Cat. No. | Product Name | Field of Application | Chemical Structure |
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DCC5401 | Veratridine |
Natural Janus-Faced Modulator of Voltage-Gated Sodium Ion Channels, acting on the channel as either an agonist or antagonist depending on the nature of the electrophysiological stimulation protocol
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DCC5400 | veratramine Hydrochloride |
Antitumor agent
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DCC5398 | Venlafaxine |
Serotonin-norepinephrine reuptake inhibitor (SNRI); Antidepressant
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DCC5397 | Veledimex |
Activator for Proprietary Gene Therapy Promoter System
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DCC5396 | Vegfr-in-v |
Potent, Vascular Endothelial Growth Factor Receptor-2 (VEGFR-2) Tyrosine Kinase Inhibitor
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DCC5395 | Ve-465 |
Novel Aurora kinase inhibitor
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DCC5394 | Vdr Modulator I8 |
Novel nonsecosteroidal vitamin D receptor (VDR) modulator, enhancing pancreatic cancer therapy through remodeling of the tumor microenvironment by combination with gemcitabine
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DCC5393 | Vdr Modulator I5 |
Novel nonsecosteroidal vitamin D receptor (VDR) modulator, enhancing pancreatic cancer therapy through remodeling of the tumor microenvironment by combination with gemcitabine
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DCC5392 | Vdr Modulator C4 |
Novel nonsecosteroidal vitamin D receptor (VDR) modulator, enhancing pancreatic cancer therapy through remodeling of the tumor microenvironment by combination with gemcitabine
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DCC5391 | Vd12-09 |
Novel potent and selective CA IX inhibitor
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DCC5390 | Vd11-4-2 |
Novel potent and selective CA IX inhibitor
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DCC5389 | Vchcaγ Inhibitor 40 |
Novel selective inhibitor of the γ-class enzyme of bacteria Vibrio cholerae A (VchCAγ)
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DCC5388 | Vch-759 |
Novel non-nucleoside inhibitor of HCV RNA-dependent polymerase
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DCC5387 | Vbit-3 |
Novel inhibitor of VDAC1 oligomerization and apoptosis
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DCC5386 | Vbit-12 |
Novel potent inhibitor of VDAC1, directly interacting with purified VDAC1 and reducing its channel conductance
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DCC5385 | Vb-703 |
Novel potent TLR‐4 activation inhibitor, attenuating the expression of fibrosis hallmark genes collagen, fibronectin (FN) and transforming growth factor β (TGF‐β) in kidneys and improved albumin/creatinine ratio with higher efficacy
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DCC5383 | Variegatic Acid |
Natural inhibitor of β-hexosaminidase release and tumor necrosis factor (TNF)-α secretion from rat basophilic leukemia (RBL 2H3) cells, with IC50 values of 10.4 μM and 16.8 μM, respectively, also inhibiting PKC β1 activity with an IC50 value of 36.2 μM
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DCC5382 | Varenicline Dihydrochloride |
Partial α4ß2 nicotinic receptor agonist and α7 full agonist
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DCC5381 | Vanillylidenacetone |
Novel osteoclastogenesis inhibitor, preventing ovariectomy-induced osteoporosis in ddY mice
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DCC5380 | Vandetanib Fumarate |
Novel selective inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2), blocking VEGF-stimulated endothelial cell proliferation and migration and reducing tumor vessel permeability
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DCC5379 | Valoluc |
Novel prodrug of luciferin to mimic the transport and activation of valacyclovir, , being a robust and functional determinant of VACVase activity
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DCC5378 | Validamine |
Natural pseudo-aminosugar
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DCC5377 | Valganciclovir |
Prodrug of ganciclovir for treatment of cytomegalovirus (CMV) infection in those with HIV/AIDS or following organ transplant
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DCC5376 | Vadaclidine |
Orally acting antinociceptive muscarinic agonist
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DCC5375 | Vabicaserin Hydrochloride |
Selective 5-HT2C receptor full agonist
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DCC5374 | Va999024 |
Specific inhibitor of tissue Kallikrein>kallikrein
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DCC5373 | V4-015 |
Novel potent inhibitor of FGFR4 kinase activity
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DCC5372 | V30-sp-8 |
Novel Mycobacterium Tuberculosis VapC-Activating Stapled Peptide, successfully penetrated Mycobacterium smegmatis cell membranes and exerted bactericidal activity at a minimum inhibitory concentration that inhibited 50% of the isolates (MIC50) < 6.25 μM
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DCC5371 | V2 Inhibitor 4b |
Novel Long Residence Time Superior Inhibitor of the Vasopressin V2 Receptor
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DCC5370 | V-10367 |
Non-immunosuppressive immunophilins ligand, demonstrating enhanced neuroregeneration in the peripheral nervous system and CNS
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