Anti-genotoxic hydrazide from Crinum defixum

被引:14
作者
Bordoloi, Manobjyoti [1 ]
Kotoky, Rumi [2 ]
Mahanta, Jiban J. [2 ]
Sarma, Tarun C. [2 ]
Kanjilal, Purnendu B. [2 ]
机构
[1] CSIR, NE Inst Sci & Technol, Nat Prod Chem Div, Jorhat 785006, Assam, India
[2] CSIR, NE Inst Sci & Technol, Med Aromat & Econ Plants Div, Jorhat 785006, Assam, India
关键词
Crinum defixum Ker-Gawl; Amaryllidaceae; Bon-naharu; Anti-genotoxicity; Onion root tip assay; (E)-N '-[(E)-2-Butenoyl]-2-butenoylhydrazide; AQUEOUS EXTRACT; AMARYLLIDACEAE; L;
D O I
10.1016/j.ejmech.2008.09.041
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Crinum defixum Ker-Gawl popularly known as Bon-naharu (meaning wild garlic) in Assam. It is found abundantly growing wild on riverbanks of Dhansiri River in Golaghat District of Assam. It is used as ethnomedicine in this part of India for a number of ailments. Bioassay guided chemical investigation of the bulbs of Crinum defixum Ker-Gawl afforded to isolate a new hydrazide derivative and its structure was determined as (E)-N'-[(E)-2-butenoyl]-2-butenoylhydrazide by spectroscopic methods. The compound was assayed for anti-genotoxic activity by onion root tip assay (by observing different types of chromosomal aberrations such as chromosomal bridges, stickiness, delayed anaphase, polyploidy and vagrant chromosome). The phyto-compound was found to have anti-genotoxic activity and imparted a clear dose dependent protective effect against the genotoxic effect of H2O2. Further, the compound seems to be more effective against clastogenic aberrations than physiological aberration at the highest concentration used (250 ppm). (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:2754 / 2757
页数:4
相关论文
共 20 条
  • [1] Central inhibitory activity of the aqueous extract of Crinum giganteum
    Amos, S
    Binda, L
    Akah, P
    Wambebe, C
    Gamaniel, K
    [J]. FITOTERAPIA, 2003, 74 (1-2) : 23 - 28
  • [2] ALKALOIDE AUS CRINUM-, ZEPHYRANTHES-, LEUCOJUM- UND CLIVIA-ARTEN
    BOIT, HG
    DOPKE, W
    STENDER, W
    [J]. CHEMISCHE BERICHTE-RECUEIL, 1957, 90 (10): : 2203 - 2206
  • [3] Isolation and structure elucidation of a new antifungal and antibacterial antibiotic produced by Streptomyces sp 201
    Bordoloi, GN
    Kumari, B
    Guha, A
    Bordoloi, M
    Yadav, RNS
    Roy, MK
    Bora, TC
    [J]. BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2001, 65 (08) : 1856 - 1858
  • [4] Sapidolide A: An unprecedented spherical carbocyclic lactone from Baccaurea sapida seed kernels: Is it a meroisoprenoid?
    Bordoloi, M
    Barua, NC
    Mohan, S
    Dutta, SC
    Mathur, RK
    Ghosh, AC
    Rychlewska, U
    [J]. TETRAHEDRON LETTERS, 1996, 37 (37) : 6791 - 6792
  • [5] An alkylated coumarin from Kayea assamica
    Bordoloi, M
    Mohan, S
    Barua, NC
    Dutta, SC
    Mathur, RK
    Ghosh, AC
    [J]. PHYTOCHEMISTRY, 1997, 44 (05) : 939 - 942
  • [6] CABERERA GL, 1999, MUTAT RES, V426, P211
  • [7] Synthesis and antigenotoxic activity of some naphtho[2,1-b] pyrano[3,2-e][1,2,4]triazolo[1,5-c]pyrimidine derivatives
    Chabchoub, Fakher
    Messaad, Mehdi
    Ben Mansour, Hedi
    Chekir-Ghedira, Leila
    Salem, Mansour
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2007, 42 (05) : 715 - 718
  • [8] Chakraborty V, 2003, INDIAN J CHEM B, V42, P944
  • [9] DYER JR, 1978, APPL ABSORPTION SPEC, P95
  • [10] HOOKER JD, 1954, FLORA BRIT INDIA, V6, P281