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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DCC4988 | Syk-524 |
Novel universal opioid receptor agonist
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