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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2227 | Gca-186 |
Highly potent non-nucleoside inhibitor of HIV-1 reverse transcriptase
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| DCC2226 | Gc-205 |
Selective inhibitor of carbonic anhydrase IX (CAIX)
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| DCC2225 | Gc-204 |
Selective inhibitor of carbonic anhydrase IX (CAIX)
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| DCC2224 | Gbs-149 |
Novel non-toxic and mammalian-specific LINE-1 inhibitor
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| DCC2223 | Gb-115 |
Antagonist of central cholecystokinin receptors
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| DCC2222 | Gat593 |
Novel CB1R allosteric agonist-positive modulator (ago-PAM), exhibiting augmented allosteric-agonist and PAM activities in neuronal cultures, improved metabolic stability, and enhanced orthosteric agonist binding (CP55940)
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| DCC2221 | Gat592 |
Novel CB1R allosteric agonist-positive allosteric modulator (ago-PAM), exhibiting moderate ago-PAM potency and improved aqueous solubility with therapeutic reduction of intraocular pressure in murine glaucoma models
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| DCC2220 | Gat591 |
Novel CB1R allosteric agonist-positive modulator (ago-PAM), exhibiting augmented allosteric-agonist and PAM activities in neuronal cultures, improved metabolic stability, and enhanced orthosteric agonist binding (CP55940)
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| DCC2219 | Gat1601 |
Novel CB1R allosteric agonist biased toward G protein- vs β-arrestin1/2-dependent signaling
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| DCC2218 | Gat1600 |
Novel potent CB1R ago-PAM
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| DCC2217 | Gat107 |
Novel allosteric activator and positive modulator of α7 nicotinic acetylcholine receptors (nAChR), more active (+)-enantiomer of 4BP-TQS
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| DCC2216 | Gas41 Inhibitor 19 |
Novel GAS41 YEATS inhibitor, blocking proliferation of NSCLC cells, and modulating expression of GAS41-dependent genes, demonstrating on-target inhibition of GAS41 in cancer cells
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| DCC2215 | Ganstigmine |
Novel acetylcholinesterase inhibitor
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| DCC2214 | Gamma-glu-gln |
Mammalian metabolite, identified in plasma and cerebrospinal fluid from hyperammonaemic patients
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| DCC2213 | Gamma-actinorhodin |
Natural antibiotic, displaying potent and selective bactericidal activity against key Gram-positive pathogens (including Staphylococcus aureus and enterococci)
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| DCC2212 | Gamillus |
Novel acid-tolerant green RSFP, exhibiting negative switching with especially high contrast in acidic conditions, and its off switching is caused by trans-to-cis isomerization of the chromophore hydroxyphenyl ring that accompanies protonation
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| DCC2211 | Gamendazole |
Novel male contraceptive agent, blocking spermatogenesis
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| DCC2210 | Galunisertib Monohydrate |
First-in-class transforming growth factor-β receptor type I inhibitor
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| DCC2209 | Galk-in-36 |
Novel inhibitor of galactokinase (GALK)
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| DCC2208 | Galidesivir Dihydrochloride |
Novel viral RNA-dependent RNA polymerase (RdRP) inhibitor
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| DCC2207 | Gadoxetate Disodium |
Liver-specific magnetic resonance imaging (MRI) contrast agent
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| DCC2204 | gabra5-agonist-6 |
Potent and selective
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| DCC2203 | Gabaar Antagonist 1e |
Novel potent competitive γ-aminobutyric acid type A receptor (GABA A R) antagonist (K i = 180 nM), targeting extrasynaptic α4βδ subtype, showing efficiently rescue inhibition of T cell proliferation
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| DCC2202 | G6pdi-1 |
Novel G6PD inhibitor, revealing immune dependence on pentose phosphate pathway. depleting NADPH most strongly in lymphocytes, markedly decreasing inflammatory cytokine production in T calls, suppressing respiratory burst in neutrophils
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| DCC2201 | G6 Hydrochloride |
Novel antibacterial and anti-biofilm agent against antibiotic resistant clinical isolates
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| DCC2200 | G514-0206 |
Inhibitor of NLRP3 inflammasome
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| DCC2199 | G4-dna Ligand-3 |
Novel fluorescent specific ligand of human telomeric G-quadruplex DNA, binding to both G-tetrad and the lateral loop near the 5-end, reducing the telomere length and downregulating hTERC and hTERT mRNA expression in HeLa cells
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| DCC2198 | G-38963 |
Novel potent and highly specific MEK inhibitor (MEKi)
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| DCC2197 | G202-0362 |
Novel antiviral agent against Rift Valley fever virus (RVFV) by blocking virus budding from the trans Golgi.
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| DCC2196 | fxr-in-12u |
Novel, Potent, and Nonsteroidal Farnesoid X Receptor (FXR) Selective Antagonist
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