| 词条 | 2,3-Bis(acetylmercaptomethyl)quinoxaline |
| 释义 |
| ImageFile = 2,3-Bis(acetylmercaptomethyl)quinoxaline.svg | ImageSize = | ImageAlt = | IUPACName = S-[[3-(acetylsulfanylmethyl)quinoxalin-2-yl]methyl] ethanethioate | OtherNames = | Section1 = {{Chembox Identifiers | CASNo = 36014-40-1 | PubChem = 188227 | SMILES = CC(=O)SCC1=NC2=CC=CC=C2N=C1CSC(=O)C | ChemSpiderID = 163612 | InChI = 1/C14H14N2O2S2/c1-9(17)19-7-13-14(8-20-10(2)18)16-12-6-4-3-5-11(12)15-13/h3-6H,7-8H2,1-2H3 | InChIKey = KIYGADXCTZZZDG-UHFFFAOYAA | StdInChI = 1S/C14H14N2O2S2/c1-9(17)19-7-13-14(8-20-10(2)18)16-12-6-4-3-5-11(12)15-13/h3-6H,7-8H2,1-2H3 | StdInChIKey = KIYGADXCTZZZDG-UHFFFAOYSA-N }} | Section2 = {{Chembox Properties | C=14|H=14|N=2|O=2|S=2 | MolarMass = | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}2,3-Bis(acetylmercaptomethyl)quinoxaline ia an antiviral agent which can inhibits poliovirus RNA synthesis in vitro and in vivo and inhibits human herpesvirus 1 multiplication in vitro. It does not interfere with attachment, penetration or DNA synthesis, but interrupts a late stage in virus assembly and/or maturation.[1][2] References1. ^{{cite journal |title=none| author = Bucchini D and Girard M | date = 1975–1976 | journal = Intervirology | volume = 6 | pages = 285 | doi=10.1159/000149482}} {{DEFAULTSORT:Bis(acetylmercaptomethyl)quinoxaline, 2,3-}}{{organic-compound-stub}}2. ^{{cite book|last=Mahy|first=Brian W J|title=A dictionary of virology|year=2001|publisher=Academic Press|location=San Diego, Calif. [u.a.]|isbn=0-12-465327-8|pages=2|edition=3.}} 3 : Quinoxalines|Thioesters|Antivirals |
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