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T27373FR-181157；化合物 T27373FR-181157 Free Base；FR-181157 Free Base
FR-181157, a novel prostaglandin (PG) mimetic, shows high potency and agonist efficacy at the IP receptor and has good bioavailability.
价 格：￥电议型 号：T27373产 地：中国大陆
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T27372FR-168888 mesylate；化合物 T27372FR-168888|||FR-168888 Free Base|||FR168888|||FR 168888；FR-168888|||FR-1
FR-168888, a new Na+/H+ exchange inhibitor, can protect the heart from arrhythmia and myocardial cell death in ischemic and reperfused situations.
价 格：￥电议型 号：T27372产 地：中国大陆
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T27347Fonsartan free acid；化合物 T27347HR720|||HOE720|||HR-720|||HOE-720；HR720|||HOE720|||HR-720|||HOE-720
Fonsartan is an angiotensin receptor antagonist. Fonsartan inhibits the angiotensin II-induced trophic effects, fibronectin release and fibronectin-EIIIA+ expression in rat aortic vascular smooth muscle cells in vitro.
价 格：￥电议型 号：T27347产 地：中国大陆
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T27342LFlurocitabine HCl；氟西他滨盐酸盐Flurocitabine HCl(37717-21-8 Free base)；Flurocitabine HCl(37717-21-8 Free b
Flurocitabine HCl is a fluorinated anhydride analog of cytarabine, which is partially hydrolyzed in vivo to two active antitumor substances (arabinosyl-fluorouracil (ara-FC) and arabinosyl-fluorouracil (ara-FU)).Flurocitabine HCl has demonstrated antitumor activity in phase I studies in acute leukemia and solid tumors.
价 格：￥电议型 号：T27342L产 地：中国大陆
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T27325FK-739 free acid；化合物 T27325FK-739|||FK 739|||FK739；FK-739|||FK 739|||FK739
FK-739 is an angiotensin type 1 receptor antagonist. FK 739 inhibits the specific binding of [125I]-angiotensin II to rat aortic smooth muscle cell membrane (IC50 = 8.6 nM) without displacing the specific binding of [125I]-angiotensin II to bovine cerebellum membrane.
价 格：￥电议型 号：T27325产 地：中国大陆
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T27307LFasnall HCl；Fasnall盐酸盐Fasnall HCl（929978-58-5 Free base）；Fasnall HCl（929978-58-5 Free base）
Fasnall HCl is a selective FASN inhibitor that acts through its co-factor binding sites. Fasnall HCl also shows potent anti-tumor activity in the MMTV-Neu model of HER2(+) breast cancer, particularly when combined with carboplatin.
价 格：￥电议型 号：T27307L产 地：中国大陆
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T27286LEsprolol；化合物 EsprololACC-9369 free base；ACC-9369 free base
Esprolol (ACC-9369 free base) is a novel β-adrenergic receptor antagonist for the study of exertional angina.
价 格：￥电议型 号：T27286L产 地：中国大陆
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T27275LEpaminurad HCl（1198153-15-9 Free base）；化合物 Epaminurad HCl（1198153-15-9 Free base）Epaminurad HCl（1198
产品可用于生物细胞实验
价 格：￥电议型 号：T27275L产 地：中国大陆
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T27272EO-122；化合物 T27272EO-122 free|||PFS 1144|||PFS-1144|||EO122；EO-122 free|||PFS 1144|||PFS-1144|||EO122
EO-122, a calcium channel antagonist and sodium channel antagonist, is used potentially for the treatment of arrhythmia.
价 格：￥电议型 号：T27272产 地：中国大陆
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T27250LElarofiban TFA；艾罗非班三氟乙酸盐Elarofiban TFA（198958-88-2 Free base）|||RWJ-53308 TFA；Elarofiban TFA（198958-
Elarofiban TFA (RWJ-53308 TFA) is a novel and orally active and selective GPIIb/IIIa antagonist for the study of cardiovascular disease.
价 格：￥电议型 号：T27250L产 地：中国大陆
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T27241EF1502 free base；化合物 T27241EF 1502 racemic|||Rac-EF 1502|||EF1502|||EF 1502|||EF-1502|||(R,S)-EF 150
EF1502 is a potent and selective GABA transporter inhibitor.
价 格：￥电议型 号：T27241产 地：中国大陆
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T27228E-3030 free acid；化合物 T27228E-3030|||E3030|||E 3030；E-3030|||E3030|||E 3030
E-3030 free acid is a peroxisome proliferator-activated receptor (PPAR) agonist. E-3030 decreased blood glucose, triglyceride, non-esterified fatty acids, and insulin levels and increased blood adiponectin levels. Triglyceride- and non-high-density lipoprotein cholesterol-lowering actions of E-3030 involve combined effects on reduction of apo C-III and elevation of lipoprotein lipase, resulting in increased lipolysis.
价 格：￥电议型 号：T27228产 地：中国大陆
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T27211DS-8587；化合物 T27211DS 8587|||DS8587|||DS-8587 free；DS 8587|||DS8587|||DS-8587 free
DS-8587 is a DNA topoisomerase inhibitor. DS-8587 exhibits potent antibacterial activity against quinolone-resistant A. baumannii isolates that harbor mutations in quinolone resistance-determining regions. DS-8587 significantly reduces the number of viable bacteria in a murine model of F. necrophorum-induced liver abscess. In the presence of the efflux pump inhibitor 1-(1-napthylmethyl)-piperazine, no significant changes were observed in the MIC for DS-8587.
价 格：￥电议型 号：T27211产 地：中国大陆
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T27202DPC-423；化合物 T27202DPC-423 Free；DPC-423 Free
DPC-423 is a factor Xa inhibitor potentially for the treatment of thrombosis.
价 格：￥电议型 号：T27202产 地：中国大陆
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T27158LDF-1012 FA；DF-1012 甲酸盐DF-1012 FA（163220-65-3 Free base）；DF-1012 FA（163220-65-3 Free base）
DF-1012 FA is a structural analog of DF-1012, a neuropeptide inhibitor used in the study of asthma and cough.
价 格：￥电议型 号：T27158L产 地：中国大陆
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T26893Branaplam mesylate (1562338-42-4 free base)；化合物 T26893LMI070|||Branaplam mesylate|||LMI 070|||LMI-07
Branaplam is a highly potent, selective and orally active SMN2 splicing modulator. Branaplam increases the amount of functional SMN protein produced by the SMN2 gene through modifying its splicing.
价 格：￥电议型 号：T26893产 地：中国大陆
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T26848BMS-433771 free base；化合物 T26848BMS-433771|||BMS 433771|||BMS433771；BMS-433771|||BMS 433771|||BMS4337
BMS-433771, a novel inhibitor of respiratory syncytial virus (RSV), binds the RSV F glycoprotein and inhibits membrane fusion.
价 格：￥电议型 号：T26848产 地：中国大陆
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T26835BL-1021；化合物 T26835BL-1021 free|||AN 228|||AN-228；BL-1021 free|||AN 228|||AN-228
BL-1021, an adrenergic receptor antagonist, is used potentially for the treatment of neuropathic pain.
价 格：￥电议型 号：T26835产 地：中国大陆
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T26778LBesipirdine hydrochloride；贝西吡啶盐酸盐HP 749 hydrochloride|||Besipirdine hydrochloride（119257-34-0 Free b
Besipirdine hydrochloride is a non-receptor-dependent cholinomimetic compound with alpha-adrenergic and cardiovascular activities.Besipirdine hydrochloride inhibits voltage-dependent sodium-potassium channels and inhibits biogenic amine uptake.Besipirdine hydrochloride reduces schedule-induced thirst and enhances cholinergic and adrenergic neurotransmission in the central nervous system in rats.
价 格：￥电议型 号：T26778L产 地：中国大陆
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T26778Besipirdine；贝西吡啶HP 749 free base|||P-867493|||P867493|||HP 749|||HP749|||P 867493；HP 749 free base||
Besipirdine (HP 749 free base) is a non-receptor-dependent cholinomimetic compound with alpha-adrenergic and cardiovascular activities.Besipirdine inhibits voltage-dependent sodium-potassium channels and inhibits biogenic amine uptake.Besipirdine reduces schedule-induced irritability and thirst and enhances cholinergic and adrenergic activity in the CNS in the rat. Besipirdine reduces schedule-induced thirst and enhances cholinergic and adrenergic neurotransmission in the central nervous system.
价 格：￥电议型 号：T26778产 地：中国大陆
