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  • T4346SPDB

    SPDB is a small fragment linked to DM4 conjugates. It conjugates to antibodies utilizing disulfide linkers: anti-EGFR-SPDB-DM4 has been widely used.

    价 格：￥电议型 号：T4346产 地：中国大陆

  • T4332c-Kit-IN-1PDGFR inhibitor 1；DCC-2618

    DCC-2618 is an effective inhibitor of c-Met and c-Kit (IC50s<200 nM).

    价 格：￥电议型 号：T4332产 地：中国大陆

  • T4046BX517BX 517；BX-517；PDK1 inhibitor 2

    BX-517 is a potent and selective inhibitor of PDK1.

    价 格：￥电议型 号：T4046产 地：中国大陆

  • T38737LSDKPDMAEIEKFDKSK acetateSDKPDMAEIEKFDKSK acetate(1339864-27-5 free base)

    SDKPDMAEIEKFDKSK acetate is a thymosin β4 derivative. Thymosin β4 inhibits PDGF-BB-induced fibrogenesis, proliferation and migration of HSC by blocking Akt phosphorylation.

    价 格：￥电议型 号：T38737L产 地：中国大陆

  • T3655BMS-1PD1-PDL1 inhibitor 1；PD-1/PD-L1 inhibitor 1

    PD1-PD-L1 inhibitor 1 (PD1-PD-L1-IN-1) is an inhibitor of the PD1-PD-L1 protein-protein interaction. It also acts as an immunomodulator. Programmed death ligand 1 (PD-L1) is a protein in humans that is encoded by the CD274 gene and the upregulation of PD-

    价 格：￥电议型 号：T3655产 地：中国大陆

  • T3558EBE-A22PD153035 Analog 63

    EBE-A22 is a derivative of PD 153035 which can inhibit ErbB-1-phosphorylation, whereas EBE-A22 is inactive.

    价 格：￥电议型 号：T3558产 地：中国大陆

  • T3492PD-166866PD166866；PD 166866

    PD166866 is a selective FGFR tyrosine kinase inhibitor.

    价 格：￥电议型 号：T3492产 地：中国大陆

  • T3484trans-ACPD(±)-trans-ACPD；1-amino-1,3-dicarboxycyclopentane；Trans-(±)-ACP

    (±)-trans-ACPD is an equimolecular mixture of (1S, 3R)- and (1R, 3S)-ACPD. (±)-trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/15/23/800 μM, mGluR2/1/5/4).

    价 格：￥电议型 号：T3484产 地：中国大陆

  • T3199PTACHNCH-51；Cpd 51

    PTACH (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the growth of various human Y cells (EC50: 1 to 10 μM).

    价 格：￥电议型 号：T3199产 地：中国大陆

  • T3176APD597JNJ-38431055

    APD597 is a GPR119 agonist, used in the treatment of type 2 diabetes.

    价 格：￥电议型 号：T3176产 地：中国大陆

  • T3146BMS-202PD1-PDL1 inhibitor 2；PD-1/PD-L1 inhibitor 2

    PD1-PDL1 inhibitor 2 is an inhibitor of the PD-1 (Programmed death- 1) /PD-Ll (Programmed death-ligand 1) protein/protein interaction, extracted from patent WO/2015034820 A1.

    价 格：￥电议型 号：T3146产 地：中国大陆

  • T3112Verteporfin维替泊芬；CL 318952；BPD-MA

    Verteporfin, a benzoporphyrin derivative monoacid ring A, can inhibit the activity of YAP.

    价 格：￥电议型 号：T3112产 地：中国大陆

  • T3063PD173955PD 173955；PD-173955

    PD173955 is src family-selective tyrosine kinase inhibitor with IC50 of ~22 nM for Src, Yes and Abl kinase; less potent for FGFRα and no activity on InsR and PKC.

    价 格：￥电议型 号：T3063产 地：中国大陆

  • T28353PDP-EA

    PDP-EA is an activator of fatty acid amide hydrolase(FAAH) and enhances the amidohydrolase activity of FAAH.

    价 格：￥电议型 号：T28353产 地：中国大陆

  • T28352PDE9-IN-(S)-C33(S)-C33；PDE9IN(S)C33；PDE9 IN (S) C33

    PDE9-IN-(S)-C33 is a potent and selective inhibitor of PDE9 (IC50 = 11 nM). PDE9-IN-(S)-C33 can be used for central nervous system diseases and diabetes research.

    价 格：￥电议型 号：T28352产 地：中国大陆

  • T2799(20S)-Protopanaxadiol20 (S)-原人参二醇；原人参二醇；20(S)-APPD；20-Epiprotopanaxadiol

    (20S)-Protopanaxadiol (20-Epiprotopanaxadiol), an apoptosis inducer, is an aglycon metabolic derivative of the protopanaxadiol-type ginseng saponin.

    价 格：￥电议型 号：T2799产 地：中国大陆

  • T2753AvasimibePD-148515；CI-1011；阿伐麦布

    Avasimibe is an orally bioavailable inhibitor of acyl-Coenzyme A: cholesterol acyltransferase (ACAT, IC50: 3.3 μM) that prevents cholesterol deposition in the arterial wall. It also inhibits human P450 isoenzymes CYP2C9/1A2/2C19 (IC50: 2.9/13.9/26.5 μM).

    价 格：￥电议型 号：T2753产 地：中国大陆

  • T2623PD98059PD 98059

    PD98059 is a non-ATP competitive MEK inhibitor (IC50: 2/50 μM for MEK1/MEK2).

    价 格：￥电议型 号：T2623产 地：中国大陆

  • T2501Canertinib dihydrochlorideCI-1033 dihydrochloride；Canertinib；PD-183805 dihydrochloride；卡奈替尼二盐酸盐

    Canertinib dihydrochloride is the hydrochloride salt of an orally bio-available quinazoline with potential antineoplastic and radiosensitizing activities.

    价 格：￥电议型 号：T2501产 地：中国大陆

  • T2493PD 151746

    PD 151746 is a selective, cell-permeable calpain inhibitor (Ki: 0.26/5.33 μM, μ-Calpain/m-calpain).

    价 格：￥电议型 号：T2493产 地：中国大陆

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