Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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A299594-50mg | 50mg | In stock | $162.90 | |
A299594-250mg | 250mg | In stock | $643.90 | |
A299594-1g | 1g | In stock | $2,060.90 |
Synonyms | BCP04187 | Malaphos | 6-Bromo-4-dimethylaminomethyl-5-hydroxy-1-methyl-2-phenylsulfanylmethyl-1H-indole-3-carboxylic acid ethyl ester | BSPBio_001223 | DB13609 | Oprea1_384852 | Umifenovir [INN] | D10558 | AR-1I9514 | ethyl 6-bromo-4-(dimethylaminomethyl) |
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Specifications & Purity | Moligand™, ≥98% |
Shipped In | Normal |
Grade | Moligand™ |
Action Type | NEGATIVE MODULATOR |
Mechanism of action | Hemagglutinin negative modulator |
ALogP | 4.4 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Pubchem Sid | 488187811 |
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Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488187811 |
IUPAC Name | ethyl 6-bromo-4-[(dimethylamino)methyl]-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-carboxylate |
INCHI | InChI=1S/C22H25BrN2O3S/c1-5-28-22(27)20-18(13-29-14-9-7-6-8-10-14)25(4)17-11-16(23)21(26)15(19(17)20)12-24(2)3/h6-11,26H,5,12-13H2,1-4H3 |
InChi Key | KCFYEAOKVJSACF-UHFFFAOYSA-N |
Canonical SMILES | CCOC(=O)C1=C(N(C2=CC(=C(C(=C21)CN(C)C)O)Br)C)CSC3=CC=CC=C3 |
Isomeric SMILES | CCOC(=O)C1=C(N(C2=CC(=C(C(=C21)CN(C)C)O)Br)C)CSC3=CC=CC=C3 |
PubChem CID | 131411 |
Molecular Weight | 477.43 |
PubChem CID | 131411 |
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CAS Registry No. | 131707-25-0 |
ChEMBL Ligand | CHEMBL1214598 |
BindingDB Ligand | 83797 |
DrugBank Ligand | DB13609 |
RCSB PDB Ligand | 75U |
DrugCentral Ligand | 4868 |
PubChem SID | 488187811 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
J2009370 | Certificate of Analysis | Jul 03, 2024 | A299594 |
E2007016 | Certificate of Analysis | Jan 30, 2024 | A299594 |
E2324193 | Certificate of Analysis | Jun 01, 2023 | A299594 |
B2302891 | Certificate of Analysis | Feb 15, 2023 | A299594 |
1. Ting Zhang, Ge Bai, Nan Cai, Yongqian Lei, Pengran Guo, Jingwei Xu. (2023) The carbon-doped Fe3O4 montmorillonite particle electrode for the degradation of antiviral drugs in electro-Fenton system. APPLIED CLAY SCIENCE, 243 (107056). [PMID:] |
2. Hongrui Yang, Chen Wang, Wenjuan Zhu, Xia Zhang, Tiemei Li, Jing Fan. (2022) A Sustainable Strategy for Solid-Phase Extraction of Antiviral Drug from Environmental Waters by Immobilized Hydrogen Bond Acceptor. Nanomaterials, 12 (8): (1287). [PMID:35457995] |
3. Dai Tianming, Wang Min, Wang Pengzhen, Dai Libing, Dai Renke, Meng Qingqi. (2021) Inhibition effects of eight anti-coronavirus drugs on glycosides metabolism and glycosidases in human gut microflora. PHARMAZIE, 76 (5): (195-201). [PMID:33964992] |
1. Leneva IA, Russell RJ, Boriskin YS, Hay AJ. (2009) Characteristics of arbidol-resistant mutants of influenza virus: implications for the mechanism of anti-influenza action of arbidol.. Antiviral Res, 81 (2): (132-40). [PMID:19028526] |
2. Pécheur EI, Borisevich V, Halfmann P, Morrey JD, Smee DF, Prichard M, Mire CE, Kawaoka Y, Geisbert TW, Polyak SJ. (2016) The Synthetic Antiviral Drug Arbidol Inhibits Globally Prevalent Pathogenic Viruses.. J Virol, 90 (6): (3086-92). [PMID:26739045] |
3. Hulseberg CE, Fénéant L, Szymańska-de Wijs KM, Kessler NP, Nelson EA, Shoemaker CJ, Schmaljohn CS, Polyak SJ, White JM. (2019) Arbidol and Other Low-Molecular-Weight Drugs That Inhibit Lassa and Ebola Viruses.. J Virol, 93 (8): (1755-70). [PMID:30700611] |
4. Ianevski A, Yao R, Fenstad MH, Biza S, Zusinaite E, Reisberg T, Lysvand H, Løseth K, Landsem VM, Malmring JF et al.. (2020) Potential Antiviral Options against SARS-CoV-2 Infection.. Viruses, 12 (6): (1755-70). [PMID:32545799] |
5. Ting Zhang, Ge Bai, Nan Cai, Yongqian Lei, Pengran Guo, Jingwei Xu. (2023) The carbon-doped Fe3O4 montmorillonite particle electrode for the degradation of antiviral drugs in electro-Fenton system. APPLIED CLAY SCIENCE, 243 (107056). [PMID:] |
6. Hongrui Yang, Chen Wang, Wenjuan Zhu, Xia Zhang, Tiemei Li, Jing Fan. (2022) A Sustainable Strategy for Solid-Phase Extraction of Antiviral Drug from Environmental Waters by Immobilized Hydrogen Bond Acceptor. Nanomaterials, 12 (8): (1287). [PMID:35457995] |
7. Dai Tianming, Wang Min, Wang Pengzhen, Dai Libing, Dai Renke, Meng Qingqi. (2021) Inhibition effects of eight anti-coronavirus drugs on glycosides metabolism and glycosidases in human gut microflora. PHARMAZIE, 76 (5): (195-201). [PMID:33964992] |