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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC4999 T-10106 Novel potent PPARγ antagonist with much improved drug-like properties and promising pharmacokinetic profile
DCC5000 T16a(inh)-b01 Selective class B inhibitor of the Ca -activated Cl- Channel, Ano1(TMEM16A)
DCC5001 T16a(inh)-d01 Selective class D inhibitor of the Ca -activated Cl- Channel, Ano1(TMEM16A)
DCC5002 T-2 Toxin Triol Type-A trichothecene mycotoxin
DCC5003 T3ss Inhibitor Iii-7 Novel inhibitor of the type III secretion system (T3SS), acting as a anti-microbial agent against Xanthomonas oryzae pv. oryzae (Xoo)
DCC5004 t5660136 Novel Inhibitor of Adenovirus Gene Transfer
DCC5005 t5660138 Novel Inhibitor of Adenovirus Gene Transfer
DCC5006 T5975164 Inhibitor of HIV-1 Assembly that Targets the Phosphatidylinositol (4,5)-bisphosphate Binding Site of the HIV-1 Matrix Protein
DCC5007 T6603185 Novel inhibitor of the catalytic functions of peroxiredoxin (Prx) and thioredoxin (Trx) systems
DCC5008 Tachioside Natural radical scavenger on ABTS
DCC5009 Tachyplegina Novel Inhibitor of Parasite Motility and Invasion
DCC5010 Tachyplegina-2 Novel Inhibitor of Parasite Motility and Invasion
DCC5011 Tachyplegina-4 Novel Irriversible Inhibitor of Parasite Motility and Invasion
DCC5012 Tacrine-pyrimidone Hybrid 27g Novel Potent Dual AChE/GSK-3 Inhibitor for the Treatment of Alzheimers Disease
DCC5013 Tah-19 Novel potent p53-MDM2/X antagonist, inhibiting MDM2 potently with a Ki value of 58 nmol/L, inducing accumulation of p53, p21 and MDM2, inhibiting cell cycle progression of U-2 OS cells at G1 phase in a p53-dependent manner
DCC5014 Ta-in-2 Novel inhibitor of the Klebsiella pneumoniae VapBC toxin-antitoxin (TA) system, acting as antimicrobial agents by disrupting the VapBC complex and activating VapC
DCC5015 Tak-137 Novel AMPA receptor potentiator with little agonistic effect, producing antidepressant-like effect without causing psychotomimetic effects
DCC5016 tak-187 Long-lasting ergosterol biosynthesis inhibitor
DCC5017 Tak-21d Potent FAAH Inhibitor
DCC5018 Tak-220 Hydrochloride Novel anti-HIV CCR5 antagonist
DCC5019 Tak-233 Novel selective 5-hydroxytryptamine type 2C (5-HT2C) receptor agonist
DCC5020 Tak-418 Novel inhibitor of the epigenetic modulator lysine-specific demethylase 1A (LSD1)
DCC5021 Talaroconvolutin A Natural ferroptosis inducer, killing colorectal cancer cells in vitro and in vivo
DCC5022 Talarozole CYP26 inhibitor, potentiating the effects of all-trans retinoic acid on cultured human epidermal keratinocytes
DCC5023 Talaumidin Natural neurotrophic agent, promoting neurite outgrowth from neurons through PI3K/Akt pathway
DCC5024 Talirine Novel Antibody-Drug Conjugate PBD Dimer Payload
DCC5025 Taltirelin Superagonist at the human thyrotropin-releasing hormone receptor, reversing opioid-induced respiratory depression in isoflurane anesthetized rats
DCC5026 Tamra-edatp Novel Fluorescent dATP for DNA Synthesis In Vivo, exhibited high brightness, low toxicity, and rapid incorporation and depletion kinetics in both a vertebrate (zebrafish) and a nematode (Caenorhabditis elegans)
DCC5027 Tan-67 Potent and selective non-peptide δ1 opioid receptor agonist
DCC5028 Tanshinol Borneol Ester Novel angiogenesis stimulator, promoting multiple key steps of angiogenesis parially via Akt and MAPK signalling pathways, showing anti-ischemic and anti-atherosclerosis activities, also acting as a putative PPARγ agonist

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