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  • T69819ALM2;化合物 ALM2ALM2

    ALM2 is an USP7 inhibitor.

    价 格:¥电议型 号:T69819产 地:中国大陆

  • T69818GNTI TFA;化合物 GNTI TFAGNTI TFA

    GNTI TFA is a selective kappa opioid receptor antagonist.

    价 格:¥电议型 号:T69818产 地:中国大陆

  • T69817Eprociclovir Na;化合物 Eprociclovir NaEprociclovir Na

    Eprociclovir Na is the salt form of Eprociclovir, also known as A-5021, a new acyclovir analogue and a potent inhibitor of EHV1 replication and may have potential for the treatment and/or prophylaxis of infections with this virus. Eprociclovir possess potent anti-herpetic activity against most human herpesviruses. A-5021 proved to be about 15-fold more potent than acyclovir in inhibiting viral replication. Eprociclovir inhibits murine herpetic keratitis. A-5021 eyedrops, which are easily applie

    价 格:¥电议型 号:T69817产 地:中国大陆

  • T69816ATZ-1993;化合物 ATZ-1993ATZ-1993

    ATZ-1993 is an Endothelin Receptor Antagonist.

    价 格:¥电议型 号:T69816产 地:中国大陆

  • T69815SB-284851-BT;化合物 SB-284851-BTSB-284851-BT

    SB-284851-BT is a chemical compound that serves as an inhibitor of BRD4, p38α, and BRDT, exhibiting varying degrees of affinity and inhibition for each. Specifically, it inhibits BRD4-BD1 with an IC50 value of 1.7 ?M, p38α with a Kd of 0.47 nM, BRDT (1) with an IC50 value of 18 ?M, and BRD4 (1) with an IC50 value of 3.7 ?M. By targeting p38α, SB-284851-BT effectively reduces IL-8 production and, through inhibiting BRD4, down-regulates both the c-Myc and NF-κB gene pathways, crucial in cancer pat

    价 格:¥电议型 号:T69815产 地:中国大陆

  • T69814Neramexane Free Base;化合物 Neramexane Free BaseNeramexane Free Base

    Neramexane Free Base is a drug related to memantine, which acts as an NMDA antagonist and has neuroprotective effects. It is being developed for various possible applications, including treatment of tinnitus, Alzheimer´s disease, drug addiction and as an analgesic.

    价 格:¥电议型 号:T69814产 地:中国大陆

  • T69813AZD-6126;化合物 AZD-6126AZD-6126

    AZD6126, also known as ANG-453, a water-soluble phosphate prodrug of N-acetylcolchinol with potential antiangiogenesis and antineoplastic activities. AZD-6126 is an angiogenesis inhibitor and tubulin inhibitor potentially for the treatment of solid tumours. AZD6126 is converted in vivo into N-acetylcolchinol. N-acetylcolchinol binds to and destabilizes the tubulin cytoskeleton of endothelial cells in tumor blood vessels, which may result in tumor endothelial cel apoptosis, the selective occlusio

    价 格:¥电议型 号:T69813产 地:中国大陆

  • T69812AFN941;化合物 AFN941AFN941

    AFN941 is a staurosporine analog, acting as a Jak3-specific inhibitor.

    价 格:¥电议型 号:T69812产 地:中国大陆

  • T69811AGI25696;化合物 AGI25696AGI25696

    AGI-25696 is a MATA2 inhibitor that are useful as therapeutic agents for treating malignancies. AGI-25696 showed in vivo activity in MTAP null tumors. Note: The correct structure of AGI-25696 is CAS#2201065-84-9. Many vendors mistakenly listed CAS#2201066-35-3 as its AGI25696. J. Med. Chem. 2021, 64, 8, 4430–4449 published AGI25696 structure (it is CAS#2201065-84-9).

    价 格:¥电议型 号:T69811产 地:中国大陆

  • T69810N-2733 HCl;化合物 N-2733 HClN-2733 HCl

    N-2733 HCl is a nuclear factor (NF)-kappaB activation inhibitor.

    价 格:¥电议型 号:T69810产 地:中国大陆

  • T6981Nudifloric Acid;化合物 Nudifloric AcidNudifloric Acid;1-甲基-6-氧代-1,6-二氢吡啶-3-羧酸|||Nudifloric Acid

    1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (Nudifloric Acid) is from Cordyceps bassiana. Nudifloric Acid targets to block AP-1-mediated luciferase activity, implying it has an anti-inflammatory function.

    价 格:¥电议型 号:T6981产 地:中国大陆

  • T68981PD-321852;化合物 PD-321852PD-321852

    PD-321852 is a small-molecule Chk1 inhibitor, which potentiates gemcitabine-induced clonogenic death in a panel of pancreatic cancer cell lines and evaluated the relationship between endpoints associated with Chk1 inhibition and chemosensitization. Gemcitabine chemosensitization by minimally toxic concentrations of PD-321852 ranged from minimal (<3-fold change in survival) in Panc1 cells to >30-fold in MiaPaCa2 cells. PD-321852 inhibited Chk1 in all cell lines as evidenced by stabilization of Cd

    价 格:¥电议型 号:T68981产 地:中国大陆

  • T68539CEP-11981;化合物 CEP-11981BOL 303213X|||ESK981 ; BOL 303213X|||ESK981;BOL 303213X|||ESK981 ; BOL 3032

    CEP-11981 (ESK981; BOL 303213X) is an orally active tyrosine kinase inhibitor (TKI) that targets TIE2, VEGFR1-3, and FGFR1. It exhibits potential anti-tumor and anti-angiogenic effects.

    价 格:¥电议型 号:T68539产 地:中国大陆

  • T68240AZD-9819;化合物 AZD-9819AZD-9819

    AZD-9819 is an inhibitor of human neutrophil elastase for potential treatment of chronic obstructive pulmonary disease (COPD).

    价 格:¥电议型 号:T68240产 地:中国大陆

  • T67981Copper histidine;组氨酸铜Copper histidine

    Copper histidine inhibited Ctr1-mediated cellular uptake of oxaliplatin in vitro without altering oxaliplatin accumulation of platinum or neurotoxicity in DRG tissues in vivo. Copper histidine is administered orally for the treatment of Menkes disease.

    价 格:¥电议型 号:T67981产 地:中国大陆

  • T66981(2S,4R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxyli

    (2S,4R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid is a useful organic compound for research related to life sciences. The catalog number is T66981 and the CAS number is 176486-63-8.

    价 格:¥电议型 号:T66981产 地:中国大陆

  • T65981Ethyl 4-(1-methyl-5-nitro-1H-benzo[d]imidazol-2-yl)butanoate;化合物 Ethyl 4-(1-methyl-5-nitro-1H-benzo[

    Ethyl 4-(1-methyl-5-nitro-1H-benzo[d]imidazol-2-yl)butanoate is a useful organic compound for research related to life sciences. The catalog number is T65981 and the CAS number is 3543-72-4.

    价 格:¥电议型 号:T65981产 地:中国大陆

  • T649811,2-Bis(chloromethyl)benzene;化合物 1,2-Bis(chloromethyl)benzene1,2-Bis(chloromethyl)benzene

    1,2-Bis(chloromethyl)benzene is a useful organic compound for research related to life sciences. The catalog number is T64981 and the CAS number is 612-12-4.

    价 格:¥电议型 号:T64981产 地:中国大陆

  • T6399AZD1981;化合物AZD1981Prostaglandin Receptor|||AZD 1981|||AZD1981|||Inhibitor|||AZD 1981|||AZD-1981|||AZ

    AZD1981 is an effective and specific CRTh2 (DP2) receptor antagonist (IC50: 4 nM), showing >1000-fold selectivity over more than 340 other enzymes and receptors, including DP1. AZD1981 has been used in trials studying the treatment and basic science of Asthma, Postmenopausal, Pharmakokinetic, Asthma Patients, and Drug Interaction, among others.

    价 格:¥电议型 号:T6399产 地:中国大陆

  • T63981Cap-dependent endonuclease-IN-17;化合物 Cap-dependent endonuclease-IN-17Cap-dependent endonuclease-IN-1

    Cap-dependent endonuclease-IN-17 is a cap-dependent endonuclease (CEN) inhibitor. cap-dependent endonuclease-IN-17 exhibits antiviral activity (IC50: 1.29 μM) against influenza virus A/Hanfang/359/95 (H3N2).

    价 格:¥电议型 号:T63981产 地:中国大陆

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