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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC5309 Ufp512
Novel selective delta-opioid receptor agonist
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DCC5308 Ue2316
Potent and selective 11ß-HSD1 inhibitor, improving memory, including after intracerebroventricular drug administration to the central nervous system alone
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DCC5307 Ucph-102f
Fluorescent excitatory amino acid transporter subtype 1 (EAAT1) selective inhibitor
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DCC5306 Ucp1172
Novel dual inhibitor of dihydrofolate reductase (DHFR) and its functional analog, Rv2671
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DCC5305 Ucn-02
Stereoisomer of UCN-01, inhibiting protein kinase C with a slightly reduced potency than UCN-01
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DCC5304 Ucm710
Dual inhibitor of fatty acid amide hydrolase (FAAH) and α/β hydrolase domain 6 (ABHD6)
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DCC5303 Ucm-1336
Novel potent isoprenylcysteine carboxylmethyltransferase (ICMT) inhibitor, improving survival in Ras-driven acute myeloid leukemia
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DCC5302 Ucm-05194
Novel Agonist of the Type 1 Lysophosphatidic Acid Receptor (LPA1), Showing Efficacy in Neuropathic Pain Amelioration
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DCC5301 Ucl-2190 Hydrogen Maleate
The first potent nonimidazole H3 receptor antagonist (pKi=8.40)
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DCC5300 ucl-1972
Histamine H3 Receptor Antagonist in Treatments of Cognition Disorders
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DCC5299 Uck2-in-20874830
Novel non-competitive UCK2 inhibitor, suppressing nucleoside salvage in cells both in the presence and absence of DHODH inhibitors
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DCC5298 Uck2-in-135546812
Novel non-competitive UCK2 inhibitor, suppressing nucleoside salvage in cells both in the presence and absence of DHODH inhibitors
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DCC5297 Uck2-in-135546734
Novel non-competitive UCK2 inhibitor, suppressing nucleoside salvage in cells both in the presence and absence of DHODH inhibitors
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DCC5295 uc-ddc-966791
Competitive dual inhibitor of the hydrolysis FS-3 and the phosphodiesterase substrate p-nitrophenyl thymidine 5'-monophosphate
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DCC5294 uc-ddc-931126
Selective competitive inhibitor of ATX-mediated hydrolysis of the lysophospholipase substrate FS-3
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DCC5293 uc-ddc-918013
Selective competitive inhibitor of ATX-mediated hydrolysis of the lysophospholipase substrate FS-3
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DCC5292 Ucb-fcrn-303
Novel allosteric modulator of neonatal Fc receptor (FcRn), binding to the extracellular domain of FcRn
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DCC5291 Ucb-6876
Novel inhibitor of TNF signalling by stabilising an asymmetric form of the trimer, displaying a concentration-dependent response curve and selectivity over the TNFR1 extracellular domain and control proteins
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DCC5290 Ucb-6786
Novel inhibitor of TNF signalling by stabilising an asymmetric form of the trimer, displaying a concentration-dependent response curve and selectivity over the TNFR1 extracellular domain and control proteins
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DCC5289 ucb30889
Potent ligand of synaptic vesicle protein 2A (SV2A)
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DCC5288 Ucb-11056
Modulator of cyclic AMP generation, amplifing induced cyclic AMP formation in rat brain tissue; Nootropic
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DCC5287 Ubtr008295a
Novel Antagonist of the USP5 Zinc Finger Ubiquitin-Binding Domain (USP5 ZnF-UBD)
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DCC5286 Ubp684
Novel NMDAR positive allosteric modulator (PAM), robustly potentiating responses at all GluN1/GluN2 subtypes and at neuronal NMDARs
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DCC5285 Ubp646
Novel pan potentiator of GluN1/GluN2 receptors
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DCC5284 Ubp618
Novel pan-inhibitor of GluN1/GluN2 receptors
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DCC5283 Ubp512
Selective modulator of NMDA_receptor>NMDA receptors, potentiates responses at GluN1/GluN2A
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DCC5282 Uawj172
Novel potent and broad-spectrum antiviral agent against multiple strains of EV-D68, EV-A71, and CVB3, targeting the viral protein 2C
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DCC5281 Ua62784
Novel potent inhibitor of microtubule polymerization, binding directly to tubulin α/β heterodimers via the colchicine-binding site, perturbing mitotic spindles, delaying cells in mitosis and promotes apoptosis
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DCC5280 U-101958 Maleate [224170-09-6]
Potent and selective dopamine D4 receptor antagonist
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DCC5279 Tyrosinase Inhibitor Thio-2
Novel competitive inhibitor of tyrosinase enzyme
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