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  • T4345CeMMEC1化合物CeMMEC1CeMMEC1 HCl

    CeMMEC1 is an inhibitor of BRD4, and also has a great affinity for TAF1(IC50=0.9 μM).

    价 格：￥电议型 号：T4345产 地：中国大陆

  • T4330CaCCinh-A01；化合物CaCCinh-A01CaCCinh-A01

    CaCCinh-A01 is an inhibitor of the calcium-activated chloride channel (CaCC, 10 μM) and TMEM16A (IC50: 2.1 μM).

    价 格：￥电议型 号：T4330产 地：中国大陆

  • T4306CCG-203971；化合物CCG203971CCG203971；CCG203971

    CCG-203971 is an inhibitor of SRE activation in the prostate cancer cell line PC-3 (IC50: 6.4 μM), with 87% inhibition of SRE activation achieved at 100 μM. This compound also inhibits PC-3 cell migration (IC50: 4.2 μM), as determined by a scratch wound assay. CCG-203971(CCG203971) causes no cytotoxicity when evaluated by the WST-1 assay. It is well tolerated in normal mice up to doses of 100 mg/kg given intraperitoneally over five days.

    价 格：￥电议型 号：T4306产 地：中国大陆

  • T41200cis MZ 1；cis MZ 1cis MZ 1

    cis MZ 1 is a negative Control for MZ1. Exhibits no significant VHL binding affinity.

    价 格：￥电议型 号：T41200产 地：中国大陆

  • T41199cis-SIM1；cis-SIM1cis-SIM1；cis-SIM1

    cis-SIM1 is the negative control for SIM1.

    价 格：￥电议型 号：T41199产 地：中国大陆

  • T40996Coppersensor 1化合物Coppersensor 1Coppersensor 1|||CS1

    Coppersensor 1 (CS1) is a boron dipyrromethene-based fluorescent sensor for selective and sensitive detection of copper(I) ions (Cu + ) in biological samples. Coppersensor 1 can be imaged using any type of fluorescence microscope, including epifluorescence, confocal and multiphoton.

    价 格：￥电议型 号：T40996产 地：中国大陆

  • T40675CP-610431；CP-610431CP-610431

    CP-610431 is a reversible, ATP-uncompetitive inhibitor of acetyl-CoA carboxylase (ACC), exhibiting isozyme nonselectivity. It inhibits both ACC1 and ACC2 with IC50 values of approximately 50 nM. CP-610431 offers potential application in metabolic syndrome research.

    价 格：￥电议型 号：T40675产 地：中国大陆

  • T40437Caloxin 2A1；Caloxin 2A1Caloxin 2A1

    Caloxin 2A1 is an inhibitor peptide of the plasma membrane Ca 2+-ATPase (PMCA) responsible for extracellular signaling. Importantly, Caloxin 2A1 has no impact on the basal Mg 2+-ATPase or Na+-K+-ATPase activities.

    价 格：￥电议型 号：T40437产 地：中国大陆

  • T40353CDK7/9-IN-1CDK7/9-IN-1CDK7/9-IN-1

    CDK7/9-IN-1 is a specific inhibitor of cyclin-dependent kinases 7/9 (CDK7/9). It specifically targets CDK7, while also displaying inhibitory activity against CDK9. CDK7/9-IN-1 demonstrates excellent inhibitory potency against CDK7, with IC50 values of 0.0656 μM and 0.00574 μM without pre-incubation and after 3 hours pre-incubation, respectively. Furthermore, CDK7/9-IN-1 inhibits CDK9 with an IC50 of 2.14 μM after 3 hours pre-incubation. Its application in cancer research makes it valuable for su

    价 格：￥电议型 号：T40353产 地：中国大陆

  • T40263CDK5-IN-1CDK5-IN-1CDK5-IN-1

    CDK5-IN-1 is a highly potent inhibitor of CDK5, displaying an inhibitory activity of less than 10 nM. This potent compound is specifically employed in scientific investigations relating to kidney diseases.

    价 格：￥电议型 号：T40263产 地：中国大陆

  • T40237Carboxylesterase-IN-1；Carboxylesterase-IN-1Carboxylesterase-IN-1

    Carboxylesterase-IN-1, a novel pesticide, acts as an inhibitor of carboxylesterase at a concentration of 50 μg/mL, displaying comparable inhibitory activity to the established inhibitor triphenyl phosphate.

    价 格：￥电议型 号：T40237产 地：中国大陆

  • T40071Cavα2δ-IN-1；Cavα2δ-IN-1Cavα2δ-IN-1

    Cavα2δ-IN-1 demonstrates exceptional specificity for voltage-gated calcium channels Cavα2δ-1 (with a Ki value of 6 nM), in comparison to Cavα2δ-2 (with a Ki value greater than 10,000 nM).

    价 格：￥电议型 号：T40071产 地：中国大陆

  • T40063CBR-470-1；化合物CBR-470-1CBR-470-1

    CBR-470-1 is a potent inhibitor of glycolytic phosphoglycerate kinase 1 (PGK1) that activates NRF2 by increasing methylglyoxal levels. CBR-470-1 is a non-covalent Nrf2 activator with neuroprotective activity that protects SH-SY5Y neuronal cells from MPP+-induced cytotoxicity by activating the Keap1-Nrf2 cascade. cytotoxicity induced by MPP+.

    价 格：￥电议型 号：T40063产 地：中国大陆

  • T40047CDK6/9-IN-1CDK6/9-IN-1CDK6/9-IN-1

    CDK6/9-IN-1 (compound 66) is a potent dual inhibitor of CDK 6 and CDK 9 that can be administered orally. It exhibits inhibitory activity with IC 50 values of 40.5 nM and 39.5 nM against CDK6 and CDK9, respectively.

    价 格：￥电议型 号：T40047产 地：中国大陆

  • T39827c-ABL-IN-1；c-ABL-IN-1c-ABL-IN-1

    C-ABL-IN-1 is a new and specific inhibitor of the c-Abl protein, which effectively prevents the progression of neurodegeneration observed in Parkinson´s disease.

    价 格：￥电议型 号：T39827产 地：中国大陆

  • T39676CM121CM121CM121

    CM121 is a reversible inhibitor of ALDH1A2 that acts specifically on the active site, exhibiting an IC50 of 0.54 μM and a Kd of 1.1 μM. It exerts its inhibitory effect through multiple hydrophobic interactions.

    价 格：￥电议型 号：T39676产 地：中国大陆

  • T3964Glutaminase C-IN-1；化合物Glutaminase C-IN-1Compound 968|||Glutaminase Inhibitor Compound 968；Compound 9

    Glutaminase C-IN-1 (Compound 968) is a Glutaminase C allosteric inhibitor.

    价 格：￥电议型 号：T3964产 地：中国大陆

  • T39631Chst15-IN-1Chst15-IN-1Chst15-IN-1

    Chst15-IN-1 is a powerful, reversible, covalent inhibitor of the Chst15 enzyme. It effectively suppresses the sulfation levels of chondroitin sulfate-E (CS-E) and other closely related sulfotransferases responsible for glycosaminoglycans (GAGs) synthesis. Acting as a selective sulfotransferase inhibitor, Chst15-IN-1 can attenuate the inhibitory actions of chondroitin sulfate proteoglycans (CSPGs), making it a promising candidate for enhancing neuronal repair.

    价 格：￥电议型 号：T39631产 地：中国大陆

  • T3961CYM-5541；化合物CYM 5541CYM 5541|||ML249|||CID-17253208；CYM 5541|||ML249|||CID-17253208

    CYM-5541 (ML249) is a selective and allosteric S1P3 receptor agonist.

    价 格：￥电议型 号：T3961产 地：中国大陆

  • T39606CE3F4 analog 1；CE3F4 analog 1CE3F4 analog 1

    CE3F4 analog 1 is an analogue of CE3F4.

    价 格：￥电议型 号：T39606产 地：中国大陆

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