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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC1410 | Cid-1792579 |
Novel Selective Agonist of GPR55
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| DCC1409 | Cid-16672637 |
Novel inhibitor against the NS3/4A serine protease of Hepatitis C virus genotype 3
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| DCC1408 | Cid15997213 |
Novel specific anti-VEEV (Anti-Venezuelan Equine Encephalitis Virus) agent
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| DCC1407 | Cid-1304264 |
HIV-1 Rev pre-integration inhibitor
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| DCC1406 | Cid-1252842 |
Novel Selective Agonist of GPR55
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| DCC1405 | Cid-1011163 |
Novel Selective Agonist of GPR55
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| DCC1404 | cicletanine |
Stimulator of nitric oxide release and scavenger of superoxide
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| DCC1403 | Cic-37 |
Novel SOCE modulator, displaying selectivity over other calcium channels, such as TRPV1, TRPM8, and voltage-operated calcium channels
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| DCC1402 | Ciap1-in-d19-14 |
Novel inhibitor of E3 ligase activity of cIAP1, antagonizing c-MYC by stabilizing MAD1 protein in cells
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| DCC1401 | Chymase-in-1 |
Novel chymase inhibitor, exhibiting concentration-dependent chymase inhibitory activity
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| DCC1400 | Chu-128 |
Novel Non-peptide GLP-1R Agonist, adopting a unique binding mode with a more open receptor conformation at the extracellular face
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| DCC1399 | Chs-111 |
Novel inhibitor of superoxide anion (O2(-)) generation; Inhibitor of phospholipase D activation; Modulator of immune cell migration via RhoA activity inhibition; Inhibitor of Rac2 activation in stimulated neutrophils
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| DCC1398 | Chrysotoxine |
Novel inhibitor of 6-hydroxydopamine induced apoptosis in SH-SY5Y cells via mitochondria protection and NF-κB modulation
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| DCC1397 | Chromenone 1 |
Novel potent BMP potentiator with osteogenic efficacy, enhancing canonical BMP outputs at the expense of TGFβ-Smads in an unprecedented manner
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| DCC1396 | chromafenozide |
Potent and selective partial agonist of ecdysone receptor (EcR)
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| DCC1395 | Chondrillasterol |
Natural phytosterol, showing antidiabetes activities
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| DCC1394 | Choerospondin |
Antioxidant; Aldose reductase inhibitor
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| DCC1393 | Chmfl-kit-64 |
Novel Orally Available Potent Inhibitor against Broad-Spectrum Mutants of c-KIT Kinase for Gastrointestinal Stromal Tumors
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| DCC1392 | Chmfl-flt3-335 |
Novel Potent Fms-like Tyrosine Kinase 3 Internal Tandem Duplications (FLT3-ITD) Mutant Selective Inhibitor for Acute Myeloid Leukemia
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| DCC1391 | Chmfl-flt3-122 |
Potent and selective FLT3 inhibitor
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| DCC1390 | Chmfl-btk-01 |
Novel potent and highly selective irreversible Brutons tyrosine kinase (BTK) inhibitor, inhibiting BTK Y223 auto-phosphorylation
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| DCC1389 | Chm-1-p-na |
Hydrophilic prodrug of CHM-1
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| DCC1388 | Chlorphentermine Hydrochloride |
Serotonin transporter substrate
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| DCC1387 | Chlorphentermine |
Sympathomimetic agent, facilitating the release of catecholamines, especially noradrenaline and dopamine, from nerve terminals in the brain and also inhibiting their uptake
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| DCC1386 | Chlorphenoctium Amsonate |
Widely used biocidal agent
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| DCC1385 | Chlorokojic Acid |
Antiviral and antifungal agent
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| DCC1384 | Cx14442 |
Novel potent inhibitor of HIV-1 integrase
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| DCC1383 | Chikv-in-11 |
Novel Potent and Selective Chikungunya Virus Envelope Protein Inhibitor
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| DCC1382 | Chf5407 |
Potent, long-acting, and selective muscarinic M3 receptor antagonist
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| DCC1381 | Chf-4227 |
Potent, tissue-selective estrogen receptor modulator
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