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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC1372 | Chalkophomycin |
Novel inhibitor of mitochondrial respiration, targeting drug-resistant cancer cells with stem-like features by inhibiting mitochondrial respiration complex I (NADH:ubiquinone oxidoreductase, complex I [CI])
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| DCC1371 | Ch5138303 |
Novel Hsp90 inhibitor
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| DCC1370 | Ch-5137291 |
Potent Androgen_receptor>androgen receptor (AR) pure antagonist which did not produce the agonist metabolite
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| DCC1369 | Ch5015765 |
Novel Hsp90 inhibitor
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| DCC1368 | Ch-3-8 |
Novel microtubule polymerization inhibitor with little susceptible to transporter-mediated chemoresistance
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| DCC1367 | Ch24h Inhibitor 17 |
Novel Highly Potent and Selective Cholesterol 24-Hydroxylase (CH24H) Inhibitor
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| DCC1366 | Ch1055 |
The first small-molecule based MCM2-targeted NIR-II probe
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| DCC1365 | cgs-9896 |
Benzodiazepine receptor partial agonist
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| DCC1364 | Cgs-8612 |
Benzodiazepine antagonist
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| DCC1363 | Cycluc3 Sodium Salt |
Water soluble CycLuc3, mutant firefly luciferase variant with enhanced light emission
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| DCC1362 | Cgs27023a |
Matrix metalloproteinase (MMP) inhibitor
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| DCC1361 | Cycluc3 |
Mutant firefly luciferase variant with enhanced light emission
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| DCC1360 | cgs-25966 |
Broad spectrum matrix metalloproteinase (MMP) inhibitor
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| DCC1359 | cgs-23425 |
Liver specific thyromimetic agonist of thyroid hormone receptor-
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| DCC1358 | Cgp64222 |
Peptoid Tat/transactivation response element inhibitor, inhibiting human immunodeficiency virus replication by blocking CXC-chemokine receptor 4-mediated virus entry
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| DCC1357 | Cgp-53437 |
Novel HIV-1 protease inhibitor, also potently inhibiting major aspartyl peptidase 1 (May1), a secreted Cryptococcus neoformans protease
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| DCC1356 | Cgp52608 |
Activator of RORalpha, inducing growth arrest in androgen-independent DU 145 prostate cancer cells
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| DCC1355 | Cgp-49823 |
Non-peptide tachykinin NK1 receptor antagonist
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| DCC1354 | Cgk062 |
Novel inhibitor of Wnt/β-catenin signaling; Anticancer agent promoting PKCα-mediated β-catenin phosphorylation/degradation
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| DCC1353 | Cgi-560 |
Novel Bruton's tyrosine kinase (BTK) inhibitor
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| DCC1352 | C-gboxin |
Novel functional Gboxin analogue that is suitable for live-cell ultraviolet crosslink conjugation and click chemistry
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| DCC1350 | Cg-707 |
Novel PRL-3 inhibitor, blocking the migration and invasion of metastatic cancer cells
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| DCC1349 | Cg500354 |
Novel inducer of neural differentiation and growth arrest in human primary GBM-derived cells, playing a tumor-suppressive role via cAMP/CREB signaling pathway
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| DCC1348 | Cg0009 |
Novel GSK3 inhibitor, inducing cell death through cyclin D1 depletion in breast cancer cells
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| DCC1347 | Cfi-402257 Hcl |
Novel Highly Potent, Selective, Bioavailable TTK (threonine tyrosine kinase) Inhibitor
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| DCC1346 | Cfi-400936 |
Potent inhibitor of TTK kinase
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| DCC1345 | Cfg920 |
Novel non-steroid reversible dual inhibitor of CYP17 and CYP11B2 against prostate cancer with fewer cardiac side effects
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| DCC1344 | Cf-ahx-lflv-dpp |
Novel Probe for the High Temperature Requirement A (HTRA) Serine Proteases
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| DCC1343 | Cestrin |
Novel probe for cellulose synthase trafficking, inhibiting cellulose deposition and interferes with the trafficking of cellulose synthase complexes and their associated proteins KORRIGAN1 and POM2/CSI1
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| DCC1342 | Ceph-ams |
Novel small molecule prodrug for use with SEAKER cells, exhibiting enhanced anticancer activity
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