Eco-friendly synthesis and study of new plant growth promoters: 3,3′-Diindolylmethane and its derivatives

Bioorganic and Medicinal Chemistry Letters

Volumn 17, Issue 17, 2007, Pages 4924-4928

  Pal, Churala ^a   Dey, Sumit ^a   Mahato, Sanjit Kumar ^a   Vinayagam, Jayaraman ^a   Pradhan, Prasun K ^a   Giri, Venkatachalam Sesha ^a   Jaisankar, Parasuraman ^a   Hossain, Tanvir ^a   Baruri, Shikhi ^a   Ray, Debjit ^a   Biswas, Suparna Mandal ^b  

^a INDIAN INSTITUTE OF CHEMICAL BIOLOGY   (India)

^b INDIAN STATISTICAL INSTITUTE   (India)

Author keywords

Auxin; Diindolylmethane; Ionic liquid; Oryza sativa; Plant growth promoter

Indexed keywords

3,3' DIINDOLYLMETHANE; INDOLE DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; DRUG POTENCY; DRUG SYNTHESIS; PLANT GROWTH; RICE;

CATALYSIS; CHEMISTRY, PHARMACEUTICAL; CONSERVATION OF NATURAL RESOURCES; DRUG DESIGN; INDOLES; MODELS, CHEMICAL; ORYZA SATIVA; PLANT EXTRACTS; PLANT GROWTH REGULATORS; PLANT PHYSIOLOGY; PLANTS;

ORYZA SATIVA;

EID: 34547602435     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2007.06.025     Document Type: Article

References (32)

1. Went F.W. Proc. Kon. Ned. Akad 37 (1934) 445
2. Thimann K.V., and Went F.W. Proc. Kon. Med. Akad. Wet. 37 (1934) 456
3. Thimann K.V., and Koepfli J.B. Nature 135 (1935) 101
4. Haissig B.E., and Davis T.D. A Historical Evaluation of Adventitious Rooting Research to 1993. In: Davis T.D., and Haissig B.E. (Eds). Biology of Adventitious Root Formation (1994), Plenum Press, New York, NY
5. Hartmann H.T., Kestar D.E., Davies F.T., and Geneve Jr. R.L. Plant Propagation: Principles and Practices (1997), Prentice Hall, Upper Saddle River, NJ
6. Macdonald B. Practical Woody Plant Propagation for Nursery Growers (1986), Timber Press, Portland, OR Chapter 10
7. Armstrong D.W., Liu Y.S., He L., Ekborg-Ott K.H., Barnes C.L., and Hammer C.F. J. Agric. Food. Chem. 50 (2002) 473
8. Anderton M.J., Manson M.M., Verschoyle R., Gescher A., Steward W.P., Williams M.L., and Mager D.E. Drug Metab. Dispos. 32 (2004) 632
9. Bonnesen C., Eggleston I.M., and Hayes J.D. Cancer Res. 61 (2001) 6120
10. Cang Y.C., Riby J., Chang G.H., Peng B., Firestone G., and Bjeldanes L.F. Biochem. Pharmacol. 58 (1999) 825
11. Le H.T., Schaldach C.M., Firestone G.L., and Bjeldanes L.F. J. Biol. Chem. 278 (2003) 21136
12. Zeligs, M.A. U.S. Patent Appl. Publ. 2004, 12 pp. 6689, 387.
13. Hong C., Firestone G.L., and Bjeldanes L.F. Biochem. Pharmacol. 63 (2002) 1085
14. Grubbs C., Steele V., Casebolt T., Juliana M.M., Eto I., and Whitaker L.M. Anticancer Res. 15 (1995) 709
15. Bailey G.S., Dashwood R.H., Fong A.T., Williams D.E., Scanlan R.A., and Hendricks J.D. Anticancer Res. 78 (1991) 275
16. Kojima T., Tanaka T., and Mori H. Cancer Res. 54 (1994) 1446
17. Morse M.A., LaGreca S.A., Amin S.G., and Chung F.L. Cancer Res. 50 (1990) 2613
18. Shertzer H.G., Tabor M.W., Hogan I.T., Brown S.J., and Sainsbury M. Arch. Toxicol. 70 (1996) 830
19. Arnao M.B., Sanchez-Bravo J., and Acosta M. Biochem. Mol. Biol. Int. 39 (1996) 1125
20. Benabadji S.H., Wen R., Zheng J., Dong X., and Yuan S. Acta Pharmacol. Sin. 25 (2004) 666
21. Carter T.H., Liu K., Ralph Jr. W., Chen D., Qi M., Fan S., Yuan F., Rosen E.M., and Auborn K.J. J. Nutr. 132 (2002) 3314
22. Welton T. Chem. Rev. 99 (1999) 2071
23. Wasserscheid P., and Keim W. Angew. Chem. Int. Ed. 39 (2000) 3772
24. Jain N., Kumar A., Chauhan S., and Chauhan S.M.S. Tetrahedron 61 (2005) 1015
25. Gordon C.M. Appl. Catal., A. Gen. 222 (2001) 101
26. Meshram H.M., Reddy P.N., Vishnu P., Sadshiv K., and Yadav J.S. Tetrahedron Lett. 47 (2006) 991
27. Yadav J.S., Reddy B.V.S., and Baishya G. J. Org. Chem. 68 (2003) 7098 and references cited therein
28. Jarikote D.V., Siddiqui S.A., Rajagopal R., Daniel T., Lahoti R.J., and Srinivasan K.V. Tetrahedron Lett. 44 (2003) 1835
29. Palimkar S.S., Siddiqui S.A., Daniel T., Lahoti R.J., and Srinivasan K.V. J. Org. Chem. 68 (2003) 9371
30. Pradhan P.K., Dey S., Giri V.S., and Jaisankar P. Synthesis (2005) 1779
31. 4, and the solvent removed to give a solid mass. Column chromatography of the residue over silica gel using increasing concentration of chloroform in petroleum ether yielded 3h as white solid (154 mg, 77%).
32. 2 solution followed by washing with distilled water. Seeds (42) of the same type were placed on each of the above Petri dishes in horizontal manner; otherwise their growth could be affected. The Petri dishes were placed in greenhouse in which the temperature varied from ∼15 °C (night) to ∼30 °C (day). Level of water was maintained at the 15 mL mark of each Petri dish before start of the days experiment to compensate the water loss. Readings of the shoot and root growths were measured in millimeter scale on day 5.