Synthesis and characterization of novel 1,2,4-triazine derivatives with antiproliferative activity

被引:83
|
作者
Krauth, Fabian [1 ]
Dahse, Hans-Martin [2 ]
Ruettinger, Hans-Hermann [1 ]
Frohberg, Petra [1 ]
机构
[1] Univ Halle Wittenberg, Inst Pharm, D-06120 Halle, Germany
[2] HKI, Leibniz Inst Nat Prod Res & Infect Biol, D-07745 Jena, Germany
关键词
1,2,4-triazin-5-ones; Small molecules; Leukemia; K-562; Rule-of-five; log P; Imatinib; Serum albumin binding; HUMAN SERUM-ALBUMIN; 5-LIPOXYGENASE INHIBITORS; ARYLHYDRAZONIC ACIDS; PROTEIN-BINDING; AGENTS; DRUGS; IDENTIFICATION; ANTIBACTERIAL; AMIDRAZONES; CYCLIZATION;
D O I
10.1016/j.bmc.2010.01.053
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of novel small molecules with a 1,2,4-triazine scaffold was obtained according to a recently published and highly efficient synthetic route. Screening for antiproliferative and cytotoxic activity revealed distinct anticancer effects against the human leukemia cell line K-562 combined with a remarkable low cytotoxicity. All compounds were in agreement with the 'rule-of-five' claims by Lipinski and calculated log P(calc) values were experimentally confirmed (log P(exp)). For the most active compounds, in vitro serum albumin binding was investigated and structure-activity relationships were established. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1816 / 1821
页数:6
相关论文
共 50 条
  • [21] Xanthone-1,2,4-triazine and Acridone-1,2,4-triazine Conjugates: Synthesis and Anticancer Activity
    Santra, Sougata
    Sharapov, Ainur D.
    Fatykhov, Ramil F.
    Potapova, Anastasya P.
    Khalymbadzha, Igor A.
    Valieva, Maria I.
    Kopchuk, Dmitry S.
    Zyryanov, Grigory V.
    Bunev, Alexander S.
    Melekhin, Vsevolod V.
    Gaviko, Vasiliy S.
    Zonov, Andrey A.
    PHARMACEUTICALS, 2023, 16 (03)
  • [22] Synthesis, characterization and biological activity of some 1,2,4-triazine derivatives (vol 42, pg 935, 2005)
    El-Barbary, AA
    Sakran, MA
    El-Madani, AM
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2005, 42 (06) : 1243 - 1244
  • [23] Synthesis, spectral characterization and antihaemostatic activity of 1,2,4-triazoles incorporating 1,2,4-triazine rings
    Ravindra R. Kamble
    Belgur S. Sudha
    Journal of Chemical Sciences, 2006, 118 : 191 - 194
  • [24] Synthesis, spectral characterization and antihaemostatic activity of 1,2,4-triazoles incorporating 1,2,4-triazine rings
    Kamble, RR
    Sudha, BS
    JOURNAL OF CHEMICAL SCIENCES, 2006, 118 (02) : 191 - 194
  • [25] A Short Review on the Synthesis of 1,2,4-Triazine Derivatives as Bioactive Compounds
    Hashem, Heba E.
    MINI-REVIEWS IN ORGANIC CHEMISTRY, 2021, 18 (08) : 1127 - 1133
  • [26] SYNTHESIS, REACTIONS AND BIOLOGICAL EVALUATION OF SOME 1,2,4-TRIAZINE DERIVATIVES
    MANSOUR, AK
    EID, MM
    HASSAN, RA
    HAEMERS, A
    PATTYN, SR
    VANDENBERGHE, DA
    VANHOOF, L
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1988, 25 (01) : 279 - 283
  • [27] Microwave assisted synthesis and antifungal activity of 1,2,4-triazine, 1,2,4-triazole, tetrazole and pyrazole derivatives
    Kidwai, M
    Goel, Y
    Kumar, R
    INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 1998, 37 (02): : 174 - 179
  • [28] Biological Activity Evaluation of Novel 1,2,4-Triazine Derivatives Containing Thiazole/Benzothiazole Rings
    Yurttas, Leyla
    Ciftci, Gulsen Akalin
    Temel, Halide Edip
    Saglik, Begum Nurpelin
    Demir, Bahar
    Levent, Serkan
    ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2017, 17 (13) : 1846 - 1853
  • [29] Design, synthesis and biological evaluation of novel anti-cytokine 1,2,4-triazine derivatives
    Khoshneviszadeh, Mehdi
    Ghahremani, Mohammad H.
    Foroumadi, Alireza
    Miri, Ramin
    Firuzi, Omidreza
    Madadkar-Sobhani, Armin
    Edraki, Najmeh
    Parsa, Maliheh
    Shafiee, Abbas
    BIOORGANIC & MEDICINAL CHEMISTRY, 2013, 21 (21) : 6708 - 6717
  • [30] Synthesis and Study Impaction Antibacterial, Antifungal Activity Newly Pyridazine and 1,2,4-Triazine Derivatives
    Al-Dahlaki, Mohammed Hasan Mohammed
    Al-Majidi, Suaad M. H.
    CHEMICAL METHODOLOGIES, 2022, 6 (04): : 269 - 279