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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC1828 | Dmnpe-caged Luciferin |
Novel cell permeable caged Luciferin
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| DCC1827 | Dmcl1-2 |
Novel potent and selective PROTAC degrader of myeloid cell leukemia 1 (MCL1)
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| DCC1826 | Dmb213 |
Novel non-nucleoside inhibitor of Zika viral RNA-dependent RNA polymerase (RdRp) enzymes
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| DCC1825 | D-mannuronic Acid [6906-37-2] |
Novel blocker of the TLR2 and TLR4 downstream signaling pathway, effectively inhibiting mRNA expression of MyD88 and p65, major subunit of nuclear factor-kappaB
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| DCC1824 | Dmako-5 |
Novel antineoplastic agent, exhibiting remarkable anticancer activity as well as excellent cellular selectivity
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| DCC1823 | Dmako-20 |
Novel multi-target anticancer prodrug activated by the tumor specific CYP1B1 enzyme, potently inhibiting HCT-15, HCT-116 and K562 cells growth, showing moderate anti-proliferative activity towards MDA-MB-231, HepG2, PANC, Bel7402 and MGC803 cancer cells,
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| DCC1822 | Dma-cpptl |
Prodrug of CPPTL, inducing apoptosis in a dose-dependent manner via the ROS/JNK pathway in acute myeloid leukemia
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| DCC1821 | D-lys(z)-pro-arg-pna |
Chromogenic peptide substrate, being highly sensitive for the measurement of activated Protein C.
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| DCC1820 | D-luciferin Phosphate Sodium Salt |
Ultrasensitive bioluminogenic enzyme substrate
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| DCC1819 | Dl-threo-dihydrosphingosine |
Competitive inhibitor of both SPHK1 and SPHK2
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| DCC1818 | Dlc27-14 |
Specific protein disorder catalyzer of HIV-1 Nef
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| DCC1817 | D-lana-14 |
Novel potent anti-MRSA agent, disrupting biofilms with no resistance development, sensitizing rifampicin and tetracycline against multidrug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa
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| DCC1816 | Dl0410 |
Novel acetylcholinesterase inhibitor, promoting synaptic function and neuronal survival, ameliorating cognitive deficits in SAMP8 mice via improved mitochondrial dynamics and increased activity of the NMDAR-CREB-BDNF pathway
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| DCC1815 | Dk-1-49 |
Novel autophagonizer, inducing autophagic cell death in apoptosis-defective cell line
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| DCC1814 | Dk-139 |
Inhibitor of NF-kappaB-mediated GROalpha expression, suppressing the TNFalpha-induced invasive capability of MDA-MB-231 human breast cancer cells
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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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