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T7360GSK2018682LPL Receptor,Inhibitor,inhibit,Lysophospholipid Receptor,GSK-2018682,GSK 2018682,GSK201868
GSK2018682 is an agonist of sphingosine-1-phosphate receptor (s1p1) and (s1p5) agonist(pEC50s of 7.7 and 7.2,respectively).
价 格：￥电议型 号：T7360产 地：中国大陆
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T27392FT001FT001,FT-001
FT001 is a potent, selective and orally available inhibitor of BET Bromodomain with antitumor activity. FT001 inhibited the expression of MYC with the IC50 value of 0.46 μM). FT001 has potent antiproliferative effects against MV-4-11 and demonstrates significant MYC mRNA suppression both in vitro and in vivo.
价 格：￥电议型 号：T27392产 地：中国大陆
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TN6773AcetoxyvalerensreAcetoxyvalerensre
Acetoxyvalerensre (acetylvalerenolic acid) is a derivative of valerenic acid, which is a a GABAA receptor modulator.
价 格：￥电议型 号：TN6773产 地：中国大陆
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T7572RN-1734RN1734,Inhibitor,RN-1734,Transient receptor potential channels,TRP Channel,inhibit,RN 1734
RN-1734 is selective TRPV4 channel antagonist(IC50 of 2.3 μM,5.9 μM,3.2 μM for hTRPV4, mTRPV4 and rTRPV4,respectively)
价 格：￥电议型 号：T7572产 地：中国大陆
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T8733Antrodin AAntrodin A,inhibit,Inhibitor,anti-inflammatory,acute alcoholic liver injury,antioxidant
Antrodin A (AdA) is one of the main active ingredients in the solid-state fermented A. camphorata mycelium. It protects the liver from alcohol damage by improving the antioxidant and anti-inflammatory capacity of the liver and maintaining the stability of the intestinal flora.
价 格：￥电议型 号：T8733产 地：中国大陆
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TN4673(+)-NortrachelogeninPhosphoinositide 3-kinase,(+)-Nortrachelogenin,Inhibitor,inhibit,Apoptosis,(+)No
(+)-Nortrachelogenin is a lignan isolated from Wikstroemia indica C.A. Meyer (Thymelaeaceae). (+)-Nortrachelogenin possesses antileukemic activity.
价 格：￥电议型 号：TN4673产 地：中国大陆
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T11321FR194738 free baseFR194738 free base,FR-194738 free base
FR194738 free base inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM.?
价 格：￥电议型 号：T11321产 地：中国大陆
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T7699AZD7325modulator,effect,inhibit,Cytochrome P450,Dravet,syndrome,Inhibitor,γ-Aminobutyric acid Recept
AZD-7325 is a GABA-Aα2,3 -selective receptor modulator.
价 格：￥电议型 号：T7699产 地：中国大陆
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T10733CDDO-EA
CDDO-EA is an activator of the Nrf2/antioxidant response element.
价 格：￥电议型 号：T10733产 地：中国大陆
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T7369LGemigliptin Tartrate(911637-19-9 free base)type,Gemigliptin,products,mellitus,peptidase-4,Gemiglipti
Gemigliptin tartrate is a highly selective, reversible and competitive inhibitor of dipeptidyl peptidase-4 (DPP-4). It has an IC50 of 10.3 nM for human recombinant DPP-4. Gemigliptin tartrate exhibits potent anti-glycation properties.
价 格：￥电议型 号：T7369L产 地：中国大陆
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T7316LY2828360Inhibitor,LY2828360,inhibit,LY-2828360,LY 2828360,Cannabinoid Receptor
LY2828360 is a cannabinoid (CB) receptor 2 agonist (Ki = 40.3 nM). It selectively activates CB2 over CB1 in a GTPγS binding assay (EC50s = 20.1 and >100,000 nM, respectively).
价 格：￥电议型 号：T7316产 地：中国大陆
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T77362-Chloroadenosine2-Chloroadenosine,permeant,Inhibitor,influx,nitrobenzylthioinosine,inhibit,cell,hum
2-Chloroadenosine (CADO) is a metabolically stable analog of adenosine that binds to adenosine A1, A2A, and A3 receptors( Ki:300, 80, and 1,900 nM, respectively)
价 格：￥电议型 号：T7736产 地：中国大陆
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T7392RevefenacinRevefenacin,TD4208,TD 4208,inhibit,Muscarinic acetylcholine receptor,Inhibitor,mAChR,GSK
Revefenacin is a mAChR antagonist has a high affinity on M3 receptor( Ki : 0.18 nM),and potentially useful for the treatment of respiratory disease.
价 格：￥电议型 号：T7392产 地：中国大陆
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T7300GDC-0575GDC 0575,GDC-0575,RG-7741,inhibit,ARRY575,Inhibitor,Checkpoint Kinase (Chk),ARRY 575,GDC0575
GDC-0575 is a highly-selective oral small-molecule Chk1 inhibitor(IC50 of 1.2 nM).
价 格：￥电议型 号：T7300产 地：中国大陆
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T9273SI 60SI 60
Sanaid SI 60 is an aromatic sulfonium salt and is initiator for thermosetting polymerization at low temperature.
价 格：￥电议型 号：T9273产 地：中国大陆
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T7766RemdesivirDNA/RNA Synthesis,Remdesivir,GS 5734,COVID-19,MERS-CoV,2019-nCoV,antiviral,SARS coronaviru
Remdesivir is a nucleoside analogue, with effective antiviral activity( EC50s of 74 nM for SARS-CoV and MERS-CoV in HAE cells)
价 格：￥电议型 号：T7766产 地：中国大陆
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TN1733Hesperetin 7-O-glucosideInhibitor,enzymatic,Antihypertensive,Hesperetin 7Oglucoside,antibacterial,He
Hesperetin 7-O-glucoside and prunin are direct precursors of naringin and neohesperidin, respectively, in C. aurantium. Hesperetin 7-O-glucoside shows inhibition of human HMG-CoA reductase, it also exhibits effective inhibition of the growth of Helicobacter pylori. Hesperetin 7-O-glucoside can reduce blood pressure in healthy volunteers.
价 格：￥电议型 号：TN1733产 地：中国大陆
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T7387Ceftaroline fosamilN-phosphono,PPI 0903,inhibit,TAK599,MRSA,TAK 599,PPI-0903,T-91825,Bacterial,Inhib
Ceftaroline fosamil is a cephalosporin, with activity against Gram-positive pathogens.
价 格：￥电议型 号：T7387产 地：中国大陆
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T97356-(4-methylpiperazin-1-yl)-4-o-tolylnicotinamide6(4methylpiperazin1yl)4otolylnicotinamide,6 (4 methy
6-(4-methylpiperazin-1-yl)-4-o-tolylnicotinamide can be used in the synthesis of befetupitant and netupitant.
价 格：￥电议型 号：T9735产 地：中国大陆
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T6730WAY-600inhibit,Inhibitor,mTOR,WAY 600,WAY-600,Mammalian target of Rapamycin
WAY-600 is a potent, ATP-competitive and selective inhibitor of mTOR with IC50 of 9 nM; blocks mTORC1/P-S6K(T389) and mTORC2/P-AKT(S473) but not P-AKT(T308); selective for mTOR than PI3Kα (>100-fold) and PI3Kγ (>500-fold).
价 格：￥电议型 号：T6730产 地：中国大陆
