NP-MRD: Showing NP-Card for 16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one (NP0154349)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 11:08:27 UTC

Updated at

2022-09-02 11:08:28 UTC

NP-MRD ID

NP0154349

Secondary Accession Numbers

None

Natural Product Identification

Common Name

16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one

Description

16-Benzyl-5,18-dihydroxy-9,14,15-trimethyl-2H,5H,6H,7H,8H,9H,10H,15H,15aH,16H,18bH-oxacyclotetradeca[3,2-e]isoindol-2-one belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone. 16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one is found in Boeremia exigua. 16-Benzyl-5,18-dihydroxy-9,14,15-trimethyl-2H,5H,6H,7H,8H,9H,10H,15H,15aH,16H,18bH-oxacyclotetradeca[3,2-e]isoindol-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171517392D          

 34 37  0  0  0  0            999 V2000
    6.6427   -0.4406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6033   -0.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3917   -0.6660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5757   -1.4703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9712   -2.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1828   -1.7889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7937   -1.4254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5783   -2.3504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9139   -1.9100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7299   -1.1057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6626   -1.0028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9414   -0.8630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6334   -0.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2379    0.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1504    0.2599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6308    0.6237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4193    0.3810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9581   -0.0464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2103   -0.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2184   -0.9842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5376   -1.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7104   -2.4195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7491   -1.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1094   -1.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9878   -2.3522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2403   -2.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0914   -3.4299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3143   -3.7067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6860   -3.1720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8348   -2.3606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6120   -2.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4878   -0.9416    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8117   -0.1828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3622    0.5447    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
  8  6  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  2 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  0  0  0  0
 13 33  1  0  0  0  0
 33 34  2  0  0  0  0
M  END

     RDKit          3D

 71 74  0  0  0  0  0  0  0  0999 V2000
    1.5267   -3.1838   -2.3742 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2211   -2.3275   -1.2117 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0093   -2.3433   -0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1519   -1.4319    0.4720 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3460   -1.5592    1.2702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5939   -1.8639    0.9727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1722   -2.1819   -0.3451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6611   -1.7707   -0.2936 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4054   -2.4380    0.8056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8386   -0.2969   -0.4093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6179    0.5002    0.8267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2658    1.1876    0.8526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3647    2.6833    0.6895 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4977    2.8834   -0.1367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1853    3.3307    0.1337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9066    3.1010    0.3658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2762    2.1462    1.2302 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2438    2.6259    2.3284 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1083    0.8003    1.1237 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3173   -0.0379    0.1357 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0160    0.4777   -1.1816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9248    0.1732   -1.9848 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0005    1.4906   -1.3819 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2399    0.9965   -0.8181 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0155    2.0606   -0.1059 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3216    1.5953    0.4617 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4235    1.1705    1.7618 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6404    0.7458    2.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7882    0.7247    1.4866 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6362    1.1624    0.1840 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4456    1.5893   -0.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8422   -0.1786   -0.0150 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2574   -1.4633   -0.6354 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3739   -1.3915   -1.6425 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8552   -2.5348   -3.2383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847   -3.6444   -2.7293 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3039   -3.9459   -2.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7889   -2.9494   -1.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6949   -1.8006    1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1886   -1.3491    2.3726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3565   -1.9090    1.8002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7050   -1.6568   -1.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1080   -3.2696   -0.5883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0615   -2.2161   -1.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4584   -2.5970    0.4650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3879   -1.9641    1.7831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9888   -3.4856    0.8861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8310   -0.0444   -0.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0963    0.0908   -1.1711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3701    1.3457    0.8174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8276   -0.0215    1.7812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7685    0.9003    1.8003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6168    0.8403    0.0262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6836    3.0763    1.6799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2511    3.2168   -1.0195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4140    4.1417   -0.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1797    3.7675   -0.1838 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8842    2.4035   -1.8459 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9427    0.6974   -1.6753 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2702    2.8726   -0.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4775    2.4846    0.7665 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5763    1.1640    2.4494 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7351    0.4028    3.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7481    0.3897    1.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5261    1.1611   -0.4557 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3495    1.9337   -1.3752 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3010   -0.0870    0.9892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7000   -2.0936    0.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8073   -2.4312   -1.7905 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1183   -1.0545   -2.6351 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2366   -0.8104   -1.2738 H   0  0  0  0  0  0  0  0  0  0  0  0
 34 33  1  0
 33 32  1  0
 32 24  1  0
 24 25  1  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
 24 23  1  0
 23 21  1  0
 21 22  2  0
 21 20  1  0
 20 19  1  1
 19 17  1  0
 17 18  2  0
 17 16  1  0
 16 15  2  0
 15 13  1  0
 13 14  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  1  0
  8  7  1  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 33  1  0
 20 32  1  0
  4 20  1  0
 31 26  1  0
 34 69  1  0
 34 70  1  0
 34 71  1  0
 33 68  1  1
 32 67  1  1
 24 59  1  6
 25 60  1  0
 25 61  1  0
 27 62  1  0
 28 63  1  0
 29 64  1  0
 30 65  1  0
 31 66  1  0
 23 58  1  0
 16 57  1  0
 15 56  1  0
 13 54  1  1
 14 55  1  0
 12 52  1  0
 12 53  1  0
 11 50  1  0
 11 51  1  0
 10 48  1  0
 10 49  1  0
  8 44  1  6
  9 45  1  0
  9 46  1  0
  9 47  1  0
  7 42  1  0
  7 43  1  0
  6 41  1  0
  5 40  1  0
  4 39  1  1
  3 38  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
M  END


  Mrv1533004171517392D          

 34 37  0  0  0  0            999 V2000
    6.6427   -0.4406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6033   -0.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3917   -0.6660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5757   -1.4703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9712   -2.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1828   -1.7889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7937   -1.4254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5783   -2.3504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9139   -1.9100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7299   -1.1057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6626   -1.0028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9414   -0.8630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6334   -0.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2379    0.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1504    0.2599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6308    0.6237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4193    0.3810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9581   -0.0464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2103   -0.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2184   -0.9842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5376   -1.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7104   -2.4195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7491   -1.1693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1094   -1.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9878   -2.3522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2403   -2.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0914   -3.4299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3143   -3.7067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6860   -3.1720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8348   -2.3606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6120   -2.0838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4878   -0.9416    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8117   -0.1828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3622    0.5447    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
  8  6  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  4  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  2 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  0  0  0  0
 13 33  1  0  0  0  0
 33 34  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0154349

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CC3=CC=CC=C3)NC(=O)C22OC(=O)C=CC(O)CCCC(C)CC=CC2C=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C29H37NO4/c1-19-9-7-13-23-17-20(2)21(3)27-25(18-22-11-5-4-6-12-22)30-28(33)29(23,27)34-26(32)16-15-24(31)14-8-10-19/h4-7,11-13,15-17,19,21,23-25,27,31H,8-10,14,18H2,1-3H3,(H,30,33)

> <INCHI_KEY>
ILLALIWIXIHHKP-UHFFFAOYSA-N

> <FORMULA>
C29H37NO4

> <MOLECULAR_WEIGHT>
463.618

> <EXACT_MASS>
463.272258675

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
52.43674450400995

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
16-benzyl-5-hydroxy-9,14,15-trimethyl-2H,5H,6H,7H,8H,9H,10H,15H,15aH,16H,17H,18H,18bH-oxacyclotetradeca[3,2-e]isoindole-2,18-dione

> <ALOGPS_LOGP>
4.55

> <JCHEM_LOGP>
5.213677513

> <ALOGPS_LOGS>
-5.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.844197689514186

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.21477938155552

> <JCHEM_PKA_STRONGEST_BASIC>
-2.871612284856008

> <JCHEM_POLAR_SURFACE_AREA>
75.63

> <JCHEM_REFRACTIVITY>
136.07280000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.39e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
16-benzyl-5-hydroxy-9,14,15-trimethyl-5H,6H,7H,8H,9H,10H,15H,15aH,16H,17H,18bH-oxacyclotetradeca[3,2-e]isoindole-2,18-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      12.400  -0.822   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.193  -0.790   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.665  -1.243   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.008  -2.744   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.880  -3.793   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.408  -3.339   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      12.682  -2.661   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      12.279  -4.387   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.039  -3.565   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.696  -2.064   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.437  -1.872   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       9.224  -1.611   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.649  -0.479   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.777   0.569   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.481   0.485   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.378   1.164   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.849   0.711   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.122  -0.087   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.593  -1.385   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.474  -1.837   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.337  -2.636   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.659  -4.516   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.865  -2.183   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.671  -2.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.444  -4.391   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.049  -4.888   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.771  -6.402   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.320  -6.919   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.147  -5.921   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.425  -4.406   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.876  -3.890   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       6.511  -1.758   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       7.115  -0.341   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       6.276   1.017   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   17                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   23   33                                             
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    2                                                       
CONECT   18   14   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   13   24                                                  
CONECT   24   23   25   32                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26                                                       
CONECT   32   24   33                                                       
CONECT   33   32   13   34                                                  
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₃₇NO₄

Average Mass

463.6180 Da

Monoisotopic Mass

463.27226 Da

IUPAC Name

16-benzyl-5-hydroxy-9,14,15-trimethyl-2H,5H,6H,7H,8H,9H,10H,15H,15aH,16H,17H,18H,18bH-oxacyclotetradeca[3,2-e]isoindole-2,18-dione

Traditional Name

16-benzyl-5-hydroxy-9,14,15-trimethyl-5H,6H,7H,8H,9H,10H,15H,15aH,16H,17H,18bH-oxacyclotetradeca[3,2-e]isoindole-2,18-dione

CAS Registry Number

Not Available

SMILES

CC1C2C(CC3=CC=CC=C3)NC(=O)C22OC(=O)C=CC(O)CCCC(C)CC=CC2C=C1C

InChI Identifier

InChI=1S/C29H37NO4/c1-19-9-7-13-23-17-20(2)21(3)27-25(18-22-11-5-4-6-12-22)30-28(33)29(23,27)34-26(32)16-15-24(31)14-8-10-19/h4-7,11-13,15-17,19,21,23-25,27,31H,8-10,14,18H2,1-3H3,(H,30,33)

InChI Key

ILLALIWIXIHHKP-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
Phoma exigua	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Isoindolines

Direct Parent

Isoindolones

Alternative Parents

Substituents

Isoindolone
Isoindole
Monocyclic benzene moiety
Benzenoid
Pyrroline
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Cyclic carboximidic acid
Carboxylic acid ester
Lactone
Secondary alcohol
Oxacycle
Azacycle
Carboxylic acid derivative
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Carbonyl group
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Alcohol
Organic oxide
Organic nitrogen compound
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	4.55	ALOGPS
logP	5.21	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	13.21	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.63 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	136.07 m³·mol⁻¹	ChemAxon
Polarizability	52.44 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one (NP0154349)

MOL for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)

3D MOL for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)

3D SDF for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)

3D-SDF for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)

PDB for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)

3D PDB for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)

SMILES for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)

INCHI for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)

Structure for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)

3D Structure for NP0154349 (16-benzyl-5,18-dihydroxy-9,14,15-trimethyl-5h,6h,7h,8h,9h,10h,12ah,15h,15ah,16h-oxacyclotetradeca[3,2-d]isoindol-2-one)