NP-MRD: Showing NP-Card for 21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one (NP0154348)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 11:08:24 UTC

Updated at

2022-09-02 11:08:24 UTC

NP-MRD ID

NP0154348

Secondary Accession Numbers

None

Natural Product Identification

Common Name

21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one

Description

21-Hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]Tetracosa-4,16,18,23-tetraen-15-one belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position. 21-Hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]Tetracosa-4,16,18,23-tetraen-15-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241510202D          

 42 46  0  0  0  0            999 V2000
   -0.0267   -5.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6027   -5.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4556   -4.2381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0850   -3.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9379   -2.8930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5673   -2.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4202   -1.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6345   -1.2552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4386   -0.4240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3029    0.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2832    0.8984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0051    1.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4433    1.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9967    2.0485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5492    2.7416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8240    2.2736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5858    1.9062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9087    1.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1587    1.9164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6074    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4246    1.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8103    2.1853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9780    0.8441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2987    1.6043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0087    0.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8331    0.0504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8025    0.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9651    1.6836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5970    1.0971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5023   -0.6316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6957   -0.8049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664   -0.4193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3545   -0.9727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5279   -1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6556    0.3450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9381   -0.1542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0526   -0.9986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1221    0.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8263    0.7647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5610    1.1402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9410   -1.3302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5554   -2.0595    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
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 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
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  4  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  1  0  0  0  0
 18 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
  7 37  1  0  0  0  0
 36 38  1  0  0  0  0
  9 38  1  0  0  0  0
 38 39  2  0  0  0  0
 13 39  1  0  0  0  0
 39 40  1  0  0  0  0
 30 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END

     RDKit          2D

 90 94  0  0  0  0  0  0  0  0999 V2000
    6.2573   -4.7857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8084   -5.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3595   -5.5622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9107   -5.9504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4618   -6.3386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9871   -6.7269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4360   -7.1151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6647   -7.9755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0242   -7.3415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0375   -7.1654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0981   -6.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5470   -6.4930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7099   -4.6558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6492   -5.7165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2832   -7.0760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1549   -5.8472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9262   -4.9869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5667   -5.6208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5380   -3.5380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1785   -4.1719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1757   -5.2924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6447   -4.9891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7296   -3.7837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1307   -2.5550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5796   -2.9432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0285   -3.3314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0607    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0607    2.1213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0607    2.1213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0607    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5737    1.4095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5550    0.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0011    1.5248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7837   -0.7296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1719   -2.1785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8058   -0.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5314   -1.5446    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9803   -1.9328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8406   -3.1615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2895   -2.7733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7062   -4.3975    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8691   -3.3368    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6455   -6.2346    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4202   -3.7251    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1967   -6.6228    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5165   -4.0704    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7478   -7.0111    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3487   -4.5596    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2989   -7.3993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2530   -4.8532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8500   -7.7875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1958   -5.2415    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5989   -8.1757    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8021   -8.4746    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6041   -9.0361    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5251   -9.2042    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2462   -8.6508    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6077   -5.4323    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0781   -8.3480    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7811   -7.1546    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9237   -7.7099    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4299   -4.8824    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7431   -4.8100    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2413   -5.3431    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1137   -4.6858    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2945   -6.3411    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3414   -3.5201    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2741   -4.8984    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0177   -4.3339    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069   -1.6313    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9103   -4.5449    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4095   -1.5737    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2427    0.9235    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3465   -0.7725    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1213    3.1820    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1372    3.3034    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4952    1.6829    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1213    3.1820    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1372    3.3034    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2427    1.1979    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0509    1.6700    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6094    1.1976    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9315    2.7014    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4255    0.6261    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1280   -0.0641    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4398    0.5404    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2783   -1.1052    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6402    0.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 29 31  1  0
 29 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  2  0
 18  7  1  0
 37 19  1  0
 16  9  1  0
 32 27  1  0
 41 13  1  0
  1 43  1  0
  1 44  1  0
  1 45  1  0
  2 46  1  0
  2 47  1  0
  3 48  1  0
  3 49  1  0
  4 50  1  0
  4 51  1  0
  5 52  1  0
  5 53  1  0
  6 54  1  0
  6 55  1  0
  7 56  1  0
  8 57  1  0
  8 58  1  0
 10 59  1  0
 12 60  1  0
 15 61  1  0
 15 62  1  0
 15 63  1  0
 17 64  1  0
 19 65  1  0
 20 66  1  0
 22 67  1  0
 22 68  1  0
 22 69  1  0
 23 70  1  0
 25 71  1  0
 25 72  1  0
 26 73  1  0
 27 74  1  0
 28 75  1  0
 28 76  1  0
 30 77  1  0
 30 78  1  0
 30 79  1  0
 31 80  1  0
 31 81  1  0
 31 82  1  0
 33 83  1  0
 34 84  1  0
 35 85  1  0
 36 86  1  0
 36 87  1  0
 38 88  1  0
 38 89  1  0
 38 90  1  0
M  END


  Mrv1533004241510202D          

 42 46  0  0  0  0            999 V2000
   -0.0267   -5.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6027   -5.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4556   -4.2381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0850   -3.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9379   -2.8930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5673   -2.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4202   -1.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6345   -1.2552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4386   -0.4240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3029    0.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2832    0.8984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0051    1.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4433    1.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9967    2.0485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5492    2.7416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8240    2.2736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5858    1.9062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9087    1.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1587    1.9164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6074    1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4246    1.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8103    2.1853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9780    0.8441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2987    1.6043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0087    0.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8331    0.0504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8025    0.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9651    1.6836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5970    1.0971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5023   -0.6316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6957   -0.8049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9664   -0.4193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3545   -0.9727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5279   -1.7793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6556    0.3450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9381   -0.1542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0526   -0.9986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1221    0.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8263    0.7647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5610    1.1402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9410   -1.3302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5554   -2.0595    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
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 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
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  4  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  1  0  0  0  0
 18 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
  7 37  1  0  0  0  0
 36 38  1  0  0  0  0
  9 38  1  0  0  0  0
 38 39  2  0  0  0  0
 13 39  1  0  0  0  0
 39 40  1  0  0  0  0
 30 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154348

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCC1CC2=CC(O)=C3C(C)=C2C(O1)C1C(OC)C=C(CO)C2CC(C)(C)C2(O)C(O)CC1(C)OOC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H48O9/c1-7-8-9-10-11-21-12-19-13-23(35)27-18(2)26(19)29(40-21)28-24(39-6)14-20(17-34)22-15-31(3,4)33(22,38)25(36)16-32(28,5)42-41-30(27)37/h13-14,21-22,24-25,28-29,34-36,38H,7-12,15-17H2,1-6H3

> <INCHI_KEY>
MFHAAVYSAAPBIZ-UHFFFAOYSA-N

> <FORMULA>
C33H48O9

> <MOLECULAR_WEIGHT>
588.738

> <EXACT_MASS>
588.329833126

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
65.73393928293797

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one

> <ALOGPS_LOGP>
4.41

> <JCHEM_LOGP>
5.124865274333334

> <ALOGPS_LOGS>
-4.79

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.204574741449552

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.623805426082571

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7397363939011656

> <JCHEM_POLAR_SURFACE_AREA>
134.91000000000003

> <JCHEM_REFRACTIVITY>
158.01180000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.45e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -0.050 -10.422   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.125  -9.426   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.850  -7.911   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.025  -6.916   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.751  -5.400   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.926  -4.405   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.651  -2.889   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.184  -2.343   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.819  -0.792   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.565   0.054   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.529   1.677   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.876   2.422   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.827   2.572   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.861   3.824   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.025   5.118   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       3.405   4.244   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.827   3.558   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.430   2.110   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.896   3.577   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.734   2.929   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.259   2.718   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.979   4.079   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.292   1.576   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.891   2.995   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.350   0.037   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.889   0.094   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.831   1.633   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.135   3.143   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.314   2.048   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.404  -1.179   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.899  -1.503   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.537  -0.783   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.395  -1.816   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.719  -3.321   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.957   0.644   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.618  -0.288   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       3.831  -1.864   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       2.095   0.070   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.543   1.428   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.914   2.128   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.223  -2.483   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       8.503  -3.844   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   37                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   38                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   39                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   35                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25   27                                             
CONECT   24   23                                                            
CONECT   25   23   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   23   28   29                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   31   41                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   35                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   32   18   36                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36    7                                                       
CONECT   38   36    9   39                                                  
CONECT   39   38   13   40                                                  
CONECT   40   39                                                            
CONECT   41   30   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₈O₉

Average Mass

588.7380 Da

Monoisotopic Mass

588.32983 Da

IUPAC Name

21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one

Traditional Name

21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one

CAS Registry Number

Not Available

SMILES

CCCCCCC1CC2=CC(O)=C3C(C)=C2C(O1)C1C(OC)C=C(CO)C2CC(C)(C)C2(O)C(O)CC1(C)OOC3=O

InChI Identifier

InChI=1S/C33H48O9/c1-7-8-9-10-11-21-12-19-13-23(35)27-18(2)26(19)29(40-21)28-24(39-6)14-20(17-34)22-15-31(3,4)33(22,38)25(36)16-32(28,5)42-41-30(27)37/h13-14,21-22,24-25,28-29,34-36,38H,7-12,15-17H2,1-6H3

InChI Key

MFHAAVYSAAPBIZ-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 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

2-benzopyrans

Direct Parent

2-benzopyrans

Alternative Parents

Substituents

2-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Tertiary alcohol
Vinylogous acid
Carboxylic acid salt
Cyclobutanol
Secondary alcohol
Carboxylic acid derivative
Polyol
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Oxacycle
Organic oxide
Organic oxygen compound
Primary alcohol
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic salt
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	4.41	ALOGPS
logP	5.12	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	9.62	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	134.91 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	158.01 m³·mol⁻¹	ChemAxon
Polarizability	65.73 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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 21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one (NP0154348)

MOL for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)

3D MOL for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)

3D SDF for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)

3D-SDF for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)

PDB for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)

3D PDB for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)

SMILES for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)

INCHI for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)

Structure for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)

3D Structure for NP0154348 (21-hexyl-9,10,17-trihydroxy-5-(hydroxymethyl)-3-methoxy-8,8,12,24-tetramethyl-13,14,22-trioxapentacyclo[14.6.2.0²,¹².0⁶,⁹.0¹⁹,²³]tetracosa-4,16,18,23-tetraen-15-one)