99 Results for "

VP

" in MedChemExpress (MCE) Product Catalog:
Products (99)

99 Results for "VP" in MCE Product Catalog:

Cat. No.: HY-154585
CAS No.: 2361324-80-1
Purity:  ≥95.0%
Research Areas:  

Others

VP-U-6 is a nucleoside analog that can be used in oligonucleotide synthesis .
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Cat. No.: HY-12994
CAS No.: 235106-62-4
Purity:  98.68%
Synonyms: MDT-637
Target:  

RSV

Research Areas:  

Infection

MDT-637 (VP 14637) is a novel respiratory syncytial virus (RSV) fusion inhibitor with an IC50 of 1.42 ng/mL.
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Cat. No.: HY-B0502R
CAS No.: 93106-60-6
Synonyms: BAY VP 2674 (Standard); PD160788 (Standard)
Enrofloxacin (Standard) is the analytical standard of Enrofloxacin. This product is intended for research and analytical applications. Enrofloxacin (BAY Vp 2674) is an effective antibiotic with an MIC90 of 0.312 μg/mL for Mycoplasma bovis.
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Cat. No.: HY-P99438
CAS No.: 2370896-63-0
Synonyms: KIND-030

Target:  

Inhibitory Antibodies

Research Areas:  

Infection

Anivovetmab (KIND-030) is an anti-VP2 protein (canine parvovirus major capsid protein) monoclonal antibody (IgG2 isotype). Anivovetmab has the potential for studying canine parvovirus infection .
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Cat. No.: HY-111233
CAS No.: 87495-31-6
Synonyms: WIN-51711
Target:  

Enterovirus

Research Areas:  

Infection

Disoxaril (WIN-51711) is an antivirus agent with activity against poliovirus types 1 and 2. Disoxaril inserts into the hydrophobic interior of virus capsid protein VP1 to stabilize virion conformation, inhibits poliovirus uncoating, and prevents viral RNA release and synthesis. Disoxaril can be used for the research of poliovirus infection .
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Cat. No.: HY-128879
CAS No.: 1281681-54-6
Research Areas:  

Neurological Disease

VP3.15 is a potent, orally bioavailable and CNS-penetrant dual phosphodiesterase (PDE)7- glycogen synthase kinase (GSK)3 inhibitor, with IC50s of 1.59 μM and 0.88 μM for PDE7 and GSK-3, respectively. VP3.15 has neuroprotective and neuroreparative activities, thus as potential combined anti-inflammatory and pro-remyelinating therapies for multiple sclerosis (MS) .
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Cat. No.: HY-W881465
CAS No.: 2172373-55-4
5'(E)-VP-2'-OMe-U Phosphoramidite is a phosphoramidite nucleotide precursor compound, mainly used to synthesize stable and functionalized modified oligonucleotides for the research and synthesis of nucleic acid drugs.
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Cat. No.: HY-B0502S
CAS No.: 1173021-92-5
Synonyms: BAY VP 2674-d5; PD160788-d5
Research Areas:  

Infection

Enrofloxacin-d5 is the deuterium labeled Enrofloxacin. Enrofloxacin (BAY Vp 2674) is an effective antibiotic with an MIC90 of 0.312 μg/mL for Mycoplasma bovis.
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Cat. No.: HY-113761
CAS No.: 957513-35-8
Purity:  99.61%
Target:  

Filovirus

Research Areas:  

Infection

ASN03576800 could be a potent inhibitor for Ebola virus matrix protein VP40 in process of viral assembly and budding process. ASN03576800 occupies the RNA binding region of VP40 .
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Cat. No.: HY-W015815R
CAS No.: 6960-22-1
6-Methylnicotinamide (Standard) is the analytical standard of 6-Methylnicotinamide (HY-W015815). This product is intended for research and analytical applications. 6-Methylnicotinamide is a derivative of Nicotinamide (HY-B0150). 6-Methylnicotinamide coordinates with undercoordinated Pb 2+ ions through its carbonyl group, passivating Pb-related defects. 6-Methylnicotinamide reduces trap density and non-radiative recombination in the perovskite absorber layer while inducing interfacial dipole formation. 6-Methylnicotinamide enhances the hydrophobicity, grain size, and environmental, thermal, and photostability of perovskite films. 6-Methylnicotinamide induces complementation of VP16-deficient HSV-1 replication and stimulates immediate-early gene expression. 6-Methylnicotinamide is upregulated in the acute phase of intracerebral hemorrhage and may exacerbate neurological injury. 6-Methylnicotinamide can be used for research on intracerebral hemorrhage and herpes simplex virus type 1 infection .
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Cat. No.: HY-122046
CAS No.: 956571-77-0
Purity:  98.87%
Target:  

Endogenous Metabolite

Research Areas:  

Infection

Amb123203 is an antiviral compound with the activity of inhibiting viral budding. Amb123203 exerts its effect by blocking the interaction between mVP40 and Nedd4 proteins. Amb123203 has a significant inhibitory effect on the budding of VP40 virus-like particles (VLPs) of Marburg (MARV) and Ebola viruses. Amb123203 can effectively target RNA viruses that rely on the PPxY L domain for efficient budding, showing broad-spectrum antiviral activity. The discovery of Amb123203 provides an important basis for the development of new broad-spectrum antiviral compounds .
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Cat. No.: HY-CE01868
CAS No.: 86029-72-3
Synonyms: VP-Coenzyme A; Valproyl-CoA; Valproyl-coenzyme A
Research Areas:  

Metabolic Disease

VP-CoA (VP-Coenzyme A) is a coenzyme A derivative .
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Cat. No.: HY-14805S
CAS No.: 2923753-84-6
Purity:  99.14%
Synonyms: ST-246-d4
Tecovirimat-d4 (ST-246-d4) is a deuterium-labelled Tecovirimat (HY-14805). Tecovirimat is an orally bioavailable and selective compound against orthopoxviruses [including vaccinia, monkeypox, camelpox, cowpox, ectromelia (mousepox), smallpox and variola viruses]. Tecovirimat is evaluated against vaccinia, cowpox virus, ectromelia virus with EC50 values of 0.01 μM, 0.48 μM and 0.05 μM, respectively. Tecovirimat targets the orthopoxvirus protein VP37 which is necessary for membrane envelopment of intracellular mature virus particles to form enveloped virus. Tecovirimat exerts antiviral activity on the target of the cowpox virus V061 gene, which is homologous to vaccinia virus F13L, encoding a major envelope protein (p37) required for production of extracellular virus. Tecovirimat could be used in the study for orthopoxvirus-induced diseases .
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Cat. No.: HY-W744243
Synonyms: VP-16-d4; VP-16-213-d4
Etoposide-d4 (VP-16-d4; VP-16-213-d4) is the deuterium labeled Etoposide (HY-13629). Etoposide (VP-16; VP-16-213) is an anti-cancer chemotherapy agent. Etoposide inhibits topoisomerase II, thus stopping DNA replication. Etoposide induces cell cycle arrest, apoptosis and autophagy .
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Cat. No.: HY-W1119957
CAS No.: 1882067-09-5
Research Areas:  

Others

5'-VP-2'-OMe-U phosphoramidite is a phosphoramidite that contains 5’ DMT and uridine with 2’-O-methyl protection. 5'-VP-2'-OMe-U Phosphoramidite can be used to synthesize oligonucleotide.
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Cat. No.: HY-P1163
CAS No.: 42061-33-6
D[LEU4,LYS8]-VP is a selective agonist of vasopressin V1b receptor, with the Kis of 0.16 nM, 0.52 nM, and 0.1.38 nM for rat, human and mouse V1b receptor, respectively. D[LEU4,LYS8]-VP has weak antidiuretic, vasopressor, and in vitro oxytocic activities .
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Cat. No.: HY-W881466
CAS No.: 2419895-65-9
Research Areas:  

Others

5'(E)-VP-2'-OMe-Bz-A Phosphoramidite is a phosphoramidate nucleotide precursor compound, which is mainly used to synthesize stable and functionalized modified oligonucleotides and is used in the development and synthesis of nucleic acid drugs .
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Cat. No.: HY-P991153
CAS No.: 2923558-06-7

Target:  

Virus Protease

Research Areas:  

Infection

Potravitug is a humanized immunoglobulin G1-κ monoclonal antibody targeting the major capsid protein VP1 of BK polyomavirus (BKV). Potravitug is promising for research of BKV-infection-related diseases, such as BKV-induced nephropathy after organ transplantation .
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Cat. No.: HY-145850
CAS No.: 2413648-96-9
Target:  

Enterovirus

Research Areas:  

Infection

EV-A71-IN-1 is a human enterovirus A71 (EV-A71) capsid protein inhibitor with an EC50 of 0.27 μM against EV-A71. EV-A71-IN-1 is a capsid binder that blocks the interaction between the viral VP1 and the host receptor hSCARB2. EV-A71-IN-1 inhibits a series of different human enteroviruses without significant cytotoxicity (CC50>56.2 μM) .
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Cat. No.: HY-115965R
CAS No.: 64268-93-5
Research Areas:  

Infection

VP-4604 (Standard) is the analytical standard of VP-4604. This product is intended for research and analytical applications. VP-4604 is a potent anti-methicillin-resistant Staphylococcus aureus (MRSA) agent. VP-4604 exhibits significant microbial growth inhibition toward Staphylococcus aureus (ATCC 43300) with MIC of 4-8 μg/mL. VP-4604 inhibits the growth of methicillin‐resistant Staphylococcus aureus with growth inhibition >95%[1].
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