NP-MRD: Showing NP-Card for Dihydrosolanidine (NP0069802)

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Record Information

Version

2.0

Created at

2022-04-28 15:08:18 UTC

Updated at

2022-04-28 15:08:18 UTC

NP-MRD ID

NP0069802

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Dihydrosolanidine

Description

Demissidine belongs to the class of organic compounds known as solanidines and derivatives. These are steroids with a structure based on the solanidane skeleton. Solanidane arises from the conversion of a cholestane side-chain into a bicyclic system. Thus, demissidine is considered to be a sterol lipid molecule. Dihydrosolanidine is found in Solanum demissum and Solanum tuberosum. Demissidine is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

Demissidine
  Mrv1572004231619372D          

 29 34  0  0  1  0            999 V2000
    9.3080   -1.3550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5766   -2.1350    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.3655   -2.3762    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0727   -1.9513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7943   -2.3513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8086   -3.1762    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.5302   -3.5761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1015   -3.6011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3799   -3.2012    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.5999   -3.4697    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1266   -4.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3377   -3.9043    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6306   -4.3292    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6449   -5.1541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9378   -5.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2163   -5.1790    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5090   -5.6040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -5.2040    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0804   -5.6289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7731   -4.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4803   -3.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2018   -4.3542    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1874   -3.5293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9090   -3.9293    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8946   -3.1043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6017   -2.6794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3233   -3.0795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3953   -2.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1034   -2.8108    0.0000 C   0  0  1  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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  1  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 13 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 12 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  2 29  1  0  0  0  0
 29 10  1  1  0  0  0
M  END

     RDKit          3D

 74 79  0  0  0  0  0  0  0  0999 V2000
    5.7341    2.2983    1.3477 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1136    1.8959    0.0483 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7519    0.6950   -0.5869 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4794   -0.5902    0.1064 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1864   -0.7055    0.8011 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1125   -1.4310   -0.0220 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4610   -2.8751   -0.2212 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9195   -1.2365    0.8550 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2113    0.1151    1.5155 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1230    1.0415    0.9522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0009    0.0852    0.8484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2354    0.5482    0.1878 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7535    1.8039    0.7584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1949    2.0481    0.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0946    0.8988    0.4376 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3416    1.3980   -0.2515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2966    0.3679   -0.6753 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.9766    0.8374   -1.8229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7860   -0.9955   -0.9363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4520   -1.3277   -0.3859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4704   -0.1801   -0.4003 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2591    0.2371   -1.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2264   -0.6111    0.2862 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6712   -1.8902   -0.2260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3229   -2.2445    0.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6241   -1.1011    0.1504 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8443   -0.8605   -1.3207 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5232    0.5027    1.1407 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6236    1.5635    0.2013 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4080    1.6825    2.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8373    2.1541    1.2535 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5943    3.3910    1.5166 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1950    2.7376   -0.6585 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5117    0.6756   -1.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8667    0.8689   -0.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2955   -0.8657    0.8340 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5332   -1.4073   -0.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2745   -1.3191    1.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0678   -0.8791   -0.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4911   -3.0474    0.1687 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3646   -3.2071   -1.2753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7519   -3.4946    0.3966 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9216   -2.0499    1.6192 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0617    0.0245    2.6008 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9448    1.8196    1.7306 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3946    1.4664   -0.0100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2594   -0.2628    1.8791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0358    0.6803   -0.9067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3954    1.8654    1.8304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1971    2.6555    0.2614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5531    2.5058    1.7025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4244    2.8567   -0.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4326    0.4101    1.3781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9779    2.0092   -1.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7907    2.1533    0.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1110    0.2913    0.0988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4806    1.5812   -2.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7563   -1.1950   -2.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5046   -1.7804   -0.5517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0515   -2.2191   -0.9397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5521   -1.6559    0.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4140   -0.2970   -2.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1282    1.3525   -1.9152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1577    0.0104   -2.4431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4426   -0.7288    1.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7344   -1.9625   -1.3515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3749   -2.7048    0.1209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4419   -2.4893    1.3872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0245   -3.1673   -0.1824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1152   -0.8485   -1.8911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3824   -1.7716   -1.7018 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3574    0.0748   -1.5525 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2634    1.3315   -0.8159 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1634    2.4676    0.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  2 29  1  0
 29 28  1  0
 28  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  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
 26  8  1  0
  8  6  1  0
 28  5  1  0
  8  9  1  0
 26 11  1  0
 23 12  1  0
 21 15  1  0
  7 40  1  0
  7 41  1  0
  7 42  1  0
  6 39  1  6
  5 38  1  1
  4 36  1  0
  4 37  1  0
  3 34  1  0
  3 35  1  0
  2 33  1  6
  1 30  1  0
  1 31  1  0
  1 32  1  0
 29 73  1  0
 29 74  1  0
  9 44  1  1
 10 45  1  0
 10 46  1  0
 11 47  1  1
 12 48  1  6
 13 49  1  0
 13 50  1  0
 14 51  1  0
 14 52  1  0
 15 53  1  1
 16 54  1  0
 16 55  1  0
 17 56  1  1
 18 57  1  0
 19 58  1  0
 19 59  1  0
 20 60  1  0
 20 61  1  0
 22 62  1  0
 22 63  1  0
 22 64  1  0
 23 65  1  1
 24 66  1  0
 24 67  1  0
 25 68  1  0
 25 69  1  0
 27 70  1  0
 27 71  1  0
 27 72  1  0
  8 43  1  1
M  END

Demissidine
  Mrv1572004231619372D          

 29 34  0  0  1  0            999 V2000
    9.3080   -1.3550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5766   -2.1350    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.3655   -2.3762    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0727   -1.9513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7943   -2.3513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8086   -3.1762    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.5302   -3.5761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1015   -3.6011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3799   -3.2012    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.5999   -3.4697    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1266   -4.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3377   -3.9043    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6306   -4.3292    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6449   -5.1541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9378   -5.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2163   -5.1790    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5090   -5.6040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -5.2040    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0804   -5.6289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7731   -4.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4803   -3.9542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2018   -4.3542    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1874   -3.5293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9090   -3.9293    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8946   -3.1043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6017   -2.6794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3233   -3.0795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3953   -2.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1034   -2.8108    0.0000 C   0  0  1  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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  1  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 13 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 12 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  2 29  1  0  0  0  0
 29 10  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0069802

> <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[C@H]5C[C@@H](O)CC[C@]5(C)[C@H]4CC[C@]3(C)[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C27H45NO/c1-16-5-8-23-17(2)25-24(28(23)15-16)14-22-20-7-6-18-13-19(29)9-11-26(18,3)21(20)10-12-27(22,25)4/h16-25,29H,5-15H2,1-4H3/t16-,17+,18-,19-,20+,21-,22-,23+,24-,25-,26-,27-/m0/s1

> <INCHI_KEY>
JALVTHFTYRPDMB-HRRTYWNUSA-N

> <FORMULA>
C27H45NO

> <MOLECULAR_WEIGHT>
399.663

> <EXACT_MASS>
399.350115073

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
50.853215016475986

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5S,7S,10S,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²³.0¹⁷,²²]tetracosan-7-ol

> <ALOGPS_LOGP>
5.02

> <JCHEM_LOGP>
5.288114703000001

> <ALOGPS_LOGS>
-6.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.296396321121705

> <JCHEM_PKA_STRONGEST_BASIC>
12.437052139202105

> <JCHEM_POLAR_SURFACE_AREA>
23.47

> <JCHEM_REFRACTIVITY>
120.00739999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.21e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
demissidine

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 23-APR-16   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: Demissidine                                       
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-16         0                                  
HETATM    1  C   UNK     0      17.375  -2.529   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.876  -3.985   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      19.349  -4.436   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.669  -3.642   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      22.016  -4.389   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.043  -5.929   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.390  -6.675   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      20.723  -6.722   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      19.376  -5.976   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      17.920  -6.477   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.036  -7.738   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.564  -7.288   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.244  -8.081   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.270  -9.621   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.951 -10.414   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.604  -9.667   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.283 -10.461   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.937  -9.714   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.617 -10.507   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.910  -8.174   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.230  -7.381   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.577  -8.128   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.550  -6.588   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.897  -7.335   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.870  -5.795   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.190  -5.002   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.537  -5.748   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      15.671  -4.214   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      16.993  -5.247   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8    3   10                                                  
CONECT   10    9   11   29                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   27                                                  
CONECT   13   12   14   24                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   16   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   13   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   12   28   29                                             
CONECT   28   27                                                            
CONECT   29   27    2   10                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₄₅NO

Average Mass

399.6630 Da

Monoisotopic Mass

399.35012 Da

IUPAC Name

(1S,2R,5S,7S,10S,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²³.0¹⁷,²²]tetracosan-7-ol

Traditional Name

demissidine

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[C@H]5C[C@@H](O)CC[C@]5(C)[C@H]4CC[C@]3(C)[C@@H]12

InChI Identifier

InChI=1S/C27H45NO/c1-16-5-8-23-17(2)25-24(28(23)15-16)14-22-20-7-6-18-13-19(29)9-11-26(18,3)21(20)10-12-27(22,25)4/h16-25,29H,5-15H2,1-4H3/t16-,17+,18-,19-,20+,21-,22-,23+,24-,25-,26-,27-/m0/s1

InChI Key

JALVTHFTYRPDMB-HRRTYWNUSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Solanum demissum	LOTUS Database	35616633
Solanum tuberosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as solanidines and derivatives. These are steroids with a structure based on the solanidane skeleton. Solanidane arises from the conversion of a cholestane side-chain into a bicyclic system.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal alkaloids

Direct Parent

Solanidines and derivatives

Alternative Parents

Substituents

Solanidane skeleton
3-hydroxysteroid
Hydroxysteroid
3-beta-hydroxysteroid
Azasteroid
Indolizidine
Alkaloid or derivatives
Piperidine
N-alkylpyrrolidine
Cyclic alcohol
Pyrrolidine
Tertiary aliphatic amine
Secondary alcohol
Tertiary amine
Organoheterocyclic compound
Azacycle
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Amine
Organic nitrogen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Solanidines and alkaloid derivatives (LMST01150001 )

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	5.02	ALOGPS
logP	5.29	ChemAxon
logS	-6.3	ALOGPS
pKa (Strongest Acidic)	18.3	ChemAxon
pKa (Strongest Basic)	12.44	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	23.47 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	120.01 m³·mol⁻¹	ChemAxon
Polarizability	50.85 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

101379

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Dihydrosolanidine (NP0069802)

MOL for NP0069802 (Dihydrosolanidine)

3D MOL for NP0069802 (Dihydrosolanidine)

3D SDF for NP0069802 (Dihydrosolanidine)

3D-SDF for NP0069802 (Dihydrosolanidine)

PDB for NP0069802 (Dihydrosolanidine)

3D PDB for NP0069802 (Dihydrosolanidine)

SMILES for NP0069802 (Dihydrosolanidine)

INCHI for NP0069802 (Dihydrosolanidine)

Structure for NP0069802 (Dihydrosolanidine)

3D Structure for NP0069802 (Dihydrosolanidine)