NP-MRD: Showing NP-Card for β-chaconine (NP0198597)

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Record Information

Version

1.0

Created at

2022-09-04 17:04:50 UTC

Updated at

2022-09-04 17:04:50 UTC

NP-MRD ID

NP0198597

Secondary Accession Numbers

None

Natural Product Identification

Common Name

β-chaconine

Description

Solanidine 3-o-alpha-l-rhamnopyranosyl-(1-2)-beta-d-glucopyranoside, also known as beta(1)-chaconine, belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative. Thus, solanidine 3-O-alpha-L-rhamnopyranosyl-(1-2)-beta-D-glucopyranoside is considered to be a sterol. β-chaconine is found in Fritillaria stenanthera, Fritillaria thunbergii, Solanum chacoense and Solanum tuberosum. It was first documented in 2008 (PMID: 18075898). Based on a literature review very few articles have been published on Solanidine 3-o-alpha-l-rhamnopyranosyl-(1-2)-beta-d-glucopyranoside (PMID: 30989914).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042219042D          

 50 57  0  0  1  0            999 V2000
    4.0885   -2.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6330   -2.8879    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3684   -3.6693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9129   -4.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7219   -4.1276    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3833   -4.6207    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3732   -5.4456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0567   -4.1440    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8114   -3.3563    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4848   -2.8796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1462   -3.3727    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9552   -3.2111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2198   -2.4297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0288   -2.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5732   -2.8879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3823   -2.7263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9267   -3.3461    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.7357   -3.1845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0003   -2.4031    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.4559   -1.7833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7204   -1.0019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1760   -0.3820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3669   -0.5436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5294   -0.8403    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.7940   -0.0588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0739   -1.4601    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.8829   -1.2985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8093   -2.2415    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.3538   -2.8614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0892   -3.6428    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2802   -3.8044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0156   -4.5858    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.2066   -4.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5601   -5.2056    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2955   -5.9871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3691   -5.0441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.9136   -5.6639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.6337   -4.2626    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4427   -4.1010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6622   -4.1276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8531   -4.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3087   -3.6693    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0441   -4.4508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4997   -3.8309    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2351   -4.6124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4261   -4.7740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8816   -4.1541    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5368   -4.9036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9865   -3.3461    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4420   -2.7263    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
  6  7  1  6  0  0  0
  8  6  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  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  0  0  0  0
 17 18  1  1  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 19 28  1  0  0  0  0
 28 29  1  1  0  0  0
 30 29  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 30 38  1  0  0  0  0
 38 39  1  6  0  0  0
 17 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 15 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 12 44  1  0  0  0  0
 44 45  1  1  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 11 47  1  0  0  0  0
  8 47  1  0  0  0  0
 47 48  1  1  0  0  0
  9 49  1  1  0  0  0
  5 49  1  1  0  0  0
 49 50  1  0  0  0  0
  2 50  1  0  0  0  0
M  END

     RDKit          3D

113120  0  0  0  0  0  0  0  0999 V2000
   -8.7249    4.0724   -1.1046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3425    3.0551   -0.0475 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.4175    2.0364    0.1401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7539    0.7095    0.5056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9802    0.2922   -0.7301 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1834   -0.9585   -0.4994 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.9327   -2.1174   -1.1357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9058   -0.7318   -1.2164 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9128    0.7311   -1.6547 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6159    1.3277   -1.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7411    0.0983   -1.1177 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4412    0.2355   -0.4306 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5063    1.0555   -1.3405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1184    1.0145   -0.8149 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3074    0.1425    0.0497 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7213    0.1203    0.5694 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3531   -1.1561    0.0727 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4932   -1.4856    0.7937 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6714   -1.5086    0.1292 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3701   -2.6692    0.1586 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1045   -2.8026    1.3150 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2272   -4.2639    1.7348 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9808   -4.3070    2.9088 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5382   -2.0357    2.4817 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2486   -2.3227    3.6545 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6265   -0.5509    2.1597 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5065    0.0733    2.7223 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5566   -0.3697    0.6763 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7738   -0.4168    0.0466 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4399    1.5357   -2.7810 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1298    2.2404   -2.8935 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3956   -2.3160   -0.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6582   -0.8727   -0.3839 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8518   -0.5522    1.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0931    1.3146   -1.1543 N   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.8333    4.1716   -1.0780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3475    3.7959   -2.0996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3017    5.0657   -0.8152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2893    3.6381    0.9199 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.6033   -3.0048    0.0440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9193   -2.4546   -1.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9139   -0.2400    1.5147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1356   -1.5224    1.5654 H   0  0  0  0  0  0  0  0  0  0  0  0
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 43102  1  0
 43103  1  0
 44104  1  6
 45105  1  0
 45106  1  0
 46107  1  0
 46108  1  0
 48109  1  0
 48110  1  0
 48111  1  0
  8 64  1  6
 19 76  1  6
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 25 82  1  0
 26 83  1  1
 27 84  1  0
 28 85  1  1
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 33 88  1  0
 33 89  1  0
 33 90  1  0
 34 91  1  6
 35 92  1  0
 36 93  1  1
 37 94  1  0
 38 95  1  1
 39 96  1  0
M  END


  Mrv1652309042219042D          

 50 57  0  0  1  0            999 V2000
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    4.6330   -2.8879    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3684   -3.6693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9129   -4.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7219   -4.1276    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3833   -4.6207    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3732   -5.4456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0567   -4.1440    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8114   -3.3563    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4848   -2.8796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1462   -3.3727    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9552   -3.2111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2198   -2.4297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0288   -2.2681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5732   -2.8879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3823   -2.7263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9267   -3.3461    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.7357   -3.1845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0003   -2.4031    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.4559   -1.7833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7204   -1.0019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1760   -0.3820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3669   -0.5436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5294   -0.8403    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.7940   -0.0588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0739   -1.4601    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.8829   -1.2985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8093   -2.2415    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.3538   -2.8614    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0892   -3.6428    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2802   -3.8044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.0156   -4.5858    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.2066   -4.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5601   -5.2056    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2955   -5.9871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3691   -5.0441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.9136   -5.6639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.6337   -4.2626    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4427   -4.1010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6622   -4.1276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8531   -4.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3087   -3.6693    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0441   -4.4508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4997   -3.8309    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2351   -4.6124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4261   -4.7740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8816   -4.1541    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5368   -4.9036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9865   -3.3461    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4420   -2.7263    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
  6  7  1  6  0  0  0
  8  6  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  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  0  0  0  0
 17 18  1  1  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 19 28  1  0  0  0  0
 28 29  1  1  0  0  0
 30 29  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 30 38  1  0  0  0  0
 38 39  1  6  0  0  0
 17 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 15 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 12 44  1  0  0  0  0
 44 45  1  1  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 11 47  1  0  0  0  0
  8 47  1  0  0  0  0
 47 48  1  1  0  0  0
  9 49  1  1  0  0  0
  5 49  1  1  0  0  0
 49 50  1  0  0  0  0
  2 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198597

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@H]2CC[C@H](C)CN2[C@H]2C[C@H]3[C@@H]4CC=C5C[C@H](CC[C@]5(C)[C@H]4CC[C@]3(C)[C@@H]12)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C39H63NO10/c1-18-6-9-26-19(2)29-27(40(26)16-18)15-25-23-8-7-21-14-22(10-12-38(21,4)24(23)11-13-39(25,29)5)48-37-35(33(45)31(43)28(17-41)49-37)50-36-34(46)32(44)30(42)20(3)47-36/h7,18-20,22-37,41-46H,6,8-17H2,1-5H3/t18-,19+,20-,22-,23+,24-,25-,26+,27-,28+,29-,30-,31+,32+,33-,34+,35+,36-,37+,38-,39-/m0/s1

> <INCHI_KEY>
ZLSYCIYRYZUJCZ-MTXMLOAPSA-N

> <FORMULA>
C39H63NO10

> <MOLECULAR_WEIGHT>
705.93

> <EXACT_MASS>
705.445197233

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
113

> <JCHEM_AVERAGE_POLARIZABILITY>
80.81749813439953

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[(1S,2S,7S,10R,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{15,23}.0^{17,22}]tetracos-4-en-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

> <JCHEM_LOGP>
1.5086522093064294

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.854619980100022

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.945434291156102

> <JCHEM_PKA_STRONGEST_BASIC>
12.43013484948969

> <JCHEM_POLAR_SURFACE_AREA>
161.54000000000002

> <JCHEM_REFRACTIVITY>
184.14030000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[(1S,2S,7S,10R,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{15,23}.0^{17,22}]tetracos-4-en-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       7.632  -4.234   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.648  -5.391   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.154  -6.849   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.171  -8.006   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.681  -7.705   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.916  -8.625   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.897 -10.165   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.172  -7.735   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.715  -6.265   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.972  -5.375   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.206  -6.296   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.716  -5.994   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.210  -4.535   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      18.720  -4.234   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      19.737  -5.391   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.247  -5.089   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      22.263  -6.246   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      23.773  -5.944   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      24.267  -4.486   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      23.251  -3.329   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      23.745  -1.870   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      22.728  -0.713   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      21.218  -1.015   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      25.255  -1.568   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      25.749  -0.110   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      26.271  -2.726   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      27.781  -2.424   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      25.777  -4.184   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      26.794  -5.341   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      26.300  -6.800   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      24.790  -7.102   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      24.296  -8.560   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      22.786  -8.862   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      25.312  -9.717   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      24.818 -11.176   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      26.822  -9.416   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      27.839 -10.573   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      27.316  -7.957   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      28.826  -7.655   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      21.769  -7.705   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      20.259  -8.006   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      19.243  -6.849   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      18.749  -8.308   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      17.733  -7.151   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      17.239  -8.610   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      15.729  -8.911   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      14.712  -7.754   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      14.069  -9.153   0.000  0.00  0.00           C+0
HETATM   49  N   UNK     0      11.175  -6.246   0.000  0.00  0.00           N+0
HETATM   50  C   UNK     0      10.158  -5.089   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   50                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   49                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   47                                                  
CONECT    9    8   10   49                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   47                                                  
CONECT   12   11   13   44                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   42                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   40                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   19   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   38                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   30   39                                                  
CONECT   39   38                                                            
CONECT   40   17   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   15   43   44                                             
CONECT   43   42                                                            
CONECT   44   42   12   45                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   11    8   48                                             
CONECT   48   47                                                            
CONECT   49    9    5   50                                                  
CONECT   50   49    2                                                       
MASTER        0    0    0    0    0    0    0    0   50    0  114    0
END

View in JSmol

Synonyms

Value	Source
Solanidine 3-O-a-L-rhamnopyranosyl-(1-2)-b-D-glucopyranoside	Generator
Solanidine 3-O-α-L-rhamnopyranosyl-(1-2)-β-D-glucopyranoside	Generator
beta(1)-Chaconine	MeSH

Chemical Formula

C₃₉H₆₃NO₁₀

Average Mass

705.9300 Da

Monoisotopic Mass

705.44520 Da

IUPAC Name

(2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[(1S,2S,7S,10R,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{15,23}.0^{17,22}]tetracos-4-en-7-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@H]2CC[C@H](C)CN2[C@H]2C[C@H]3[C@@H]4CC=C5C[C@H](CC[C@]5(C)[C@H]4CC[C@]3(C)[C@@H]12)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O

InChI Identifier

InChI=1S/C39H63NO10/c1-18-6-9-26-19(2)29-27(40(26)16-18)15-25-23-8-7-21-14-22(10-12-38(21,4)24(23)11-13-39(25,29)5)48-37-35(33(45)31(43)28(17-41)49-37)50-36-34(46)32(44)30(42)20(3)47-36/h7,18-20,22-37,41-46H,6,8-17H2,1-5H3/t18-,19+,20-,22-,23+,24-,25-,26+,27-,28+,29-,30-,31+,32+,33-,34+,35+,36-,37+,38-,39-/m0/s1

InChI Key

ZLSYCIYRYZUJCZ-MTXMLOAPSA-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
Fritillaria stenanthera	LOTUS Database	35616633
Fritillaria thunbergii	LOTUS Database	35616633
Solanum chacoense	LOTUS Database	35616633
Solanum tuberosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal saponins. These are saponins in which the aglycone moiety is a steroid. The steroidal aglycone is usually a spirostane, furostane, spirosolane, solanidane, or curcubitacin derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal saponins

Alternative Parents

Substituents

Steroidal saponin
Diterpene glycoside
Solanidane skeleton
Diterpenoid
Steroidal alkaloid
Terpene glycoside
Delta-5-steroid
Azasteroid
Glycosyl compound
O-glycosyl compound
Disaccharide
Alkaloid or derivatives
Indolizidine
N-alkylpyrrolidine
Oxane
Piperidine
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Acetal
Organoheterocyclic compound
Azacycle
Oxacycle
Polyol
Alcohol
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Amine
Primary alcohol
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	1.51	ChemAxon
pKa (Strongest Acidic)	11.95	ChemAxon
pKa (Strongest Basic)	12.43	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	161.54 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	184.14 m³·mol⁻¹	ChemAxon
Polarizability	80.82 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

10181229

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

119393

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zong JF, Hu Z, Hajiakber A, Lei C, Abulimiti Y, Hou AJ: [Studies on alkaloid constituents of Fritillaria yuminensis]. Zhongguo Zhong Yao Za Zhi. 2019 Feb;44(3):495-499. doi: 10.19540/j.cnki.cjcmm.20181121.005. [PubMed:30989914 ]
Abouzid S, Fawzy N, Darweesh N, Orihara Y: Steroidal glycoalkaloids from the berries of Solanum distichum. Nat Prod Res. 2008 Jan 20;22(2):147-53. doi: 10.1080/14786410701592141. [PubMed:18075898 ]
LOTUS database [Link]

Showing NP-Card for β-chaconine (NP0198597)

MOL for NP0198597 (β-chaconine)

3D MOL for NP0198597 (β-chaconine)

3D SDF for NP0198597 (β-chaconine)

3D-SDF for NP0198597 (β-chaconine)

PDB for NP0198597 (β-chaconine)

3D PDB for NP0198597 (β-chaconine)

SMILES for NP0198597 (β-chaconine)

INCHI for NP0198597 (β-chaconine)

Structure for NP0198597 (β-chaconine)

3D Structure for NP0198597 (β-chaconine)