ID Name Structure References (top 5) Molecular Target(s)
1ID:249
AMAROGENTIN

Freqency:
in 1 ingredients:

  • 82
  • in 14 recipes:

  • 187
  • 279
  • 289
  • 318
  • 331
  • 339
  • 343
  • 352
  • 355
  • 434
  • 479
  • 502
  • 521
  • 523

  • Properties
    C28H30O14    590.53





    1:  Medda S, Mukhopadhyay S, Basu MK.
    Evaluation of the in-vivo activity and toxicity of amarogentin, an antileishmanial agent, in both liposomal and niosomal forms.
    J Antimicrob Chemother.    impact factor:   2.964
    1999;  44(6): 791-4

    2:  Wang CZ, Maier UH, Zenk MH.
    Synthesis of 3,3',5-trihydroxybiphenyl-2-carboxylic acid, a component of the bitterest natural product amarogentin and its coenzyme A and N-acetyl cysteamine thiol esters.
    J Nat Prod.    impact factor:   1.652
    2000;  63(3): 371-4

    3:  Ray S, Majumder HK, Chakravarty AK, Mukhopadhyay S, Gil RR, Cordell GA.
    Amarogentin, a naturally occurring secoiridoid glycoside and a newly recognized inhibitor of topoisomerase I from Leishmania donovani.
    J Nat Prod.    impact factor:   1.652
    1996;  59(1): 27-9

    4:  Keil M, Hartle B, Guillaume A, Psiorz M.
    Production of amarogentin in root cultures of Swertia chirata.
    Planta Med.    impact factor:   1.438
    2000;  66(5): 452-7

    5:  Kikuzaki H, Kawasaki Y, Kitamura S, Nakatani N.
    Secoiridoid glucosides from Swertia mileensis.
    Planta Med.    impact factor:   1.438
    1996;  62(1): 35-8

    LC
     
    Time used: 125 milliseconds.

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