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Others

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Cat. No. Product Name Field of Application Chemical Structure
DCC5413 Vidarabine Monohydrate
Broad spectrum antibiotic, inhibiting adenylyl cyclase type 5 (AC5) and protecting against chronic coronary artery occlusion (CAO)
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DCC5412 Vicagrel
Clopidogrel analog as an antiplatelet agent
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DCC5411 Vibsanin A
Natural protein kinase C (PKC) activator and HSP90 inhibitor, sensitizing human acute myeloid leukemia cells to tyrosine kinase inhibitor-induced myeloid differentiation via activation of PKC and upregulation of Lyn
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DCC5410 Vhl-hif1α Inhibitor-tg0
The first sub-micromolar inhibitor of the VHL-HIF1α interaction
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DCC5409 Vezf1-in-t4
Novel Inhibitor of the Pro-Angiogenic Activity of the Zinc Finger Transcription Factor Vezf1
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DCC5408 Vesiculopolin B
Novel anti-vesiculoviral agent, inhibiting transcription initiation of vesiculoviruses
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DCC5407 Vesamicol Hydrochloride
Potent inhibitor of acetylcholine transport
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DCC5406 Verticillin A
Apoptosis inducer, inhibiting Leiomyosarcoma and Malignant peripheral nerve sheath tumor growth
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DCC5405 Verticilide
Natural insect ryanodine receptor (RyR) antagonist
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DCC5404 Vernolepin
Natural Reversible Plant Growth Inhibitor
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DCC5403 Vernakalant
Novel blocker of atrial potassium channels
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DCC5402 Verminoside
Natural anti-inflammatory and antioxidant agent, inhibiting both iNOS expression and NO release in the LPS-induced J774.A1 macrophage cell line, enhancing protein expression levels of PARP-1 and p53, and attenuating intracellular ROS and stress (oxidative
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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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