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  • T68113Naluzotan hydrochloride；Naluzotan盐酸盐PRX 00023 hydrochloride；PRX 00023 hydrochloride

    Naluzotan hydrochloride (PRX 00023 hydrochloride) is a hERG K+ channel blocker with an IC50 value of 3800 nM and is commonly used in the study of anxiety and depression.Naluzotan hydrochloride is also a novel, potent, and selective 5-HT1A agonist, with an IC50 value of about 20 nM and a Ki value of about 5.1 Naluzotan hydrochloride is also a novel, potent and selective 5-HT1A agonist with an IC50 of approximately 20 nM and a Ki of approximately 5.1 nM.

    价 格：￥电议型 号：T68113产 地：中国大陆

  • T68112Nafimidone；萘咪酮Nafimidone

    Nafimidone shows anticonvulsant activity in a rat model of amygdala epilepsy and can be used in the treatment of chronic intractable epilepsy.

    价 格：￥电议型 号：T68112产 地：中国大陆

  • T68110Moxnidazole；吗硝唑Moxnidazole

    Moxnidazole, a 5-nitroimidazole, is mutagenic in microbial assays and in Drosophila, inducing genetic alterations in mouse somatic cells.

    价 格：￥电议型 号：T68110产 地：中国大陆

  • T6811CPI-637；化合物CPI637CPI 637；CPI 637

    CPI-637 is a selective and cell-active benzodiazepinone CBP/EP300 bromodomain inhibitor.

    价 格：￥电议型 号：T6811产 地：中国大陆

  • T67956LLitoxetine HCl；利托西汀盐酸盐litoxetine HCL(86811-09-8 Free base)；litoxetine HCL(86811-09-8 Free base)

    Litoxetine HCl is a selective 5-hydroxytryptamine (5-HT) reuptake inhibitor (SSRI) and mixed 5-hydroxytryptamine antagonist used in the treatment of urinary incontinence. Litoxetine HCl in the absence of antimuscarinic concentrations without antimuscarinic properties (10 nM-1 microM) caused concentration-dependent relaxation of isolated oesophageal muscle mucosa in rats, reducing carbachol tone by up to 37%. Higher concentrations of Litoxetine HCl (3 microM-300 microM) were associated with signi

    价 格：￥电议型 号：T67956L产 地：中国大陆

  • T67811Tefludazine；替氟达嗪Tefludazine

    Tefludazine, a novel neuroleptic with a benzindone structure, is a compound with good oral activity and antagonistic effects on dopamine and 5-hydroxytryptamine receptors. Tefludazine has shown potent dopamine (DA) antagonistic activity in in vitro and in vivo test models in mice, rats and dogs. Tefludazine is a therapeutic agent used to treat psychiatric disorders.

    价 格：￥电议型 号：T67811产 地：中国大陆

  • T66811H-D-Chg-OH.HCl；化合物 H-D-Chg-OH.HClH-D-Chg-OH.HCl

    H-D-Chg-OH.HCl is an amino acid derivative and has a wide range of applications in life science related research.

    价 格：￥电议型 号：T66811产 地：中国大陆

  • T65811Fmoc-D-Phe(4-NO2)-OH；化合物 Fmoc-D-Phe(4-NO2)-OHFmoc-D-Phe(4-NO2)-OH

    Fmoc-D-Phe(4-NO2)-OH is an amino acid derivative and has a wide range of applications in life science related research.

    价 格：￥电议型 号：T65811产 地：中国大陆

  • T6574311β-HSD1-IN-8；化合物 11β-HSD1-IN-811β-HSD1-IN-8

    11β-HSD1-IN-8 is a useful organic compound for research related to life sciences. The catalog number is T65743 and the CAS number is 386704-15-0.

    价 格：￥电议型 号：T65743产 地：中国大陆

  • T64811Benzyl-PEG5-acid；化合物 Benzyl-PEG5-acidBenzyl-PEG5-acid

    Benzyl-PEG5-acid is a useful organic compound for research related to life sciences and the catalog number is T64811.

    价 格：￥电议型 号：T64811产 地：中国大陆

  • T63811EPI-7170；化合物 EPI-7170EPI-7170

    EPI-7170 is a ralaniten analogue and a potent antagonist of the androgen receptor N-terminal structural domain, blocking the transcriptional activity of the full-length AR (FL-AR) and AR splice variants (AR-Vs). EPI-7170 exhibits antitumor activity against enzalutamide resistant debulking resistant prostate cancer (CRPC).

    价 格：￥电议型 号：T63811产 地：中国大陆

  • T63038WAY-181187 oxalate；化合物 WAY-181187 oxalateWAY-181187 oxalate

    WAY-181187 (SAX-187) oxalate is a selective and potent agonist of the 5-HT6 receptor (Ki: 2.2 nM; EC50: 6.6 nM). wAY-181187 oxalate is a specific agonist that mediates 5-HT6 receptor-dependent signalling pathways (e.g. cAMP, Fyn and ERK1/2 kinases).

    价 格：￥电议型 号：T63038产 地：中国大陆

  • T62695GFB-12811；化合物 GFB-12811GFB-12811

    GFB-12811 is a highly selective and orally active inhibitor of cyclin-dependent kinase 5 (CDK5), exhibiting an inhibitory concentration (IC50) of 2.3 nM. It demonstrates notable specificity, with minimal activity against other tested kinases, including CDK1, CDK2, CDK6, CDK7, and CDK9 [1].

    价 格：￥电议型 号：T62695产 地：中国大陆

  • T62694(S)-GFB-12811；化合物 (S)-GFB-12811(S)-GFB-12811

    (S)-GFB-12811 (compound 596) is a selective and selective inhibitor of CDK5 (IC50<10 nM). (S)-GFB-12811 can be used in studies of cell cycle progression, neuronal development, and tumorigenesis.

    价 格：￥电议型 号：T62694产 地：中国大陆

  • T61811GPVI antagonist 3；化合物 GPVI antagonist 3GPVI antagonist 3

    GPVI antagonist 3 (Compound 2) is a potential antagonist that shows promising antiplatelet activity by selectively inhibiting the interaction between the Glycoprotein VI (GPVI) receptor and its ligands. It demonstrates potent inhibitory effects, with IC50 values of 1.01 μM for collagen, 1.92 μM for CRP, 7.24 μM for convulxin, and 51.74 μM for thrombin. GPVI is a major collagen receptor on platelets, making it an ideal target for safe and effective antithrombotic treatment. Therefore, GPVI antago

    价 格：￥电议型 号：T61811产 地：中国大陆

  • T60811CXCR4 antagonist 7；化合物 CXCR4 antagonist 7CXCR4 antagonist 7

    CXCR4 antagonist 7 (Compound PARA-B) is able to be used in the HIV infection, inflammatory diseases, cancer, and WHIM syndrome research which is a antagonist of CXCR4 (IC 50 = 9.3 nM) [1].

    价 格：￥电议型 号：T60811产 地：中国大陆

  • T60734NSC81111；化合物 NSC81111NSC81111

    NSC81111 shows anticaner effects which is a potent and orally active inhibitor of EGFR-TK (IC50 = 0.15 nM) [1].

    价 格：￥电议型 号：T60734产 地：中国大陆

  • T4811D-Alanine；D-丙氨酸D-α-Alanine|||Ba 2776|||(R)-Alanine|||(R)-2-Aminopropionic acid；D-α-Alanine|||Ba 2776

    Alanine is a nonessential amino acid made in the body from the conversion of the carbohydrate pyruvate or the breakdown of DNA and the dipeptides carnosine and anserine. D-Alanine ((R)-Alanine) is a weak GlyR (inhibitory glycine receptor) and PMBA agonist, with an EC50 of 9 mM for GlyR.

    价 格：￥电议型 号：T4811产 地：中国大陆

  • T4635Ralinepag；化合物RalinepagAPD811；APD811

    Ralinepag (APD811) is a potent, orally bioavailable agonist of non-prostanoid prostacyclin (IP) receptor, with EC50s of 8.5 nM, 530 nM and 850 nM for human and rat IP receptor and human DP1 receptor, respectively.

    价 格：￥电议型 号：T4635产 地：中国大陆

  • T40811Eflornithine依氟乌氨酸RMI71782|||DFMO|||α-difluoromethylornithine|||MDL71782

    Eflornithine (DFMO) is a selective and orally available ornithine decarboxylase inhibitor that delays hair overgrowth.Eflornithine is used in the study of African trypanosomiasis, malignant glioma, and sleeping sickness.

    价 格：￥电议型 号：T40811产 地：中国大陆

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