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  • T3766(-)-vibo-Quercitol(-)-Viburnitol；(-)-VIBO-栎醇

    (-)-vibo-Quercitol is a carbaglycosylamine glycosidase inhibitor.

    价 格：￥电议型 号：T3766产 地：中国大陆

  • T3706BDA366BDA 366；BDA-366

    BDA-366 specifically targets the BH4 domain of Bcl2 BDA-366 and suppresses human myeloma growth. BDA-366 induces robust apoptosis in MM cell lines and primary MM cells by inducing BCL2 conformational change. Delivery of BDA-366 substantially suppressed th

    价 格：￥电议型 号：T3706产 地：中国大陆

  • T3705GDC0084RG7666；GDC-0084；GDC 0084

    GDC-0084 (RG7666) is a PI3K inhibitor with potential antineoplastic activity. GDC-0084 specifically inhibits PI3K in the PI3K/AKT kinase (or protein kinase B) signaling pathway, thereby inhibiting the activation of the PI3K signaling pathway. This may res

    价 格：￥电议型 号：T3705产 地：中国大陆

  • T36879LH-Leu-Leu-OMe . HBrH-Leu-Leu-OMe . HBr (16689-14-8 Free base)

    H-Leu-Leu-OMe . HBr is a dipeptide condensation product of L-leucine methyl ester generated by human monocytes or polymorphonuclear leukocytes. H-Leu-Leu-OMe . HBr induces endolysosomal pathway stress and selectively eliminates lymphocytes with cytotoxic

    价 格：￥电议型 号：T36879L产 地：中国大陆

  • T368663-DeazauridineNSC 126849；4-羟基-1-Β-D-呋喃核糖苷-2(1H)吡啶酮

    3-Deazauridine is a structural analog of uridine that inhibits the biosynthesis of Cytidine-5´-Triphosphate by competitive inhibition of Cytidine Triphosphate synthetase which is considered to be the primary mode of action of this nucleoside analog.

    价 格：￥电议型 号：T36866产 地：中国大陆

  • T36694XY028-140XY028-140

    XY028-140 is a selective CDK4/CDK6 degrade and inhibits both CDK4/6 expression and activity in cancer cells. XY028-140 is a PROTAC connected by ligands for Cereblon and CDK.

    价 格：￥电议型 号：T36694产 地：中国大陆

  • T36692Fanotaprim

    Fanotaprim is a dihydrofolate reductase (DHFR) inhibitor. Fanotaprim inhibits the growth of T. gondii strains with a TgDHFR IC50 of 1.57 ± 0.11 nM and a hDHFR IC50 of 308?±?71 nM and a hDHFR to TgDHFR selectivity ratio of 196.

    价 格：￥电议型 号：T36692产 地：中国大陆

  • T3669Curcumenol莪术醇；(+)-Curcumenol

    Curcumenol, one of the major components of Zedoary turmeric oil, is an antibiotic drug which has anti-Y, anti-inflammation activity. Curcumenol may be safely used without inducing metabolic drug-drug interaction through P450 inhibition.

    价 格：￥电议型 号：T3669产 地：中国大陆

  • T36687Ac-rC Phosphoramidite

    Ac-rC Phosphoramidite can modify phosphodisulfide oligonucleotides.

    价 格：￥电议型 号：T36687产 地：中国大陆

  • T36682USP30 inhibitor 18

    USP30 inhibitor 18 is a selective inhibitor of USP30 (IC50 = 0.02 μM). USP30 inhibitor 18 is able to accelerate mitophagy and increase protein ubiquitination.

    价 格：￥电议型 号：T36682产 地：中国大陆

  • T3668GalanginNorizalpinin；3,5,7-Trihydroxyflavone；高良姜素

    Galangin is an agonist/antagonist of the arylhydrocarbon receptor, and also shows inhibition of CYP1A1 activity.

    价 格：￥电议型 号：T3668产 地：中国大陆

  • T36674DMU-212

    DMU-212, a methylated form of Resveratrol, shows antimitotic, antiproliferative, and antioxidant activities. DMU-212 induces mitotic arrest through the activation of ERK1/2 protein and the promotion of apoptosis.

    价 格：￥电议型 号：T36674产 地：中国大陆

  • T36670JNJ-67856633

    JNJ-67856633 is an orally active, first-in-class, potent, selective and allosteric MALT1 protease inhibitor. JNJ-67856633 in some cases lead to tumor stasis[1][2][3].

    价 格：￥电议型 号：T36670产 地：中国大陆

  • T3667Kalii Dehydrographolidi Succinas穿琥宁；Ddhads；Dehydroandrographolide Succinate Potasium Salt

    Dehydroandrographolide Succinate Potasium Salt is a natural compound with anti-virus infection activity.

    价 格：￥电议型 号：T3667产 地：中国大陆

  • T3666AtractylodinAtractydin；苍术素

    Atractylodin has high lipase inhibitory activity (IC5:39.12 μM); Atractylodin possesses strong repellency activities against T. castaneum adults (LD50: 1.83 μg/cm). The repellency of Atractylodin (0.63 μg/cm) can achieve >90%.

    价 格：￥电议型 号：T3666产 地：中国大陆

  • T3665Tectoridin射干苷；Shekanin

    Tectoridin possesses an estrogenic and thyroid hormone-like agent by activating estrogen and thyroid hormone receptors. Tectoridin has anti-oxidant, anti-inflammatory and hypoglycemic activities; Tectoridin and its five metabolites inhibits the activities

    价 格：￥电议型 号：T3665产 地：中国大陆

  • T3664THZ1CDK7 inhibitor；THZ1 2HCl

    THZ1 is a novel selective and potent covalent CDK7 inhibitor.

    价 格：￥电议型 号：T3664产 地：中国大陆

  • T36631BAY-6035

    BAY-6035 is an inhibitor of SET and MYND domain-containing protein 3 (SMYD3). It is 100-fold selective for SMYD3 over other histone methyltransferases. BAY-6035 inhibits methylation of MEKK2 peptide in a cell-free assay and in cells (IC50s = 88 and 70 nM,

    价 格：￥电议型 号：T36631产 地：中国大陆

  • T3663Eliglustat依利格鲁司特；GENZ-112638；Genz 99067

    Eliglustat is an oral inhibitor of glucosylceramide synthase which is used in the therapy of type 1 Gaucher disease.

    价 格：￥电议型 号：T3663产 地：中国大陆

  • T3662Eleutheroside E

    Eleutheroside E has anti-inflammatory effects by inhibiting NF-κB activities. Eleutheroside E significantly decreases the inflammatory cell infiltration, pannus formation, cartilage damage, bone erosion of CIA mice, the generation of TNF-α and IL-6, the m

    价 格：￥电议型 号：T3662产 地：中国大陆

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