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T5399GeA-69
GeA-69 (GeA69) is a selective and allosteric PARP14 macrodomain 2 (MD2) inhibitor (Kd: 0.86 μM in ITC assays).
价 格：￥电议型 号：T5399产 地：中国大陆
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T5398BMS 599626 2HCl (873837-23-1(HCl))AC480 dihydrochloride
BMS-599626 (AC480) is a selective inhibitor of HER1 and HER2 (IC50s: 20 nM and 30 nM), ~8-fold less potent to HER4, >100-fold to Lck, VEGFR2, c-Kit, MET, etc.
价 格：￥电议型 号：T5398产 地：中国大陆
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T5396Letermovir莱莫维韦；MK-8828；AIC246
Letermovir (AIC246) is a novel anti-CMV compound (EC50: about 5 nM in fibroblast cells). It targets the pUL56 subunit of the viral terminase complex.
价 格：￥电议型 号：T5396产 地：中国大陆
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T5395BSJ-03-123
BSJ-03-123 is a potent, CDK6-selective small-molecule degrader.
价 格：￥电议型 号：T5395产 地：中国大陆
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T5394Prulifloxacin普卢利沙星；Pruvel；NM441；AF 3012
Prulifloxacin is a broad-spectrum fluoroquinolone antibiotic. It Inhibits bacterial DNA synthesis by inhibiting the activity of bacterial DNA topoisomerase II and IV.
价 格：￥电议型 号：T5394产 地：中国大陆
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T5393CK1-IN-1PUN51207
CK1-IN-1, compound 1c reported in patent WO2015119579A1, is a casein kinase 1 (CK1) inhibitor. It has IC50s of 15 nM, 16 nM, 73 nM for CK1δ, and CK1ε, p38σ MAPK, respectively.
价 格：￥电议型 号：T5393产 地：中国大陆
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T5392TP0463518
TP-0463518 is a highly potent HIF prolyl hydroxylase (PHD) inhibitor (IC50s: 13 nM and 18 nM for human and rat PHD2, respectively).
价 格：￥电议型 号：T5392产 地：中国大陆
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T5391Bepridil hydrochlorideCERM 1978；盐酸苄普地尔
Bepridil is a calcium channel blocker and also inhibits Na+/Ca2+ exchange (NCX), sodium channels and cardiac sarcolemmal KATP channels.
价 格：￥电议型 号：T5391产 地：中国大陆
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T5389Volinanserin氟利色林；MDL100907；M 100907
Volinanserin (MDL 100907) is a potent and selective antagonist of the serotonin receptor 5-HT2 (Ki: 0.36 nM) and shows 300-fold selectivity for 5-HT2 receptor over 5-HT1c, alpha-1 adrenergic and sigma receptors.
价 格：￥电议型 号：T5389产 地：中国大陆
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T53882,5-PYRIDINEDICARBOXYLIC ACID
2,5-Pyridinedicarboxylic Acid is used in the preparation of new derivatives as antiviral agents.
价 格：￥电议型 号：T5388产 地：中国大陆
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T5387LP-211
LP-211 is a brain penetrant selective agonist for a 5-HT7 receptor (Ki: 0.58 nM), and >300-fold selectivity over the 5-HT1A receptor.
价 格：￥电议型 号：T5387产 地：中国大陆
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T5386Asapiprant
Asapiprant (S-555739) is a potent and selective DP1 receptor antagonist (Ki: 0.44 nM). It exhibited high affinity and selectivity for the DP1 receptor.
价 格：￥电议型 号：T5386产 地：中国大陆
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T5385RadiprodilRGH-896
Radiprodil (RGH-896) is an orally active and selective NMDA NR2B receptors antagonist. It was a potential treatment of neuropathic pain associated with diabetic peripheral neuropathy (DPNP).
价 格：￥电议型 号：T5385产 地：中国大陆
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T5384RS 504393
RS 504393 is a highly selective CCR2 chemokine receptor antagonist (IC50s: 89 nM and > 100 μM for human recombinant CCR2 and CCR1).
价 格：￥电议型 号：T5384产 地：中国大陆
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T5383D3-βArrNCGC00379308
D3-βArr is a positive allosteric modulator for thyrotropin receptor (TSHR), which initiates translocation of β-Arr 1 (EC50: 11.6 μM) by direct TSHR activation.
价 格：￥电议型 号：T5383产 地：中国大陆
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T5382RitlecitinibPF-06651600
PF-06651600 is a potent JAK3-selective inhibitor (IC50: 33.1 nM).
价 格：￥电议型 号：T5382产 地：中国大陆
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T5380Ansofaxine hydrochlorideAnsofaxine盐酸盐；LPM570065；LY03005
Ansofaxine (LY03005; LPM570065) is a serotonin-norepinephrine-dopamine reuptake inhibitor (IC50s: 723, 763 and 491 nM, respectively).
价 格：￥电议型 号：T5380产 地：中国大陆
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T5379(Rac)-Antineoplaston A103-苯基乙酰氨基-2,6-哌啶二酮；Antineoplaston A10
(Rac)-Antineoplaston A10 is a naturally occurring substance and the first antineoplaston in the human body to be chemically identified. It displayed anti-proliferative action inhibiting cell growth.
价 格：￥电议型 号：T5379产 地：中国大陆
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T5378alpha-Cypermethrin右旋反式苯醚菊酯；Fendana
α-Cypermethrin is a synthetic pyrethroid pesticide used in large-scale commercial agricultural applications.
价 格：￥电议型 号：T5378产 地：中国大陆
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T5377Dimethyl itaconate
Dimethyl Itaconate is a chemical reagent used in the synthesis of functionalized 2-isoxazolines used in fragment-based drug discovery.
价 格：￥电议型 号：T5377产 地：中国大陆
