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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
918 Results for "
N2
" in MedChemExpress (MCE) Product Catalog:
Products (918)
918 Results for "N2" in MCE Product Catalog:
Cat. No.: HY-N17963
CAS No.: 229483-41-4
Target:
Research Areas:
Oxiran-2-ylmethanol (Glycidol) is an ester product. Oxiran-2-ylmethanol induces base pair point mutations in bacterial strains and structural chromosome aberrations in cultured cells. Oxiran-2-ylmethanol forms N-(2,3-dihydroxypropyl)valine hemoglobin adducts. Oxiran-2-ylmethanol acts as an animal carcinogen but does not significantly induce micronucleated immature erythrocytes in animal bone marrow. Oxiran-2-ylmethanol enables anionic polymerization to produce linear poly(glycidol). Oxiran-2-ylmethanol can be used for cancer-related research [2] .
Cat. No.: HY-P71816
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: DPYSL2; ULIP-2; Dihydropyrimidinase Like 2; ULIP2; DRP-2; N2A3; CRMP2; Collapsin Response Mediator Protein HCRMP-2; Dihydropyrimidinase-Related Protein 2; Collapsin Response Mediator Protein 2; DHPRP2; Dihydropyrimidinase-Like 2 Short Form; DRP2; Dihydrop
Species:
Human
Source:
P. pastoris
Cat. No.: HY-103658R
CAS No.: 15809-19-5
Synonyms: Miramistin (Standard)
Research Areas:
Myramistin (Miramistin) (Standard) is the analytical standard of Myramistin (HY-103658). This product is intended for research and analytical applications. Myramistin is a cationic surfactant and disinfectant preservative. Myramistin exhibits high bactericidal activity against Staphylococcus aureus and Escherichia coli, shows lower activity against yeasts and fungi, and is active against HIV, measles virus, mumps virus, as well as influenza viruses of the H3N2 and H5N1 subtypes. Myramistin adsorbs to the negatively charged microbial cell membrane, leading to increased membrane permeability and disruption of membrane integrity, which ultimately results in leakage of intracellular contents, enzyme inactivation, and the death of bacteria/fungi/enveloped viruses [2] .
Cat. No.: HY-136820S1
Cat. No.: HY-143494
CAS No.: 2395007-81-3
Target:
Research Areas:
RSV/IAV-IN-3 (compound 14'i) is a dual inhibitor of respiratory syncytial virus (RSV) and influenza A virus (IAV) with EC50 values of 2.92 µM and 1.90 µM,respectively. RSV/IAV-IN-3 has antiviral effect against H1N1 and H3N2 with EC50 values of 3.25 µM and 1.50 µM in MDCK cells, respectively. RSV/IAV-IN-3 significantly inhibits the activity of luciferase in a dose-dependent manner, with an EC50 of 3.89 µM. RSV/IAV-IN-3 inhibits IAV infectivity and RdRp activity. RSV/IAV-IN-3 inhibits IAV and RSV replication at the post-entry stage .
Cat. No.: HY-P702064
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: UBE2L5; Ubiquitin Conjugating Enzyme E2 L5; UBE2L5P; Ubiquitin-Conjugating Enzyme E2 L5; Ubiquitin-Protein Ligase L5; Ubiquitin Conjugating Enzyme E2L 5 (Pseudogene); Ubiquitin Conjugating Enzyme E2 L5, Pseudogene; UBCH7N2
Species:
Human
Source:
Sf9 insect cells
Cat. No.: HY-P702066
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: UBE2L5; Ubiquitin Conjugating Enzyme E2 L5; UBE2L5P; Ubiquitin-Conjugating Enzyme E2 L5; Ubiquitin-Protein Ligase L5; Ubiquitin Conjugating Enzyme E2L 5 (Pseudogene); Ubiquitin Conjugating Enzyme E2 L5, Pseudogene; UBCH7N2
Species:
Human
Source:
Sf9 insect cells
Cat. No.: HY-P5377
CAS No.: 221055-89-6
Synonyms: Cathepsin K substrate
Target:
Research Areas:
Cat. No.: HY-P992482
Research Areas:
Target:
Research Areas:
Oxiran-2-ylmethanol (Standard) is the analytical standard of Oxiran-2-ylmethanol (Glycidol) (HY-Y1010). This product is intended for research and analytical applications. Oxiran-2-ylmethanol is an ester product. Oxiran-2-ylmethanol induces base pair point mutations in bacterial strains and structural chromosome aberrations in cultured cells. Oxiran-2-ylmethanol forms N-(2,3-dihydroxypropyl)valine hemoglobin adducts. Oxiran-2-ylmethanol acts as an animal carcinogen but does not significantly induce micronucleated immature erythrocytes in animal bone marrow. Oxiran-2-ylmethanol enables anionic polymerization to produce linear poly(glycidol). Oxiran-2-ylmethanol can be used for cancer-related research [2] .
Cat. No.: HY-Y1010S
CAS No.: 1246819-20-4
Synonyms: Glycidol-d5
Cat. No.: HY-P77107
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: NOTCH2NLA; Notch Homolog 2 (Drosophila) N-Terminal Like; Prev. NOTCH2NL; Notch Homolog 2 N-Terminal-Like Protein; N2N; Notch 2 N-Terminal Like; Notch Homolog 2 N-Terminal-Like Protein A; Notch 2 N-Terminal Like A; Notch Homolog 2 N-Terminal Like Protein
Species:
Human
Source:
HEK293
Cat. No.: HY-P1837
CAS No.: 186302-15-8
Target:
Research Areas:
Cat. No.: HY-189215
CAS No.: 3087067-85-1
Target:
Influenza Virus RIG-I-like receptor (RLR) Toll-like Receptor (TLR) NF-κB Interleukin Related IFNAR Apoptosis Reactive Oxygen Species (ROS)
Research Areas:
Anti-Influenza agent 12 is an orally active inhibitor of influenza A virus infection. Anti-Influenza agent 12 inhibits RIG-I-mediated innate immune signaling and TLR3-mediated signaling pathways. Anti-Influenza agent 12 inhibits NF-κB phosphorylation and downregulates the expression levels of IRF3, ASC, iNOS, IL-4, IL-6, and IFN-α inflammatory genes. Anti-Influenza agent 12 inhibits viral nucleoprotein (NP) and matrix protein 2 (M2) mRNA transcription and protein synthesis. Anti-Influenza agent 12 inhibits virus-induced apoptosis, reduces ROS and NO production, and maintains mitochondrial membrane potential. Anti-Influenza agent 12 exhibits broad-spectrum activity against H1N1 and H3N2 subtypes, reduces viral load, and alleviates lung tissue damage. Anti-Influenza agent 12 can be used for research on influenza A virus infection .
Cat. No.: HY-P706279
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ¹⁵N-Neuron-specific enolase; ¹⁵N-γ-Enolase; ¹⁵N-Enolase 2; ¹⁵N-2-Phosphoglycerate dehydratase; ENO2; Neural Enolase; Enolase 2; HEL-S-279; NSE; Epididymis Secretory Protein Li 279; 2-Phospho-D-Glycerate Hydro-Lyase; 2-Phospho-D-Glycerate Hydrolyase; Gamma-Enolase; Neuron Specific Gamma Enolase; Enolase 2 (Gamma, Neuronal); Phosphopyruvate Hydratase; Neuronal Enriched Enolase; Neurone-Specific Enolase; Neuron-Specific Enolase; Neuron Specific Enolase
Species:
Human
Source:
E. coli
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
