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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DCC1380 | Chf-2060 |
Novel acetylcholinesterase inhibitor
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| DCC1379 | Ches/aß-in-9q |
Novel dual inhibitor of cholinergic dysfunction and amyloid deposition for AD treatment, penetrating the blood-brain barrier (BBB) and enhancing the cerebral acetylcholine level
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| DCC1378 | Chemr23 Inhibitor 14f |
Novel potent and orally active ChemR23 inhibitor (IC 80 = 12 nM), showing a long-acting effect in cynomolgus monkeys
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| DCC1377 | Chembl94431 |
Inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase
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| DCC1376 | Chembl1784973 |
Novel inhibitor against Lactate Dehydrogenase (LDH) of Cryptosporidium parvum
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| DCC1375 | Chelator 1a |
Novel intracellular chelator, disrupting iron homeostasis in bacteria
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| DCC1374 | Chdi-340246 |
Novel potent and selective kynurenine mono-oxygenase (KMO) inhibitor
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| DCC1373 | Chdi-180-oh |
The desmethyl precursor of CHDI-180R which is a first-in-class high-affinity PET imaging ligand specific for mHTT aggregates
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