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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DCC1818 |
Dlc27-14 |
Specific protein disorder catalyzer of HIV-1 Nef |
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DCC1819 |
Dl-threo-dihydrosphingosine |
Competitive inhibitor of both SPHK1 and SPHK2 |
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DCC1820 |
D-luciferin Phosphate Sodium Salt |
Ultrasensitive bioluminogenic enzyme substrate |
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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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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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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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DCC1824 |
Dmako-5 |
Novel antineoplastic agent, exhibiting remarkable anticancer activity as well as excellent cellular selectivity |
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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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DCC1826 |
Dmb213 |
Novel non-nucleoside inhibitor of Zika viral RNA-dependent RNA polymerase (RdRp) enzymes |
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DCC1827 |
Dmcl1-2 |
Novel potent and selective PROTAC degrader of myeloid cell leukemia 1 (MCL1) |
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DCC1828 |
Dmnpe-caged Luciferin |
Novel cell permeable caged Luciferin |
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DCC1829 |
Dmocptl |
Novel inducer of ferroptosis and apoptosis through ubiquitination of GPX4 in triple negative breast cancer cells |
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DCC1830 |
Dmt-dalda |
Potent and highly selective µ opioid agonist |
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DCC1831 |
Dmxb-a |
Novel,orally active and selective alpha-7 nicotinic acetylcholine (nACh) receptor |
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DCC1832 |
Dna Primase Inhibitor-1 |
Novel DNA primase inhibitor |
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DCC1833 |
Dna Primase Inhibitor-13 |
Novel DNA primase inhibitor |
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DCC1834 |
Dnac-1 |
Novel potentiator of β-lactam activity against Gram positive and Gram negative pathogens |
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DCC1835 |
Dndi-0690 |
Novel antitubercular and antiparasitic agent, possessing excellent in vitro activity against both L. donovani and Leishmania infantum as well as displaying a better safety profile |
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DCC1836 |
Do-601 |
Analeptic agent, stimulating central nervous system; Anti-barbiturate-overdose |
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DCC1837 |
Dolastatin 10
Featured
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Highly potent cytotoxic microtubule inhibitor |
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DCC1838 |
Doot-2d |
Selective MAO-B inhibitor |
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DCC1839 |
Dora 42 |
Dual orexin receptor antagonist (OX1R and OX2R antagonist or DORA) |
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DCC1840 |
Doramectin |
Anthelmintic, for the treatment of parasites such as gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice and mange mites in cattle |
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DCC1841 |
Dothiepin Hydrochloride |
Tricyclic antidepressant (TCA), acting as a serotonin–norepinephrine reuptake inhibitor (SNRI) and also having other activities including antihistamine, antiadrenergic, antiserotonergic, anticholinergic, and sodium channel-blocking effects |
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DCC1842 |
Dov51892 |
Agonist of GABAA receptors α15 subunits |
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DCC1843 |
Dp-326 |
Novel antibacterial with activity against the Gram-negative bacteria associated with nosocomial infections |
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DCC1844 |
Dpa-154 |
Novel effective and selective inhibitor of E. coli topoisomerase I |
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DCC1845 |
Dpb163-ae |
Novel 2-aminoethyl diphenylborinate (2-APB) analogue, inducing a profound activation of SOCE in DT40 cells, albeit at low concentrations (10 nM), blocking the melatonin-induced [Ca ] cyt increase and SOCE in P. falciparum. |
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DCC1846 |
Dpbx-l-dopa |
Novel boron-containing dopa-derivative, acting as a bladder relaxant through non-catecholamine receptors |
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