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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC0162 | 17-hydroxywortmannin |
Irreversible inhibitor of PI3K and mTOR
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| DCC0161 | 17-hydroxycativic Acid |
Acetylcholinesterase (AChE) inhibitor
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| DCC0160 | 17-dmag |
Potent HSP90 inhibitor
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| DCC0159 | 17beta-hsd12 Activator A1 |
Novel potent 17β-HSD12 activator
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| DCC0158 | 17,18-dihete |
Major metabolite of eicosapentaenoic acid (EPA)
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| DCC0157 | 163-bpyne |
Notch-sparing
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| DCC0156 | 163-bp3 |
Potent clickable photoaffinity probe, targeting gamma-secretase
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| DCC0155 | 15-hete |
Inhibitor of monocyte/macrophage infiltration and the expressions of intercellular adhesion molecules under hypoxia
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| DCC0154 | 15-epi-lipoxin A4 |
Natural inhibitor of TNF-α-induced tissue factor (TF) expression via the PI3K/AKT/ NF-κB axis in human umbilical vein endothelial cells
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| DCC0153 | 14-3-3 Dimer Ligand |
The First Ligand Targeting the Dimerization Interface of the 14-3-3ζ Adapter Protein
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| DCC0152 | 14,15-eeze |
Antagonist of EpETrE-induced relaxation of vascular smooth muscle
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| DCC0151 | 13b-1c |
Potent highly active irreversible inhibitor of myeloperoxidase (MPO)
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| DCC0150 | 12oh-ja |
Novel regulator of plant growth and immunity, promoting flower and tuber development but prevents induction of JA signaling, plant defense or both
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| DCC0149 | 12-hydroxynevirapine |
Metabolite of Nevirapine
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| DCC0148 | 12-crown-4 |
Aß40 fibril disrupter
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| DCC0147 | 11ßhsd1-in-1 |
Novel potent and selective inhibitor of 11ß-hydroxysteroid dehydrogenase type 1 enzyme
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| DCC0146 | 11ß-hsd1 Inhibitor 544 |
Potent inhibitor of both mouse and human 11β-HSD1
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| DCC0145 | 11-oxo-ete |
Cellular antiproliferative agent, inhibiting BrdU incorporation acrossing multiple cell lines with varying potency
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| DCC0144 | 11-deoxy-pgf2a |
Selective activator of TREK-2 channels, stimulating DRG c-fiber nociceptor K2P currents and limiting calcium influx
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| DCC0143 | 10-fthf |
Donor of formyl groups in anabolism used as a substrate in formyltransferase reactions, which is important in purine biosynthesis
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| DCC0142 | 10074-a4 |
Novel Myc-Max-specific inhibitor
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| DCC0141 | 1.16-hexadecanedithiol |
Long chain dithiol for self-assembled monolayers (SAMs) in sensors
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| DCC0140 | 1,4-nhq |
Inhibitor of the Cdc42-PBD interaction, blocking the association of Cdc42 with the PBD
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| DCC0139 | 1,3,6-trihydroxyxanthone |
Anti-androgenic, Antimicrobial, and anticancer agent
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| DCC0138 | 1(r)-(trifluoromethyl)oleyl Alcohol |
Novel potent ferroptosis inhibitor
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| DCC0137 | 0026-59-kk |
Novel inhibitor of the biosynthesis of DNA, RNA and proteins; Antimicrobial agent
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| DCC0136 | 002-04-kk |
Novel inhibitor of the biosynthesis of DNA, RNA and proteins; Antimicrobial agent
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| DCC0135 | [n9a]lvia |
Novel α-Conotoxin LvIA Analogue, highly selectively trgeting α3β2 nicotinic acetylcholine receptors with >2000-fold higher selectivity than LvIA
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| DCC0134 | [d-trp]cj-15208 |
Short-duration κ opioid receptor antagonist with weak KOR agonist activity
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| DCC0133 | [dmt1,5]n/ofq(1-13)-nh2 |
Novel highly potent dual NOP/mu receptor peptide agonist, exerting antitussive effects in an in vivo model of cough
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