NP-MRD: Showing NP-Card for 4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate (NP0319047)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 19:53:03 UTC

Updated at

2022-09-11 19:53:03 UTC

NP-MRD ID

NP0319047

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate

Description

4-Formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-1H,3H,6H,6aH,7H,8H,9H,10H,10bH-naphtho[4,4a-c]furan-10-yl 2-hydroxydecanoate belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. 4-Formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-1H,3H,6H,6aH,7H,8H,9H,10H,10bH-naphtho[4,4a-c]furan-10-yl 2-hydroxydecanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241500112D          

 33 35  0  0  0  0            999 V2000
    7.1620   -0.0298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8621    0.4066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6041    0.0110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3378    0.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0477   -0.0279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7670    0.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4182   -0.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0019    0.4855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6629   -0.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5813   -0.8291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4204    0.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3068    1.1515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2178    0.0110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.1585    0.3427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0958    1.0872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2369    1.5568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8209    1.4805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5242    1.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9410    1.8222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3852    0.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5022    0.2244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2055   -0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1836   -1.0316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4584   -1.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5180   -2.2896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1541   -2.8413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7551   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9640   -1.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6518   -2.0352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.4970   -0.5475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.9995    0.1068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5272    0.8822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7771   -0.1689    0.0000 C   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  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 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
 18 21  1  0  0  0  0
 21 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  2  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 14 33  1  0  0  0  0
 21 33  1  0  0  0  0
 27 33  1  0  0  0  0
M  END

     RDKit          3D

 71 73  0  0  0  0  0  0  0  0999 V2000
    8.8768   -0.0826    0.7826 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9997   -0.5768   -0.6233 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8838   -1.3964   -1.1406 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5365   -0.7729   -1.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9391   -0.2571   -0.0156 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5316    0.3266   -0.2010 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6285   -0.7487   -0.6995 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2135   -0.2179   -0.8761 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6216    0.3113    0.3873 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5271   -0.6087    1.4164 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2682    0.8521    0.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1910    1.6687   -0.8818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8720    0.4844    0.7032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1676    0.9408    0.4427 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6692    1.7851    1.6160 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8597    2.9226    1.6562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0863    2.1630    1.2874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9254    0.9072    1.4585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2186    1.1461    0.7202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2908    0.8881    2.9519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2051   -0.3323    1.1308 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0662   -1.4810    0.7494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5043   -1.4723   -0.6461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8733   -0.8000   -1.5849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4459   -0.8980   -2.9176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4526   -1.5866   -3.1405 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6746   -0.0020   -1.3174 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5344   -0.5467   -2.1474 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8565   -0.8810   -3.4443 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1664   -1.6762   -1.3787 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3455   -1.4057   -0.0349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8802   -2.1547    0.8677 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1317   -0.1567    0.0697 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8732   -0.2824    1.2782 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1390   -0.6807    1.3295 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7270    1.0203    0.8433 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9348   -1.2153   -0.7051 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2295    0.2941   -1.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7903   -2.3459   -0.5375 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1764   -1.7214   -2.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6259    0.0892   -1.9983 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8354   -1.4706   -1.7981 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8490   -1.0487    0.7387 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5292    0.6319    0.3411 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5593    1.1855   -0.8782 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2297    0.6629    0.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9461   -1.0034   -1.7516 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6074   -1.6448   -0.0829 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2099    0.6123   -1.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5950   -1.0231   -1.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2708    1.1467    0.7453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6493   -1.5261    1.1215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1217    1.6487   -0.4080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6792    1.2237    2.5586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3623    3.7119    1.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4844    2.9470    1.9647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1376    2.5909    0.2706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9417    1.5969   -0.2798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8007    0.2515    0.5045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8240    1.9532    1.2104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3877    0.7743    3.5871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9322   -0.0028    3.0955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8694    1.7967    3.2123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6290   -0.6502    2.0528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5348   -2.4602    0.9466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9943   -1.5608    1.3807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4147   -2.0709   -0.9003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9904   -0.3635   -3.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8455    1.0889   -1.5655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6917    0.1763   -2.2155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1267   -0.6733   -4.0755 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  1  0
  9 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 31 32  2  0
 33 31  1  6
 33 14  1  0
 33 21  1  0
 33 27  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  2 37  1  0
  2 38  1  0
  3 39  1  0
  3 40  1  0
  4 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  6 45  1  0
  6 46  1  0
  7 47  1  0
  7 48  1  0
  8 49  1  0
  8 50  1  0
  9 51  1  1
 10 52  1  0
 14 53  1  6
 15 54  1  1
 16 55  1  0
 17 56  1  0
 17 57  1  0
 19 58  1  0
 19 59  1  0
 19 60  1  0
 20 61  1  0
 20 62  1  0
 20 63  1  0
 21 64  1  1
 22 65  1  0
 22 66  1  0
 23 67  1  0
 25 68  1  0
 27 69  1  6
 28 70  1  6
 29 71  1  0
M  END


  Mrv1533004241500112D          

 33 35  0  0  0  0            999 V2000
    7.1620   -0.0298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8621    0.4066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6041    0.0110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3378    0.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0477   -0.0279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7670    0.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4182   -0.1286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0019    0.4855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6629   -0.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5813   -0.8291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4204    0.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3068    1.1515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2178    0.0110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.1585    0.3427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0958    1.0872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2369    1.5568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8209    1.4805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5242    1.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9410    1.8222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.3852    0.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5022    0.2244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2055   -0.2069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1836   -1.0316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4584   -1.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5180   -2.2896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1541   -2.8413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7551   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9640   -1.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6518   -2.0352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.4970   -0.5475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.9995    0.1068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5272    0.8822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7771   -0.1689    0.0000 C   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  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 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
 18 21  1  0  0  0  0
 21 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  2  0  0  0  0
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 14 33  1  0  0  0  0
 21 33  1  0  0  0  0
 27 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0319047

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCC(O)C(=O)OC1C(O)CC(C)(C)C2CC=C(C=O)C3C(O)OC(=O)C123

> <INCHI_IDENTIFIER>
InChI=1S/C25H38O8/c1-4-5-6-7-8-9-10-16(27)21(29)32-20-17(28)13-24(2,3)18-12-11-15(14-26)19-22(30)33-23(31)25(18,19)20/h11,14,16-20,22,27-28,30H,4-10,12-13H2,1-3H3

> <INCHI_KEY>
JFWFXOAWDVOLHC-UHFFFAOYSA-N

> <FORMULA>
C25H38O8

> <MOLECULAR_WEIGHT>
466.571

> <EXACT_MASS>
466.256668184

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
50.44120301314149

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-1H,3H,6H,6aH,7H,8H,9H,10H,10bH-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate

> <ALOGPS_LOGP>
2.88

> <JCHEM_LOGP>
2.8512354843333334

> <ALOGPS_LOGS>
-3.82

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.75403083248787

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.85154349924951

> <JCHEM_PKA_STRONGEST_BASIC>
-3.184617635059234

> <JCHEM_POLAR_SURFACE_AREA>
130.36

> <JCHEM_REFRACTIVITY>
119.85719999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.99e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3H,6H,6aH,8H,9H,10H,10bH-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate

> <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      13.369  -0.056   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.676   0.759   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.061   0.020   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.431   0.823   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.756  -0.052   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      20.098   0.778   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.314  -0.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.404   0.906   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      23.637  -0.015   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      23.485  -1.548   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      25.051   0.624   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      24.839   2.150   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      26.540   0.020   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      28.296   0.640   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      28.179   2.029   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      26.575   2.906   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      29.532   2.764   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      30.845   1.958   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      31.623   3.401   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      32.452   1.818   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      30.804   0.419   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      32.117  -0.386   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      32.076  -1.926   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      30.722  -2.660   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      30.834  -4.274   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      32.021  -5.304   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      29.410  -1.855   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      27.933  -2.292   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      27.350  -3.799   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      27.061  -1.022   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      27.999   0.199   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      27.117   1.647   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      29.451  -0.315   0.000  0.00  0.00           C+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                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   33                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22   33                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28   33                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   14   21   27                                             
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Value	Source
4-Formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-1H,3H,6H,6ah,7H,8H,9H,10H,10BH-naphtho[4,4a-c]furan-10-yl 2-hydroxydecanoic acid	Generator

Chemical Formula

C₂₅H₃₈O₈

Average Mass

466.5710 Da

Monoisotopic Mass

466.25667 Da

IUPAC Name

4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-1H,3H,6H,6aH,7H,8H,9H,10H,10bH-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate

Traditional Name

4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3H,6H,6aH,8H,9H,10H,10bH-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCC(O)C(=O)OC1C(O)CC(C)(C)C2CC=C(C=O)C3C(O)OC(=O)C123

InChI Identifier

InChI=1S/C25H38O8/c1-4-5-6-7-8-9-10-16(27)21(29)32-20-17(28)13-24(2,3)18-12-11-15(14-26)19-22(30)33-23(31)25(18,19)20/h11,14,16-20,22,27-28,30H,4-10,12-13H2,1-3H3

InChI Key

JFWFXOAWDVOLHC-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 naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Fatty alcohol
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Gamma butyrolactone
Monosaccharide
Cyclic alcohol
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Hemiacetal
Lactone
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Aldehyde
Carbonyl group
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.88	ALOGPS
logP	2.85	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	11.85	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.36 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	119.86 m³·mol⁻¹	ChemAxon
Polarizability	50.44 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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 4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate (NP0319047)

MOL for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)

3D MOL for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)

3D SDF for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)

3D-SDF for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)

PDB for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)

3D PDB for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)

SMILES for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)

INCHI for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)

Structure for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)

3D Structure for NP0319047 (4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate)