ID Name Structure References (top 5) Molecular Target(s)

in 1 ingredients:

  • 614
  • in 3 recipes:

  • 18
  • 236
  • 473

  • Properties
    C9H17NO5    219.23

    1:  Shigenobu S, Watanabe H, Hattori M, Sakaki Y, Ishikawa H.
    Genome sequence of the endocellular bacterial symbiont of aphids Buchnera sp. APS.
    Nature.    impact factor:   29.491
    2000;  407(6800): 81-6

    2:  Sambandamurthy VK, Wang X, Chen B, Russell RG, Derrick S, Collins FM, Morris SL, Jacobs WR Jr.
    A pantothenate auxotroph of Mycobacterium tuberculosis is highly attenuated and protects mice against tuberculosis.
    Nat Med.    impact factor:   26.584
    2002;  8(10): 1171-4

    3:  Daugherty M, Polanuyer B, Farrell M, Scholle M, Lykidis A, de Crecy-Lagard V, Osterman A.
    Complete reconstitution of the human coenzyme A biosynthetic pathway via comparative genomics.
    J Biol Chem.    impact factor:   7.666
    2002;  277(24): 21431-9

    4:  Strauss E, Begley TP.
    The antibiotic activity of N-pentylpantothenamide results from its conversion to ethyldethia-coenzyme a, a coenzyme a antimetabolite.
    J Biol Chem.    impact factor:   7.666
    2002;  277(50): 48205-9

    5:  Kupke T, Hernandez-Acosta P, Steinbacher S, Culianez-Macia FA.
    Arabidopsis thaliana flavoprotein AtHAL3a catalyzes the decarboxylation of 4'-Phosphopantothenoylcysteine to 4'-phosphopantetheine, a key step in coenzyme A biosynthesis.
    J Biol Chem.    impact factor:   7.666
    2001;  276(22): 19190-6

    Time used: 78 milliseconds.

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