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  • T16380OGT 2115OGT 2115

    OGT 2115 is an effective and cell-permeable heparanase inhibitor (IC50: 0.4 μM). OGT 2115 also suppresses heparan sulfate degradation activity. OGT 2115 has anti-angiogenic properties (IC50: 1 μM).

    价 格：￥电议型 号：T16380产 地：美洲

  • T16382OleandomycinOleandomycin

    Oleandomycin is similar to Erythromycin has antimicrobial activity. Oleandomycin is a macrolide antibiotic structurally closely related to Erythromycin.

    价 格：￥电议型 号：T16382产 地：美洲

  • T16384OlutasidenibOlutasidenib,FT-2102,

    Olutasidenib is under the study in the treatment of acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). Olutasidenib is a highly effective, brain penetrant, and selective inhibitor of the mutant Isocitrate dehydrogenase 1 (IDH1) (IC50: 21.2 nM

    价 格：￥电议型 号：T16384产 地：美洲

  • T16385OmapatrilatOmapatrilat,BMS-186716,

    Omapatrilat is a metalloprotease ACE and NEP dual inhibitor (Ki: 0.64 and 0.45 nM, respectively).

    价 格：￥电议型 号：T16385产 地：美洲

  • T16386Ombrabulin hydrochlorideOmbrabulin hydrochloride,AVE8062 (hydrochloride),AC7700 (hydrochloride)

    Ombrabulin hydrochloride is a derivative of CA-4 phosphate. It is known to show antivascular effects through selective disruption of the tubulin cytoskeleton of endothelial cells.

    价 格：￥电议型 号：T16386产 地：美洲

  • T1639AmlexanoxAmlexanox,Amoxanox,CHX3673

    Amlexanox is an anti-aphthous ulcer drug. Amlexanox inhibits the synthesis and release of inflammatory mediators, including leukotrienes and histamine, from mast cells, neutrophils, and mononuclear cells. Amlexanox also acts as a leukotriene D4 antagonist

    价 格：￥电议型 号：T1639产 地：美洲

  • T16390OmtriptolideOmtriptolide

    Omtriptolide, triptolide purified from the Chinese herb, is a water-soluble derivative prodrug.

    价 格：￥电议型 号：T16390产 地：美洲

  • T16391ON-013100ON-013100

    ON-013100 is an antineoplastic drug. It also acts as a mitotic inhibitor that could inhibit Cyclin D1 expression.

    价 格：￥电议型 号：T16391产 地：美洲

  • T16392ONC206ONC206

    ONC206 is an analogue of TRAIL inducer ONC201 and is a selective antagonist of the D2-like dopamine receptors (DRD2/3/4) at nanomolar concentrations. ONC206 also has broad-spectrum anti-tumor activity.

    价 格：￥电议型 号：T16392产 地：美洲

  • T16398OpicaponeOpicapone,BIA 9-1067,

    Opicapone reduces the ATP content of the cells (IC50: 98 μM). Opicapone is an effective third-generation catechol-O-methyltransferase inhibitor for the research of Parkinson´s disease and motor fluctuations.

    价 格：￥电议型 号：T16398产 地：美洲

  • T16490PF-06380101PF-06380101,Aur0101,Auristatin-0101

    PF-06380101 is an auristatin microtubule inhibitor and is a cytotoxic Dolastatin 10 analogue. When compared to other synthetic auristatin analogues that are used in the preparation of ADCs, PF-06380101 displays excellent potencies in tumor cell proliferat

    价 格：￥电议型 号：T16490产 地：美洲

  • T1663Deoxythymidine triphosphateDeoxythymidine triphosphate

    Deoxythymidine triphosphate (dTTP) is one of the four nucleoside triphosphates that are used in the in vivo synthesis of DNA.

    价 格：￥电议型 号：T1663产 地：美洲

  • T16663Bis-NH2-PEG2Bis-NH2-PEG2,PROTAC Linker 19,

    Bis-NH2-PEG2 (PROTAC Linker 19) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1].

    价 格：￥电议型 号：T16663产 地：美洲

  • T16678PSN632408PSN632408

    PSN632408 is an optimized agonist of GPR119 receptors that display similar potency to OEA at both recombinant mouse and human GPR119 receptors (EC50: 5.6 and 7.9 uM, respectively).

    价 格：￥电议型 号：T16678产 地：美洲

  • T16700QC6352QC6352

    QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM).

    价 格：￥电议型 号：T16700产 地：美洲

  • T16781RogaratinibRogaratinib,BAY1163877,

    Rogaratinib is an aberrant inhibitor of fibroblast growth factor receptor (FGFR). Rogaratinib is as an orally available, selective and potent inhibitor of FGFR-1, -2 and -3 kinase activity.

    价 格：￥电议型 号：T16781产 地：美洲

  • T16791RottlerinRottlerin,Mallotoxin,NSC 56346

    Rottlerin is a natural product purified from Mallotus Philippinensis and is a specific PKC inhibitor (IC50: PKCδ of 3-6 μM, PKCα,β,γ of 30-42 μM, PKCε,η,ζ of 80-100 μM). Rottlerin causes apoptosis via caspase 3 activation.

    价 格：￥电议型 号：T16791产 地：美洲

  • T1725Y-27632 dihydrochlorideY-27632 dihydrochloride,Y-27632 2HCl,

    Y-27632 is a selective inhibitor of ROCKs including p160ROCK (Ki: 140 nM) and ROCK2 (IC50: 800 nM).

    价 格：￥电议型 号：T1725产 地：美洲

  • T1745TAK-063TAK-063,TAK063,TAK 063

    TAK-063 is a highly effective and selective PDE10A inhibitor (IC50: 0.30 nM); Its selectivity is >15000-fold over other PDEs.

    价 格：￥电议型 号：T1745产 地：美洲

  • T1763SB525334SB525334

    SB-525334 is a potent and selective inhibitor of the TGF-β1R and ALK5 (IC50: 14.3 nM).

    价 格：￥电议型 号：T1763产 地：美洲

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