NP-MRD: Showing NP-Card for scutelaterin a (NP0256259)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 21:00:52 UTC

Updated at

2022-09-07 21:00:52 UTC

NP-MRD ID

NP0256259

Secondary Accession Numbers

None

Natural Product Identification

Common Name

scutelaterin a

Description

Scutelaterin A belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. scutelaterin a is found in Scutellaria lateriflora. Based on a literature review very few articles have been published on Scutelaterin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072223002D          

 35 39  0  0  1  0            999 V2000
    1.2753    1.8883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0308    1.5570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6955    2.0457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1217    0.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8773    0.4057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.4142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2186    0.3718    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6632    0.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9137    1.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8228    2.5878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7197    1.9439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0246    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5801   -0.0621    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3861    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3296   -0.8481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3631   -1.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1472   -0.9583    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7170   -0.3616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4605   -0.7191    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2721   -0.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6636   -1.2975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0938   -1.8942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3503   -1.5367    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5386   -1.6846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5236   -1.0242    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2731   -1.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4671   -1.9863    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2166   -2.7724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4106   -2.9485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1601   -3.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8552   -2.3385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116   -1.3764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622   -0.5903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3761   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9861    0.2157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  6  0  0  0
 17 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  6  0  0  0
 15 25  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
  6 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 33 35  1  1  0  0  0
M  END

     RDKit          3D

 71 75  0  0  0  0  0  0  0  0999 V2000
   -4.7603   -2.4459   -2.9356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4210   -1.8320   -2.9075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7234   -1.6973   -3.9535 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8458   -1.3635   -1.7219 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5330   -0.7719   -1.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1832   -0.3721   -0.3744 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2100   -1.6004    0.5167 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4158   -2.2989    0.4533 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1420   -2.5684    1.5895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4155   -3.3099    1.4896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7748   -2.2095    2.7444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0937   -2.4912    0.0360 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2204   -1.8406    0.2493 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3034   -2.8101   -0.1159 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3800   -0.4849   -0.4717 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7226   -0.7888   -1.8849 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5593    0.1333    0.2585 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1330    1.3803   -0.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6083    1.2703    0.1918 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8980    2.0181    1.4404 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1998    1.1709    2.3994 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1535   -0.1391    1.9497 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7515   -0.1403    0.6016 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5705   -0.8166    0.3959 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1593    0.2914   -0.2117 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0412    1.6442   -0.8436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7699    2.5238    0.1295 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0918    3.2548    0.9823 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0671    4.6256    0.9285 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9514    5.4789    1.8014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7209    5.1855    0.1227 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6776    1.6965    0.9741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2341    0.5566    0.1628 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6199    0.2671    0.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1581    1.1294   -0.8488 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5666   -1.7295   -3.1551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9878   -3.0133   -2.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7657   -3.1922   -3.7668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9100   -1.4833   -2.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6434    0.1026   -2.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9910   -1.3377    1.5756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1367   -2.8059    2.1663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8405   -3.2970    0.4701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3028   -4.3459    1.8856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2769   -2.8584   -0.9719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1175   -3.3858    0.7076 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3429   -1.6124    1.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8698   -3.8285   -0.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0018   -3.0415    0.7373 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9098   -2.5560   -0.9806 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8414   -0.7792   -1.9780 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3654   -0.0302   -2.6107 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4553   -1.8233   -2.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2342    0.2998    1.3413 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7991    2.3042    0.3097 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1250    1.6070   -1.2960 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2780    1.6159   -0.6025 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8675    3.0814    1.5495 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4564    1.4327    3.4216 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5272   -0.6264   -0.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2168    0.4974    0.9070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303    1.5794   -1.8181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9387    2.2075   -1.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3883    3.1953   -0.5080 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8863    5.7290    1.2989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1477    4.8733    2.7207 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3640    6.3672    2.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2687    1.3979    1.9533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5467    2.3696    1.2368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2449   -0.5075   -0.1224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2213    0.9486    0.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 12  1  0
 12  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
  7  6  1  0
  6  5  1  6
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  6 25  1  0
 25 26  1  0
 26 27  1  0
 27 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 29 31  2  0
 25 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 15 13  1  0
 24 17  1  0
 33  6  1  0
 33 35  1  6
 23 19  1  0
 14 48  1  0
 14 49  1  0
 14 50  1  0
 13 47  1  1
 12 45  1  0
 12 46  1  0
  7 41  1  1
 10 42  1  0
 10 43  1  0
 10 44  1  0
  5 39  1  0
  5 40  1  0
  1 36  1  0
  1 37  1  0
  1 38  1  0
 25 61  1  1
 26 62  1  0
 26 63  1  0
 27 64  1  6
 32 68  1  0
 32 69  1  0
 34 70  1  0
 34 71  1  0
 30 65  1  0
 30 66  1  0
 30 67  1  0
 16 51  1  0
 16 52  1  0
 16 53  1  0
 17 54  1  1
 18 55  1  0
 18 56  1  0
 19 57  1  6
 20 58  1  0
 21 59  1  0
 23 60  1  6
M  END


  Mrv1652309072223002D          

 35 39  0  0  1  0            999 V2000
    1.2753    1.8883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0308    1.5570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6955    2.0457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1217    0.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8773    0.4057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.4142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2186    0.3718    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6632    0.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9137    1.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8228    2.5878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7197    1.9439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0246    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5801   -0.0621    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3861    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3296   -0.8481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3631   -1.6724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1472   -0.9583    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7170   -0.3616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4605   -0.7191    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2721   -0.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6636   -1.2975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0938   -1.8942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3503   -1.5367    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5386   -1.6846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5236   -1.0242    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2731   -1.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4671   -1.9863    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2166   -2.7724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4106   -2.9485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1601   -3.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8552   -2.3385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116   -1.3764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622   -0.5903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3761   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9861    0.2157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  6  0  0  0
 17 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  6  0  0  0
 15 25  1  0  0  0  0
  6 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
  6 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 33 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0256259

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H](OC(C)=O)[C@]2(COC(C)=O)[C@H](C[C@@H](C[C@]22CO2)OC(C)=O)[C@@]1(C)[C@@H]1C[C@H]2C=CO[C@H]2O1

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O9/c1-14-8-22(34-17(4)29)26(13-31-15(2)27)20(10-19(33-16(3)28)11-25(26)12-32-25)24(14,5)21-9-18-6-7-30-23(18)35-21/h6-7,14,18-23H,8-13H2,1-5H3/t14-,18-,19+,20-,21+,22+,23+,24+,25+,26+/m1/s1

> <INCHI_KEY>
QPZJPRFBKONNBN-ROXXLOQASA-N

> <FORMULA>
C26H36O9

> <MOLECULAR_WEIGHT>
492.565

> <EXACT_MASS>
492.235932739

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
51.37809855603024

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1R,3S,4aR,5S,6R,8S,8aR)-5-[(2S,3aS,6aS)-2H,3H,3aH,6aH-furo[2,3-b]furan-2-yl]-3,8-bis(acetyloxy)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-yl]methyl acetate

> <JCHEM_LOGP>
1.253725424999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9201815717761304

> <JCHEM_POLAR_SURFACE_AREA>
109.89000000000001

> <JCHEM_REFRACTIVITY>
121.11479999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,4aR,5S,6R,8S,8aR)-5-[(2S,3aS,6aS)-2H,3H,3aH,6aH-furo[2,3-b]furan-2-yl]-3,8-bis(acetyloxy)-5,6-dimethyl-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-ylmethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       2.381   3.525   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.791   2.906   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.032   3.819   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.961   1.376   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.371   0.757   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.541  -0.773   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.008   0.694   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.971   1.833   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.439   3.300   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.269   4.831   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.943   3.629   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.513   1.023   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.550  -0.116   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.054   0.213   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.082  -1.583   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.144  -3.122   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.608  -1.789   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.672  -0.675   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.060  -1.342   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.575  -1.066   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.305  -2.422   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      13.242  -3.536   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      11.854  -2.869   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.339  -3.145   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.577  -1.912   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.110  -3.379   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.605  -3.708   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.138  -5.175   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.633  -5.504   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.166  -6.971   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.596  -4.365   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       3.568  -2.569   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.036  -1.102   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.569  -0.634   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.707   0.403   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   25   33                                             
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17   25                                             
CONECT   16   15                                                            
CONECT   17   15   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   19   24                                                  
CONECT   24   23   17                                                       
CONECT   25   15    6   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   27   33                                                       
CONECT   33   32    6   34   35                                             
CONECT   34   33   35                                                       
CONECT   35   34   33                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₆O₉

Average Mass

492.5650 Da

Monoisotopic Mass

492.23593 Da

IUPAC Name

[(1R,3S,4aR,5S,6R,8S,8aR)-5-[(2S,3aS,6aS)-2H,3H,3aH,6aH-furo[2,3-b]furan-2-yl]-3,8-bis(acetyloxy)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-yl]methyl acetate

Traditional Name

(1R,3S,4aR,5S,6R,8S,8aR)-5-[(2S,3aS,6aS)-2H,3H,3aH,6aH-furo[2,3-b]furan-2-yl]-3,8-bis(acetyloxy)-5,6-dimethyl-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-8a-ylmethyl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H](OC(C)=O)[C@]2(COC(C)=O)[C@H](C[C@@H](C[C@]22CO2)OC(C)=O)[C@@]1(C)[C@@H]1C[C@H]2C=CO[C@H]2O1

InChI Identifier

InChI=1S/C26H36O9/c1-14-8-22(34-17(4)29)26(13-31-15(2)27)20(10-19(33-16(3)28)11-25(26)12-32-25)24(14,5)21-9-18-6-7-30-23(18)35-21/h6-7,14,18-23H,8-13H2,1-5H3/t14-,18-,19+,20-,21+,22+,23+,24+,25+,26+/m1/s1

InChI Key

QPZJPRFBKONNBN-ROXXLOQASA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Scutellaria lateriflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Furofuran
Dihydrofuran
Tetrahydrofuran
Carboxylic acid ester
Acetal
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	1.25	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	109.89 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	121.11 m³·mol⁻¹	ChemAxon
Polarizability	51.38 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00044308

Chemspider ID

34985368

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

76963770

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for scutelaterin a (NP0256259)

MOL for NP0256259 (scutelaterin a)

3D MOL for NP0256259 (scutelaterin a)

3D SDF for NP0256259 (scutelaterin a)

3D-SDF for NP0256259 (scutelaterin a)

PDB for NP0256259 (scutelaterin a)

3D PDB for NP0256259 (scutelaterin a)

SMILES for NP0256259 (scutelaterin a)

INCHI for NP0256259 (scutelaterin a)

Structure for NP0256259 (scutelaterin a)

3D Structure for NP0256259 (scutelaterin a)