CAS: 60784-46-5; Elmustine

该化合物是一种合成有机化合物,属于硝基硫素类别,以其碳酸盐特性著称;该化合物的特点是能够与DNA形成共价联系,导致细胞复制和功能的中断,使其对癌症化学治疗感兴趣;它一般是白色至白固体的白色,在有机溶剂中可溶解;CENU特别注意到它对某些类型的癌症细胞,包括古力瘤和其他肿瘤有选择性的细胞具有细胞毒性;然而,它也具有重大的副作用,包括乳油压抑和潜在的...

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    上下游产品

    1,2,2,2-Tetrachloroethyl N-(2-chloroethyl) N-nitroso-carbamate ethanolamine

    合成工艺路线路线简述

      📜1,2,2,2-四氯乙基n-(2-氯乙基)N-亚硝基氨基甲酸酯,C.I.酸性橙108置于potassium Carbonate体系中,用 四氢呋喃 作为反应溶剂,化学反应 2.0H,反应生成 依莫司汀
      参考文献:1,2,2,2-Tetrachloroethyl Carbamates: Versatile Intermediates For The Synthesis Ofn-Nitrosoureas
      标题:1,2,2,2-Tetrachloroethyl Carbamates: Versatile Intermediates For The Synthesis Ofn-Nitrosoureas
      摘要:1,2,2,2-四氯乙基氨基甲酸酯3是通过1,1,2,2-四氯乙基碳酰氯与胺反应制备的.随后,氨基甲酸酯3被亚硝化并与胺反应,反应生成n-亚硝基脲.
      DOI:10.1055/s-1987-28160

      海关参考信息

      专利信息


      专利号:US-9574189-B2
      优先权日:2005-12-01
      标题:Enzymatic encoding methods for efficient synthesis of large libraries
      发明人:FRANCH THOMAS; LUNDORF MIKKEL DYBRO; JACOBSEN SØREN NYBOE; OLSEN EVA KAMPMANN; ANDERSEN ANNE LEE; HOLTMANN ANETTE; HANSEN ANDERS HOLM; SØRENSEN ANDERS MALLING; GOLDBECH ANNE; DE LEON DAEN; KALDOR DITTE KIEVSMOSE; SLØK FRANK ABILDGAARD; HUSEMOEN GITTE NYSTRUP; DOLBERG JOHANNES; Jensen Kim Birkebæ; PEDERSEN LENE; NØRREGAARD-MADSEN MADS; GODSKESEN MICHAEL ANDERS; GLAD SANNE SCHRØDER; NEVE SØREN; THISTED THOMAS; KRONBORG TINE TITILOLA AKINLEMINU; SAMS CHRISTIAN KLARNER; FELDING JAKOB; FRESKGÃ…RD PER-OLA; GOULIAEV ALEX HAAHR; PEDERSEN HENRIK
      权利人:FRANCH THOMAS; LUNDORF MIKKEL DYBRO; JACOBSEN SØREN NYBOE; OLSEN EVA KAMPMANN; ANDERSEN ANNE LEE; HOLTMANN ANETTE; HANSEN ANDERS HOLM; SØRENSEN ANDERS MALLING; GOLDBECH ANNE; DE LEON DAEN; KALDOR DITTE KIEVSMOSE; SLØK FRANK ABILDGAARD; HUSEMOEN GITTE NYSTRUP; DOLBERG JOHANNES; Jensen Kim Birkebæ; PEDERSEN LENE; NØRREGAARD-MADSEN MADS; GODSKESEN MICHAEL ANDERS; GLAD SANNE SCHRØDER; NEVE SØREN; THISTED THOMAS; KRONBORG TINE TITILOLA AKINLEMINU; SAMS CHRISTIAN KLARNER; FELDING JAKOB; FRESKGÃ…RD PER-OLA; GOULIAEV ALEX HAAHR; PEDERSEN HENRIK; NUEVOLUTION AS
      摘要:Disclosed is a method for obtaining a bifunctional complex comprising a molecule linked to a single stranded identifier oligonucleotide, wherein a nascent bifunctional complex comprising a chemical reaction site and a priming site for enzymatic addition of a tag is a) reacted at the chemical reaction site with one or more reactants, and b) reacted enzymatically at the priming site with one or more tag(s) identifying the reactant(s).

      专利号:US-6787668-B2
      优先权日:2000-04-13
      标 题 :2-amino-4,5 heptenoic acid derivatives useful as nitric oxide synthase inhibitors
      发明人:PITZELE BARNETT S; SIKORSKI JAMES A; WEBBER RONALD KEITH
      权利人:PHARMACIA CORP
      摘要:The present invention is directed to a compound of formula I:or a pharmaceutically acceptable salt thereof, wherein:R1 is selected from the group consisting of H and methyl; andR2 is selected from the group consisting of H and methyl.The compounds possess useful nitric oxide synthetase inhibiting activity, and are expected to be useful in the treatment or prophylaxis of a disease or condition in which the synthesis or over synthesis of nitric oxide forms a contributory part.

      专利号:US-11702652-B2
      优先权日:2005-12-01
      标题:Enzymatic encoding methods for efficient synthesis of large libraries

      专利号:US-2009264300-A1
      优先权日:2005-12-01
      标题 :Enzymatic encoding methods for efficient synthesis of large libraries

      专利号:WO-2006040676-A1
      优先权日:2004-10-12
      标题 :Nitrosated benzopyran compounds as novel cyclooxygenase-2 selective inhibitors
      发明人:TJOENG FOE SIONG; CARTER JEFFERY; SPRINGER JOHN ROBERT; ZUPEC MARK E
      权利人:PHARMACIA & UPJOHN CO LLC; TJOENG FOE SIONG; CARTER JEFFERY; SPRINGER JOHN ROBERT; ZUPEC MARK E
      摘要:This invention specifically relates to novel cyclooxygenase 2 (COX-2) selective inhibitor compounds that donate, transfer or release nitric oxide, stimulate endogenous synthesis of nitric oxide, elevate endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase. Compounds of particular interest and their analogs defined by formula (I) wherein Z, X, R1, R2, R3, and R4 are as described in the specification. This invention also relates to pharmaceutical compositions and methods for treating COX-2 mediated disorders, such as inflammation and inflammation related disorders.

      专利号:US-2020216836-A1
      优先权日:2005-12-01
      标题 :Enzymatic encoding methods for efficient synthesis of large libraries

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      📌 第三方产品分析报告

      ✅ COA系统入驻 | 共享模式

      主要参考文献

      1. Eisenbrand G, Müller N, Denkel E, Sterzel W. DNA adducts and DNA damage by antineoplastic and carcinogenic N-nitrosocompounds. J Cancer Res Clin Oncol. 1986;112(3):196-204. doi:10.1007/BF00395912 2. Karplus PA, Krauth-Siegel RL, Schirmer RH, Schulz GE. Inhibition of human glutathione reductase by the nitrosourea drugs 1,3-bis(2-chloroethyl)-1-nitrosourea and 1-(2-chloroethyl)-3-(2-hydroxyethyl)-1-nitrosourea. A crystallographic analysis. Eur J Biochem. 1988;171(1-2):193-198. doi:10.1111/j.1432-1033.1988.tb13775.x

      合成参考文献


      摘要:INSERM Symposium., 19(123), 1981
      摘要:Oncology., 37(177), 1980 []
      参考文献:10.1007/bf00717727
      摘要:Postma NS, Zuidema J, Mommérs EC, Eling WMC. Oxidative stress in malaria; implications for prevention and therapy. International Journal of Clinical Pharmacy. 1996 Jul;18(4):121–9. doi: 10.1007/bf00717727.
      参考文献:10.1007/bf00689967
      摘要:Sobottka SB, Berger MR. Assessment of antineoplastic agents by MTT assay: partial underestimation of antiproliferative properties. Cancer Chemother Pharmacol. 1992;30(5):385–93. doi: 10.1007/bf00689967.
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