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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (203) Show 203 proteins XML

Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2021-09-14 14:57:20 UTC

HMDB ID

HMDB0000221

Secondary Accession Numbers

HMDB0000799
HMDB0006341
HMDB00221
HMDB00799
HMDB06341

Metabolite Identification

Common Name

NADPH

Description

NADPH is the reduced form of NADP+, and NADP+ is the oxidized form of NADPH. Nicotinamide adenine dinucleotide phosphate (NADP) is a coenzyme composed of ribosylnicotinamide 5'-phosphate (NMN) coupled with a pyrophosphate linkage to 5'-phosphate adenosine 2',5'-bisphosphate. NADP serves as an electron carrier in a number of reactions, being alternately oxidized (NADP+) and reduced (NADPH). NADP is formed through the addition of a phosphate group to the 2' position of the adenosyl nucleotide through an ester linkage (Dorland, 27th ed). This extra phosphate is added by the enzyme NAD+ kinase and removed via NADP+ phosphatase. NADP is also known as TPN (triphosphopyridine nucleotide) and it is an important cofactor used in anabolic reactions in all forms of cellular life. Examples include the Calvin cycle, cholesterol synthesis, fatty acid elongation, and nucleic acid synthesis (Wikipedia ).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652309032023572D          

 48 52  0  0  0  0            999 V2000
 9997.3578 9998.0438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.8653 9999.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5818 9999.4911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.2961 9999.9046    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10000.0167 9999.5054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.7302 9999.9168    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10001.4459 9999.5054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.1573 9999.9168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.6358 9998.0583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.4258 9998.0663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10007.0717 9999.5177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10007.7873 9999.9292    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10007.0717 9998.6928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.317810000.6318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.142710000.6318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.882710000.6194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.707610000.6194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.5378 9999.9992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.8704 9999.5142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.1253 9998.7296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10003.9503 9998.7296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10004.2052 9999.5142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.4809 9999.9854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0684 9998.7158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.8934 9998.7158    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9997.1483 9999.5004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10006.351610000.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10005.637110001.1544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.922610000.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.9225 9999.9170    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10005.6370 9999.5044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10006.3516 9999.9170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9993.033010000.2714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9992.6975 9999.5178    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9993.1825 9998.8503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9994.0029 9998.9365    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9994.3385 9999.6901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9993.853510000.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9992.548010000.9388    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9995.1231 9999.9450    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9995.123110000.7700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9994.338610001.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9995.7905 9999.4600    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.7195 9997.2073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.8990 9997.2936    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
 9995.8141 9996.4731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.5614 9998.0514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.1466 9996.9580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4 16  2  0  0  0  0
  4 17  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6 14  2  0  0  0  0
  7  8  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 19  1  0  0  0  0
 18 22  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 26  1  0  0  0  0
 26  2  1  6  0  0  0
 25  1  1  1  0  0  0
 19  8  1  1  0  0  0
 21 10  1  6  0  0  0
 20  9  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 31 32  2  0  0  0  0
 32 27  1  0  0  0  0
 32 11  1  0  0  0  0
 37 38  2  0  0  0  0
 38 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 33 39  1  0  0  0  0
 41 42  2  0  0  0  0
 38 42  1  0  0  0  0
 40 41  1  0  0  0  0
 37 40  1  0  0  0  0
 43 40  1  6  0  0  0
 43 24  1  0  0  0  0
 23 43  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 45 47  1  0  0  0  0
 45 48  1  0  0  0  0
 24 47  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 22 30  1  1  0  0  0
  6 15  1  0  0  0  0
M  END

HMDB0000221
     RDKit          3D
NADPH
 78 82  0  0  0  0  0  0  0  0999 V2000
   10.1531   -2.1020   -0.4812 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.1001   -1.1643   -0.6005 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9539   -0.5546   -1.7315 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1501   -0.8062    0.4424 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2252    0.0995    0.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2348    0.5512    1.0736 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2911    1.5427    0.6642 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0501    1.1819    0.3037 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1785    0.8138   -1.1037 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8065   -0.6473   -1.0841 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3865   -0.5750   -1.0877 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5980   -1.2660    0.1915 P   0  0  0  0  0  5  0  0  0  0  0  0
    2.3512   -2.1442    1.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2847    0.1730    1.2695 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0607   -1.6994   -0.2588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4111   -0.6237   -1.5097 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.7549    0.0902   -2.1190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2334   -1.5689   -2.6665 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5225    0.5286   -0.9701 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0546    0.2020    0.2437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1379    1.2027    0.6519 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0830    1.2088   -0.3843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2450    1.5451    0.2156 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.4398    1.1222   -0.5473 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5603    1.8463   -0.7184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4715    1.0709   -1.3783 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9326   -0.1347   -1.6238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4513   -1.2487   -2.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7889   -1.3026   -2.7306 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6369   -2.3115   -2.3303 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3702   -2.2569   -1.8106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8854   -1.1677   -1.2060 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6654   -0.0713   -1.0993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2652    0.6347    1.4815 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1070    1.0765    2.4400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1217   -0.2122    2.8769 P   0  0  0  0  0  5  0  0  0  0  0  0
   -7.2442   -0.2208    4.3994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6493   -0.0394    2.2360 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4247   -1.6870    2.4592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8308    0.5240    1.8543 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5088    1.1161    3.0433 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2385    1.5296   -1.6865 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7919    2.5131   -2.6546 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8017    2.3459   -0.5160 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1602    3.5815   -0.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2181   -0.0017    2.3792 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1499   -0.9133    2.6865 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2084   -1.4029    1.7727 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9428   -3.1006   -0.5764 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1030   -1.7171   -0.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2207    0.5437   -0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1788    2.2489    1.5496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1902    1.3031   -1.5501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1576   -1.1651   -0.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1125   -1.1535   -1.9863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0972    0.8963    0.5856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8850   -2.1326   -2.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3196    0.2881    1.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5093   -0.7945    0.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7745    2.1551    0.9715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3599    2.5779    0.5171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7440    2.8552   -0.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0944   -1.7794   -3.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5784   -0.8200   -2.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7265   -3.1421   -1.9008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6345   -0.3833    1.0938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6472    0.2538    1.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7922   -2.1015    1.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5570   -0.5686    1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3103    0.3631    3.7045 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9223    0.9425   -2.2630 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6384    2.7718   -3.0782 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8579    2.5037   -0.5363 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4094    3.6143   -1.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5000    0.2764    3.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1654   -1.3786    3.6792 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2239   -1.2033    2.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1061   -2.5314    1.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 12 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 23 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  2  0
 36 38  1  0
 36 39  1  0
 34 40  1  0
 40 41  1  0
  9 42  1  0
 42 43  1  0
 42 44  1  0
 44 45  1  0
  6 46  1  0
 46 47  2  0
 47 48  1  0
 48  4  1  0
 44  7  1  0
 40 21  1  0
 33 24  1  0
 33 27  1  0
  1 49  1  0
  1 50  1  0
  5 51  1  0
  7 52  1  1
  9 53  1  6
 10 54  1  0
 10 55  1  0
 14 56  1  0
 18 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  1
 23 61  1  1
 25 62  1  0
 29 63  1  0
 29 64  1  0
 31 65  1  0
 34 66  1  6
 38 67  1  0
 39 68  1  0
 40 69  1  1
 41 70  1  0
 42 71  1  6
 43 72  1  0
 44 73  1  6
 45 74  1  0
 46 75  1  0
 47 76  1  0
 48 77  1  0
 48 78  1  0
M  END


  Mrv1652309032023572D          

 48 52  0  0  0  0            999 V2000
 9997.3578 9998.0438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.8653 9999.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5818 9999.4911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.2961 9999.9046    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10000.0167 9999.5054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.7302 9999.9168    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10001.4459 9999.5054    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.1573 9999.9168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.6358 9998.0583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.4258 9998.0663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10007.0717 9999.5177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10007.7873 9999.9292    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10007.0717 9998.6928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.317810000.6318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.142710000.6318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.882710000.6194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.707610000.6194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.5378 9999.9992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.8704 9999.5142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.1253 9998.7296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10003.9503 9998.7296    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10004.2052 9999.5142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.4809 9999.9854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0684 9998.7158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.8934 9998.7158    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9997.1483 9999.5004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10006.351610000.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10005.637110001.1544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.922610000.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.9225 9999.9170    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10005.6370 9999.5044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10006.3516 9999.9170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9993.033010000.2714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9992.6975 9999.5178    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9993.1825 9998.8503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9994.0029 9998.9365    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9994.3385 9999.6901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9993.853510000.3577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9992.548010000.9388    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9995.1231 9999.9450    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9995.123110000.7700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9994.338610001.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9995.7905 9999.4600    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9996.7195 9997.2073    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.8990 9997.2936    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
 9995.8141 9996.4731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.5614 9998.0514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.1466 9996.9580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4 16  2  0  0  0  0
  4 17  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6 14  2  0  0  0  0
  7  8  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 18 19  1  0  0  0  0
 18 22  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
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 26  2  1  6  0  0  0
 25  1  1  1  0  0  0
 19  8  1  1  0  0  0
 21 10  1  6  0  0  0
 20  9  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 31 32  2  0  0  0  0
 32 27  1  0  0  0  0
 32 11  1  0  0  0  0
 37 38  2  0  0  0  0
 38 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 33 39  1  0  0  0  0
 41 42  2  0  0  0  0
 38 42  1  0  0  0  0
 40 41  1  0  0  0  0
 37 40  1  0  0  0  0
 43 40  1  6  0  0  0
 43 24  1  0  0  0  0
 23 43  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 45 47  1  0  0  0  0
 45 48  1  0  0  0  0
 24 47  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 22 30  1  1  0  0  0
  6 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0000221

> <DATABASE_NAME>
hmdb

> <SMILES>
NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H30N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1

> <INCHI_KEY>
ACFIXJIJDZMPPO-NNYOXOHSSA-N

> <FORMULA>
C21H30N7O17P3

> <MOLECULAR_WEIGHT>
745.4209

> <EXACT_MASS>
745.091102105

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
63.542294008111696

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3R,4R,5R)-2-(6-amino-9H-purin-9-yl)-5-[({[({[(2R,3S,4R,5R)-5-(3-carbamoyl-1,4-dihydropyridin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)methyl]-4-hydroxyoxolan-3-yl]oxy}phosphonic acid

> <ALOGPS_LOGP>
-1.13

> <JCHEM_LOGP>
-6.376368250362743

> <ALOGPS_LOGS>
-2.14

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-4

> <JCHEM_PKA>
1.8806160343962963

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.6557894226872323

> <JCHEM_PKA_STRONGEST_BASIC>
4.00201652313229

> <JCHEM_POLAR_SURFACE_AREA>
364.1500000000001

> <JCHEM_REFRACTIVITY>
153.8726

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.45e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
nadph

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000221
     RDKit          3D
NADPH
 78 82  0  0  0  0  0  0  0  0999 V2000
   10.1531   -2.1020   -0.4812 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.1001   -1.1643   -0.6005 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9539   -0.5546   -1.7315 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1501   -0.8062    0.4424 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2252    0.0995    0.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2348    0.5512    1.0736 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2911    1.5427    0.6642 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0501    1.1819    0.3037 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1785    0.8138   -1.1037 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8065   -0.6473   -1.0841 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3865   -0.5750   -1.0877 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5980   -1.2660    0.1915 P   0  0  0  0  0  5  0  0  0  0  0  0
    2.3512   -2.1442    1.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2847    0.1730    1.2695 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0607   -1.6994   -0.2588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4111   -0.6237   -1.5097 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.7549    0.0902   -2.1190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2334   -1.5689   -2.6665 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5225    0.5286   -0.9701 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0546    0.2020    0.2437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1379    1.2027    0.6519 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0830    1.2088   -0.3843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2450    1.5451    0.2156 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.4398    1.1222   -0.5473 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5603    1.8463   -0.7184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4715    1.0709   -1.3783 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9326   -0.1347   -1.6238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4513   -1.2487   -2.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7889   -1.3026   -2.7306 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6369   -2.3115   -2.3303 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3702   -2.2569   -1.8106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8854   -1.1677   -1.2060 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6654   -0.0713   -1.0993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2652    0.6347    1.4815 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1070    1.0765    2.4400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1217   -0.2122    2.8769 P   0  0  0  0  0  5  0  0  0  0  0  0
   -7.2442   -0.2208    4.3994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6493   -0.0394    2.2360 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4247   -1.6870    2.4592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8308    0.5240    1.8543 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5088    1.1161    3.0433 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2385    1.5296   -1.6865 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7919    2.5131   -2.6546 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8017    2.3459   -0.5160 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1602    3.5815   -0.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2181   -0.0017    2.3792 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1499   -0.9133    2.6865 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2084   -1.4029    1.7727 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9428   -3.1006   -0.5764 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1030   -1.7171   -0.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2207    0.5437   -0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1788    2.2489    1.5496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1902    1.3031   -1.5501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1576   -1.1651   -0.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1125   -1.1535   -1.9863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0972    0.8963    0.5856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8850   -2.1326   -2.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3196    0.2881    1.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5093   -0.7945    0.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7745    2.1551    0.9715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3599    2.5779    0.5171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7440    2.8552   -0.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0944   -1.7794   -3.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5784   -0.8200   -2.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7265   -3.1421   -1.9008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6345   -0.3833    1.0938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6472    0.2538    1.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7922   -2.1015    1.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5570   -0.5686    1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3103    0.3631    3.7045 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9223    0.9425   -2.2630 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6384    2.7718   -3.0782 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8579    2.5037   -0.5363 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4094    3.6143   -1.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5000    0.2764    3.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1654   -1.3786    3.6792 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2239   -1.2033    2.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1061   -2.5314    1.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 12 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 23 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  2  0
 36 38  1  0
 36 39  1  0
 34 40  1  0
 40 41  1  0
  9 42  1  0
 42 43  1  0
 42 44  1  0
 44 45  1  0
  6 46  1  0
 46 47  2  0
 47 48  1  0
 48  4  1  0
 44  7  1  0
 40 21  1  0
 33 24  1  0
 33 27  1  0
  1 49  1  0
  1 50  1  0
  5 51  1  0
  7 52  1  1
  9 53  1  6
 10 54  1  0
 10 55  1  0
 14 56  1  0
 18 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  1
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 25 62  1  0
 29 63  1  0
 29 64  1  0
 31 65  1  0
 34 66  1  6
 38 67  1  0
 39 68  1  0
 40 69  1  1
 41 70  1  0
 42 71  1  6
 43 72  1  0
 44 73  1  6
 45 74  1  0
 46 75  1  0
 47 76  1  0
 48 77  1  0
 48 78  1  0
M  END

HEADER    PROTEIN                                 03-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-20         0                                  
HETATM    1  O   UNK     0    8661.7358663.015   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0    8662.6828666.489   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0    8664.0198665.717   0.000  0.00  0.00           O+0
HETATM    4  P   UNK     0    8665.3538666.489   0.000  0.00  0.00           P+0
HETATM    5  O   UNK     0    8666.6988665.743   0.000  0.00  0.00           O+0
HETATM    6  P   UNK     0    8668.0308666.511   0.000  0.00  0.00           P+0
HETATM    7  O   UNK     0    8669.3668665.743   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0    8670.6948666.511   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0    8671.5878663.042   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0    8674.9288663.057   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0    8679.8678665.766   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0    8681.2038666.535   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0    8679.8678664.227   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0    8667.2608667.846   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0    8668.8008667.846   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0    8664.5818667.823   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0    8666.1218667.823   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0    8673.2718666.665   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0    8672.0258665.760   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8672.5018664.295   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8674.0418664.295   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8674.5168665.760   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0    8660.0988666.639   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0    8659.3288664.269   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0    8660.8688664.269   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0    8661.3438665.734   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0    8678.5238668.052   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0    8677.1898668.822   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0    8675.8568668.052   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0    8675.8558666.512   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0    8677.1898665.742   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0    8678.5238666.512   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0    8653.6628667.173   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0    8653.0358665.767   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0    8653.9418664.521   0.000  0.00  0.00           C+0
HETATM   36  N   UNK     0    8655.4728664.681   0.000  0.00  0.00           N+0
HETATM   37  C   UNK     0    8656.0998666.088   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0    8655.1938667.334   0.000  0.00  0.00           C+0
HETATM   39  N   UNK     0    8652.7568668.419   0.000  0.00  0.00           N+0
HETATM   40  N   UNK     0    8657.5638666.564   0.000  0.00  0.00           N+0
HETATM   41  C   UNK     0    8657.5638668.104   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0    8656.0998668.580   0.000  0.00  0.00           N+0
HETATM   43  C   UNK     0    8658.8098665.659   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0    8660.5438661.454   0.000  0.00  0.00           O+0
HETATM   45  P   UNK     0    8659.0118661.615   0.000  0.00  0.00           P+0
HETATM   46  O   UNK     0    8658.8538660.083   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0    8658.3818663.029   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0    8657.6078660.988   0.000  0.00  0.00           O+0
CONECT    1   25                                                            
CONECT    2    3   26                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   16   17                                             
CONECT    5    4    6                                                       
CONECT    6    5    7   14   15                                             
CONECT    7    6    8                                                       
CONECT    8    7   19                                                       
CONECT    9   20                                                            
CONECT   10   21                                                            
CONECT   11   12   13   32                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    6                                                            
CONECT   15    6                                                            
CONECT   16    4                                                            
CONECT   17    4                                                            
CONECT   18   19   22                                                       
CONECT   19   20   18    8                                                  
CONECT   20   19   21    9                                                  
CONECT   21   20   22   10                                                  
CONECT   22   21   18   30                                                  
CONECT   23   26   43                                                       
CONECT   24   25   43   47                                                  
CONECT   25   24   26    1                                                  
CONECT   26   25   23    2                                                  
CONECT   27   28   32                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   22                                                  
CONECT   31   32   30                                                       
CONECT   32   31   27   11                                                  
CONECT   33   38   34   39                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   38   36   40                                                  
CONECT   38   37   33   42                                                  
CONECT   39   33                                                            
CONECT   40   41   37   43                                                  
CONECT   41   42   40                                                       
CONECT   42   41   38                                                       
CONECT   43   40   24   23                                                  
CONECT   44   45                                                            
CONECT   45   44   46   47   48                                             
CONECT   46   45                                                            
CONECT   47   45   24                                                       
CONECT   48   45                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  104    0
END

COMPND    HMDB0000221
HETATM    1  N1  UNL     1      10.153  -2.102  -0.481  1.00  0.00           N  
HETATM    2  C1  UNL     1       9.100  -1.164  -0.601  1.00  0.00           C  
HETATM    3  O1  UNL     1       8.954  -0.555  -1.731  1.00  0.00           O  
HETATM    4  C2  UNL     1       8.150  -0.806   0.442  1.00  0.00           C  
HETATM    5  C3  UNL     1       7.225   0.099   0.173  1.00  0.00           C  
HETATM    6  N2  UNL     1       6.235   0.551   1.074  1.00  0.00           N  
HETATM    7  C4  UNL     1       5.291   1.543   0.664  1.00  0.00           C  
HETATM    8  O2  UNL     1       4.050   1.182   0.304  1.00  0.00           O  
HETATM    9  C5  UNL     1       4.178   0.814  -1.104  1.00  0.00           C  
HETATM   10  C6  UNL     1       3.806  -0.647  -1.084  1.00  0.00           C  
HETATM   11  O3  UNL     1       2.386  -0.575  -1.088  1.00  0.00           O  
HETATM   12  P1  UNL     1       1.598  -1.266   0.191  1.00  0.00           P  
HETATM   13  O4  UNL     1       2.351  -2.144   1.101  1.00  0.00           O  
HETATM   14  O5  UNL     1       1.285   0.173   1.269  1.00  0.00           O  
HETATM   15  O6  UNL     1       0.061  -1.699  -0.259  1.00  0.00           O  
HETATM   16  P2  UNL     1      -0.411  -0.624  -1.510  1.00  0.00           P  
HETATM   17  O7  UNL     1       0.755   0.090  -2.119  1.00  0.00           O  
HETATM   18  O8  UNL     1      -1.233  -1.569  -2.666  1.00  0.00           O  
HETATM   19  O9  UNL     1      -1.523   0.529  -0.970  1.00  0.00           O  
HETATM   20  C7  UNL     1      -2.055   0.202   0.244  1.00  0.00           C  
HETATM   21  C8  UNL     1      -3.138   1.203   0.652  1.00  0.00           C  
HETATM   22  O10 UNL     1      -4.083   1.209  -0.384  1.00  0.00           O  
HETATM   23  C9  UNL     1      -5.245   1.545   0.216  1.00  0.00           C  
HETATM   24  N3  UNL     1      -6.440   1.122  -0.547  1.00  0.00           N  
HETATM   25  C10 UNL     1      -7.560   1.846  -0.718  1.00  0.00           C  
HETATM   26  N4  UNL     1      -8.471   1.071  -1.378  1.00  0.00           N  
HETATM   27  C11 UNL     1      -7.933  -0.135  -1.624  1.00  0.00           C  
HETATM   28  C12 UNL     1      -8.451  -1.249  -2.248  1.00  0.00           C  
HETATM   29  N5  UNL     1      -9.789  -1.303  -2.731  1.00  0.00           N  
HETATM   30  N6  UNL     1      -7.637  -2.311  -2.330  1.00  0.00           N  
HETATM   31  C13 UNL     1      -6.370  -2.257  -1.811  1.00  0.00           C  
HETATM   32  N7  UNL     1      -5.885  -1.168  -1.206  1.00  0.00           N  
HETATM   33  C14 UNL     1      -6.665  -0.071  -1.099  1.00  0.00           C  
HETATM   34  C15 UNL     1      -5.265   0.635   1.481  1.00  0.00           C  
HETATM   35  O11 UNL     1      -6.107   1.076   2.440  1.00  0.00           O  
HETATM   36  P3  UNL     1      -7.122  -0.212   2.877  1.00  0.00           P  
HETATM   37  O12 UNL     1      -7.244  -0.221   4.399  1.00  0.00           O  
HETATM   38  O13 UNL     1      -8.649  -0.039   2.236  1.00  0.00           O  
HETATM   39  O14 UNL     1      -6.425  -1.687   2.459  1.00  0.00           O  
HETATM   40  C16 UNL     1      -3.831   0.524   1.854  1.00  0.00           C  
HETATM   41  O15 UNL     1      -3.509   1.116   3.043  1.00  0.00           O  
HETATM   42  C17 UNL     1       5.239   1.530  -1.687  1.00  0.00           C  
HETATM   43  O16 UNL     1       4.792   2.513  -2.655  1.00  0.00           O  
HETATM   44  C18 UNL     1       5.802   2.346  -0.516  1.00  0.00           C  
HETATM   45  O17 UNL     1       5.160   3.582  -0.495  1.00  0.00           O  
HETATM   46  C19 UNL     1       6.218  -0.002   2.379  1.00  0.00           C  
HETATM   47  C20 UNL     1       7.150  -0.913   2.687  1.00  0.00           C  
HETATM   48  C21 UNL     1       8.208  -1.403   1.773  1.00  0.00           C  
HETATM   49  H1  UNL     1       9.943  -3.101  -0.576  1.00  0.00           H  
HETATM   50  H2  UNL     1      11.103  -1.717  -0.319  1.00  0.00           H  
HETATM   51  H3  UNL     1       7.221   0.544  -0.789  1.00  0.00           H  
HETATM   52  H4  UNL     1       5.179   2.249   1.550  1.00  0.00           H  
HETATM   53  H5  UNL     1       3.190   1.303  -1.550  1.00  0.00           H  
HETATM   54  H6  UNL     1       4.158  -1.165  -0.191  1.00  0.00           H  
HETATM   55  H7  UNL     1       4.113  -1.154  -1.986  1.00  0.00           H  
HETATM   56  H8  UNL     1       1.097   0.896   0.586  1.00  0.00           H  
HETATM   57  H9  UNL     1      -1.885  -2.133  -2.146  1.00  0.00           H  
HETATM   58  H10 UNL     1      -1.320   0.288   1.095  1.00  0.00           H  
HETATM   59  H11 UNL     1      -2.509  -0.795   0.197  1.00  0.00           H  
HETATM   60  H12 UNL     1      -2.775   2.155   0.972  1.00  0.00           H  
HETATM   61  H13 UNL     1      -5.360   2.578   0.517  1.00  0.00           H  
HETATM   62  H14 UNL     1      -7.744   2.855  -0.401  1.00  0.00           H  
HETATM   63  H15 UNL     1     -10.094  -1.779  -3.579  1.00  0.00           H  
HETATM   64  H16 UNL     1     -10.578  -0.820  -2.183  1.00  0.00           H  
HETATM   65  H17 UNL     1      -5.726  -3.142  -1.901  1.00  0.00           H  
HETATM   66  H18 UNL     1      -5.635  -0.383   1.094  1.00  0.00           H  
HETATM   67  H19 UNL     1      -8.647   0.254   1.313  1.00  0.00           H  
HETATM   68  H20 UNL     1      -6.792  -2.102   1.669  1.00  0.00           H  
HETATM   69  H21 UNL     1      -3.557  -0.569   1.842  1.00  0.00           H  
HETATM   70  H22 UNL     1      -3.310   0.363   3.705  1.00  0.00           H  
HETATM   71  H23 UNL     1       5.922   0.943  -2.263  1.00  0.00           H  
HETATM   72  H24 UNL     1       5.638   2.772  -3.078  1.00  0.00           H  
HETATM   73  H25 UNL     1       6.858   2.504  -0.536  1.00  0.00           H  
HETATM   74  H26 UNL     1       4.409   3.614  -1.154  1.00  0.00           H  
HETATM   75  H27 UNL     1       5.500   0.276   3.167  1.00  0.00           H  
HETATM   76  H28 UNL     1       7.165  -1.379   3.679  1.00  0.00           H  
HETATM   77  H29 UNL     1       9.224  -1.203   2.190  1.00  0.00           H  
HETATM   78  H30 UNL     1       8.106  -2.531   1.711  1.00  0.00           H  
CONECT    1    2   49   50
CONECT    2    3    3    4
CONECT    4    5    5   48
CONECT    5    6   51
CONECT    6    7   46
CONECT    7    8   44   52
CONECT    8    9
CONECT    9   10   42   53
CONECT   10   11   54   55
CONECT   11   12
CONECT   12   13   13   14   15
CONECT   14   56
CONECT   15   16
CONECT   16   17   17   18   19
CONECT   18   57
CONECT   19   20
CONECT   20   21   58   59
CONECT   21   22   40   60
CONECT   22   23
CONECT   23   24   34   61
CONECT   24   25   33
CONECT   25   26   26   62
CONECT   26   27
CONECT   27   28   28   33
CONECT   28   29   30
CONECT   29   63   64
CONECT   30   31   31
CONECT   31   32   65
CONECT   32   33   33
CONECT   34   35   40   66
CONECT   35   36
CONECT   36   37   37   38   39
CONECT   38   67
CONECT   39   68
CONECT   40   41   69
CONECT   41   70
CONECT   42   43   44   71
CONECT   43   72
CONECT   44   45   73
CONECT   45   74
CONECT   46   47   47   75
CONECT   47   48   76
CONECT   48   77   78
END

HMDB0000221
     RDKit          3D
NADPH
 78 82  0  0  0  0  0  0  0  0999 V2000
   10.1531   -2.1020   -0.4812 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.1001   -1.1643   -0.6005 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9539   -0.5546   -1.7315 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1501   -0.8062    0.4424 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2252    0.0995    0.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2348    0.5512    1.0736 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2911    1.5427    0.6642 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0501    1.1819    0.3037 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1785    0.8138   -1.1037 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8065   -0.6473   -1.0841 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3865   -0.5750   -1.0877 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5980   -1.2660    0.1915 P   0  0  0  0  0  5  0  0  0  0  0  0
    2.3512   -2.1442    1.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2847    0.1730    1.2695 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0607   -1.6994   -0.2588 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4111   -0.6237   -1.5097 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.7549    0.0902   -2.1190 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2334   -1.5689   -2.6665 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5225    0.5286   -0.9701 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0546    0.2020    0.2437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1379    1.2027    0.6519 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0830    1.2088   -0.3843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2450    1.5451    0.2156 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.4398    1.1222   -0.5473 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5603    1.8463   -0.7184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4715    1.0709   -1.3783 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9326   -0.1347   -1.6238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4513   -1.2487   -2.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7889   -1.3026   -2.7306 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6369   -2.3115   -2.3303 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3702   -2.2569   -1.8106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8854   -1.1677   -1.2060 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6654   -0.0713   -1.0993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2652    0.6347    1.4815 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1070    1.0765    2.4400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1217   -0.2122    2.8769 P   0  0  0  0  0  5  0  0  0  0  0  0
   -7.2442   -0.2208    4.3994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6493   -0.0394    2.2360 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4247   -1.6870    2.4592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8308    0.5240    1.8543 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5088    1.1161    3.0433 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2385    1.5296   -1.6865 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7919    2.5131   -2.6546 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8017    2.3459   -0.5160 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1602    3.5815   -0.4947 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2181   -0.0017    2.3792 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1499   -0.9133    2.6865 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2084   -1.4029    1.7727 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9428   -3.1006   -0.5764 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1030   -1.7171   -0.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2207    0.5437   -0.7890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1788    2.2489    1.5496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1902    1.3031   -1.5501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1576   -1.1651   -0.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1125   -1.1535   -1.9863 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0972    0.8963    0.5856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8850   -2.1326   -2.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3196    0.2881    1.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5093   -0.7945    0.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7745    2.1551    0.9715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3599    2.5779    0.5171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7440    2.8552   -0.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0944   -1.7794   -3.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5784   -0.8200   -2.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7265   -3.1421   -1.9008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6345   -0.3833    1.0938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6472    0.2538    1.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7922   -2.1015    1.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5570   -0.5686    1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3103    0.3631    3.7045 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9223    0.9425   -2.2630 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6384    2.7718   -3.0782 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8579    2.5037   -0.5363 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4094    3.6143   -1.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5000    0.2764    3.1667 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1654   -1.3786    3.6792 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2239   -1.2033    2.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1061   -2.5314    1.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 12 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 23 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  2  0
 36 38  1  0
 36 39  1  0
 34 40  1  0
 40 41  1  0
  9 42  1  0
 42 43  1  0
 42 44  1  0
 44 45  1  0
  6 46  1  0
 46 47  2  0
 47 48  1  0
 48  4  1  0
 44  7  1  0
 40 21  1  0
 33 24  1  0
 33 27  1  0
  1 49  1  0
  1 50  1  0
  5 51  1  0
  7 52  1  1
  9 53  1  6
 10 54  1  0
 10 55  1  0
 14 56  1  0
 18 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  1
 23 61  1  1
 25 62  1  0
 29 63  1  0
 29 64  1  0
 31 65  1  0
 34 66  1  6
 38 67  1  0
 39 68  1  0
 40 69  1  1
 41 70  1  0
 42 71  1  6
 43 72  1  0
 44 73  1  6
 45 74  1  0
 46 75  1  0
 47 76  1  0
 48 77  1  0
 48 78  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
Dihydronicotinamide-adenine dinucleotide phosphate	ChEBI
NADPH dihydro-nicotinamide-adenine-dinucleotide phosphATE	ChEBI
Reduced nicotinamide adenine dinucleotide phosphate	ChEBI
Reduced nicotinamide-adenine dinucleotide phosphate	ChEBI
TPNH	ChEBI
Dihydronicotinamide-adenine dinucleotide phosphoric acid	Generator
NADPH dihydro-nicotinamide-adenine-dinucleotide phosphoric acid	Generator
Reduced nicotinamide adenine dinucleotide phosphoric acid	Generator
Reduced nicotinamide-adenine dinucleotide phosphoric acid	Generator
Nadph dihydro-nicotinamide-adenine-dinucleotidephosphoric acid	Generator
Coenzyme II	MeSH
Dinucleotide phosphate, nicotinamide-adenine	MeSH
NADP	MeSH
Nicotinamide adenine dinucleotide phosphate	MeSH
Nicotinamide-adenine dinucleotide phosphate	MeSH
Nucleotide, triphosphopyridine	MeSH
Phosphate, nicotinamide-adenine dinucleotide	MeSH
Triphosphopyridine nucleotide	MeSH
NADPH	HMDB
Nicotinamide-adenine dinucleotide phosphate, reduced	HMDB
Reduced triphosphopyridine nucleotide	HMDB
Triphosphopyridine nucleotide, reduced	HMDB
beta-NADPH	HMDB
beta-Nicotinamide-adenine-dinucleotide-phosphoric acid	HMDB
beta-TPNH	HMDB
β-NADPH	HMDB
β-Nicotinamide-adenine-dinucleotide-phosphoric acid	HMDB
β-TPNH	HMDB

Chemical Formula

C₂₁H₃₀N₇O₁₇P₃

Average Molecular Weight

745.4209

Monoisotopic Molecular Weight

745.091102105

IUPAC Name

{[(2R,3R,4R,5R)-2-(6-amino-9H-purin-9-yl)-5-[({[({[(2R,3S,4R,5R)-5-(3-carbamoyl-1,4-dihydropyridin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)methyl]-4-hydroxyoxolan-3-yl]oxy}phosphonic acid

Traditional Name

nadph

CAS Registry Number

53-57-6

SMILES

NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O

InChI Identifier

InChI=1S/C21H30N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1

InChI Key

ACFIXJIJDZMPPO-NNYOXOHSSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as (5'->5')-dinucleotides. These are dinucleotides where the two bases are connected via a (5'->5')-phosphodiester linkage.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

(5'->5')-dinucleotides

Sub Class

Not Available

Direct Parent

(5'->5')-dinucleotides

Alternative Parents

Substituents

(5'->5')-dinucleotide
Purine nucleotide sugar
Purine ribonucleoside 2',5'-bisphosphate
Purine ribonucleoside bisphosphate
Purine ribonucleoside diphosphate
Nicotinamide-nucleotide
Pentose phosphate
Pentose-5-phosphate
N-glycosyl compound
Glycosyl compound
N-substituted nicotinamide
Monosaccharide phosphate
Organic pyrophosphate
6-aminopurine
Imidazopyrimidine
Dihydropyridinecarboxylic acid derivative
Purine
Dihydropyridine
Monoalkyl phosphate
Aminopyrimidine
N-substituted imidazole
Phosphoric acid ester
Hydropyridine
Alkyl phosphate
Monosaccharide
Organic phosphoric acid derivative
Imidolactam
Pyrimidine
Azole
Tetrahydrofuran
Heteroaromatic compound
Imidazole
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Carboximidic acid
Carboximidic acid derivative
Enamine
Hydrocarbon derivative
Organopnictogen compound
Organic oxide
Amine
Organic oxygen compound
Primary amine
Alcohol
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

NADP (CHEBI:16474 )
NAD(P)H (CHEBI:16474 )

Ontology

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	5.45 g/L	ALOGPS
logP	-1.1	ALOGPS
logP	-6.4	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	0.66	ChemAxon
pKa (Strongest Basic)	4	ChemAxon
Physiological Charge	-4	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	364.15 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	153.87 m³·mol⁻¹	ChemAxon
Polarizability	63.54 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	221.176	30932474
DeepCCS	[M-H]-	219.281	30932474
DeepCCS	[M-2H]-	252.763	30932474
DeepCCS	[M+Na]+	226.797	30932474
AllCCS	[M+H]+	237.9	32859911
AllCCS	[M+H-H2O]+	237.6	32859911
AllCCS	[M+NH4]+	238.0	32859911
AllCCS	[M+Na]+	238.0	32859911
AllCCS	[M-H]-	234.0	32859911
AllCCS	[M+Na-2H]-	236.5	32859911
AllCCS	[M+HCOO]-	239.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
NADPH	NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O	5599.8	Standard polar	33892256
NADPH	NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O	3976.0	Standard non polar	33892256
NADPH	NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O	6479.9	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_16) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - NADPH GC-MS (TMS_2_17) - 70eV, Positive	Not Available	2021-10-18	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH Quattro_QQQ 10V, Positive-QTOF (Annotated)	splash10-02tj-1838493720-b38b37650e8976905bb0	2019-11-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH Quattro_QQQ 25V, Positive-QTOF (Annotated)	splash10-0a4r-0841393100-6e4cbc8ac576e3e8b195	2019-11-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH Quattro_QQQ 40V, Positive-QTOF (Annotated)	splash10-0550-2694875730-0dc522520957880672cb	2019-11-22	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 15V, negative-QTOF	splash10-0006-0000000900-1448a5a4a9a9ec30bc1d	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 17V, negative-QTOF	splash10-0006-0000000900-84c6720ae2b6d0d9ca35	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 20V, negative-QTOF	splash10-0006-0000100900-4ddda02ddc90d193fba1	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 23V, negative-QTOF	splash10-0006-0000201900-cbb70a91b1ac1fcb6e18	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 25V, negative-QTOF	splash10-0006-0001301900-2ec6727d0b32f09b91b6	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 27V, negative-QTOF	splash10-0006-0101502900-1d110f57242fe6b3d4eb	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 30V, negative-QTOF	splash10-054o-1213903700-aa4ca72e492f0f0b7f75	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 33V, negative-QTOF	splash10-0a6u-1313903400-9a6e4df99ff5a68effea	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 35V, negative-QTOF	splash10-0a6r-1324903300-069588f3537afa016ac8	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 40V, negative-QTOF	splash10-0a6r-3535903000-746e661fe41dfe08b6d1	2020-07-21	HMDB team, MONA	View Spectrum
Experimental LC-MS/MS	LC-MS/MS Spectrum - NADPH QTOF 45V, negative-QTOF	splash10-0a6r-5946701000-9407142d1340518483bf	2020-07-21	HMDB team, MONA	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 10V, Positive-QTOF	splash10-000i-0921103300-a94dc77e4683c53f1e1c	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 20V, Positive-QTOF	splash10-000i-0901000000-5fcc7bc2ff00254e837a	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 40V, Positive-QTOF	splash10-000i-0920000000-91a94a0d16f7db6907e1	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 10V, Negative-QTOF	splash10-0036-6900111800-7f73a4ecf431645a13cf	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 20V, Negative-QTOF	splash10-003r-3901000000-b9bf964190caf0afebde	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 40V, Negative-QTOF	splash10-057i-6900000000-f6e201cd60ed9314f31a	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 10V, Positive-QTOF	splash10-000i-0900000200-c30f8bbbadabff3b10f6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 20V, Positive-QTOF	splash10-000i-0911003300-322bf2f4fc18dbf667d6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 40V, Positive-QTOF	splash10-002r-1901300000-6129e75df61dcc44c45a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 10V, Negative-QTOF	splash10-0006-0000000900-b62da30b8e49b793af7d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - NADPH 20V, Negative-QTOF	splash10-004i-8301205900-8cec7794d03fc25fae8b	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View

Biological Properties

Cellular Locations

Cytoplasm (predicted from logP)

Biospecimen Locations

Blood

Tissue Locations

All Tissues

Pathways

Name	SMPDB/PathBank	KEGG
Histidine metabolism
Glycerolipid Metabolism
Glucose-Alanine Cycle		Not Available
Glutathione metabolism	Not Available
Phytanic Acid Peroxisomal Oxidation		Not Available

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected and Quantified	51.0 (34.0-81.0) uM	Adult (>18 years old)	Both	Normal	Geigy Scientific ...	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

DB02338

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Not Available

Wikipedia Link

Nicotinamide adenine dinucleotide phosphate

METLIN ID

3691

PubChem Compound

5884

PDB ID

Not Available

ChEBI ID

16474

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Seelbach, Karsten; Riebel, Bettina; Hummel, Werner; Kula, Maria-Regina; Tishkov, Vladimir I.; Egorov, Alexey M.; Wandrey, Christian; Kragl, Udo. A novel, efficient regenerating method of NADPH using a new formate dehydrogenase. Tetrahedron Letters (1996), 37(9), 1377-80.

Material Safety Data Sheet (MSDS)

Not Available

General References

Nakayama Y, Kinoshita A, Tomita M: Dynamic simulation of red blood cell metabolism and its application to the analysis of a pathological condition. Theor Biol Med Model. 2005 May 9;2:18. [PubMed:15882454 ]
Shindo Y, Witt E, Han D, Epstein W, Packer L: Enzymic and non-enzymic antioxidants in epidermis and dermis of human skin. J Invest Dermatol. 1994 Jan;102(1):122-4. [PubMed:8288904 ]
Iwata H, Tezuka Y, Kadota S, Hiratsuka A, Watabe T: Mechanism-based inactivation of human liver microsomal CYP3A4 by rutaecarpine and limonin from Evodia fruit extract. Drug Metab Pharmacokinet. 2005 Feb;20(1):34-45. [PubMed:15770073 ]
Birkmayer GJ, Birkmayer W: Stimulation of endogenous L-dopa biosynthesis--a new principle for the therapy of Parkinson's disease. The clinical effect of nicotinamide adenine dinucleotide (NADH) and nicotinamide adenine dinucleotidephosphate (NADPH). Acta Neurol Scand Suppl. 1989;126:183-7. [PubMed:2618590 ]
Lee AJ, Zhu BT: NADPH-dependent formation of polar and nonpolar estrogen metabolites following incubations of 17 beta-estradiol with human liver microsomes. Drug Metab Dispos. 2004 Aug;32(8):876-83. [PubMed:15258114 ]
Kochansky CJ, Xia YQ, Wang S, Cato B, Creighton M, Vincent SH, Franklin RB, Reed JR: Species differences in the elimination of a peroxisome proliferator-activated receptor agonist highlighted by oxidative metabolism of its acyl glucuronide. Drug Metab Dispos. 2005 Dec;33(12):1894-904. Epub 2005 Sep 23. [PubMed:16183782 ]
Karanam BV, Hop CE, Liu DQ, Wallace M, Dean D, Satoh H, Komuro M, Awano K, Vincent SH: In vitro metabolism of MK-0767 [(+/-)-5-[(2,4-dioxothiazolidin-5-yl)methyl]-2-methoxy-N-[[(4-trifluoromethyl) phenyl]methyl]benzamide], a peroxisome proliferator-activated receptor alpha/gamma agonist. I. Role of cytochrome P450, methyltransferases, flavin monooxygenases, and esterases. Drug Metab Dispos. 2004 Sep;32(9):1015-22. [PubMed:15319344 ]
Soglia JR, Contillo LG, Kalgutkar AS, Zhao S, Hop CE, Boyd JG, Cole MJ: A semiquantitative method for the determination of reactive metabolite conjugate levels in vitro utilizing liquid chromatography-tandem mass spectrometry and novel quaternary ammonium glutathione analogues. Chem Res Toxicol. 2006 Mar;19(3):480-90. [PubMed:16544956 ]
Afanas'ev IB, Suslova TB, Cheremisina ZP, Abramova NE, Korkina LG: Study of antioxidant properties of metal aspartates. Analyst. 1995 Mar;120(3):859-62. [PubMed:7741242 ]
Lin CC, Wong BK, Burgey CS, Gibson CR, Singh R: In vitro metabolism of a thrombin inhibitor and quantitation of metabolically generated cyanide. J Pharm Biomed Anal. 2005 Oct 4;39(5):1014-20. Epub 2005 Jul 14. [PubMed:16023819 ]
Conley AJ, Pattison JC, Bird IM: Variations in adrenal androgen production among (nonhuman) primates. Semin Reprod Med. 2004 Nov;22(4):311-26. [PubMed:15635499 ]

Only showing the first 10 proteins. There are 203 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details

1. Fatty acid synthase

General function:: Involved in transferase activity
Specific function:: Fatty acid synthetase catalyzes the formation of long-chain fatty acids from acetyl-CoA, malonyl-CoA and NADPH. This multifunctional protein has 7 catalytic activities and an acyl carrier protein.
Gene Name:: FASN
Uniprot ID:: P49327
Molecular weight:: 273424.06

Reactions

(3R)-3-hydroxyacyl-[acyl-carrier-protein] + NADP → 3-oxoacyl-[acyl-carrier-protein] + NADPH	details
Acyl-[acyl-carrier-protein] + NADP → trans-2,3-dehydroacyl-[acyl-carrier-protein] + NADPH	details
Butyryl-[acp] + NADP → But-2-enoyl-[acyl-carrier protein] + NADPH + Hydrogen Ion	details
(3R)-3-Hydroxybutanoyl-[acyl-carrier protein] + NADP → Acetoacetyl-[acp] + NADPH + Hydrogen Ion	details
(3R)-3-Hydroxydecanoyl-[acyl-carrier protein] + NADP → 3-Oxodecanoyl-[acp] + NADPH	details
(3R)-3-Hydroxyoctanoyl-[acyl-carrier protein] + NADP → 3-Oxooctanoyl-[acp] + NADPH + Hydrogen Ion	details
(3R)-3-Hydroxypalmitoyl-[acyl-carrier protein] + NADP → 3-Oxohexadecanoyl-[acp] + NADPH + Hydrogen Ion	details
(3R)-3-Hydroxytetradecanoyl-[acyl-carrier protein] + NADP → 3-Oxotetradecanoyl-[acp] + NADPH + Hydrogen Ion	details
Dodecanoyl-[acyl-carrier protein] + NADP → trans-Dodec-2-enoyl-[acp] + NADPH + Hydrogen Ion	details
(R)-3-Hydroxyhexanoyl-[acp] + NADP → 3-Oxohexanoyl-[acp] + NADPH + Hydrogen Ion	details
Hexanoyl-[acp] + NADP → trans-Hex-2-enoyl-[acp] + NADPH + Hydrogen Ion	details
Octanoyl-[acp] + NADP → trans-Oct-2-enoyl-[acp] + NADPH + Hydrogen Ion	details
Decanoyl-[acp] + NADP → trans-Dec-2-enoyl-[acp] + NADPH + Hydrogen Ion	details
Tetradecanoyl-[acp] + NADP → trans-Tetradec-2-enoyl-[acp] + NADPH + Hydrogen Ion	details
Hexadecanoyl-[acp] + NADP → trans-Hexadec-2-enoyl-[acp] + NADPH + Hydrogen Ion	details

Enzyme Details

2. Methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial

General function:: Involved in oxidoreductase activity
Specific function:: Plays a role in valine and pyrimidine metabolism. Binds fatty acyl-CoA.
Gene Name:: ALDH6A1
Uniprot ID:: Q02252
Molecular weight:: 57839.31

Reactions

Malonic semialdehyde + Coenzyme A + NADP → Acetyl-CoA + Carbon dioxide + NADPH + Hydrogen Ion	details
Malonic semialdehyde + Coenzyme A + NADP → Malonyl-CoA + NADPH + Hydrogen Ion	details

Enzyme Details

3. Aldo-keto reductase family 1 member C4

General function:: Involved in oxidoreductase activity
Specific function:: Catalyzes the transformation of the potent androgen dihydrotestosterone (DHT) into the less active form, 5-alpha-androstan-3-alpha,17-beta-diol (3-alpha-diol). Also has some 20-alpha-hydroxysteroid dehydrogenase activity. The biotransformation of the pesticide chlordecone (kepone) to its corresponding alcohol leads to increased biliary excretion of the pesticide and concomitant reduction of its neurotoxicity since bile is the major excretory route.
Gene Name:: AKR1C4
Uniprot ID:: P17516
Molecular weight:: 37094.57

Reactions

Chlordecone alcohol + NADP → Chlordecone + NADPH	details
Androsterone + NADP → Androstanedione + NADPH + Hydrogen Ion	details
Etiocholanolone + NADP → Etiocholanedione + NADPH + Hydrogen Ion	details
3a,7a-Dihydroxy-5b-cholestane + NADP → 7a-Hydroxy-5b-cholestan-3-one + NADPH + Hydrogen Ion	details
5beta-Cholestane-3alpha,7alpha,12alpha-triol + NADP → 7a,12a-Dihydroxy-5b-cholestan-3-one + NADPH + Hydrogen Ion	details
17a,21-Dihydroxy-5b-pregnane-3,11,20-trione + Hydrogen Ion + NADPH → Tetrahydrocortisone + NADP	details
Tetrahydrocortisol + NADP → Dihydrocortisol + NADPH + Hydrogen Ion	details
3a,11b,21-Trihydroxy-20-oxo-5b-pregnan-18-al + NADP → 11b,21-Dihydroxy-3,20-oxo-5b-pregnan-18-al + NADPH + Hydrogen Ion	details
Tetrahydrocorticosterone + NADP → 11b,21-Dihydroxy-5b-pregnane-3,20-dione + NADPH + Hydrogen Ion	details
3a,21-Dihydroxy-5b-pregnane-11,20-dione + NADP → 21-Hydroxy-5b-pregnane-3,11,20-trione + NADPH + Hydrogen Ion	details
3a-Hydroxy-5b-pregnane-20-one + NADP → 5a-Pregnane-3,20-dione + NADPH + Hydrogen Ion	details
Dihydrotestosterone + NADPH + Hydrogen Ion → Androstan-3alpha,17beta-diol + NADP	details

Enzyme Details

4. Carbonyl reductase [NADPH] 1

General function:: Involved in oxidoreductase activity
Specific function:: NADPH-dependent reductase with broad substrate specificity. Catalyzes the reduction of a wide variety of carbonyl compounds including quinones, prostaglandins, menadione, plus various xenobiotics. Catalyzes the reduction of the antitumor anthracyclines doxorubicin and daunorubicin to the cardiotoxic compounds doxorubicinol and daunorubicinol. Can convert prostaglandin E2 to prostaglandin F2-alpha. Can bind glutathione, which explains its higher affinity for glutathione-conjugated substrates. Catalyzes the reduction of S-nitrosoglutathione.
Gene Name:: CBR1
Uniprot ID:: P16152
Molecular weight:: 30374.73

Reactions

R-CHOH-R' + NADP → R-CO-R' + NADPH	details
(5Z,13E)-(15S)-9-alpha,11-alpha,15-trihydroxyprosta-5,13-dienoate + NADP → (5Z,13E)-(15S)-11-alpha,15-dihydroxy-9-oxoprosta-5,13-dienoate + NADPH	details
(13E)-(15S)-11-alpha,15-dihydroxy-9-oxoprost-13-enoate + NADP → (13E)-11-alpha-hydroxy-9,15-dioxoprost-13-enoate + NADPH	details
Prostaglandin F2a + NADP → Prostaglandin E2 + NADPH + Hydrogen Ion	details
4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone + NADPH + Hydrogen Ion → 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol + NADP	details

Enzyme Details

5. Dehydrogenase/reductase SDR family member 4

General function:: Involved in oxidoreductase activity
Specific function:: Reduces all-trans-retinal and 9-cis retinal. Can also catalyze the oxidation of all-trans-retinol with NADP as co-factor, but with much lower efficiency. Reduces alkyl phenyl ketones and alpha-dicarbonyl compounds with aromatic rings, such as pyrimidine-4-aldehyde, 3-benzoylpyridine, 4-benzoylpyridine, menadione and 4-hexanoylpyridine. Has no activity towards aliphatic aldehydes and ketones (By similarity).
Gene Name:: DHRS4
Uniprot ID:: Q9BTZ2
Molecular weight:: 29536.885

Reactions

R-CHOH-R' + NADP → R-CO-R' + NADPH	details

Enzyme Details

6. Carbonyl reductase [NADPH] 3

General function:: Involved in oxidoreductase activity
Specific function:: Has low NADPH-dependent oxidoreductase activity towards 4-benzoylpyridine and menadione (in vitro).
Gene Name:: CBR3
Uniprot ID:: O75828
Molecular weight:: 30849.97

Reactions

R-CHOH-R' + NADP → R-CO-R' + NADPH	details
Prostaglandin F2a + NADP → Prostaglandin E2 + NADPH + Hydrogen Ion	details
4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone + NADPH + Hydrogen Ion → 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol + NADP	details

Enzyme Details

7. Aldose reductase

General function:: Involved in oxidoreductase activity
Specific function:: Catalyzes the NADPH-dependent reduction of a wide variety of carbonyl-containing compounds to their corresponding alcohols with a broad range of catalytic efficiencies.
Gene Name:: AKR1B1
Uniprot ID:: P15121
Molecular weight:: 35853.125

Reactions

Glycerol + NADP → Glyceraldehyde + NADPH + Hydrogen Ion	details
beta-D-Galactose + NADPH + Hydrogen Ion → Galactitol + NADP	details
D-Xylitol + NADP → D-Xylose + NADPH + Hydrogen Ion	details
L-Arabitol + NADP → L-Arabinose + NADPH + Hydrogen Ion	details
Sorbitol + NADP → alpha-D-Glucose + NADPH + Hydrogen Ion	details
Propylene glycol + NADP → Lactaldehyde + NADPH + Hydrogen Ion	details

Enzyme Details

8. Thioredoxin reductase 1, cytoplasmic

General function:: Involved in oxidoreductase activity
Specific function:: Isoform 1 may possess glutaredoxin activity as well as thioredoxin reductase activity and induces actin and tubulin polymerization, leading to formation of cell membrane protrusions. Isoform 4 enhances the transcriptional activity of estrogen receptors alpha and beta while isoform 5 enhances the transcriptional activity of the beta receptor only. Isoform 5 also mediates cell death induced by a combination of interferon-beta and retinoic acid.
Gene Name:: TXNRD1
Uniprot ID:: Q16881
Molecular weight:: 70905.58

Reactions

Thioredoxin + NADP → thioredoxin disulfide + NADPH	details
Thioredoxin + NADP → Thioredoxin disulfide + NADPH + Hydrogen Ion	details
Hydrogen selenide + NADP + Water → Selenite + NADPH + Hydrogen Ion	details
NADPH + Hydrogen Ion + Methylselenic acid → NADP + Water + Methaneselenol	details

Enzyme Details

9. Lathosterol oxidase

General function:: Involved in iron ion binding
Specific function:: Catalyzes a dehydrogenation to introduce C5-6 double bond into lathosterol.
Gene Name:: SC5DL
Uniprot ID:: O75845
Molecular weight:: 35300.55

Reactions

Lathosterol + NADPH + Hydrogen Ion + Oxygen → 7-Dehydrocholesterol + NADP + Water	details
Episterol + NADP → 5,7,24(28)-Ergostatrienol + NADPH + Hydrogen Ion	details

Enzyme Details

10. Dimethylaniline monooxygenase [N-oxide-forming] 5

General function:: Involved in flavin-containing monooxygenase activity
Specific function:: In contrast with other forms of FMO it does not seem to be a drug-metabolizing enzyme.
Gene Name:: FMO5
Uniprot ID:: P49326
Molecular weight:: 32480.04

Reactions

N,N-Dimethylaniline + NADPH + Oxygen → Dimethylaniline-N-oxide + NADP + Water	details
Trimethylamine + NADPH + Hydrogen Ion + Oxygen → Trimethylamine N-oxide + NADP + Water	details
Tamoxifen + Oxygen + NADPH + Hydrogen Ion → Tamoxifen N-oxide + NADP + Water	details

Only showing the first 10 proteins. There are 203 proteins in total.

Show all enzymes and transporters

Showing metabocard for NADPH (HMDB0000221)

MOL for HMDB0000221 (NADPH)

3D MOL for HMDB0000221 (NADPH)

3D SDF for HMDB0000221 (NADPH)

3D-SDF for HMDB0000221 (NADPH)

PDB for HMDB0000221 (NADPH)

3D PDB for HMDB0000221 (NADPH)

SMILES for HMDB0000221 (NADPH)

INCHI for HMDB0000221 (NADPH)

Structure for HMDB0000221 (NADPH)

3D Structure for HMDB0000221 (NADPH)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

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