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 |
|