NP-MRD: Showing NP-Card for (1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid (NP0177076)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 14:51:36 UTC

Updated at

2022-09-03 14:51:36 UTC

NP-MRD ID

NP0177076

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid

Description

(22R,25R)-1beta,2beta,3beta-Trihydroxy-21-norspirosta-4-ene-19-oic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid is found in Asparagus racemosus. Based on a literature review very few articles have been published on (22R,25R)-1beta,2beta,3beta-Trihydroxy-21-norspirosta-4-ene-19-oic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032216512D          

 33 38  0  0  1  0            999 V2000
    4.3030   -3.2858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1170   -3.1521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4082   -2.3802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2223   -2.2464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7452   -2.8845    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3319   -3.4645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0648   -3.0857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9311   -2.2716    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6640   -1.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2507   -2.4728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0743   -2.4249    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.4446   -1.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2682   -1.6397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7215   -2.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5451   -2.2811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9984   -2.9704    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.8221   -2.9224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6282   -3.7076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0815   -4.3969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8046   -3.7555    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.4343   -4.4928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3512   -3.0662    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9810   -3.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3428   -4.3264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9425   -4.6276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5276   -3.1142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1573   -3.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3337   -3.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8804   -3.2101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4351   -3.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1155   -2.1473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4540   -3.6564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6399   -3.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 22 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 10 29  1  0  0  0  0
  7 29  1  0  0  0  0
 29 30  1  1  0  0  0
  8 31  1  1  0  0  0
  5 31  1  6  0  0  0
  5 32  1  0  0  0  0
 32 33  1  0  0  0  0
  2 33  1  0  0  0  0
M  END

     RDKit          3D

 71 76  0  0  0  0  0  0  0  0999 V2000
    7.8991    0.1732    0.9477 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4177    0.2604    0.7438 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6118   -0.2826    1.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5602   -1.2931    1.4167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8703   -0.6952    0.2378 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1204    0.5641    0.6298 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0410    0.6307   -0.3783 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2928   -0.6225   -1.2294 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9186   -1.1035   -1.6758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0066   -0.0451   -1.1956 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4278   -0.4621   -0.9731 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0548   -0.8626   -2.2611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2891   -0.1382   -2.6692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1603    0.3021   -1.5632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3932    0.6911   -1.8073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3171    1.1475   -0.7233 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6018    0.6628   -0.9038 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8250    0.7282    0.6210 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9503   -0.6173    0.8859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3620    1.1725    0.7483 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9907    0.8413    2.0531 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5836    0.2877   -0.1909 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6567   -1.1109    0.3134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1339   -2.0688   -0.3452 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1787   -1.4365    1.5944 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1505    0.7131   -0.3891 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5120    1.2508    0.8616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0738    1.5622    0.6212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6555    0.3447    0.1369 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6139   -0.7939    1.0976 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8692   -1.4884   -0.2977 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7301   -0.3526   -0.7914 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0613   -0.5341   -0.4970 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4172   -0.1295    0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3353    1.1846    1.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1742   -0.5554    1.7464 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1888    1.3424    0.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2976   -0.7322    2.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0150    0.5338    2.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0154   -2.2575    1.1751 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8551   -1.4349    2.2347 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7923    1.4576    0.4666 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8260    0.5987    1.6747 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0153    1.5284   -0.9938 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9582   -0.4122   -2.0781 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9168   -1.0782   -2.7918 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6929   -2.1206   -1.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0043    0.8248   -1.8539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4667   -1.3380   -0.2602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2308   -1.9802   -2.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3187   -0.7014   -3.1089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9192   -0.8581   -3.2757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0890    0.6957   -3.3872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8210    0.7048   -2.8246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3908    2.2677   -0.7166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0226    1.1803   -1.6362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3906    1.2649    1.4206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6283   -0.9872    0.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2709    2.2387    0.5449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6007    0.2000    2.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6474   -2.2960    1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0777    1.5406   -1.1546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0276    2.2282    1.0816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6880    0.6226    1.7553 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4227    1.9682    1.5129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0115    2.3315   -0.1672 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5829   -1.0126    1.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1196   -0.6656    1.9271 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3205   -1.7727    0.6165 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2496   -1.5972   -0.3086 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6469   -0.2090   -1.3762 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  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  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  0
 22 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  1
 22 23  1  1
 23 25  1  0
 23 24  2  0
  8 31  1  0
  5 32  1  6
 32 33  1  0
 33  2  1  0
 31  5  1  0
 29  7  1  0
 29 10  1  0
 26 11  1  0
 22 14  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  6
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  6 42  1  0
  6 43  1  0
  7 44  1  6
  8 45  1  6
  9 46  1  0
  9 47  1  0
 10 48  1  6
 11 49  1  1
 12 50  1  0
 12 51  1  0
 13 52  1  0
 13 53  1  0
 15 54  1  0
 16 55  1  1
 17 56  1  0
 18 57  1  1
 19 58  1  0
 20 59  1  6
 21 60  1  0
 26 62  1  6
 27 63  1  0
 27 64  1  0
 28 65  1  0
 28 66  1  0
 30 67  1  0
 30 68  1  0
 30 69  1  0
 25 61  1  0
 33 70  1  0
 33 71  1  0
M  END


  Mrv1652309032216512D          

 33 38  0  0  1  0            999 V2000
    4.3030   -3.2858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1170   -3.1521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4082   -2.3802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2223   -2.2464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7452   -2.8845    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3319   -3.4645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0648   -3.0857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9311   -2.2716    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6640   -1.8929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2507   -2.4728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0743   -2.4249    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.4446   -1.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2682   -1.6397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7215   -2.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5451   -2.2811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9984   -2.9704    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.8221   -2.9224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6282   -3.7076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0815   -4.3969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8046   -3.7555    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.4343   -4.4928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3512   -3.0662    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9810   -3.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3428   -4.3264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9425   -4.6276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5276   -3.1142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.1573   -3.8514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3337   -3.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8804   -3.2101    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4351   -3.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1155   -2.1473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4540   -3.6564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6399   -3.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 22 26  1  0  0  0  0
 11 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 10 29  1  0  0  0  0
  7 29  1  0  0  0  0
 29 30  1  1  0  0  0
  8 31  1  1  0  0  0
  5 31  1  6  0  0  0
  5 32  1  0  0  0  0
 32 33  1  0  0  0  0
  2 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0177076

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@@]2(C[C@H]3[C@H](C[C@H]4[C@@H]5CCC6=C[C@@H](O)[C@@H](O)[C@@H](O)[C@@]6([C@H]5CC[C@]34C)C(O)=O)O2)OC1

> <INCHI_IDENTIFIER>
InChI=1S/C26H38O7/c1-13-5-8-25(32-12-13)11-18-20(33-25)10-17-15-4-3-14-9-19(27)21(28)22(29)26(14,23(30)31)16(15)6-7-24(17,18)2/h9,13,15-22,27-29H,3-8,10-12H2,1-2H3,(H,30,31)/t13-,15-,16+,17+,18+,19-,20+,21-,22-,24+,25-,26-/m1/s1

> <INCHI_KEY>
PCCYKZMWMSQXBK-WBBNHULHSA-N

> <FORMULA>
C26H38O7

> <MOLECULAR_WEIGHT>
462.583

> <EXACT_MASS>
462.261753564

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
50.70480064732201

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2R,2'S,4'S,5R,8'R,9'S,12'S,13'S,14'S,15'R,16'R)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosan]-17'-ene-13'-carboxylic acid

> <JCHEM_LOGP>
1.8016821996666659

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.948660498624093

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.024977090165636

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3510736846941382

> <JCHEM_POLAR_SURFACE_AREA>
116.45

> <JCHEM_REFRACTIVITY>
119.9817

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2R,2'S,4'S,5R,8'R,9'S,12'S,13'S,14'S,15'R,16'R)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosan]-17'-ene-13'-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       8.032  -6.134   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.552  -5.884   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.095  -4.443   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.615  -4.193   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.591  -5.384   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.686  -6.467   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      15.054  -5.760   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      14.805  -4.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.173  -3.533   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.268  -4.616   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.805  -4.526   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      19.497  -3.150   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      21.034  -3.061   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      21.880  -4.347   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      23.418  -4.258   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      24.264  -5.545   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      25.801  -5.455   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      23.573  -6.921   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      24.419  -8.208   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      22.035  -7.010   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      21.344  -8.386   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      21.189  -5.724   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      20.498  -7.100   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      19.307  -8.076   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      20.426  -8.638   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      19.652  -5.813   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      18.960  -7.189   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      17.423  -7.279   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      16.577  -5.992   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.746  -7.289   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      13.282  -4.008   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      12.048  -6.825   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      10.528  -7.075   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   33                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   31   32                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   29                                                  
CONECT    8    7    9   31                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   29                                                  
CONECT   11   10   12   26                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   14   23   26                                             
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   22   11   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   10    7   30                                             
CONECT   30   29                                                            
CONECT   31    8    5                                                       
CONECT   32    5   33                                                       
CONECT   33   32    2                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   76    0
END

View in JSmol

Synonyms

Value	Source
(22R,25R)-1b,2b,3b-Trihydroxy-21-norspirosta-4-ene-19-Oate	Generator
(22R,25R)-1b,2b,3b-Trihydroxy-21-norspirosta-4-ene-19-Oic acid	Generator
(22R,25R)-1beta,2beta,3beta-Trihydroxy-21-norspirosta-4-ene-19-Oate	Generator
(22R,25R)-1Β,2β,3β-trihydroxy-21-norspirosta-4-ene-19-Oate	Generator
(22R,25R)-1Β,2β,3β-trihydroxy-21-norspirosta-4-ene-19-Oic acid	Generator

Chemical Formula

C₂₆H₃₈O₇

Average Mass

462.5830 Da

Monoisotopic Mass

462.26175 Da

IUPAC Name

(1'S,2R,2'S,4'S,5R,8'R,9'S,12'S,13'S,14'S,15'R,16'R)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosan]-17'-ene-13'-carboxylic acid

Traditional Name

(1'S,2R,2'S,4'S,5R,8'R,9'S,12'S,13'S,14'S,15'R,16'R)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosan]-17'-ene-13'-carboxylic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@@]2(C[C@H]3[C@H](C[C@H]4[C@@H]5CCC6=C[C@@H](O)[C@@H](O)[C@@H](O)[C@@]6([C@H]5CC[C@]34C)C(O)=O)O2)OC1

InChI Identifier

InChI=1S/C26H38O7/c1-13-5-8-25(32-12-13)11-18-20(33-25)10-17-15-4-3-14-9-19(27)21(28)22(29)26(14,23(30)31)16(15)6-7-24(17,18)2/h9,13,15-22,27-29H,3-8,10-12H2,1-2H3,(H,30,31)/t13-,15-,16+,17+,18+,19-,20+,21-,22-,24+,25-,26-/m1/s1

InChI Key

PCCYKZMWMSQXBK-WBBNHULHSA-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
Asparagus racemosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Spirostane skeleton
19-oxosteroid
19-hydroxysteroid
3-hydroxy-delta-4-steroid
3-hydroxysteroid
1-hydroxysteroid
2-hydroxysteroid
3-beta-hydroxysteroid
Hydroxysteroid
Oxosteroid
Delta-4-steroid
Steroid
Ketal
Beta-hydroxy acid
Cyclitol or derivatives
Hydroxy acid
Oxane
Tetrahydrofuran
Secondary alcohol
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Carboxylic acid
Carboxylic acid derivative
Acetal
Polyol
Organic oxide
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organooxygen compound
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	1.8	ChemAxon
pKa (Strongest Acidic)	4.02	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	119.98 m³·mol⁻¹	ChemAxon
Polarizability	50.7 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

51350043

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid (NP0177076)

MOL for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)

3D MOL for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)

3D SDF for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)

3D-SDF for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)

PDB for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)

3D PDB for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)

SMILES for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)

INCHI for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)

Structure for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)

3D Structure for NP0177076 ((1's,2r,2's,4's,5r,8'r,9's,12's,13's,14's,15'r,16'r)-14',15',16'-trihydroxy-5,9'-dimethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]icosan]-17'-ene-13'-carboxylic acid)