| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC0132 | (z)-5-tetradecen-1-ol | Novel ligand of the mouse orphan odorant receptor Olfr288 |
|
| 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 |
|
| DCC0134 | [d-trp]cj-15208 | Short-duration κ opioid receptor antagonist with weak KOR agonist activity |
|
| DCC0135 | [n9a]lvia | Novel α-Conotoxin LvIA Analogue, highly selectively trgeting α3β2 nicotinic acetylcholine receptors with >2000-fold higher selectivity than LvIA |
|
| DCC0136 | 002-04-kk | Novel inhibitor of the biosynthesis of DNA, RNA and proteins; Antimicrobial agent |
|
| DCC0137 | 0026-59-kk | Novel inhibitor of the biosynthesis of DNA, RNA and proteins; Antimicrobial agent |
|
| DCC0138 | 1(r)-(trifluoromethyl)oleyl Alcohol | Novel potent ferroptosis inhibitor |
|
| DCC0139 | 1,3,6-trihydroxyxanthone | Anti-androgenic, Antimicrobial, and anticancer agent |
|
| DCC0140 | 1,4-nhq | Inhibitor of the Cdc42-PBD interaction, blocking the association of Cdc42 with the PBD |
|
| DCC0141 | 1.16-hexadecanedithiol | Long chain dithiol for self-assembled monolayers (SAMs) in sensors |
|
| DCC0142 | 10074-a4 | Novel Myc-Max-specific inhibitor |
|
| DCC0143 | 10-fthf | Donor of formyl groups in anabolism used as a substrate in formyltransferase reactions, which is important in purine biosynthesis |
|
| DCC0144 | 11-deoxy-pgf2a | Selective activator of TREK-2 channels, stimulating DRG c-fiber nociceptor K2P currents and limiting calcium influx |
|
| DCC0145 | 11-oxo-ete | Cellular antiproliferative agent, inhibiting BrdU incorporation acrossing multiple cell lines with varying potency |
|
| DCC0146 | 11ß-hsd1 Inhibitor 544 | Potent inhibitor of both mouse and human 11β-HSD1 |
|
| DCC0147 | 11ßhsd1-in-1 | Novel potent and selective inhibitor of 11ß-hydroxysteroid dehydrogenase type 1 enzyme |
|
| DCC0148 | 12-crown-4 | Aß40 fibril disrupter |
|
| DCC0149 | 12-hydroxynevirapine | Metabolite of Nevirapine |
|
| 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 |
|
| DCC0151 | 13b-1c | Potent highly active irreversible inhibitor of myeloperoxidase (MPO) |
|
| DCC0152 | 14,15-eeze | Antagonist of EpETrE-induced relaxation of vascular smooth muscle |
|
| DCC0153 | 14-3-3 Dimer Ligand | The First Ligand Targeting the Dimerization Interface of the 14-3-3ζ Adapter Protein |
|
| 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 |
|
| DCC0155 | 15-hete | Inhibitor of monocyte/macrophage infiltration and the expressions of intercellular adhesion molecules under hypoxia |
|
| DCC0156 | 163-bp3 | Potent clickable photoaffinity probe, targeting gamma-secretase |
|
| DCC0157 | 163-bpyne | Notch-sparing |
|
| DCC0158 | 17,18-dihete | Major metabolite of eicosapentaenoic acid (EPA) |
|
| DCC0159 | 17beta-hsd12 Activator A1 | Novel potent 17β-HSD12 activator |
|
| DCC0160 | 17-dmag | Potent HSP90 inhibitor |
|
| DCC0161 | 17-hydroxycativic Acid | Acetylcholinesterase (AChE) inhibitor |
|
