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产品数：86101
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T9003CVT-11127Inhibitor,apoposis,GS 456332,S-phase,monounsaturated fatty acids (MUFA),Stearoyl-CoA Desatu
CVT-11127 is an StearoylCoA Desaturase-1 (SCD1) inhibitor.
价 格：￥电议型 号：T9003产 地：中国大陆
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T9906IpilimumabBMS734016,MDX010,Ipilimumab,inhibit,BMS-734016,BMS 734016,Inhibitor,MDX 010,MDX-010
Ipilimumab anti-CTLA-4) is an immunomodulatory monoclonal antibody directed against the cell surface antigen CTLA-4 and also a type of immune checkpoint inhibitor.
价 格：￥电议型 号：T9906产 地：中国大陆
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T9618HeE1-2TyrHeE12Tyr,Nile,West,SARS-CoV,HeE1 2Tyr,SARS coronavirus,RdRp,HeE1-2Tyr,inhibit,HeE-1-2Tyr,fl
HeE1-2Tyr, a pyridobenzothiazole compound, is a flavivirus RNA dependent RNA polymerases (RdRp) inhibitor. It significantly inhibits West Nile, Dengue and SARS-CoV-2 RdRps (IC50 of 27.6 ?M) activity in vitro.
价 格：￥电议型 号：T9618产 地：中国大陆
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T6907NPS-1034Mer,NPS-1034,Tyro3,c-Met/HGFR,Apoptosis,Axl,inhibit,TAM Receptor,Inhibitor
NPS-1034 is a dual Met/Axl inhibitor with IC50 of 48 nM and 10.3 nM, respectively.
价 格：￥电议型 号：T6907产 地：中国大陆
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T6760APS-2-79 hydrochlorideMAP2K,MAPKK,Inhibitor,Mitogen-activated protein kinase kinase,APS 2 79 hydroch
APS-2-79 is a MAPK antagonist that modulating KSR-dependent MAPK signalling by antagonizing RAF heterodimerization as well as the conformational changes required for phosphorylation and activation of KSR-bound MEK.
价 格：￥电议型 号：T6760产 地：中国大陆
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T9331Bemnifosbuvir hemisulfateInhibitor,antiviral,phosphoramidate,HCV,nucleotide,SARS-CoV,pangenotypic,Be
Bemnifosbuvir hemisulfate is a potent inhibitor of HCV virus replication.
价 格：￥电议型 号：T9331产 地：中国大陆
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T7216MirogabalinDS 5565,DS-5565,Calcium Channel,Mirogabalin,inhibit,Inhibitor,Ca channels,Ca2+ channels
Mirogabalin is a calcium channel blocker with analgesic effects.
价 格：￥电议型 号：T7216产 地：中国大陆
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TN1895Luteolinidin chlorideInhibitor,I/R,reperfusion,inhibit,CD38,Luteolinidin,Ischemia,trans-chalcone,Lut
Luteolinidin chloride is a natural product. It is a potent CD38 inhibitor which can protect the heart against I/R injury with preservation of eNOS function and prevention of endothelial dysfunction in vivo.
价 格：￥电议型 号：TN1895产 地：中国大陆
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T8160EGCG OctaacetateInhibitor,EGCG Octaacetate,prodrug,gram-negative bacteria,Bacterial,inhibit,colitis-
EGCG Octaacetate, a prodrug of EGCG, is utilized to enhance the stability and bioavailability of EGCG in vivo. It has high efficacy, bioavailability, anti-oxidation, and anti-angiogenesis capacities.
价 格：￥电议型 号：T8160产 地：中国大陆
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T9685DS-1971ahypersensitivity,thermal,Sodium Channel,hyperalgesia,Na channels,inhibit,Na+ channels,Inhibi
DS-1971a is a highly potent and selective NaV1.7 inhibitor. DS-1971a exhibits a favorable toxicological profile and analgesic effects.
价 格：￥电议型 号：T9685产 地：中国大陆
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T16936SS-208
SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.
价 格：￥电议型 号：T16936产 地：中国大陆
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T7058Selisistat S-enantiomerSelisistat Senantiomer,Sirtuin,(S)-Selisistat,Selisistat S enantiomer,inhibit
Selisistat S-enantiomer is an effective and specific SIRT1 inhibitor (IC50 = 98 nM) and shows >200-fold selectivity against SIRT2/3.
价 格：￥电议型 号：T7058产 地：中国大陆
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T7111Tenofovir DisoproxilInhibitor,GS-4331,Reverse Transcriptase,Tenofovir Disoproxil,HIV,GS4331,Human im
Tenofovir Disoproxil is a nucleotide reverse transcriptase inhibitor to treat HIV and chronic Hepatitis B.
价 格：￥电议型 号：T7111产 地：中国大陆
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T9305Necroptosis-IN-1NecroptosisIN1,RIP kinase,Inhibitor,inhibit,Necroptosis,RIPK,Necroptosis IN 1,Recept
Necroptosis-IN-1 is a potent necroptosis inhibitor of RIPK1. It is an analog of Necrostatin-1.
价 格：￥电议型 号：T9305产 地：中国大陆
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T8730BMS986260nuclear translocation,TGFβR1,BMS-986260,FOXP3 expression,MINK,Transforming growth factor be
BMS-986260 is a selective, and orally bioavailable TGFβR1 inhibitor(IC50 = 1.6 nM).
价 格：￥电议型 号：T8730产 地：中国大陆
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T14671BMS-193885BMS193885,BMS 193885
BMS-193885 is a selective, brain-penetrant, and competitive antagonist of the neuropeptide Y1 receptor with a Ki of 3.3 nM, and an IC50 of 5.9 nM for hY1.
价 格：￥电议型 号：T14671产 地：中国大陆
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T6798TretazicarTretazicar,NQO1,DNA Alkylator/Crosslinker,rat,bifunctional,Inhibitor,inhibit,agent,cross-l
CB1954(Tretazicar), an anticancer prodrug, is activated by NAD(P)H quinone oxidoreductase 2. It is converted in the presence of the enzyme NQO2 and co-substrate caricotamide ( EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent.
价 格：￥电议型 号：T6798产 地：中国大陆
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T8809[Des-Arg9]-Bradykinin TFA[Des Arg9] Bradykinin TFA,[DesArg9]Bradykinin TFA,[Des-Arg-9]-Bradykinin TF
[Des-Arg9]-Bradykinin is an agonist of Bradykinin (B1) receptor that displays selectivity for B1 over B2 receptors.
价 格：￥电议型 号：T8809产 地：中国大陆
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TQ0038BrensocatibDipeptidyl Peptidase,DPP,AZD 7986,inhibit,INS-1007,AZD-7986,Brensocatib,INS1007,Inhibitor
AZD7986 is a Dipeptidyl peptidase 1 (DPP1) inhibitor (pIC50s: 6.85, 7.7, 7.6, 7.8, and 7.8 in human, rat, mouse, rabbit, and dog, respectively).
价 格：￥电议型 号：TQ0038产 地：中国大陆
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T9043AS1810722AS-1810722,inhibit,CYPs,AS 1810722,Cytochrome P450,eosinophil,allergic,AS1810722,STAT,orall
AS1810722 is an orally active and potent STAT6 inhibitor(IC50 :1.9 nM). AS1810722 shows a good profile of CYP3A4 inhibition. AS1810722, a derivative of fused bicyclic pyrimidine, has the potential for allergic diseases such as asthma and atopic diseases research.
价 格：￥电议型 号：T9043产 地：中国大陆
