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Cat. No. Product Name Field of Application Chemical Structure
DCC0665 Ap24163 Novel inhibitor of the gatekeeper mutant of BCR-ABL, suppressing in vitro resistance
DCC0666 Ap44mse Potent and selective antitumor agent, effectively depleting cellular Fe, resulting in transferrin receptor-1 up-regulation, ferritin down-regulation, and increased expression of the potent metastasis suppressor, N-myc downstream regulated gene-1
DCC0667 Ap4a-in-1 Novel inhibitor of the Ap4A phosphorylase (Rv2613c) of Mycobacterium tuberculosis (Mtb)
DCC0668 Apa-apa-mpo Novel inhibitor of PCAF bromodomain/Tat-AcK50 association
DCC0669 Apadenoson Selective A2a adenosine receptor agonist
DCC0670 Apa-h-mpo Novel inhibitor of PCAF bromodomain/Tat-AcK50 association
DCC0671 Als-i-41 Novel potent and selective oxytocin receptor antagonist
DCC0672 Apj-2929 N-Type calcium channel inhibitor
DCC0673 Aplysamine Histamine H3 receptor antagonist
DCC0674 Apn Inhibitor 4cc Potent aminopeptidase N/CD13 (APN) inhibitor
DCC0675 Apn-in-6ab Novel extremely potent inhibitor of APN activity in vitro, selective against other zinc-dependent enzymes such as matrix metalloproteases, and possessed limited cytotoxicity against Ad293 cells and favorable physicochemical and metabolic stability propert
DCC0676 Apoa-i Inducer 4010b-30 Novel inducer of endogenous ApoA-I, protecting against atherosclerotic lesion development in ApoE-/- mice, upregulating the apolipoprotein A-I gene expression, enhancing its function of promoting cholesterol efflux, ABCA1 expression and activation of PPAR
DCC0677 Apoe4 Stabilizer Novel apolipoprotein E4 (apoE4) stabilizer, showing activity in an IL-6 and IL-8 cytokine release assay
DCC0678 Apogossypolone Potent inhibitor of Bcl-2 and Mcl-1, acting as a BH3 mimetic
DCC0679 Apomine Inhibitor of HMG-CoA-reductase, promoting apoptosis of myeloma cells in vitro
DCC0680 Apoptosis Inducer 5d Novel inducer of cell death by activating apoptosis in cancer cells
DCC0681 Apoptosis Inducer 6g Novel anticancer agent, arresting MCF-7 cell growth at G2/M phase and S phase, dose dependent increasing in the mitochondrial membrane potential (ΔΨm) and ROS levels, decreasing in Gal-1 protein levels
DCC0682 Apramycin Sulfate Aminoglycoside antibiotic used in veterinary medicine
DCC0683 Apratyramide Marine-Derived Peptidic Stimulator of VEGF-A and Other Growth Factors with Potential Application in Wound Healing
DCC0684 Aps5-16-2 Novel tumor calibrated inhibitor, showing unique polypharmacology and strongly improved therapeutic index in fly and human MTC xenograft models
DCC0685 Apsr-in-8 First-in-class inhibitor of APS reductase (APSR), a critical enzyme in the assimilation of sulfate for the biosynthesis of cysteine and other essential sulfur-containing molecules
DCC0686 Apx001 Prodrug of APX-001A, the first-in-class inhibitor of the fungal protein Gwt1
DCC0687 Apyrabactin Inactive analog of pyrabactin used as the negative controller
DCC0688 Aqb007 Selective blocker of the Aquaporin-1 ion channel conductance, slowing cancer cell migration
DCC0689 Aqf026 Novel agonist of the water channel aquaporin-1 (AQP1)
DCC0690 Aqx-mn115 Novel SH2-​containing inositol 5-​phosphatase (SHIP 1) modulator
DCC0691 ar Antagonist 30 Novel Antiandrogen, Suppressing Castration-Resistant and MDV3100-Resistant Prostate Cancer Growth
DCC0692 Ar Antagonist T1-12 Novel AR antagonist, targeting the AR AF2, showing excellent AR antagonistic activity (IC 50 = 0.47 μM) and peptide displacement activity (IC 50 = 18.05 μM)
DCC0693 Ar Protac A16 Novel potent androgen receptor (AR) degrader, exhibiting excellent AR binding affinity (85%) and AR degradation efficacy at 30 μM
DCC0694 Ar-12286 Novel Rho kinase inhibitor

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