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T71386GW-597901 cinnamate；化合物 GW-597901 cinnamateGW-597901 cinnamate
GW-597901 cinnamate is a long-acting beta(2)-agonist.
价 格：￥电议型 号：T71386产 地：中国大陆
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T70593GW-841819X；化合物 GW-841819XGW-841819X
GW841819X is an analogue of (+)-JQ1 and a novel inhibitor of BET bromodomains. GW841819X displayed activity in vivo against NUT-midline carcinoma, multiple myeloma, mixed-lineage leukemia, and acute myeloid leukemia. Bromodomain and extra-terminal (BET) proteins belong to a class of proteins collectively called epigenetic readers". BET bromodomains have emerged as promising drug targets for treatment of cancers
价 格：￥电议型 号：T70593产 地：中国大陆
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T70314GW297361X；化合物 GW297361XGW297361X
GW297361X is an inhibitor of active Vaccinia-Related Kinases (VRK).
价 格：￥电议型 号：T70314产 地：中国大陆
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T69790GW-475151；化合物 GW-475151GW-475151
GW-475151 inhibits human neutrophil elastase (HNE).
价 格：￥电议型 号：T69790产 地：中国大陆
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T69435GW-4511；化合物 GW-4511GW-4511
GW-4511 is a benzophenone non-nucleoside HIV-1 reverse transcriptase inhibitor.
价 格：￥电议型 号：T69435产 地：中国大陆
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T69408GW590735 sodium；化合物 GW590735 sodiumGW590735 sodium
GW590735 is a potent and selective agonist of PPARα with an EC50 value of 4 nM for the expression a GAL4-responsive reporter gene and at least 500-fold selectivity versus PPARγ and PPARδ. GW590735 significantly increased HDL cholesterol, decreased LDL and VLDL cholesterol, and significantly reduced triglycerides. Maximal increases in HDL cholesterol were 37%, 53%, and 84% with fenofibrate, torcetrapib, and GW590735, respectively.
价 格：￥电议型 号：T69408产 地：中国大陆
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T69311GW300657X；化合物 GW300657XGW300657X
GW300657X is a small molecule inhibitor that blocks toxoplasma gondii rhoptry kinase 18 and maintains moderate CDK2-cyclin A inhibitory activity.
价 格：￥电议型 号：T69311产 地：中国大陆
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T6930Pazopanib Hydrochloride；盐酸帕唑帕尼GW786034|||Pazopanib HCl|||GW786034 HCl|||Votrient HCl|||Armala；GW7860
Pazopanib Hydrochloride (Votrient HCl) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFR, FGFR, c-Kit and c-Fms with IC50 of 10 nM, 30 nM, 47 nM, 84 nM, 74 nM, 140 nM and 146 nM in cell-free assays, respectively.
价 格：￥电议型 号：T6930产 地：中国大陆
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T69220GW438014 free base；化合物 GW438014 free baseGW438014 free base
GW438014A is a selective NPY-Y5 receptor antagonist.
价 格：￥电议型 号：T69220产 地：中国大陆
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T69211GW-468816；化合物 GW-468816GW-468816
GW-468816 is a glycine site NMDA receptor antagonist.
价 格：￥电议型 号：T69211产 地：中国大陆
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T69138GW-406381X；化合物 GW-406381XGW-406381X
GW-406381X is a cyclooxygenase-2 (COX2) inhibitor.
价 格：￥电议型 号：T69138产 地：中国大陆
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T68904GW-833972A free base；化合物 GW-833972A free baseGW-833972A free base
GW833972 is a CB2 Agonist. GW 833972A inhibited capsaicin-induced depolarization of the human and guinea-pig and prostaglandin E(2) (PGE(2)) and hypertonic saline-induced depolarization of the guinea-pig isolated vagus nerve in vitro. GW 833972A also inhibited citric acid-induced cough but not plasma extravasation in the guinea-pig and this effect was blocked by a CB(2) receptor antagonist.
价 格：￥电议型 号：T68904产 地：中国大陆
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T68611GW837016X；化合物 GW837016XGW837016X
GW837016X, also known as NEU-391, is a potent inhibitor of protozoan parasite proliferation. GW837016X extended life of treated mice by 50%, compared to untreated controls. At the cellular level, GW837016X inhibited mitosis and cytokinesis in T. brucei.
价 格：￥电议型 号：T68611产 地：中国大陆
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T68556GW679769；化合物 GW679769GW679769
GW679769 is a neurokinin-1 receptor antagonist.
价 格：￥电议型 号：T68556产 地：中国大陆
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T68053Denagliptin；地格列汀GW823093；GW823093
Denagliptin is a small molecule dipeptidyl peptidase IV (DPP-4) inhibitor for the treatment of endocrine ? metabolic diseases and can be used in the study of type 2 diabetes.
价 格：￥电议型 号：T68053产 地：中国大陆
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T6603Nelarabine；奈拉滨GW 506U78|||Nelzarabine|||506U78；GW 506U78|||Nelzarabine|||奈拉滨|||506U78
Nelarabine (GW 506U78) 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：中国大陆
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T6527GW842166X化合物GW842166X2-(2,4-二氯苯基氨基)-4-三氟甲基嘧啶-5-羧酸[(四氢吡喃-4-基)甲基]酰胺
GW842166X is a potent and highly selective agonist of cannabinoid receptor CB2 receptor with EC50 of 63 nM, shows no significant activity at CB1 receptor. Phase 2.
价 格：￥电议型 号：T6527产 地：中国大陆
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T6526GW791343 trihydrochloride；化合物GW791343 3HClGW791343 3HCl；GW791343 3HCl
GW791343 trihydrochloride (GW791343 3HCl) is aHCl salt form of GW791343, which is a non-competitive allosteric modulator of human P2X7 receptor inhibitor with pIC50 of 7.
价 格：￥电议型 号：T6526产 地：中国大陆
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T6525GW 5074化合物GW5074GW5074|||3-(3,5-二溴-4-羟基苯亚甲基)-5-碘-1,3-二氢吲哚-2-酮|||Raf1 Kinase Inhibitor I
GW 5074 (Raf1 Kinase Inhibitor I)(IC50=9 nM) is an effective and specific c-Raf inhibitor. It has no effect on the activities of JNK1/2/3, MEK1, MKK6/7, CDK1/2, c-Src, p38 MAP, VEGFR2 or c-Fms.
价 格：￥电议型 号：T6525产 地：中国大陆
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T6524GW0742；化合物GW0742GW610742；GW610742|||[4-[[[2-[3-氟-4-(三氟甲基)苯基]-4-甲基-5-噻唑基]甲基]硫代]-2-甲基苯氧基]乙酸
GW0742 (GW610742) is an effective and specific PPARδ agonist (EC50: 1 nM/1.1 μM/2 μM, for human PPARδ/α/γ).
价 格：￥电议型 号：T6524产 地：中国大陆
