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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
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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