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T28373PF-06465603；化合物 T28373PF06465603|||PF 06465603|||PF-06465603|||PF 06465603|||PF06465603|||PF 0646560
PF-06465603 is a metabolite of PF-04691502, a highly potent and selective ATP competitive kinase inhibitor of class 1 PI3Ks and mTOR.
价 格：￥电议型 号：T28373产 地：中国大陆
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T28372PF-06462894；化合物 T28372PF 6462894|||PF-6462894|||PF6462894；PF 6462894|||PF-6462894|||PF6462894
PF-06462894 is a morpholinopyrimidone mGlu5 (mGlu5 Ki = 6 nM) with favorable properties. PF-06462894 did not show any evidence of immune activation in a mouse drug allergy model.
价 格：￥电议型 号：T28372产 地：中国大陆
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T27869LY 116467；化合物 T27869LY-116467|||LY116467；LY-116467|||LY116467
LY 116467 is a dopamine agonist.
价 格：￥电议型 号：T27869产 地：中国大陆
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T27646J-104118；化合物 T27646J 104118；J 104118
J-104118 potentially inhibits squalene synthase.
价 格：￥电议型 号：T27646产 地：中国大陆
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T27261Enalkiren；化合物 T27261A-64662|||A64662|||A 64662；A-64662|||A64662|||A 64662
Enalkiren is a dipeptide renin inhibitor used in treating cogenstive heart failure. Enalkiren causes a prolonged reduction in blood pressure.
价 格：￥电议型 号：T27261产 地：中国大陆
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T27135DDD85646；化合物DDD85646DDD 85646|||DDD-85646；DDD 85646|||DDD-85646
DDD85646 is an inhibitor of T. brucei N-myristoyltransferase with a Ki of 1.44 nM, an IC50 of 2 nM and an EC50 of 2 nM. The IC50 of hNMT is 4 nM.
价 格：￥电议型 号：T27135产 地：中国大陆
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T26646AQW051；化合物AQW051AQ W051|||VQW-765|||AQW-051；AQ W051|||VQW-765|||AQW-051
AQW051 (VQW-765) is an orally active alpha-7 nicotinic acetylcholine receptor (α7-nAChR) specific activator that interacts with recombinant human α7-nAChR expression (pKD value 7.56). Alpha7-nachr is considered an attractive target for the treatment of cognitive impairments associated with neurological disorders, so VQW-051 is often used in studies of anxiety disorders and acute anxiety.
价 格：￥电议型 号：T26646产 地：中国大陆
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T26469LA-176120 ammonium；A-176120 铵盐A-176120 ammonium （185049-54-1 Free base）；A-176120 ammonium （185049-54-
A-176120 ammonium is a novel farnesyl pyrophosphate analog with antitumor and antiangiogenic properties and inhibits farnesyltransferase activity.
价 格：￥电议型 号：T26469L产 地：中国大陆
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T26469A-176120；化合物 T26469A-176120
A-176120 is a potent farnesyl pyrophosphate (FPP) analogues, it selectively inhibits farnesyltransferase. It has anti-angiogenic potential and may reduce H-ras NIH3T3 tumour growth.
价 格：￥电议型 号：T26469产 地：中国大陆
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T26466A-123189；化合物 T26466A-123189
A-123189 is a potent, alpha1D-selective antagonist.
价 格：￥电议型 号：T26466产 地：中国大陆
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T26465A1-226；化合物 T26465A1226；A1226
A1-226 is a cephalosporin of the class of β-lactam antibiotics, it is originally derived from the fungus Acremonium.
价 格：￥电议型 号：T26465产 地：中国大陆
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T26464A-119637；化合物 T26464A-119637
A-119637 is a potent, alpha1D-selective antagonist.
价 格：￥电议型 号：T26464产 地：中国大陆
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T26463A110；化合物 T26463A-110|||A 110；A-110|||A 110
A110 is a potent and selective IMPDHs inhibitor. It binds to the NAD(+) cofactor site and forms a ternary complex with IMP.
价 格：￥电议型 号：T26463产 地：中国大陆
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T26462A-1062；化合物 T26462A-1062
A-1062, a resolvase-binding inhibitor, inhibits resolvase binding to the res site.
价 格：￥电议型 号：T26462产 地：中国大陆
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T26461A-10255；化合物 T26461A 10255；A 10255
A-10255 is a complex of thiopeptide antibiotics from Streptomyces gardneri.
价 格：￥电议型 号：T26461产 地：中国大陆
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T26460A 9387；化合物 T26460A-9387|||A9387；A-9387|||A9387
A 9387 is an inhibitor of resolvase protein.
价 格：￥电议型 号：T26460产 地：中国大陆
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T26095Rivipansel；化合物 T26095GMI1070|||GMI-1070|||PF 06460031|||GMI 1070|||PF-06460031；GMI1070|||GMI-1070|||
Rivipansel is a glycomimetic compound. It acts as a pan-selectin antagonist and reverses acute vascular occlusions in sickle cell mice.
价 格：￥电议型 号：T26095产 地：中国大陆
