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  • T15369gamma-DGGgamma-DGG,γDGG,γ-D-Glutamylglycine

    gamma-DGG is a competitive blocker of AMPA receptor.

    价 格：￥电议型 号：T15369产 地：美洲

  • T1537RapamycinRapamycin,AY 22989,Sirolimus

    Rapamycin, a macrolide compound obtained from Streptomyces hygroscopicus, is a potent and specific mTOR inhibitor (IC50: 0.1 nM in HEK293 cells).

    价 格：￥电议型 号：T1537产 地：美洲

  • T15370GANT 58GANT 58,NSC 75503,

    GANT 58 is a potent antagonist of Gli. Which inhibits GLI1-induced transcription (IC50: 5 μM).

    价 格：￥电议型 号：T15370产 地：美洲

  • T15372GB1107GB1107

    GB1107 is a selective, orally active Galectin-3 (Gal-3) inhibitor (Kd: 37 nM for human Galectin-3). GB1107 decreases human and mouse lung adenocarcinoma growth and blocks metastasis in the syngeneic model.

    价 格：￥电议型 号：T15372产 地：美洲

  • T15373GboxinGboxin

    Gboxin inhibits the activity of F0F1 ATP synthase. Gboxin is an oxidative phosphorylation inhibitor that targets glioblastoma. It also has antitumour activity.

    价 格：￥电议型 号：T15373产 地：美洲

  • T15375GDC-0077GDC-0077,RG6114,

    GDC-0077 is an orally available and selective inhibitor of PI3Kα (IC50=0.038 nM). GDC-0077 is more selective for mutant versus wild-type PI3Kα. GDC-0077 exerts its activity by binding to the ATP binding site of PI3K, thereby inhibiting the phosphorylati

    价 格：￥电议型 号：T15375产 地：美洲

  • T15376GDC-0339GDC-0339

    GDC-0339 is discovered as a potential treatment of multiple myeloma. GDC-0339 is an orally bioavailable and well-tolerated inhibitor of pan-Pim kinase (Kis: 0.03 nM, 0.1 nM and 0.02 nM for Pim1, Pim2 and Pim3, respectively).

    价 格：￥电议型 号：T15376产 地：美洲

  • T15377Ravoxertinib hydrochlorideRavoxertinib hydrochloride,GDC-0994 (hydrochloride),

    Ravoxertinib hydrochloride is an orally bioavailable and selective inhibitor for ERK kinase activity (IC50: 6.1 nM and 3.1 nM for ERK1 and ERK2, respectively).

    价 格：￥电议型 号：T15377产 地：美洲

  • T15378Gemcitabine (elaidate)Gemcitabine (elaidate),CP-4126,CO-101

    Gemcitabine elaidate is a lipophilic and unsaturated fatty acid ester derivative of gemcitabine (dFdC). Gemcitabine elaidate is also an antimetabolite deoxynucleoside analogue. It has a potential antineoplastic activity.

    价 格：￥电议型 号：T15378产 地：美洲

  • T15383Glesatinib hydrochlorideGlesatinib hydrochloride,MGCD265 hydrochloride,

    Glesatinib hydrochloride is an orally active and potent dual inhibitor of MET/SMO. Glesatinib hydrochloride is also a tyrosine kinase inhibitor. Which antagonizes P-glycoprotein (P-gp) mediated multidrug resistance (MDR) in non-small cell lung cancer (NSC

    价 格：￥电议型 号：T15383产 地：美洲

  • T15388GLPG0974GLPG0974

    GLPG0974 is an antagonist of free fatty acid receptor-2 (IC50: 9 nM).

    价 格：￥电议型 号：T15388产 地：美洲

  • T15389GlucagonGlucagon,Porcine glucagon,

    Glucagon is a peptide hormone, produced by pancreatic α-cells. Glucagon reduces the activity of HNF-4. Glucagon stimulates gluconeogenesis. Glucagon enhances HNF4α phosphorylation.

    价 格：￥电议型 号：T15389产 地：美洲

  • T1539IloperidoneIloperidone,HP 873,

    Iloperidone is an atypical antipsychotic agent that is used for treatment of schizophrenia.

    价 格：￥电议型 号：T1539产 地：美洲

  • T15391Glufosinate ammoniumGlufosinate ammonium

    Glufosinate ammonium is a phosphinic acid analogue of glutamic acid and is an herbicide. It is converted by plant cells into PT (L-phosphinothricin). Glufosinate ammonium has neurotoxic activity.

    价 格：￥电议型 号：T15391产 地：美洲

  • T15393Glycerol phenylbutyrateGlycerol phenylbutyrate,HPN-100,

    Glycerol phenylbutyrate (GPB) is a new generation ammonia scavenger drug and it also is a sigma-2 (σ2) receptor ligand (pKi: 8.02).

    价 格：￥电议型 号：T15393产 地：美洲

  • T15394Glyceryl monocaprateGlyceryl monocaprate,Monocaprin,

    Glyceryl monocaprate has inhibitory effect on Herpes Simplex Virus (HSV). It also offers an effective treatment for herpes labialiss. Glyceryl monocaprate is a capric acid against 1-monoglyceride gram-positive bacterial infections.

    价 格：￥电议型 号：T15394产 地：美洲

  • T15396GN44028GN44028

    GN44028 is a hypoxia-inducible factor inhibitor of (HIF)-1 (IC50: 14 nM). GN44028 inhibits hypoxia-induced HIF-1α transcriptional activity. However, It can not be suppressing HIF-1α mRNA expression, HIF-1α protein accumulation, or HIF-1α/HIF-1β heterodim

    价 格：￥电议型 号：T15396产 地：美洲

  • T15397GNE-049GNE-049

    GNE-049 is a highly potent and selective inhibitor of CBP (IC50: 1.1 nM in TR-FRET assay). GNE-049 also inhibits BRET and BRD4(1) (IC50s: 12 nM and 4200 nM, respectively).

    价 格：￥电议型 号：T15397产 地：美洲

  • T15399GNE-207GNE-207

    GNE-207 is a selective and orally bioavailable inhibitor of the bromodomain of CBP (IC50 of 1 nM). It has a selective index of?>2500-fold against BRD4 (1). GNE-207 displays excellent CBP potency (EC50: 18 nM for MYC expression in MV-4-11 cells).

    价 格：￥电议型 号：T15399产 地：美洲

  • T15691L-AlanosineL-Alanosine,NSC-153353,

    L-Alanosine inhibits adenylosuccinate synthetase, which converts inosine monophosphate (IMP) into adenylosuccinate. L-Alanosine is an antibiotic from Streptomyces alanosinicus. It has antineoplastic activity. L-Alanosine blocks the common de novo purine b

    价 格：￥电议型 号：T15691产 地：美洲

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