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T27289Etacstil；化合物 T27289GW 5638|||GW-5638|||GW5638|||DPC974|||DPC 974|||DPC-974；GW 5638|||GW-5638|||GW563
GW5638 is a estrogen receptor ligand. GW5638 is a prodrug of its active metabolite GW7604. GW5638 appears to act as an antagonist in these in vitro systems, although in a manner distinct from other known ER modulators. GW5638 is also classified as a pseudo-SERD, which could form the basis of a new paradigm of breast cancer hormonal therapy in its own right.
价 格：￥电议型 号：T27289产 地：中国大陆
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T26642Aplaviroc hydrochloride；化合物 T26642AK602|||AK 602|||GW873140A|||GW-873140|||GW873140|||AK-602|||Aplav
Aplaviroc is a human cellular CC chemokine receptor 5 (CCR5) entry inhibitor. Aplaviroc binds specifically to CCR5 and demonstrates potent anti-human immunodeficiency virus activity in vitro in the subnanomolar range. In vitro studies show that aplaviroc selectively inhibits the binding of a particular monoclonal antibody, 45531, to CCR5.
价 格：￥电议型 号：T26642产 地：中国大陆
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T2659GW2580；化合物GW 2580GW 2580|||SC-203877；GW 2580|||SC-203877
GW2580 (SC-203877) is a specific, oral-bioavailable CSF-1R inhibitor for c-FMS.
价 格：￥电议型 号：T2659产 地：中国大陆
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T2657Elacridar；依克立达GW0918|||GW120918|||GF120918|||GG918；GW0918|||依克立达|||GW120918|||GF120918|||GG918
Elacridar (GG918) (GF120918) is an effective BCRP and P-gp (MDR-1) inhibitor.
价 格：￥电议型 号：T2657产 地：中国大陆
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T25474GW-Amide；化合物 T25474Glycyl-tryptophanamide|||GW Amide；Glycyl-tryptophanamide|||GW Amide
GW-Amide is a molluscan neuropeptide that exhibits potent modulatory effects on molluscan muscles.
价 格：￥电议型 号：T25474产 地：中国大陆
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T25473GW833373X；化合物 T25473GW 833373 X|||GW-833373-X|||GW 833373X|||GW-833373X；GW 833373 X|||GW-833373-X|||
GW833373X is a GSK3beta inhibitor.
价 格：￥电议型 号：T25473产 地：中国大陆
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T25472GW0791；化合物 T25472GW 0791|||GW-0791；GW 0791|||GW-0791
GW0791 is a retinoid X receptor α (RXRα) agonist.
价 格：￥电议型 号：T25472产 地：中国大陆
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T24752S-1360；化合物 T24752GW810781|||GW-810781|||GSK-S-1360|||S1360|||S 1360；GW810781|||GW-810781|||GSK-S-136
S-1360 is an inhibitor of HIV-1 integrase.
价 格：￥电议型 号：T24752产 地：中国大陆
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T24125GW8510；化合物 T24125GW 8510|||GW-8510；GW 8510|||GW-8510
GW8510 is a cyclin kinase 2 inhibitor.
价 格：￥电议型 号：T24125产 地：中国大陆
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T24124GW827106X；化合物 T24124GW 827106 X|||GW-827106X|||GW-827106-X；GW 827106 X|||GW-827106X|||GW-827106-X
GW827106X is an effective inhibitor of GSK-3. It is highly selective over CDK-2.
价 格：￥电议型 号：T24124产 地：中国大陆
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T24123GW780056X；化合物 T24123GW-780056-X|||GW 780056 X；GW-780056-X|||GW 780056 X
GW780056X is a selective inhibitor of cyclin-dependent kinase. GW780056X is also an inhibitor of Yes1 kinase. It is an inhibitor of binding or entry into cells for the Lassa Virus.
价 格：￥电议型 号：T24123产 地：中国大陆
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T24122GW648495；化合物 T24122DSM-1|||GW-648495|||DSM 1|||GW 648495|||DSM1；DSM-1|||GW-648495|||DSM 1|||GW 64849
GW648495 is a PfDHODH inhibitor that shows greater than 4,000-fold selectivity for the malarial enzyme.
价 格：￥电议型 号：T24122产 地：中国大陆
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T24120GW-328267；化合物 T24120J2.047.755E|||GW328267X；J2.047.755E|||GW328267X
GW-328267 is an agonist of the adenosine A2 receptor.
价 格：￥电议型 号：T24120产 地：中国大陆
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T24119GW2974；化合物 T24119GW-2974|||GW 2974；GW-2974|||GW 2974
GW2974 is a potent and selective dual EGFR inhibitor.
价 格：￥电议型 号：T24119产 地：中国大陆
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T22827GW 583340 dihydrochloride；化合物 T22827GW 583340 dihydrochloride
dual EGFR/ErbB2 tyrosine kinase inhibitor
价 格：￥电议型 号：T22827产 地：中国大陆
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T22826GW 542573X；化合物GW 542573XGW 542573X
GW 542573X is a potent and selective small molecule Ca2+-activated K+ 2 (SK2) channel activator.GW 542573X induces a leftward shift in the Ca2+ response curve of hSK1 from an EC50 (Ca2+) value of 410 nM to 240 nM, which can be used to study neurological disorders.
价 格：￥电议型 号：T22826产 地：中国大陆
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T2277Losmapimod；洛批莫德GSK-AHAB|||GW856553X|||GW856553|||SB856553；GSK-AHAB|||GW856553X|||6-[5-(环丙基氨基甲酰基)-3-氟
Losmapimod (GSK-AHAB) (GW856553X; SB856553; GSK-AHAB) is a specific, potent, and orally active p38 MAPK inhibitor (pKi: 8.1/7.6 for p38α/β).
价 格：￥电议型 号：T2277产 地：中国大陆
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T2260GW96622-氯-5-硝基-N-苯基苯酰胺2-氯-5-硝基-N-苯基苯酰胺|||TIMTEC-BB SBB006523|||GW 9662
GW9662 (TIMTEC-BB SBB006523) is a specific PPARγ antagonist (IC50: 3.3 nM, in a cell-free assay), with 100 to 1000-fold functional selectivity for PPARγ than PPARα/δ in cells.
价 格：￥电议型 号：T2260产 地：中国大陆
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T2233GW 4064；化合物GW 4064GW 4064
GW 4064 is an effective farnesoid X receptor (FXR) agonist (EC50 =65 nM).
价 格：￥电议型 号：T2233产 地：中国大陆
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T21804GW 610；化合物GW 610GW 610
GW 610 is an antitumor benzothiazole that shows growth-inhibitory activity against several cancer cell lines. In MCF-7 and MDA 468 human cancer cell lines, potent antiproliferative activity (growth inhibition (GI50) < 0.1 nM) was observed.
价 格：￥电议型 号：T21804产 地：中国大陆
