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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC5189 | Toldimfos Sodium |
Stimulator of metabolism, preventing diseases associated with parturition and peri-partum period, developmental and nutritional disorders in young animals, and bone growth disorders and tetany or paresis caused by calcium, magnesium, and phosphorus metabo
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| DCC5188 | Tol8-agonist-31a |
Novel Human Toll-like Receptor 8-Selective Agonist
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| DCC5187 | Tnp-2092 |
Unique multitargeting drug conjugate with extremely low propensity for development of resistance, targeting RNA polymerase, DNA gyrase, and DNA topoisomerase IV
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| DCC5186 | Tnks-in-21 |
Novel potent and selective tankyrase (TNKS) inhibitor
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| DCC5185 | Tnks-in-1 |
Highly potent and selective tankyrase inhibitor
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| DCC5184 | Tnks2-in-5 |
Novel highly potent and selective TNKS2 inhibitor with antiproliferative effects in a colorectal cancer cell line (DLD-1) where the Wnt pathway is constitutively activated
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| DCC5183 | Tnks/usp25-in-c44 |
Novel selective inhibitor of TNKS-USP25 interaction, effectively reducing prostate cancer cell proliferation and tumor growth
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| DCC5182 | Tnk-651 |
Novel non-nucleoside reverse transcriptase inhibitor of HIV-1
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| DCC5181 | Tnk-6123 |
Emivirine analog with improved activity against drug-resistant HIV mutants
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| DCC5180 | Tnfalpha-in-5783168 |
Novel inhibitor of tumor necrosis factor-α (TNF-α)
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| DCC5179 | Tnfalpha-in-4e |
Novel potent inhibitor of TNF-α
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| DCC5178 | Tmq0153 |
Novel activator of necrostatin-1 sensitive necroptotic cell death, triggering apoptosis, autophagy and necroptosis crosstalk in chronic myeloid leukemia
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| DCC5177 | Tmppaa |
Allosteric agonist and positive allosteric modulator (PAM) of 5-HT3 receptor
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| DCC5176 | Tmp-nvoc-halo |
Novel caged protein labeling agent
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| DCC5175 | Tmp-b3a |
Novel degrader of E. coli DHFR (eDHFR), as well as eDHFR-EGFP fusion proteins, demonstrating that degradation does not require covalent attachment of the tag to the target protein
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| DCC5174 | Tm-p4-thal |
Dual Inhibitor of SIRT2 Deacetylase and Defatty-Acylase Activities
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| DCC5173 | Tmc-310911 |
Novel protease inhibitor (PI) against a variety of HIV-1 strains, including multi-PI-resistant strains, and may be less likely to generate resistance, also showing antiviral avtivity as a potential treatment for COVID-19 caused by SARS-CoV-2
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| DCC5172 | Tma-230 |
Penem beta-lactam antibiotic
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| DCC5171 | Tm5001 |
Novel inhibitor of plasminogen activator inhibitor-1 (PAI-1)
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| DCC5170 | Tm-233 |
Novel inhibitor of both JAK/STAT and proteasome activities, inducing cell death in myeloma cells
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| DCC5169 | Tm2-119 |
Potent histone methyltransferase inhibitor with rapid antimalarial activity against all blood stage forms in Plasmodium falciparum
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| DCC5168 | Tls-in-5 |
The first small molecule inhibitor of translesion synthesis (TLS) that target Rev1-CT
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| DCC5167 | Tlr8-in-5 |
Novel toll-like receptor 8 (TLR8) inhibitor, potently and selectively reducing TLR8-mediated signaling
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| DCC5166 | Tlr7/8-in-cmpd2 |
Novel potent and selective dual TLR7/8 inhibitor
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| DCC5165 | tlr4-in-c35 |
Novel Toll-Like Receptor 4 (TLR4) Inhibitor
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| DCC5164 | Tlk19781 |
Novel Insulin Receptor Modulator
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| DCC5163 | Tli3-i12 |
The first small molecule degrader, inducing anaplastic lymphoma kinase (ALK) degradation, including in non-small-cell lung cancer (NSCLC), anaplastic large-cell lymphoma (ALCL), and neuroblastoma (NB) cell lines
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| DCC5162 | Tli3-12 |
The first small molecule degrader, inducing anaplastic lymphoma kinase (ALK) degradation, including in non-small-cell lung cancer (NSCLC), anaplastic large-cell lymphoma (ALCL), and neuroblastoma (NB) cell lines
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| DCC5161 | Tl13-149 |
Novel AC220-based FLT3 degrader
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| DCC5160 | Tl13-117 |
Novel AC220-based FLT3 degrader
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