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T2357GSK1059615；化合物GSK-1059615GSK 1059615|||GSK-1059615；GSK 1059615|||GSK-1059615
GSK1059615 has been used in trials studying the treatment of Lymphoma, Solid Tumours, Endometrial Cancer, Solid Tumor Cancer, and Metastatic Breast Cancer.
价 格：￥电议型 号：T2357产 地：中国大陆
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T22821GSK J5；化合物GSK J5GSK-J5|||GSKJ5；GSK-J5|||GSKJ5
GSK J5 is an inhibitor of schistosomes and helminths and is often used as a trematode insecticide.GSK J5 promotes schistosome mortality in a dose- and time-dependent manner.GSK J5 increases the mortality rate of schistosomes and decreases the viability of adult worms.GSK J5 is an inhibitor of schistosomes and helminths and is often used as a trematode insecticide.
价 格：￥电议型 号：T22821产 地：中国大陆
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T22815GSK 1562590 hydrochloride；化合物 T22815GSK 1562590 hydrochloride
urotensin II (UT) receptor antagonist
价 格：￥电议型 号：T22815产 地：中国大陆
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T22805GR 125487 sulfamate化合物 T22805GR 125487 sulfamate
GR 125487 sulfamate is a 5-HT4 receptor antagonist.
价 格：￥电议型 号：T22805产 地：中国大陆
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T22390Olanexidine Hydrochloride semihydrate；奥兰西丁标准品HCLOPB-2045|||OPB-2045G；OPB-2045|||OPB-2045G|||奥兰西丁标准品H
Olanexidine is a monobiguanide compound with the activity of bactericidal.
价 格：￥电议型 号：T22390产 地：中国大陆
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T21831UCM05；化合物UCM05G28UCM；G28UCM
UCM05 (G28UCM) is a potent inhibitor of fatty acid synthase (FASN) with efficacy against HER2+ breast cancer xenografts, including in cell lines resistant to anti-HER2 drugs [1]. Additionally, it functions as an inhibitor of the Filamentous temperature-sensitive protein Z (FtsZ), selectively inhibiting the growth of the Gram-positive bacterium B. subtilis with minimum inhibitory concentration (MIC) values of 100 μM, while showing no activity against the Gram-negative bacterium E. coli [2].
价 格：￥电议型 号：T21831产 地：中国大陆
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T2039GSK-923295；化合物GSK923295GSK-923295
GSK923295 is a selective allosteric inhibitor of CENP-E kinesin motor ATPase(Ki=3.2 nM).
价 格：￥电议型 号：T2039产 地：中国大陆
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T20177C.I. Vat Yellow 2；还原黄 2Caledon Printing Yellow 5G|||Vat Yellow 2|||Calcoloid Yellow GCD；Caledon Prin
C.I. Vat Yellow 2 (Calcoloid Yellow GCD) is a yellow dye agent that can also be used to detect adsorption behavior on natural sediments.
价 格：￥电议型 号：T20177产 地：中国大陆
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T1945GNE-7915；化合物GNE7915GNE7915；GNE7915
GNE-7915 is a highly potent, selective and brain-penetrable leucine-rich repeat kinase 2 (LRRK2) inhibitor.
价 格：￥电议型 号：T1945产 地：中国大陆
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T1871GBR 12935 dihydrochloride；化合物GBR-12935GBR12935|||GBR-12935|||GBR 12935；GBR12935|||GBR-12935|||GBR 12
GBR 12935 dihydrochloride (GBR 12935) can induce the increase of the extracellular levels of dopamine to basal levels.
价 格：￥电议型 号：T1871产 地：中国大陆
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T1803GNF-5；化合物GNF-5GNF 5；GNF 5
GNF-5 is a specific non-ATP competitive inhibitor of Bcr-Abl (IC50: 0.22±0.1 uM, Wild-type Abl). It is an analog of GNF-2 with improved pharmacokinetic properties.
价 格：￥电议型 号：T1803产 地：中国大陆
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T17985Gemcitabine-O-Si(di-iso)-O-Mc；化合物 T17985Gemcitabine-O-Si(di-iso)-O-Mc
Gemcitabine-O-Si(di-iso)-O-Mc, a drug-linker conjugate for Antibody-Drug Conjugates (ADC), exhibits potent antitumor activity. It incorporates Gemcitabine, a pyrimidine nucleoside analog antimetabolite and antineoplastic agent, connected through the ADC linker[1].
价 格：￥电议型 号：T17985产 地：中国大陆
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T1770GNE-9605；化合物GNE9605GNE-9605
GNE-9605 is a highly effective, specifical, and brain-penetrant LRRK2 inhibitor (IC50: 19 nM).
价 格：￥电议型 号：T1770产 地：中国大陆
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T15455RGH-5526；化合物 T15455GYKI-11679；GYKI-11679
RGH-5526 is a novel antihypertensive drug. It causes an increase in hypothalamic norepinephrine (NA) turnover (utilization), and the increase in hypothalamic noradrenergic neuron activity may lead to a decrease in peripheral sympathetic nerve activity, resulting in a significant reduction in blood pressure.
价 格：￥电议型 号：T15455产 地：中国大陆
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T15437GSK3145095；化合物GSK3145095GSK3145095
GSK3145095 is an orally active inhibitor of RIPK1 with IC50 of 5 nM, with potential immunomodulatory activities and antineoplastic.
价 格：￥电议型 号：T15437产 地：中国大陆
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T15425GSK1702934A；化合物 T15425GSK1702934A
GSK1702934A is a selective TRPC3 agonist. It modulates cardiac contractility and f arrhythmogenesis by activation of TRPC3.
价 格：￥电议型 号：T15425产 地：中国大陆
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T15365G-744；化合物 T15365G-744
G-744 is a selective and orally active inhibitor of Btk (IC50: 2 nM). G-744 is well-tolerated, metabolically stable. It also has an efficacious to treat arthritis.
价 格：￥电议型 号：T15365产 地：中国大陆
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T14525Begacestat化合物 T14525GSI-953
Begacestat is a selective thiophene sulfonamide amyloid precursor protein gamma-secretase inhibitor (Aβ40,IC50=15 nM),and for the treatment of Alzheimer´s disease.
价 格：￥电议型 号：T14525产 地：中国大陆
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T14095ACH-806；化合物 T14095GS9132；GS9132
ACH-806 is an NS4A antagonist. It can inhibit Hepatitis C Virus (HCV) replication with an EC50 of 14 nM.
价 格：￥电议型 号：T14095产 地：中国大陆
