MeV-IN-1
MeV-IN-1 (OX-1) is a specific entry inhibitor targeting measles virus (MeV), with an IC50 value of 100 μM. MeV-IN-1 exhibits inhibitory activity against live MeV-Edm virus. MeV-IN-1 effectively suppresses the formation of infection foci. MeV-IN-1 can be used in studies related to measles virus infection.
연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.
- CAS No.: 313527-44-5
- 화학식: C14H12N2O
- 분자량:224.26
-
보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
제품 설명
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| Vero | CC50 |
>600 μM
Compound: 1a
|
Cytotoxicity against Vero-CD150w cells
Cytotoxicity against Vero-CD150w cells
|
[PMID: 16913698] |
| Vero | EC50 |
>8 μM
Compound: 24, OX-1
|
Inhibition of Nipah virus glycoprotein G/F-mediated cell-cell fusion expressed in african green monkey Vero cells after 24 hrs relative to untreated control
Inhibition of Nipah virus glycoprotein G/F-mediated cell-cell fusion expressed in african green monkey Vero cells after 24 hrs relative to untreated control
|
[PMID: 19499921] |
| Vero | EC50 |
0.4 μM
Compound: 24, OX-1
|
Inhibition of Measles virus hemagglutininin/F-mediated cell-cell fusion expressed in african green monkey Vero cells after 24 hrs relative to untreated control
Inhibition of Measles virus hemagglutininin/F-mediated cell-cell fusion expressed in african green monkey Vero cells after 24 hrs relative to untreated control
|
[PMID: 19499921] |
| Vero | EC50 |
8 μM
Compound: 24, OX-1
|
Cytotoxicity against african green monkey Vero cells after 16 hrs by MTT assay
Cytotoxicity against african green monkey Vero cells after 16 hrs by MTT assay
|
[PMID: 19499921] |
In Vitro
MeV-IN-1 (20-30 h) specifically inhibits the replication of live MV-Edm in Vero/HeLa cells, with an IC50 of approximately 55 μM, and induces only negligible cytotoxicity even at concentrations as high as 600 μM[1].
MeV-IN-1 (30 h) inhibits measles virus glycoprotein-mediated membrane fusion in transfected cells, with an IC50 of approximately 100 μM[1].
MeV-IN-1 (300 μM; 1 h-30 h) does not interfere with the adhesion of MV-Edm to Vero/HeLa cells, but inhibits the post-adhesion entry process of the virus by targeting membrane fusion[1].
MeV-IN-1 (300 μM; 30 min) inhibits membrane lipid fusion induced by measles virus (MV) glycoproteins in transfected cells, but has no effect on lipid fusion mediated by SV5[1].
MeV-IN-1 (0-600 μM) exhibits mutation-specific activity against measles virus (MV) recombinants in Vero/HeLa cells, with enhanced potency against MV-FV94M, MV-FV94L and MV-FV94I, reduced potency against MV-FV94A, and high resistance observed for MV-FV94G, which confirms that the cavity of the F protein is its target site[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
-
CAS No. 313527-44-5
-
분자량 224.26
-
화학식 C14H12N2O
-
SMILES
NC1=CC=C(OC(CC2=CC=CC=C2)=N3)C3=C1
-
Synonyms
OX-1
-
선적
Room temperature in continental US; may vary elsewhere.
-
보관
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocol
-
Research Protocol for Infectious Diseases
Infectious-disease experiments test how pathogens interact with host barriers, innate immune receptors, inflammatory signaling, pathogen replication, and tissue injury; pattern-recognition receptors such as TLRs, RIG-I-like receptors, NOD-like receptors, and inflammasomes detect microbial molecules and activate NF-κB, interferon, and cytokine responses. The central hypothesis is that infection severity reflects the balance between pathogen burden and host response: protective inflammation restricts pathogen growth, whereas excessive or mislocalized inflammation contributes to tissue damage and disease phenotype. Unresolved questions include which host pathways are protective versus pathogenic, why some infection models fail to translate to human disease, and which combined readouts best predict clinically relevant infection outcomes.
-
Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- MeV-IN-1
- 313527-44-5
- OX-1
- OX1
- OX 1
- Measles Virus
- Gram-positive bacteria
- measles virus
- Pseudomonas aeruginosa ATCC 10145
- Gram-negative bacteria
- measles virus fusion protein
- Candida albicans
- Bacillus subtilis ATCC 6633
- Vero/HeLa cells
- Staphylococcus aureus ATCC 25923
- Escherichia coli ATCC 23556
- Inhibitor
- inhibitor
- inhibit