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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC1813 | Dk-1-166 |
Novel inducer of apoptotic cell death in TNBC cell lines without causing cytotoxicity in the normal mammary epithelial cell line
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| DCC1812 | Dk-1-150 |
Novel inducer of apoptotic cell death in TNBC cell lines without causing cytotoxicity in the normal mammary epithelial cell line
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| DCC1811 | Djt06001 |
Novel selective Factor Xa inhibitor, reducing thrombus formation with low risk of bleeding
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| DCC1810 | Distigmine Dibromide |
Parasympathomimetic with longer duration of action
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| DCC1809 | Distamycin A Hydrochloride |
Antibiotic, specifically inhibiting the initiation of RNA synthesis, binding isohelically to the minor groove of B-DNA at A/T rich sites
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| DCC1808 | Displurigen |
Inhibitor of ATPase activity of HSP70
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| DCC1807 | Dipraglurant |
Novel negative allosteric modulator of the mGlu5 receptor
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| DCC1806 | Dipquo |
Novel activator of the bone marker alkaline phosphatase (ALP), markedly promoting osteoblast differentiation, including expression of Runx2, Osterix, and Osteocalcin, mediating osteogenesis through activation of p38-β
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| DCC1805 | Dipicrylamine Sodium Salt |
Potent antagonist of GABA A receptors that contain alpha1 and beta2 subunits
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| DCC1804 | Dinapsoline |
Natural full D1 dopamine receptor agonist
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| DCC1803 | Dinalbuphine Sebacate |
Long-lasting prodrug of nalbuphine, acting as a moderate-efficacy partial agonist or antagonist of the μ-opioid receptor and as a high-efficacy partial agonist of the κ-opioid receptor
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| DCC1802 | Dimiq Hydrochloride |
Inhibitor of Topoisomerase>DNA topoisomerase II; very potent cytotoxic antitumor agent
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| DCC1801 | Diminazene |
Anti-infective agent against certain protozoa such as Babesia, Trypanosoma, Cytauxzoon, and certain bacteria including Brucella and Streptococcus
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| DCC1800 | Dimethoxy-etomidate |
Novel analog of etomidate, potently inhibiting 11-beta-hydroxylase without GABAA receptor positive modulatory and sedative-hypnotic activities
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| DCC1799 | Dimethothiazine |
Serotonin antagonist and histamine antagonist
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| DCC1798 | dimethacrine |
Novel inhibitor of AMA1-RON2 interaction, blocking merozoite invasion from schizont-infected RBCs; Antidepressant; Acetylcholinesterase inhibitor
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| DCC1797 | Dimenthyl Succinate |
Building Block
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| DCC1796 | Dimenthyl (1s,2s)-cyclopropane-1,2-dicarboxylate |
Building Block
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| DCC1795 | Dilazep |
Vasodilator for the treatment of cardiopathy and renal disorders, acting as an adenosine reuptake inhibitor.
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| DCC1794 | Diic16'tco |
Novel lipid-based, high-density, environmentally sensitive (HIDE) probe
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| DCC1793 | Diic16tac |
Novel lipid-based, high-density, environmentally sensitive (HIDE) probe
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| DCC1792 | Dihydromotuporamine C Trihydrochloride |
Unique antimigration and antiangiogenic agent
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| DCC1791 | Dihydrocyclosporin A |
Closely related co-metabolite of cyclosporin A
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| DCC1790 | dihydro-beta-erythroidine Hydrobromide |
Competitive nicotinic receptor antagonist
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| DCC1789 | Dihydrexidine Hydrochloride |
D1-like full agonist with similar affinity for D1 and D5, and roughly 10-fold selectivity over D2-like receptors
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| DCC1788 | Dihydralazine |
Novel dose-dependent inhibitor of the SARS-CoV-2 Mac1 Macrodomain
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| DCC1787 | Diflorasone |
Corticosteroid Hormone Receptor Agonist
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| DCC1786 | Difeterol |
Agonist of the androgen receptor (AR); #333333; font-family: "Helvetica Neue", Helvetica, Arial, sans-serif; font-size: 14px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans:
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| DCC1785 | Difenidol |
Antiemetic agent used in the treatment of vomiting and vertigo
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| DCC1784 | Diethylcarbamazine Citrate |
Muscle relaxant, causing general central nervous system depression, relieving pain caused by strains, sprains, and other musculoskeletal conditions
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