ID Name Structure References (top 5) Molecular Target(s)
1ID:6113
TARTARIC ACID


NSC#:1914
NSC#:50972
NSC#:62778
NSC#:82093
NSC#:112251
NSC#:112252
NSC#:133735
NSC#:148314
NSC#:155080
NSC#:302012
NSC#:608773
Aldrich#:251380
Aldrich#:483796
Aldrich#:95308
Aldrich#:95309
Aldrich#:95310
Aldrich#:95318
Aldrich#:95320
Aldrich#:95330
Aldrich#:95350
Aldrich#:T109
Aldrich#:T206
Aldrich#:T3259
Aldrich#:T400
Aldrich#:T5259
Aldrich#:T8277
FDA approved!!!

Freqency:
in 3 ingredients:

  • 5
  • 13
  • 361
  • in 30 recipes:

  • 8
  • 20
  • 21
  • 26
  • 36
  • 77
  • 78
  • 99
  • 101
  • 107
  • 146
  • 158
  • 212
  • 232
  • 241
  • 245
  • 267
  • 288
  • 291
  • 308
  • 311
  • 312
  • 332
  • 351
  • 363
  • 381
  • 413
  • 430
  • 452
  • 490

  • Properties
    C4H6O6    150.09





    1:  Wiskur SL, Ait-Haddou H, Lavigne JJ, Anslyn EV.
    Teaching old indicators new tricks.
    Acc Chem Res.    impact factor:   11.795
    2001;  34(12): 963-72

    2:  Kim YH.
    Dual enantioselective control in asymmetric synthesis.
    Acc Chem Res.    impact factor:   11.795
    2001;  34(12): 955-62

    3:  Shakarian AM, Joshi MB, Ghedin E, Dwyer DM.
    Molecular dissection of the functional domains of a unique, tartrate-resistant, surface membrane acid phosphatase in the primitive human pathogen Leishmania donovani.
    J Biol Chem.    impact factor:   7.666
    2002;  277(20): 17994-8001

    4:  Barbosa LA, Sautet P.
    Stability of chiral domains produced by adsorption of tartaric acid isomers on the Cu(110) surface: a periodic density functional theory study.
    J Am Chem Soc.    impact factor:   5.537
    2001;  123(27): 6639-48

    5:  Li C, Pace EA, Liang MC, Lobkovsky E, Gilmore TD, Porco JA Jr.
    Total synthesis of the NF-kappa B inhibitor (-)-cycloepoxydon: utilization of tartrate-mediated nucleophilic epoxidation.
    J Am Chem Soc.    impact factor:   5.537
    2001;  123(45): 11308-9

     
    Time used: 594 milliseconds.

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