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Cat. No. Product Name Field of Application Chemical Structure
DCC5019 Tak-233
Novel selective 5-hydroxytryptamine type 2C (5-HT2C) receptor agonist
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DCC5018 Tak-220 Hydrochloride
Novel anti-HIV CCR5 antagonist
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DCC5017 Tak-21d
Potent FAAH Inhibitor
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DCC5016 tak-187
Long-lasting ergosterol biosynthesis inhibitor
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DCC5015 Tak-137
Novel AMPA receptor potentiator with little agonistic effect, producing antidepressant-like effect without causing psychotomimetic effects
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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
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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
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DCC5012 Tacrine-pyrimidone Hybrid 27g
Novel Potent Dual AChE/GSK-3 Inhibitor for the Treatment of Alzheimers Disease
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DCC5011 Tachyplegina-4
Novel Irriversible Inhibitor of Parasite Motility and Invasion
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DCC5010 Tachyplegina-2
Novel Inhibitor of Parasite Motility and Invasion
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DCC5009 Tachyplegina
Novel Inhibitor of Parasite Motility and Invasion
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DCC5008 Tachioside
Natural radical scavenger on ABTS
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DCC5007 T6603185
Novel inhibitor of the catalytic functions of peroxiredoxin (Prx) and thioredoxin (Trx) systems
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DCC5006 T5975164
Inhibitor of HIV-1 Assembly that Targets the Phosphatidylinositol (4,5)-bisphosphate Binding Site of the HIV-1 Matrix Protein
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DCC5005 t5660138
Novel Inhibitor of Adenovirus Gene Transfer
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DCC5004 t5660136
Novel Inhibitor of Adenovirus Gene Transfer
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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)
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DCC5002 T-2 Toxin Triol
Type-A trichothecene mycotoxin
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DCC5001 T16a(inh)-d01
Selective class D inhibitor of the Ca -activated Cl- Channel, Ano1(TMEM16A)
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DCC5000 T16a(inh)-b01
Selective class B inhibitor of the Ca -activated Cl- Channel, Ano1(TMEM16A)
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DCC4999 T-10106
Novel potent PPARγ antagonist with much improved drug-like properties and promising pharmacokinetic profile
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DCC4998 T-0632
Potent and selective CCKA receptor antagonist
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DCC4997 T0511-4424
Novel COX-2 inhibitor
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DCC4996 Szv558
Potent inhibitor of both rodent and human MAO-B, proved to be safe in high doses with no hERG and mutagenic activities and demonstrated neuroprotection in an in vivo chronic model of PD
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DCC4994 Synthalin Dihydrochloride
K+ channel blocker
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DCC4993 Synstab A
Novel microtubule-stablizer
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DCC4992 syn22269076
Novel Mycobacterium tuberculosis growth inhibitor
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DCC4991 Syn-1 Scr Peptide
Negative control of Syn-1 peptide, having the same amino acid composition as Syn-1 peptide, but a scrambled sequence
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DCC4990 Syn-1 Peptide
Novel potent and specific inhibitor of syncytin-mediated cell fusion, completely blocking cell fusion at 1.6 μg/ml
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DCC4989 Syk-in-ii
Novel inhibitor of the Syk kinase (spleen tyrosine kinase)
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