NP-MRD: Showing NP-Card for 2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione (NP0240733)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 00:37:33 UTC

Updated at

2022-09-07 00:37:33 UTC

NP-MRD ID

NP0240733

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione

Description

2-Hydroxy-4',4',7,7,11',14'-hexamethyl-7H-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]Tetradecane]-10',13'-dione belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position. 2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione is found in Aspergillus duricaulis. Based on a literature review very few articles have been published on 2-hydroxy-4',4',7,7,11',14'-hexamethyl-7H-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]Tetradecane]-10',13'-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202372D          

 35 41  0  0  0  0            999 V2000
   -1.3449   -0.3090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5391   -0.1319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1664    0.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6843    0.5965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2797    1.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1548    0.9831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3648    0.0921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7557   -0.6093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8885   -0.2916    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1150   -0.6585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0184   -1.4778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2224    0.1200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5663    0.8872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8734    1.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4343    2.3514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6965    1.5975    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8982    0.7976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1997    0.3585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2307   -0.4659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9601   -0.8513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6586   -0.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6277    0.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3261    0.8512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0556    0.4658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0866   -0.3586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3976   -1.1227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -0.1849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3881   -0.7976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9026    1.4003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5601    2.1508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1172    2.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5924   -0.0241    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1115   -0.6944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4599    0.7180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9388    1.3898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  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  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 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
 25 28  1  0  0  0  0
 21 28  1  0  0  0  0
 13 29  1  0  0  0  0
  6 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
  7 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
  4 34  1  0  0  0  0
 34 35  2  0  0  0  0
M  END

     RDKit          3D

 68 74  0  0  0  0  0  0  0  0999 V2000
   -6.2731    1.6196   -2.5011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8822    1.1935   -1.1241 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3880   -0.2137   -1.0282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1027   -0.1491   -0.3092 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9425   -0.8309   -1.0587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6926   -0.3328   -0.4083 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5498   -1.2568   -0.3230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8709   -2.6744    0.0260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2914   -1.2979   -1.5850 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3260   -0.6664    0.7536 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5805    0.2668    1.5652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9281    0.1895    0.9817 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6280    1.5324    0.7764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7804    1.2351   -0.0365 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7368    2.0383   -0.6744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7167    3.3001   -0.8834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8929   -0.5997    1.7454 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6595   -1.0916    3.0828 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0968   -0.8189    1.0244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0829   -1.4753    1.3793 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9739   -1.6928    1.5875 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4295   -2.7124    2.3739 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2488   -1.5407    1.5124 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6437   -0.4828    0.6905 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4853    0.0854    0.2008 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6139    1.1721   -0.6526 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8731    1.6351   -0.9736 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0258    1.0453   -0.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9082   -0.0336    0.3806 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1314   -0.6317    0.8966 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3424   -0.1964    0.5960 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4920    0.9559   -0.3085 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2982    0.4916   -1.5083 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2596    2.0986    0.3561 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2874    1.4876   -0.7718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3709    1.7922   -3.1402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7911    2.5971   -2.4235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9847    0.9307   -2.9933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7324    1.3282   -0.4244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1912   -0.5659   -2.0785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1438   -0.8737   -0.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1120   -1.9025   -0.9700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0238   -0.5224   -2.1112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3763    0.5480   -1.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4946   -2.8213    0.9052 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1204   -3.2105    0.1149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3831   -3.2185   -0.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3764   -1.3187   -1.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0996   -0.3925   -2.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0963   -2.2355   -2.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1622    1.2916    1.6003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5556   -0.1294    2.5930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8639    2.0248    1.7189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9413    2.1469    0.1543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6759   -1.3184    3.5266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1330   -2.0626    3.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2006   -0.3433    3.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8407   -3.6242    2.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7386    1.6534   -1.0628 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9636    2.4950   -1.6493 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0581   -1.4837    1.5666 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2421   -0.6644    0.9977 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3745    0.4658   -1.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0428    1.0890   -2.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9840   -0.5515   -1.7084 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3267    2.1114   -0.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8319    3.0840    0.0700 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2149    2.0313    1.4531 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  4  3  1  6
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 12 11  1  1
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 12 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 10 21  1  1
 21 22  1  0
 21 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  1  0
 32 34  1  0
 32 35  1  0
 15  2  1  0
 29 24  1  0
 14  4  1  0
 35 28  1  0
 19  4  1  0
 12  6  1  0
 25 10  1  0
  1 36  1  0
  1 37  1  0
  1 38  1  0
  2 39  1  1
  3 40  1  0
  3 41  1  0
  5 42  1  0
  5 43  1  0
  6 44  1  6
  8 45  1  0
  8 46  1  0
  8 47  1  0
  9 48  1  0
  9 49  1  0
  9 50  1  0
 11 51  1  0
 11 52  1  0
 13 53  1  0
 13 54  1  0
 18 55  1  0
 18 56  1  0
 18 57  1  0
 22 58  1  0
 26 59  1  0
 27 60  1  0
 30 61  1  0
 31 62  1  0
 33 63  1  0
 33 64  1  0
 33 65  1  0
 34 66  1  0
 34 67  1  0
 34 68  1  0
M  END


  Mrv1652309072202372D          

 35 41  0  0  0  0            999 V2000
   -1.3449   -0.3090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5391   -0.1319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1664    0.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6843    0.5965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2797    1.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1548    0.9831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3648    0.0921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7557   -0.6093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8885   -0.2916    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1150   -0.6585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0184   -1.4778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2224    0.1200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5663    0.8872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8734    1.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4343    2.3514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6965    1.5975    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8982    0.7976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1997    0.3585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2307   -0.4659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9601   -0.8513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6586   -0.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6277    0.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3261    0.8512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0556    0.4658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0866   -0.3586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3976   -1.1227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -0.1849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3881   -0.7976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9026    1.4003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5601    2.1508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1172    2.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5924   -0.0241    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1115   -0.6944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4599    0.7180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9388    1.3898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  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  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 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
 25 28  1  0  0  0  0
 21 28  1  0  0  0  0
 13 29  1  0  0  0  0
  6 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
  7 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
  4 34  1  0  0  0  0
 34 35  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0240733

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC23CC4C(C)(C)C5(CC4(CN2C1=O)N(C)C3=O)C(O)=NC1=C5C=CC2=C1C=CC(C)(C)O2

> <INCHI_IDENTIFIER>
InChI=1S/C28H33N3O4/c1-15-11-26-12-19-25(4,5)28(13-27(19,30(6)23(26)34)14-31(26)21(15)32)17-7-8-18-16(20(17)29-22(28)33)9-10-24(2,3)35-18/h7-10,15,19H,11-14H2,1-6H3,(H,29,33)

> <INCHI_KEY>
CCCBJAASKLBNPN-UHFFFAOYSA-N

> <FORMULA>
C28H33N3O4

> <MOLECULAR_WEIGHT>
475.589

> <EXACT_MASS>
475.247106555

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
52.82353679294184

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-hydroxy-4',4',7,7,11',14'-hexamethyl-7H-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecane]-10',13'-dione

> <JCHEM_LOGP>
3.180510829333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.497869436731561

> <JCHEM_PKA_STRONGEST_BASIC>
0.7104412325853736

> <JCHEM_POLAR_SURFACE_AREA>
82.44

> <JCHEM_REFRACTIVITY>
133.44050000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecane]-10',13'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.511  -0.577   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.006  -0.246   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.311   1.156   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.277   1.114   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.389   2.426   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.022   1.835   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.414   0.172   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.277  -1.137   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       1.659  -0.544   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       0.215  -1.229   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.034  -2.759   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.015   0.224   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.657   1.656   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.230   3.085   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.411   4.389   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0       8.767   2.982   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       9.143   1.489   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.839   0.669   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.897  -0.870   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.259  -1.589   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.563  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.505   0.769   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.809   1.589   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.170   0.870   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.228  -0.669   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.809  -2.096   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.734  -0.345   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.924  -1.489   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.418   2.614   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.779   4.015   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.819   4.101   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       2.973  -0.045   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       2.075  -1.296   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.725   1.340   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.619   2.594   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9   34                                             
CONECT    5    4    6                                                       
CONECT    6    5    7   29                                                  
CONECT    7    6    8   12   32                                             
CONECT    8    7    9                                                       
CONECT    9    8    4   10                                                  
CONECT   10    9    2   11                                                  
CONECT   11   10                                                            
CONECT   12    7   13                                                       
CONECT   13   12   14   18   29                                             
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   13   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   28                                                  
CONECT   22   21   17   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   21                                                       
CONECT   29   13    6   30   31                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32    7   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32    4   35                                                  
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₃N₃O₄

Average Mass

475.5890 Da

Monoisotopic Mass

475.24711 Da

IUPAC Name

2-hydroxy-4',4',7,7,11',14'-hexamethyl-7H-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecane]-10',13'-dione

Traditional Name

2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecane]-10',13'-dione

CAS Registry Number

Not Available

SMILES

CC1CC23CC4C(C)(C)C5(CC4(CN2C1=O)N(C)C3=O)C(O)=NC1=C5C=CC2=C1C=CC(C)(C)O2

InChI Identifier

InChI=1S/C28H33N3O4/c1-15-11-26-12-19-25(4,5)28(13-27(19,30(6)23(26)34)14-31(26)21(15)32)17-7-8-18-16(20(17)29-22(28)33)9-10-24(2,3)35-18/h7-10,15,19H,11-14H2,1-6H3,(H,29,33)

InChI Key

CCCBJAASKLBNPN-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

Species Name	Source	Reference
Aspergillus duricaulis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
3-alkylindole
Azaspirodecane
Alpha-amino acid or derivatives
Indolizidine
Indole or derivatives
N-alkylpiperazine
N-methylpiperazine
Piperidinone
Delta-lactam
Alkyl aryl ether
Benzenoid
N-alkylpyrrolidine
2-pyrrolidone
Pyrrolidone
Piperidine
Piperazine
1,4-diazinane
Cyclic carboximidic acid
Tertiary carboxylic acid amide
Pyrrolidine
Lactam
Carboxamide group
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	3.18	ChemAxon
pKa (Strongest Acidic)	4.5	ChemAxon
pKa (Strongest Basic)	0.71	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.44 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	133.44 m³·mol⁻¹	ChemAxon
Polarizability	52.82 Å³	ChemAxon
Number of Rings	7	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

163063859

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione (NP0240733)

MOL for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)

3D MOL for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)

3D SDF for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)

3D-SDF for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)

PDB for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)

3D PDB for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)

SMILES for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)

INCHI for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)

Structure for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)

3D Structure for NP0240733 (2-hydroxy-4',4',7,7,11',14'-hexamethyl-9',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-10',13'-dione)