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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC5416 | Vincapusine |
Natural inhibitor of 3C-like protease (3CLpro), targeting SARS-CoV-2 3CLpro, SARS-CoV 3CLpro and MERS-CoV 3CLpro
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| DCC5415 | Vincamine V2a |
Novel antagonist against hypocretin (orexin) receptor 2, significantly preventing acute morphine-conditioned place preference (CPP) and stress-induced reinstatement of extinguished morphine-CPP in mouse models of opioid reward and relapse
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| DCC5414 | Vilanterol |
Selective long-acting beta2-adrenergic agonist (LABA) with inherent 24-hour activity for once daily treatment of COPD and asthma
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| 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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