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T10595BQ-788；化合物BQ-788BQ788；BQ788
BQ-788 is a selective and potent ETB receptor antagonist with potential hypertensive activity.BQ-788 inhibits ET-1 binding to ETB receptors and inhibits exogenous ET-1-induced elevation of coronary artery perfusion pressure.
价 格：￥电议型 号：T10595产 地：中国大陆
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T10594bpV(phen)；化合物 T10594bpV(phen)
bpV(phen) is a potent protein tyrosine phosphatase (PTP) and PTEN inhibitor (IC50s: 343 nM, 920 nM, and 38 nM for PTP-β, PTP-1B, and PTEN).
价 格：￥电议型 号：T10594产 地：中国大陆
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T10593BPR1M97；化合物BPR1M97BPR1M97
BPR1M97 is a mu opioid receptor (MOP) and neuropeptide-orphin FQ (NOP) receptor agonist with blood-brain barrier permeability and potency, with Kis values of 1.8 nM for MOP and 4.2 nM for NOP.BPR1M97 exhibits anti-injurious effects and antinociceptive effects.
价 格：￥电议型 号：T10593产 地：中国大陆
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T10592BPR1K871；化合物 T10592DBPR114；DBPR114
BPR1K871, a preclinical development candidate for anti-cancer therapy [1], is a potent, selective dual inhibitor targeting FLT3 and AURKA, with IC50 values of 19 nM and 22 nM, respectively.
价 格：￥电议型 号：T10592产 地：中国大陆
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T10591L(R)-BPO-27；化合物(R)-BPO-27(R)-BPO-27
(R)-BPO-27 is an orally active and potent ATP-competitive CFTR inhibitor (IC50: 4 nM) for the study of diarrhoea and polycystic kidney.
价 格：￥电议型 号：T10591L产 地：中国大陆
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T10591BPO-27 racemate；化合物BPO-27 racemateBPO-27 (racemate)；BPO-27 (racemate)
BPO-27 racemate (BPO-27 (racemate)) is an effective CFTR inhibitor with IC50 of 8 nM.
价 格：￥电议型 号：T10591产 地：中国大陆
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T10590Zatolmilast；化合物BPN14770BPN14770；BPN14770
Zatolmilast (BPN14770) is an allosteric inhibitor of selective phosphodiesterase 4D (PDE4D; IC50s: 7.8 nM and 7.4 nM for PDE4D7 and PDE4D3).
价 格：￥电议型 号：T10590产 地：中国大陆
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T1059Retinyl palmitate；维生素A棕榈酸酯Retinol palmitate|||Vitamin A palmitate|||Retinyl (Vitamin A) Palmitate；Re
Retinyl palmitate (Vitamin A palmitate) is a naturally-occurring phenyl analogue of retinol, with potential antineoplastic and chemopreventive activities.
价 格：￥电议型 号：T1059产 地：中国大陆
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T10572LBMT-124110 Formate；BMT-124110甲酸盐BMT-124110 Formate（1679371-59-5 Free base）；BMT-124110 Formate（167937
BMT-124110 Formate is a selective AAK1 inhibitor (IC50: 0.9 nM) with anti-injury sensory activity.BMT-124110 Formate inhibits the BMP-2-inducible protein kinase BIKE with an IC50: 17 nM.BMT-124110 Formate inhibits the cell-cycle protein G-related BMT-124110 Formate inhibits the cell cycle protein G-associated kinase GAK with an IC50:99 nM.
价 格：￥电议型 号：T10572L产 地：中国大陆
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T10560P2X3 antagonist 34；化合物 T10560BLU-5937；BLU-5937
P2X3 antagonist 34, a potent, selective, and orally active antagonist, targets the P2X3 homotrimeric receptor, exhibiting IC50s of 25 nM, 92 nM, and 126 nM for human, rat, and guinea pig P2X3 receptors respectively. It shows reduced activity against P2X2/3 heterotrimeric receptors across human, rat, and guinea pig models. Notably, this compound demonstrates a significant anti-tussive effect without altering taste[1].
价 格：￥电议型 号：T10560产 地：中国大陆
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T10559Blonanserin D8；化合物 T10559AD-5423 D8；AD-5423 D8
Blonanserin D8 is a deuterium-labeled Blonanserin. Blonanserin (AD-5423) is a dopamine D2/5-HT2 receptor antagonist with an atypical antipsychotic effect.
价 格：￥电议型 号：T10559产 地：中国大陆
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T10474BAY-7598；化合物 T10474BAY-7598
BAY-7598 is a potent, selective, and orally bioavailable MMP12 inhibitor (IC50s: 0.085, 0.67, and 1.1 nM for human/murine/rat MMP12).
价 格：￥电议型 号：T10474产 地：中国大陆
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T10459Banoxantrone dihydrochloride；巴诺蒽醌盐酸盐Banoxantrone|||Banoxantrone dihydrochloride|||Banoxantrone|||AQ4
Banoxantrone dihydrochloride (AQ4N dihydrochloride) is a novel hypoxic cytotoxin that selectively kills hypoxic cells through an iNOS-dependent mechanism.
价 格：￥电议型 号：T10459产 地：中国大陆
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T10434AZD-5991；化合物 T10434AZD-5991
AZD-5991 is a potent and selective Mcl-1 inhibitor (IC50: 0.7 nM in FRET assay; Kd: 0.17 nM in SPR assay).
价 格：￥电议型 号：T10434产 地：中国大陆
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T10368Aripiprazole (D8)；化合物 T10368OPC-14597u00A0D8；OPC-14597u00A0D8
Aripiprazole D8 (OPC-14597 D8) is the deuterium-labeled Aripiprazole. Aripiprazole is a human 5-HT1A receptor partial agonist (Ki: 4.2 nM).
价 格：￥电议型 号：T10368产 地：中国大陆
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T10359AR antagonist 1；化合物AR antagonist 1AR antagonist 1
AR antagonist 1 is a potent antagonist of the androgen receptor. It binds to E3 ligase ligands with weak binding affinities to VHL protein in the synthesis of PROTAC ARD-266.
价 格：￥电议型 号：T10359产 地：中国大陆
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T10259AGI-25696；化合物AGI-25696AGI-25696
AGI-25696 is an inhibitor of methionine adenosyltransferase 2A (MATA2). AGI-25696 blocks the growth of MTAP-deleted tumors in vivo and can be used for studies about the treatment of cancer.
价 格：￥电议型 号：T10259产 地：中国大陆
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T10206A 419259；化合物 T10206RK-20449；RK-20449
A 419259 is a pyrrolo-pyrimidine inhibitor, designed to enhance selectivity towards the Src family (IC50s: 9 nM, <3 nM and <3 nM for Src, Lck and Lyn).
价 格：￥电议型 号：T10206产 地：中国大陆
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T1015948740 RP；化合物48740 RPRP-48740|||RP-55778|||RP 55779|||RP 55778；RP-48740|||RP-55778|||RP 55779|||RP 55
48740 RP (RP 55779) is an antagonist of platelet-activating factor.
价 格：￥电议型 号：T10159产 地：中国大陆
