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T9164BMS-986242glucuronidation,potent,Indoleamine 2,3-Dioxygenase (IDO),cancer,Inhibitor,BMS 986242,inhib
BMS-986242 is an orally active, potent and selective inhibitor of indoleamine-2,3-dioxygenase 1 (IDO1), and it can be used for the research of cancer.
价 格：￥电议型 号：T9164产 地：中国大陆
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T78402’,3’,5’-triacetyl-5-AzacytidineInhibitor,5-Azacytidine,2’,3’,5’ triacetyl 5 Azacytidine,2’,3’,5’tri
2´,3´,5´-triacetyl-5-Azacytidine is a prodrug form of 5-azacytidine that may be rapidly absorbed orally.
价 格：￥电议型 号：T7840产 地：中国大陆
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T8592CTK8A3536CTK-8A3536,CTK8A3536
CTK8A3536 is an inhibitor of Androgen receptor.
价 格：￥电议型 号：T8592产 地：中国大陆
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TP1166ZINC77292789inhibit,Inhibitor,ZINC77292789,ZINC-77292789
Fmoc-Thr[GalNAc(Ac)3-α-D]-OH is a reagent for the preparation of a synthetic MUC1 Glycopeptide Bearing βGalNAc-?Thr as a Tn antigen isomer which induces the antibody production against tumor cells. Fmoc-Thr[GalNAc(Ac)3-α-D]-OH is a starting material to make trimeric MUC1 immunodominant motif antigen-?based anti-?cancer vaccine candidates.
价 格：￥电议型 号：TP1166产 地：中国大陆
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TN13418-Deoxygartanin8Deoxygartanin,Parasite,8-Deoxygartanin,inhibit,Nuclear factor-kappaB,Inhibitor,Nucle
8-Deoxygartanin is a butyrylcholinesterase (BChE) selective inhibitor, it exhibits significant inhibition of self-induced α2-amyloid (Aα2) aggregation, it has multifunctional activities against Alzheimer´s disease (AD) and could be promising compounds for the therapy of AD.
价 格：￥电议型 号：TN1341产 地：中国大陆
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T8871C/EBPα inducer 1C/EBPα inducer 1,inhibit,Inhibitor
C/EBPα inducer 1 is a potential inducer of myeloid differentiation via upregulation of C/EBP.
价 格：￥电议型 号：T8871产 地：中国大陆
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T8815AzumoleneSOCE,inhibit,Azumolene,EU-4093,ryanodine,Inhibitor,Ca channels,EU 4093,Calcium Channel,rela
Azumolene
价 格：￥电议型 号：T8815产 地：中国大陆
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T8698Hydrazinium hydroxideHydrazinium hydroxide
Hydrazinium hydroxide is a bioactive compound
价 格：￥电议型 号：T8698产 地：中国大陆
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T6668SGC-CBP30inhibit,IL-17A,HAT,HATs,BRD,Histone Acetyltransferase,ankylosing,SGCCBP30,cells,epigenetic,
SGC-CBP30 is an effective CREBBP/EP300 inhibitor (IC50: 21/38 nM).
价 格：￥电议型 号：T6668产 地：中国大陆
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T81526-DemethoxytangeretinCluster of differentiation 246,6Demethoxytangeretin,Anaplastic lymphoma kinase
6-Demethoxytangeretin is a citrus flavonoid isolated from Citrus depressa.
价 格：￥电议型 号：T8152产 地：中国大陆
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T9842WAY-388264-AWAY388264A,WAY 388264 A
5-HT2B antagonist-1 is an orally active 5-HT2B receptor antagonist with an IC 50 of 33.4 nM. It can be used in studies of diseases characterized by 5-HT2B receptor signaling, such as hepatocellular carcinoma, cardiovascular disease or gastrointestinal disease [1] [2].
价 格：￥电议型 号：T9842产 地：中国大陆
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T38776LP-922056cortical,Pectinacetylesterase,thickness,orally,femur,inhibit,Wnt,lipase,bone,LP-922056,Notu
LP-922056 is an inhibitor of Notum Pectinacetylesterase with EC50 values of 21 nM, 55 nM for human and mouse, respectively.
价 格：￥电议型 号：T38776产 地：中国大陆
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TP1994LM871 acetateM871 acetate,M-871 acetate(908844-75-7 Free base)
M871 acetate is a selective galanin GAL2 receptor antagonist (Ki values are 13.1 and 420 nM at GAL2 and GAL1 receptors, respectively).It blocks pronociceptive effects of GAL2 agonists including AR-M1896.
价 格：￥电议型 号：TP1994L产 地：中国大陆
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T6588Mitoxantroneleukaemia,NSC301739,PKC,MCF-7,NSC 301739,lymphocytes,Topoisomerase,Mitoxantrone,HL60 cel
Mitoxantrone is an anthracenedione antibiotic with antineoplastic activity. Mitoxantrone intercalates into and crosslinks DNA, thereby disrupting DNA and RNA replication. This agent also binds to topoisomerase II, resulting in DNA strand breaks and inhibition of DNA repair. Mitoxantrone is less cardiotoxic compared to doxorubicin.
价 格：￥电议型 号：T6588产 地：中国大陆
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T9146ms48107Inhibitor,GPR68,GPCR,MS 48107,ms48107,brain-penetrant,BBB,inhibit,5-HT2B,MS-48107,bioavailabl
MS48107 is a potent and selective positive allosteric modulator of G protein-coupled receptor 68 (GPR68). It is selective for GPR68 over the closely related proton GPCRs, neurotransmitter transporters, and hERG ion channels. It can readily cross the blood-brain barrier (BBB) in mice.
价 格：￥电议型 号：T9146产 地：中国大陆
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T26987CF-1743CF 1743
CF-1743 is a highly potent anti-varicella zoster virus nucleoside.
价 格：￥电议型 号：T26987产 地：中国大陆
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T9328Ellagic Acid DihydrateEllagic Acid Dihydrate
Ellagic Acid Dihydrate inhibit the CYP1A1-dependent activation of benzo[a]pyrene.
价 格：￥电议型 号：T9328产 地：中国大陆
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T30855CGP77675
CGP77675 is a potent and selective inhibitor of Src family kinase with IC50s of 5-20 and 40 nM for the phosphorylation of peptide substrates and autophosphorylation of purified Src. CGP77675 exhibits anticancer activity.
价 格：￥电议型 号：T30855产 地：中国大陆
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T26520ABP688ABP688
ABP688 is a non-competitive and selective mGluR5 antagonist(Ki = 1.7 nM). ABP688 can be used as a PET tracer for clinical imaging.
价 格：￥电议型 号：T26520产 地：中国大陆
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T6438Cefoselis SulfateCefoselis,cephalosporin,Gram-negative,Gram-positive,Bacterial,barrier,FK037,Inhibit
Cefoselis is a widely used beta-lactam antibiotic.
价 格：￥电议型 号：T6438产 地：中国大陆
