| 词条 | Neosalvarsan |
| 释义 |
| verifiedrevid = 444024073 | ImageFile=Neosalvarsan.svg | ImageSize= | ImageFile2=Neosalvarsan-3D-vdW.png | IUPACName= | OtherNames= Sodium 3,3'-diamino-4,4'-dihydroxyarsenobenzene-N-formaldehydesulfoxylate; Neoarsphenamine;914 |Section1={{Chembox Identifiers | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 9586 | InChI = 1/C13H14As2N2O4S.Na/c16-10-5-8(1-3-12(10)18)14-15-9-2-4-13(19)11(6-9)17-7-22(20)21;/h1-6,17-19H,7,16H2,(H,20,21);/q;+1/p-1 | InChIKey = BGYSJUFVJUJSOL-REWHXWOFAO | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C13H14As2N2O4S.Na/c16-10-5-8(1-3-12(10)18)14-15-9-2-4-13(19)11(6-9)17-7-22(20)21;/h1-6,17-19H,7,16H2,(H,20,21);/q;+1/p-1 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = BGYSJUFVJUJSOL-UHFFFAOYSA-M | CASNo_Ref = {{cascite|correct|??}} | CASNo=457-60-3 | PubChem=9980 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = O7K7R0O4BG | SMILES = [Na+].[O-]S(=O)CNc2cc(/[As]=[As]/c1ccc(O)c(N)c1)ccc2O }} |Section2={{Chembox Properties | Formula=C13H13As2N2NaO4S | MolarMass=466.15 g/mol | Appearance= | Density= | MeltingPt= | BoilingPt= | Solubility= |Section3={{Chembox Hazards | MainHazards= | FlashPt= | AutoignitionPt = }} Neosalvarsan is a synthetic chemotherapeutic that is an organoarsenic compound. It became available in 1912 and superseded the more toxic and less water-soluble salvarsan as an effective treatment for syphilis. Because both of these arsenicals carried considerable risk of side effects, they were replaced for this indication by penicillin in the 1940s. Both salvarsan and neosalvarsan were developed in the laboratory of Paul Ehrlich in Frankfurt, Germany. Their discoveries were the result of the first organized team effort to optimize the biological activity of a lead compound through systematic chemical modifications.[1] This scheme is the basis for most modern pharmaceutical research. Both salvarsan and neosalvarsan are prodrugs — that is, they are metabolised into the active drug in the body. Although, like salvarsan, it was originally believed to contain an arsenic-arsenic double bond, this is now known to be incorrect, and exists as a mixture of differently sized rings with arsenic-arsenic single bonds.[2] References1. ^{{cite journal |vauthors=Strebhardt K, Ullrich A |title=Paul Ehrlich's magic bullet concept: 100 years of progress |journal=Nat. Rev. Cancer |volume= 8|issue= 6|pages= 473–80|date=May 2008 |pmid=18469827 |doi=10.1038/nrc2394 |url=}} 2. ^{{Cite journal|last=Lloyd|first=Nicholas C.|last2=Morgan|first2=Hugh W.|last3=Nicholson|first3=Brian K.|last4=Ronimus|first4=Ron S.|date=2005|title=The Composition of Ehrlich's Salvarsan: Resolution of a Century-Old Debate|journal=Angewandte Chemie International Edition|volume=44|issue=6|pages=941–944|doi=10.1002/anie.200461471|pmid=15624113|issn=1521-3773}} 6 : Sulfinates|Antibiotics|Organoarsenic compounds|Phenols|Paul Ehrlich|German inventions |
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