NP-MRD: Showing NP-Card for 5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol (NP0230589)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 11:05:06 UTC

Updated at

2022-09-06 11:05:07 UTC

NP-MRD ID

NP0230589

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol

Description

5-Benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]Nonadeca-6,12-diene-7,9-diol belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom. Based on a literature review very few articles have been published on 5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]Nonadeca-6,12-diene-7,9-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062213052D          

 32 37  0  0  0  0            999 V2000
    3.9254    2.3084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9979    1.4464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7461    1.0988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4221    1.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8191    0.2770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4787   -0.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2861    0.0541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8714   -0.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6695   -0.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2495   -0.9162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0312   -1.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2331   -1.9206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6532   -1.3338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2111   -0.9990    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3862   -0.9857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0416   -1.8671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1440   -0.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9559   -1.1640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6705   -1.8209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1969   -1.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4886   -0.9844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7616   -1.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6501   -2.2367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0034   -1.0494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7848   -0.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0575   -0.0794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2705    0.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0947    0.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5187    1.1568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3228    0.9723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958    0.1505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6368   -0.1728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  0  0  0  0
 17 31  1  0  0  0  0
 31 32  1  0  0  0  0
 28 32  1  0  0  0  0
 21 32  1  0  0  0  0
M  END

     RDKit          3D

 67 72  0  0  0  0  0  0  0  0999 V2000
    0.2423    3.3176    1.6702 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3623    2.2279    0.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5599    1.3298    1.0146 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8195    1.0928    2.4421 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4925    0.1790    0.0842 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3967   -0.9368    0.3407 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7874   -0.7929    0.7800 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7395   -0.0886   -0.0520 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0733    1.2243    0.1433 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9693    1.8974   -0.6635 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    1.2513   -1.7162 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2540   -0.0727   -1.9373 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3537   -0.7317   -1.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6387   -1.7088    1.3172 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3728   -1.4997    1.1814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5405   -2.1354    2.0167 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1580   -0.5529    0.0731 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1170   -1.3903   -1.1181 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6639   -2.5820   -1.1427 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5149   -1.9748   -1.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6345   -0.9252   -1.0200 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7113   -1.4168   -0.1748 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6696   -2.9169    0.1162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7936   -0.9191    0.4525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1367    0.5806    0.3667 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.5366    0.9336    1.8133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0084    1.2575   -0.1773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7441    1.6249   -0.6866 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8930    2.4047    0.1251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6481    1.8534   -0.0081 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9820    0.3838    0.2478 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9329    0.3205   -0.9348 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0524    3.5425    2.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5970    3.9817    1.6353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3754    2.0081    0.6056 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7748    0.0810    2.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1300    1.6751    3.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8354    1.4908    2.7448 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6196    0.5742   -0.9545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4794   -1.5048   -0.6462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8892   -0.4725    1.8675 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2022   -1.8539    0.8621 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6574    1.8023    0.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    2.9338   -0.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2780    1.7863   -2.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7447   -0.5565   -2.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1148   -1.7582   -1.2985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5365   -3.1447    2.0627 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0699   -0.9142   -2.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2764   -3.2326   -1.7576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5517   -2.4566   -0.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6577   -2.7295   -1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0485   -1.0128   -2.0830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1801   -3.4669   -0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6753   -3.3232    0.2028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1609   -3.0796    1.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4384   -1.5339    1.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0913    0.7285   -0.1803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5862    0.8667    2.4160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1865    0.1266    2.1490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0069    1.9154    1.8685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4271    0.8111    0.7131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1337    0.5835   -1.1085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8001    2.2414   -1.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2471    1.8952   -1.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5416    0.2545    1.1833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4113    0.5067   -1.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  6 14  1  0
 14 15  2  0
 15 16  1  0
 17 15  1  1
 17 31  1  0
 31 30  1  0
 30 29  1  0
 29 28  1  0
 28 27  1  0
 27 25  1  0
 25 26  1  0
 25 24  1  0
 24 22  2  0
 22 23  1  0
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  1  0
 21 32  1  0
 30  2  1  0
  2  1  2  3
  2  3  1  0
 17  5  1  0
 18 17  1  0
 13  8  1  0
 32 31  1  0
 32 28  1  0
  4 36  1  0
  4 37  1  0
  4 38  1  0
  3 35  1  6
  5 39  1  6
  6 40  1  6
  7 41  1  0
  7 42  1  0
  9 43  1  0
 10 44  1  0
 11 45  1  0
 12 46  1  0
 13 47  1  0
 16 48  1  0
 31 66  1  1
 30 65  1  6
 28 64  1  6
 27 62  1  0
 27 63  1  0
 25 58  1  6
 26 59  1  0
 26 60  1  0
 26 61  1  0
 24 57  1  0
 23 54  1  0
 23 55  1  0
 23 56  1  0
 21 53  1  6
 20 51  1  0
 20 52  1  0
 18 49  1  6
 19 50  1  0
 32 67  1  6
  1 33  1  0
  1 34  1  0
M  END


  Mrv1652309062213052D          

 32 37  0  0  0  0            999 V2000
    3.9254    2.3084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9979    1.4464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7461    1.0988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4221    1.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8191    0.2770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4787   -0.2186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2861    0.0541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8714   -0.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6695   -0.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2495   -0.9162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0312   -1.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2331   -1.9206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6532   -1.3338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2111   -0.9990    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3862   -0.9857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0416   -1.8671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1440   -0.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9559   -1.1640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6705   -1.8209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1969   -1.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4886   -0.9844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7616   -1.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6501   -2.2367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0034   -1.0494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7848   -0.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0575   -0.0794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2705    0.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0947    0.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5187    1.1568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3228    0.9723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958    0.1505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6368   -0.1728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  0  0  0  0
 17 31  1  0  0  0  0
 31 32  1  0  0  0  0
 28 32  1  0  0  0  0
 21 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0230589

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CC3=CC=CC=C3)N=C(O)C22C3C(OC4CC(C)C=C(C)C(CC2O)C34)C1=C

> <INCHI_IDENTIFIER>
InChI=1S/C28H35NO3/c1-14-10-15(2)19-13-22(30)28-24(20(29-27(28)31)12-18-8-6-5-7-9-18)16(3)17(4)26-25(28)23(19)21(11-14)32-26/h5-10,14,16,19-26,30H,4,11-13H2,1-3H3,(H,29,31)

> <INCHI_KEY>
WSPVFJOMQYINNH-UHFFFAOYSA-N

> <FORMULA>
C28H35NO3

> <MOLECULAR_WEIGHT>
433.592

> <EXACT_MASS>
433.261693991

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
50.105101767915734

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0^{4,8}.0^{8,18}.0^{11,17}]nonadeca-6,12-diene-7,9-diol

> <JCHEM_LOGP>
3.4236511030422223

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.671520199381085

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.441712005654768

> <JCHEM_PKA_STRONGEST_BASIC>
5.764434286284941

> <JCHEM_POLAR_SURFACE_AREA>
62.05000000000001

> <JCHEM_REFRACTIVITY>
125.66900000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0^{4,8}.0^{8,18}.0^{11,17}]nonadeca-6,12-diene-7,9-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       7.327   4.309   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.463   2.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.859   2.051   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.121   3.053   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.996   0.517   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.227  -0.408   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.734   0.101   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.827  -1.005   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.316  -0.615   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.399  -1.710   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.992  -3.195   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.502  -3.585   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.419  -2.490   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       9.727  -1.865   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       8.188  -1.840   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.544  -3.485   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.735  -0.368   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.384  -2.173   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.718  -3.399   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.968  -2.777   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.645  -1.838   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.288  -2.566   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.080  -4.175   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.873  -1.959   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.465  -0.474   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.107  -0.148   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.372   0.771   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.910   0.838   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.702   2.159   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.203   1.815   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.339   0.281   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.922  -0.323   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   17                                                  
CONECT    6    5    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14    6   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    5   18   31                                             
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   32                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29    2   31                                                  
CONECT   31   30   17   32                                                  
CONECT   32   31   28   21                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₅NO₃

Average Mass

433.5920 Da

Monoisotopic Mass

433.26169 Da

IUPAC Name

5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0^{4,8}.0^{8,18}.0^{11,17}]nonadeca-6,12-diene-7,9-diol

Traditional Name

5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0^{4,8}.0^{8,18}.0^{11,17}]nonadeca-6,12-diene-7,9-diol

CAS Registry Number

Not Available

SMILES

CC1C2C(CC3=CC=CC=C3)N=C(O)C22C3C(OC4CC(C)C=C(C)C(CC2O)C34)C1=C

InChI Identifier

InChI=1S/C28H35NO3/c1-14-10-15(2)19-13-22(30)28-24(20(29-27(28)31)12-18-8-6-5-7-9-18)16(3)17(4)26-25(28)23(19)21(11-14)32-26/h5-10,14,16,19-26,30H,4,11-13H2,1-3H3,(H,29,31)

InChI Key

WSPVFJOMQYINNH-UHFFFAOYSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azaspirodecane derivatives

Sub Class

Not Available

Direct Parent

Azaspirodecane derivatives

Alternative Parents

Substituents

Isoindolone
Azaspirodecane
Isoindole or derivatives
Isoindoline
Benzenoid
2-pyrrolidone
Pyrrolidone
Monocyclic benzene moiety
Tetrahydrofuran
Pyrrolidine
Cyclic alcohol
Secondary carboxylic acid amide
Secondary alcohol
Lactam
Carboxamide group
Oxacycle
Azacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.42	ChemAxon
pKa (Strongest Acidic)	3.44	ChemAxon
pKa (Strongest Basic)	5.76	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.05 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	125.67 m³·mol⁻¹	ChemAxon
Polarizability	50.11 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

162814733

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol (NP0230589)

MOL for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)

3D MOL for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)

3D SDF for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)

3D-SDF for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)

PDB for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)

3D PDB for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)

SMILES for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)

INCHI for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)

Structure for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)

3D Structure for NP0230589 (5-benzyl-3,12,14-trimethyl-2-methylidene-19-oxa-6-azapentacyclo[14.2.1.0⁴,⁸.0⁸,¹⁸.0¹¹,¹⁷]nonadeca-6,12-diene-7,9-diol)