ONCOGENIC PURINE DERIVATIVES - SELECTIVE BLOCKING OR REACTIVITIES BY METHYL SUBSTITUENTS

被引：0
|
作者：
BROWN, GB
BIRDSALL, NJ
TELLER, MN
LEE, TC
PARHAM, JC
机构：
来源：
PROCEEDINGS OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH | 1972年 / 13卷 / MAR期
关键词：
D O I：
暂无
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
引用
收藏
页码：14 / &
相关论文
共 50 条
  • [41] Purine-Functionalized Ferrocene Derivatives: Efficient Redox Catalysts for Oxidation of Methyl Blue and Reduction of Trinitrophenol
    Sangani, Sagar R.
    Patel, Dax
    Dabhi, Ranjitsinh C.
    Sutariya, Tushar R.
    Ahmed, Sarfaraz
    Ameta, Rakesh Kumar
    ACS ORGANIC & INORGANIC AU, 2024,
  • [42] Selective substitutions in the C10-methyl group in erythromycin derivatives
    Gunnes, Solvi
    Romming, Christian
    Undheim, Kjell
    TETRAHEDRON, 2006, 62 (25) : 6090 - 6099
  • [43] SPECTROSCOPIC STUDY OF THE EFFECT OF METHYL AND PHENYL SUBSTITUENTS ON THE BASICITY OF PHOSPHINE-LIGANDS IN TUNGSTEN CARBONYL DERIVATIVES
    BANCROFT, GM
    DIGNARDBAILEY, L
    PUDDEPHATT, RJ
    INORGANIC CHEMISTRY, 1986, 25 (20) : 3675 - 3680
  • [44] PURINE NUCLEOSIDES .27. SYNTHESIS OF I- AND 7-METHYL-8-OXOGUANOSINE AND RELATED NUCLEOSIDES . USE OF N-AMINO GROUP AS A SELECTIVE BLOCKING AGENT IN NUCLEOSIDE SYNTHESIS
    RIZKALLA, BH
    ROBINS, RK
    BROOM, AD
    BIOCHIMICA ET BIOPHYSICA ACTA, 1969, 195 (02) : 285 - &
  • [45] 2-Phenyl-9H-purine-6-carbonitrile derivatives as selective cathepsin S inhibitors
    Cai, Jiaqiang
    Bennett, D. Jonathan
    Rankovic, Zoran
    Dempster, Maureen
    Fradera, Xavier
    Gillespie, Jonathan
    Cumming, Iain
    Finlay, William
    Baugh, Mark
    Boucharens, Sylviane
    Bruin, John
    Cameron, Kenneth S.
    Hamilton, William
    Kerr, Jennifer
    Kinghorn, Emma
    McGarry, George
    Robinson, John
    Scullion, Paul
    Uitdehaag, Joost C. M.
    van Zeeland, Mario
    Potin, Dominique
    Saniere, Laurent
    Fouquet, Andre
    Chevallier, Francois
    Deronzier, Hortense
    Dorleans, Cecile
    Nicolai, Eric
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (15) : 4447 - 4450
  • [46] The SAR development of substituted purine derivatives as selective CB2 agonists for the treatment of chronic pain
    Guidetti, Rossella
    Astles, Peter C.
    Sanderson, Adam J.
    Hollinshead, Sean P.
    Johnson, Michael P.
    Chambers, Mark G.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2014, 24 (24) : 5572 - 5575
  • [47] Adsorption dynamics of benzene derivatives onto the surface of hydroxylated silica upon photoexcitation: Effect of halogen and methyl substituents
    Yang, Yonggang
    Zhao, Min
    Liu, Yang
    Guan, Tiantian
    Liu, Yufang
    JOURNAL OF APPLIED PHYSICS, 2023, 134 (08)
  • [48] INFLUENCES OF THE SUBSTITUENTS AT THE IMINIC CARBON-ATOMS (HYDROGEN VERSUS METHYL) UPON THE PROPERTIES OF FERROCENYLIMINES AND THEIR CYCLOPALLADATED DERIVATIVES
    BOSQUE, R
    LOPEZ, C
    SALES, J
    SOLANS, X
    FONTBARDIA, M
    JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1994, (05): : 735 - 745
  • [49] Binuclear Alkyne Manganese Carbonyls: Their Rearrangements to Allene, Allyl, and Vinylcarbene Derivatives by Hydrogen Migration from Methyl Substituents
    Hu, Yucheng
    Wang, Huijie
    Ji, Yupin
    Li, Huidong
    Fan, Qunchao
    King, R. Bruce
    Schaefer, Henry F., III
    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2022, 2022 (04)
  • [50] Optimization of biguanide derivatives as selective antitumor agents blocking adaptive stress responses in the tumor microenvironment
    Narise, Kosuke
    Okuda, Kensuke
    Enomoto, Yukihiro
    Hirayama, Tasuku
    Nagasawa, Hideko
    DRUG DESIGN DEVELOPMENT AND THERAPY, 2014, 8 : 701 - 717
12345