放时,IC50 值为 0.9 μg/mL。 BC-1215 降低 F
R2101018 BC-1258 密度 1.2±0.1 g/cm3 沸点 599.9±60.0 °C at 760 mmHg 闪点 316.6±32.9 °C 蒸汽压 0.0±1.7 mmHg
R2101019 BMS-191011 BMS-191011 (BMS-A) 是一种大电导钙激活钾通道 (large-conductance, Ca2++-activated potassium (m
R2101020 CRT0066101 dihydrochloride CRT0066101 is a specific inhibitor of all Protein kinase D (PKD) isoforms.
R2101021 AA92593 AA92593 (Opn4 Antagonist) is a potent antagonist of melanopsin-mediated phototra
R2101022 ML335 ML335 (CYM 51010, CID-23723457) is an agonist for OPRM1(μ-opioid receptor)-OPRD1
R2101023 VK-II-36 VK-II-36 is a carvedilol analog that suppresses sarcoplasmic reticulum (SR) Ca(2
R2101024 YMU1 ML335 (CYM 51010, CID-23723457) is an agonist for OPRM1(μ-opioid receptor)-OPRD1
R2101025 ML254 ML254 is shown to competitively interact with the MPEP allosteric binding site.
R2101026 PU-H54 A potent, selective Grp94 inhibitor.
R2101027 ML303 ML303 是一种吡唑并吡啶类化合物, 是流感病毒非结构蛋白 1 (NS1) 的拮抗剂 (IC90 为 155 nM),其对流感病毒H1N1亚型的 EC50 值
R2101028 Nisoxetine hydrochloride Nisoxetine hydrochloride 是一种有效的和选择性的去甲肾上腺素转运蛋白 (NET) 的抑制剂,Kd 值为 0.76 nM。Nisoxeti
R2101029 ASN03576800 ASN03576800 is an inhibitor of the VP40 matrix protein.
R2101030 HA-155 HA155 (Autotaxin Inhibitor IV), a boronic acid-based compound, inhibits autotaxi
R2101031 CYM5520 noncompetitive allosteric agonist of S1P2
R2101032 CRT5 CRT5 (CRT0066051), a pyrazine benzamide, is a potent and selective PKD inhibitor
R2101033 BMS453 BMS453 (BMS-189453) 是一种合成类维生素 A,是一种 RARβ 激动剂和 RARα/RARγ 拮抗剂。BMS453 主要通过诱导活性 TGFβ
R2101034 Mps1-IN-3 Mps1-IN-3 是一种有效的,选择性的 MPS1 抑制剂,IC50 值为 50 nM。
R2101035 OS-3-106 OS-3-106 is a novel dopamine D3 receptor-selective partial agonist.
R2101036 NSC-703786 A potent, selective antitumour agent through activation the aryl hydrocarbon rec
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