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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC5048 | Tbz-19 |
Novel anti-angiogenesis and vascular disrupting agent, exhibiting moderate inhibitory cell proliferation activity
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| DCC5047 | Tbz-07 |
Novel anti-angiogenesis and vascular disrupting agent, exhibiting moderate inhibitory cell proliferation activity
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| DCC5046 | Tbk1 Inhibitor-1 |
Novel TBK1/IKKε inhibitor
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| DCC5045 | Tbe-31 |
Highly potent activator of Nrf2; Potent phase 2 cytoprotective pathway inducer and liver carcinogenesis blocker
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| DCC5044 | Tbdps-chc |
Novel potent MCT1 inhibitor, exhibiting good single agent anticancer efficacy properties
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| DCC5043 | Tbbl-0000316 |
Novel antibiotic against Mycobacterium tuberculosis (Mtb), potently killing replicating, virulent Mtb H37Rv in a clavulanate-dependent manner
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| DCC5042 | Tb-2-081 |
Novel antagonist of IL-6 signaling
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| DCC5041 | Tazanolast |
Selective mast-cell-stabilizing agent, inhibiting ozone-induced airway hyperresponsiveness
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| DCC5040 | Tavarua Deoxyriboside A |
Potential neuroprotective agent, showing effects on cellular models of oxidative stress and neuroinflammation
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| DCC5039 | Tat-gap19 |
Novel brain penetrant Cx43 hemichannel blocker
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| DCC5038 | Tat Peptide (47-57) |
Trans-activator of transcription (TAT) peptide, increasing Hepta-histidine (7H) permeability into cells for treatment of iPS cell-derived neurons carrying Tau or APP mutations suppressed Tau phosphorylation
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| DCC5037 | Tasp0412098 |
Novel potent, selective, and orally active CRTH2 antagonist
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| DCC5036 | Tasp0277308 |
Potent and selective sphingosine 1-phosphate 1 (S1P1) receptor antagonist (IC50 = 7.8 nM)
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| DCC5035 | Tasp0233278 |
Potent and orally active V 1B receptor antagonist with antidepressant and anxiolytic activities in rodents
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| DCC5034 | tasidotin Hydrochloride |
Tubulin-binding dolastatin-15 analog, demostrating a wide spectrum of In Vivo antitumor activity
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| DCC5033 | Tas-303 Hydrochloride |
Novel selective norepinephrine reuptake inhibitor, displaying significant norepinephrine transporter (NET) inhibitory activity toward the serotonin or dopamine transporters
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| DCC5032 | Tariquidar Dimesylate |
Potent P-glycoprotein (P-gp) inhibitor
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| DCC5031 | Tapi-2 Acetate |
ADAM-17 (TACE) and MMP inhibitor, sensitizing cancer stem cells to the lethal effects of 5-FU and blocking shedding of TNF-α from cell membranes
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| DCC5030 | Tap1a-opt2 |
Novel potent Na V -targeting peptide, exhibiting significant increased potency for Na V 1.1, Na V 1.2, Na V 1.3, Na V 1.6 and Na V 1.7 involved in several neurological disorders including acute and chronic pain, motor neuron disease and epilepsy
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| DCC5029 | Tap1a-opt1 |
Novel potent Na V -targeting peptide, exhibiting significant increased potency for Na V 1.1, Na V 1.2, Na V 1.3, Na V 1.6 and Na V 1.7 involved in several neurological disorders including acute and chronic pain, motor neuron disease and epilepsy
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| 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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| DCC5027 | Tan-67 |
Potent and selective non-peptide δ1 opioid receptor agonist
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| 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)
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| DCC5025 | Taltirelin |
Superagonist at the human thyrotropin-releasing hormone receptor, reversing opioid-induced respiratory depression in isoflurane anesthetized rats
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| DCC5024 | Talirine |
Novel Antibody-Drug Conjugate PBD Dimer Payload
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| DCC5023 | Talaumidin |
Natural neurotrophic agent, promoting neurite outgrowth from neurons through PI3K/Akt pathway
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| DCC5022 | Talarozole |
CYP26 inhibitor, potentiating the effects of all-trans retinoic acid on cultured human epidermal keratinocytes
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| DCC5021 | Talaroconvolutin A |
Natural ferroptosis inducer, killing colorectal cancer cells in vitro and in vivo
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| DCC5020 | Tak-418 |
Novel inhibitor of the epigenetic modulator lysine-specific demethylase 1A (LSD1)
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| DCC5019 | Tak-233 |
Novel selective 5-hydroxytryptamine type 2C (5-HT2C) receptor agonist
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