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T2657ElacridarElacridar,GG918,GW0918
Elacridar (GF120918) is an effective BCRP and P-gp (MDR-1) inhibitor.
价 格：￥电议型 号：T2657产 地：美洲
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T2659GW 2580GW 2580,SC-203877,
GW2580 is a specific, oral-bioavailable CSF-1R inhibitor for c-FMS.
价 格：￥电议型 号：T2659产 地：美洲
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T5134Vilanterol trifenatateVilanterol trifenatate,GW642444 (trifenatate),
Vilanterol trifenatate is a long-acting agonist of β2-adrenoceptor (β2-AR) with inherent 24-hour activity(β2-AR, β1-AR and β3-AR pEC50s of 10.37, 6.98 and 7.36, respectively)
价 格：￥电议型 号：T5134产 地：美洲
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T6052GW 441756GW 441756
GW 441756 is a specific Tropomyosin-related kinase A (TrkA) inhibitor with an IC50 value of 2 nM.
价 格：￥电议型 号：T6052产 地：美洲
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T6235Lapatinib DitosylateLapatinib Ditosylate,GW-572016 ditosylate,Lapatinib (GW-572016) Ditosylate
Lapatinib is an effective EGFR and ErbB2 inhibitor (IC50: 10.8/9.2 nM for EGFR/ErbB2).
价 格：￥电议型 号：T6235产 地：美洲
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T6310GW3965 HClGW3965 HCl,GW3965 hydrochloride,
GW3965 HCl is an effective and specific LXR agonist for hLXRα/β (EC50: 190/30 nM).
价 格：￥电议型 号：T6310产 地：美洲
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T6603NelarabineNelarabine,GW 506U78,Nelzarabine
Nelarabine is a purine nucleoside analog and DNA synthesis inhibitor with IC50 from 0.067-2.15 μM in tumor cells.
价 格：￥电议型 号：T6603产 地：美洲
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T8486GW6471；化合物GW 6471GW 6471；GW 6471
GW6471 is a selective PPARα antagonist (IC50=0.24 μM) that enhances the binding affinity of the PPARα ligand-binding domain to the co-inhibitory proteins SMRT and NCoR. GW6471 has antitumor activity, inhibiting cell proliferation and inducing apoptosis.
价 格：￥电议型 号：T8486产 地：中国大陆
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T8238Fosamprenavir Calcium Salt；福沙那伟钙Diallyl Trisulfide|||GW433908G；福沙那伟钙|||Diallyl Trisulfide|||GW433908
Fosamprenavir Calcium Salt (GW433908G) (GW433908G) is a phosphate ester prodrug of the antiretroviral protease inhibitor Amprenavir, with improved solubility. Fosamprenavir Calcium Salt has Anti-HIV infection.
价 格：￥电议型 号：T8238产 地：中国大陆
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T82251GW274150 dihydrochloride；化合物 GW274150 dihydrochlorideGW274150 dihydrochloride
GW274150 (dihydrochloride) is a potent, selective inhibitor of human and rat inducible nitric oxide synthase (iNOS), exhibiting oral activity and NADPH-dependence with an IC50 of 2.19 μM and Kd of 40 nM for human iNOS, and an ED50 of 1.15 μM for rat iNOS. It demonstrates reduced effectiveness against endothelial NOS (eNOS) and neuronal NOS (nNOS) in both species. The compound has been shown to confer protective effects in acute lung injury inflammation models [1] [2] [3].
价 格：￥电议型 号：T82251产 地：中国大陆
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T8162Cannabidivarin；次大麻二酚Cannabidivarin|||GWP-42006|||GWP42006|||GWP 42006；Cannabidivarin|||GWP-42006|||G
Cannabidivarin (GWP42006) is a potent inhibitor against gamma 2 subunit of GABAA receptors. it may serve as a novel drug with definite control over childhood absence epilepsy.
价 格：￥电议型 号：T8162产 地：中国大陆
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T7805GW791343 dihydrochloride；化合物GW791343 dihydrochlorideGW791343 (HCl)；GW791343 (HCl)
GW791343 dihydrochloride (GW791343 (HCl)) is a P2X7 allosteric modulator.
价 格：￥电议型 号：T7805产 地：中国大陆
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T7742GW 284543 hydrochloride；化合物GW 284543 hydrochlorideGW 284543 hydrochloride
GW 284543 hydrochloride is a selective inhibitor of MEK5 .
价 格：￥电议型 号：T7742产 地：中国大陆
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T76268Mca-VDQVDGW-Lys(Dnp)-NH2；化合物 Mca-VDQVDGW-Lys(Dnp)-NH2Mca-VDQVDGW-Lys(Dnp)-NH2
Mca-VDQVDGW-Lys(Dnp)-NH2, a fluorogenic substrate specific to caspase-7, facilitates the quantification of caspase-7 activity.
价 格：￥电议型 号：T76268产 地：中国大陆
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T7614Eniluracil；化合物EniluracilGW776C85|||5-Ethynyluracil；GW776C85|||5-Ethynyluracil
Eniluracil (GW776C85) is an orally activedihydropyrimidine dehydrogenase (DPD) inhibitor,increases the oral bioavailability of 5-FU to 100%, facilitating uniform absorption and predictable toxicity.
价 格：￥电议型 号：T7614产 地：中国大陆
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T7610GW284543；化合物GW284543UNC10225170；UNC10225170
GW284543 (UNC10225170) is a selective inhibitor of MEK5 .
价 格：￥电议型 号：T7610产 地：中国大陆
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T75388FITC-GW3965；化合物 FITC-GW3965FITC-GW3965
FITC-GW3965, a fluorescence-labeled liver X receptor β (LXRβ) agonist, is derived from GW3965 by substituting its trifluoromethyl group with an amide linkage to FITC. This tracer facilitates the study of LXRβ function [1].
价 格：￥电议型 号：T75388产 地：中国大陆
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T75163GW297361；化合物GW297361GW297361
GW297361 is a potent inhibitor of the cell cycle protein-dependent kinase Cdk1 and also inhibits the Pho85 signaling pathway.The IC50s of GW297361 on yeast Cdk1 and Pho85 were 20 nM and 400 nM, respectively.
价 格：￥电议型 号：T75163产 地：中国大陆
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T72820(R)-Casopitant；化合物 (R)-Casopitant(R)-GW679769；(R)-GW679769
(R)-Casopitant ((R)-GW679769), an isomer of Casopitant, functions as an NK(1)-receptor antagonist. It has applications in the study of chemotherapy-induced nausea and vomiting [1] [2].
价 格：￥电议型 号：T72820产 地：中国大陆
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T72577Lapatinib tosylate；化合物 Lapatinib tosylateGW2016 tosylate|||GW572016 tosylate|||GW572016 tosylate ;
Lapatinib tosylate (GW572016), a robust and orally administered inhibitor specifically targeting the tyrosine kinase domains of ErbB-2 and EGFR, exhibits inhibitory concentration 50 (IC50) values of 10.2 nM and 9.8 nM against purified EGFR and ErbB-2, respectively.
价 格：￥电议型 号：T72577产 地：中国大陆
