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  • T7946AER-271Inhibitor,AER-271,AQP4,AER-270,stroke,inhibit,aquaporin-4,injury,AER 271,acute,AER271,CNS,isc

    AER-271 is an inhibitor of aquaporin-4.

    价 格：￥电议型 号：T7946产 地：中国大陆

  • T11014DFP00173AQP,Inhibitor,human,isoforms,erythrocytes,selective,homologous,DFP 00173,glycerol,DFP-00173,

    DFP00173 is a potent and selective aquaporin 3 (AQP3) inhibitor. DFP00173 inhibits mouse and human AQP3 with IC50 of ~0.1-0.4 μM. Compared with the homologous AQP subtypes AQP7 and AQP9, DFP00173 is selective for AQP3.

    价 格：￥电议型 号：T11014产 地：中国大陆

  • T2602Barasertib-HQPABarasertib；AZD1152-HQPA；1H-Pyrazole-3-acetamide；AZD2811；AZD1152-HQPA|AZD2811

    Barasertib (AZD1152-HQPA) is a highly selective Aurora B inhibitor (IC50: 0.37 nM) and demonstrates ~3,700-fold greater selectivity than Aurora A.

    价 格：￥电议型 号：T2602产 地：中国大陆

  • T24859TC-AQP1-1

    TC-AQP1-1 is a blocker of the aquaporin 1 channel.

    价 格：￥电议型 号：T24859产 地：中国大陆

  • T2429Olverembatinib dimesylateHQP1351；GZD824 Dimesylate

    GZD824 Dimesylate is a novel orally bioavailable Bcr-Abl inhibitor for Bcr-Abl(WT) and Bcr-Abl(T315I).

    价 格：￥电议型 号：T2429产 地：中国大陆

  • T22748DQP 1105

    DQP 1105 is an NMDA receptor antagonist inhibiting receptor function more potently with glutamate.

    价 格：￥电议型 号：T22748产 地：中国大陆

  • T2429GZD824 DimesylateGZD824 Dimesylate,HQP1351,

    GZD824 Dimesylate is a novel orally bioavailable Bcr-Abl inhibitor for Bcr-Abl(WT) and Bcr-Abl(T315I).

    价 格：￥电议型 号：T2429产 地：美洲

  • T2602BarasertibBarasertib,1H-Pyrazole-3-acetamide,AZD1152-HQPA

    Barasertib (AZD1152-HQPA) is a highly selective Aurora B inhibitor (IC50: 0.37 nM) and demonstrates ~3,700-fold greater selectivity than Aurora A.

    价 格：￥电议型 号：T2602产 地：美洲

  • T82528DQP-997-74；化合物 DQP-997-74DQP-997-74

    Dihydroquinoline-pyrazoline DQP-997-74 (compound 2i) is a selective N-methyl-d-aspartate receptor (NMDAR) inhibitor that preferentially targets GluN2C/D subunits, with IC50 values of 0.069 μM and 0.035 μM, respectively, and possesses blood-brain barrier permeability. It enhances its inhibitory potency in a time-dependent manner when combined with the agonist glutamate, reducing epileptogenic events in a murine model of tuberous sclerosis complex (TSC)-induced epilepsy. DQP-997-74 is potentially

    价 格：￥电议型 号：T82528产 地：中国大陆

  • T79611DQP-26；化合物 DQP-26DQP-26

    DQP-26, a potent negative allosteric modulator of NMDA receptors (NMDARs), exhibits IC50 values of 0.77 μM for GluN2C and 0.44 μM for GluN2D subunits, indicating potential application in research on NMDAR-associated neurological diseases [1].

    价 格：￥电议型 号：T79611产 地：中国大陆

  • T76451MLGFFQQPKPR-NH2；化合物 MLGFFQQPKPR-NH2MLGFFQQPKPR-NH2

    MLGFFQQPKPR-NH2 is a reversed Substance P peptide. Substance P is a neuropeptide [1] .

    价 格：￥电议型 号：T76451产 地：中国大陆

  • T76201LEESGGGLVQPGGSMK TFA；化合物 LEESGGGLVQPGGSMK TFALEESGGGLVQPGGSMK TFA

    LEESGGGLVQPGGSMK TFA, a proteolysis peptide component of Infliximab, serves for the quantitative analysis of the latter. Infliximab is a chimeric monoclonal IgG1 antibody, binding specifically to TNF-α [1].

    价 格：￥电议型 号：T76201产 地：中国大陆

  • T39521LEESGGGLVQPGGSMK；LEESGGGLVQPGGSMKLEESGGGLVQPGGSMK

    LEESGGGLVQPGGSMK, a proteolysis peptide, is a constituent of Infliximab, a chimeric monoclonal IgG1 antibody that selectively binds to TNF-α. It can be employed for quantitative assessment of Infliximab.

    价 格：￥电议型 号：T39521产 地：中国大陆

  • T38965EPQpYEEIPIYL；EPQpYEEIPIYLEPQpYEEIPIYL

    EPQpYEEIPIYL, a phosphopeptide, is a ligand for the Src homology 2 (SH2) domain. It activates members of the Src family, such as Lck, Hck, and Fyn, through the binding interaction with SH2 domains.

    价 格：￥电议型 号：T38965产 地：中国大陆

  • T38616Teprasiran；TeprasiranQPI-1002；QPI-1002

    Teprasiran (QPI-1002) is an RNA-based compound that transiently suppresses p53-dependent apoptosis, a process involved in the development of acute kidney injury (AKI).

    价 格：￥电议型 号：T38616产 地：中国大陆

  • T38202PAQPAQPAQ

    PAQ is a neuroprotective agent. It protects dopaminergic neurons from cell death without inhibiting glial cell proliferation in a rat midbrain culture model of Parkinson´s disease when used at a concentration of 10 μM. PAQ (25 or 50 mg/kg, twice per day) prevents loss of dopaminergic neurons in the substantia nigra in a mouse model of Parkinson´s disease induced by MPTP.

    价 格：￥电议型 号：T38202产 地：中国大陆

  • T38077TLQP-21 TFA；TLQP-21 TFATLQP-21 TFA

    TLQP-21 TFA, a VGF-derived peptide endowed of endocrine and extraendocrine properties, is a potent G-protein-coupled receptor complement-3a receptor1 (C3aR1) agonist (EC50: mouse TLQP-21=10.3 μM; human TLQP-21=68.8μM). TLQP-21 TFA activates C3aR1 to induce an increase of intracellular Ca2+. TLQP-21 TFA is used for the research in regulation of nociception and other relevant physiologic functions[1][2].

    价 格：￥电议型 号：T38077产 地：中国大陆

  • T36091LEESGGGLVQPGGSMK acetate；LEESGGGLVQPGGSMK acetateLEESGGGLVQPGGSMK acetate

    LEESGGGLVQPGGSMK acetate is a proteolysis peptide found in Infliximab, a chimeric monoclonal IgG1 antibody. It serves as a component of Infliximab and can be employed for the quantitative analysis of this antibody. Infliximab is specifically designed to bind to TNF-α[1].

    价 格：￥电议型 号：T36091产 地：中国大陆

  • T27625IQP-0528；化合物IQP-0528SJ-3991|||SJ3991|||IQP0528；SJ-3991|||SJ3991|||IQP0528

    IQP-0528 is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) that has potential for the treatment of HIV infection by blocking viral entry and shows antiviral activity as a microbicidal gel. . IQP-0528 showed inhibition of both HIV-1 and HIV-2, with an EC50 of 0.2 nM for HIV-1 and 100 nM for HIV-2.

    价 格：￥电议型 号：T27625产 地：中国大陆

  • T2602Barasertib-HQPA；化合物Barasertib1H-Pyrazole-3-acetamide|||Barasertib|||AZD1152-HQPA|||AZD2811|||AZD1152

    Barasertib-HQPA (AZD2811) is a highly selective Aurora B inhibitor (IC50: 0.37 nM) and demonstrates ~3,700-fold greater selectivity than Aurora A.

    价 格：￥电议型 号：T2602产 地：中国大陆

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