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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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