NP-MRD: Showing NP-Card for 7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate (NP0248036)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 10:07:26 UTC

Updated at

2022-09-07 10:07:26 UTC

NP-MRD ID

NP0248036

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate

Description

7-[6-(Hydroxymethyl)-6-methyl-5-oxo-tetrahydro-3H-spiro[furo[3,2-b]furan-2,2'-oxolane]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate belongs to the class of organic compounds known as furofurans. These are organic compounds containing a two furan rings fused to each other. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Based on a literature review very few articles have been published on 7-[6-(hydroxymethyl)-6-methyl-5-oxo-tetrahydro-3H-spiro[furo[3,2-b]furan-2,2'-oxolane]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072212072D          

 31 33  0  0  0  0            999 V2000
    7.0362   -4.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0362   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3217   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6073   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8928   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1783   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4639   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7494   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6631   -4.0438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8562   -4.2154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4437   -3.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8916   -4.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1380   -3.7784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6690   -3.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0815   -3.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9020   -3.1492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5295   -2.6224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1969   -2.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1170   -1.9079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7080   -1.9079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2242   -2.9579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0312   -2.7864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9957   -2.8878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7507   -2.8109    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4652   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4652   -4.0484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1796   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1796   -1.9859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8941   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6086   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8941   -4.0484    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
  4  3  1  4  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  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
 10 11  1  0  0  0  0
 11 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
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  1  0  0  0  0
 11 23  1  0  0  0  0
  8 23  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END

     RDKit          3D

 65 67  0  0  0  0  0  0  0  0999 V2000
   -4.2505   -0.8884   -3.1849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8997   -0.7796   -1.7124 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5588   -0.1157   -1.6195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0931    0.0537   -0.2233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9945   -0.4717    0.2288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5859   -0.2732    1.6071 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5359   -0.8209    2.0346 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3472   -1.6225    1.0983 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4815   -2.2514    1.8735 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5695   -1.1861    1.6808 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2514   -0.7807    0.2378 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0220   -1.7340   -0.6441 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2814   -0.9183   -0.9256 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1468   -0.9066    0.1799 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3451    0.3715    0.6665 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8543    0.7493    1.7481 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8179    1.2985   -0.3772 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3613    2.6029    0.1895 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9061    1.4564   -1.4136 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0568    1.9835   -0.8433 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6758    0.4863   -0.9455 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6523    0.4923   -0.0417 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8972   -0.8849    0.0802 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9374   -0.0910   -1.0826 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7463   -0.6113   -0.1026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5189   -1.7934    0.2364 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8181    0.2004    0.5015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.5675   -0.5889    1.5526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2716    1.4957    1.0147 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.6654    2.2441   -0.1419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3297    1.2432    2.0103 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3636   -0.9777   -3.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9904    0.0886   -3.6804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7006   -1.6833   -3.7021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8331   -1.7889   -1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8274   -0.7861   -2.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5359    0.8388   -2.1798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7355    0.6610    0.4340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3711   -1.0630   -0.4161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1842    0.3203    2.3047 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8687   -0.6917    3.0554 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7024   -2.4114    0.6511 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7503   -3.1869    1.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2334   -2.3832    2.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3958   -0.3706    2.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5600   -1.6481    1.7507 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3307   -2.6503   -0.1025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5163   -1.9533   -1.5930 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7533   -1.1798   -1.8747 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7477    3.4183   -0.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6963    2.8126    1.2051 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2466    2.6459    0.0701 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6098    2.0943   -2.2519 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1429    0.4344   -1.7827 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4380    1.3229   -0.1884 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4056    0.7920   -1.9686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5499    0.4591   -0.3137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1727   -0.3048    2.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3116   -1.6597    1.4009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6388   -0.4018    1.4679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1183    2.0905    1.4153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1322    1.9666   -1.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8161    3.3486    0.0046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5753    2.0789   -0.1706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5059    1.8086    1.8900 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 17 21  1  0
 21 22  1  0
 11 23  1  6
  2 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 23  8  1  0
 22 11  1  0
 21 13  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  1
  3 36  1  0
  3 37  1  0
  4 38  1  0
  5 39  1  0
  6 40  1  0
  7 41  1  0
  8 42  1  6
  9 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  6
 18 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 21 56  1  6
 27 57  1  6
 28 58  1  0
 28 59  1  0
 28 60  1  0
 29 61  1  1
 30 62  1  0
 30 63  1  0
 30 64  1  0
 31 65  1  0
M  END


  Mrv1652309072212072D          

 31 33  0  0  0  0            999 V2000
    7.0362   -4.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0362   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3217   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6073   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8928   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1783   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4639   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7494   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6631   -4.0438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8562   -4.2154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4437   -3.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8916   -4.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1380   -3.7784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6690   -3.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0815   -3.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9020   -3.1492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5295   -2.6224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1969   -2.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1170   -1.9079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7080   -1.9079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2242   -2.9579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0312   -2.7864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9957   -2.8878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7507   -2.8109    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4652   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4652   -4.0484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1796   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1796   -1.9859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8941   -3.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6086   -2.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8941   -4.0484    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
  4  3  1  4  0  0  0
  4  5  2  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  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
 10 11  1  0  0  0  0
 11 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
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  1  0  0  0  0
 11 23  1  0  0  0  0
  8 23  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0248036

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CC=CC=CC1CCC2(CC3OC(=O)C(C)(CO)C3O2)O1)OC(=O)C(C)C(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O8/c1-14(28-20(26)15(2)16(3)25)8-6-5-7-9-17-10-11-23(30-17)12-18-19(31-23)22(4,13-24)21(27)29-18/h5-7,9,14-19,24-25H,8,10-13H2,1-4H3

> <INCHI_KEY>
NQHCVEOIXCDKGY-UHFFFAOYSA-N

> <FORMULA>
C23H34O8

> <MOLECULAR_WEIGHT>
438.517

> <EXACT_MASS>
438.225368055

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
46.59911227144221

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-[6-(hydroxymethyl)-6-methyl-5-oxo-tetrahydro-3H-spiro[furo[3,2-b]furan-2,2'-oxolane]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate

> <JCHEM_LOGP>
2.490545904333332

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.229283512946992

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.597622138980867

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7867798203078022

> <JCHEM_POLAR_SURFACE_AREA>
111.52000000000002

> <JCHEM_REFRACTIVITY>
113.13000000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3H-spiro[furo[3,2-b]furan-2,2'-oxolane]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate

> <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      13.134  -7.557   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.134  -6.017   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.801  -5.247   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.467  -6.017   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.133  -5.247   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.800  -6.017   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.466  -5.247   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.132  -6.017   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.971  -7.548   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.465  -7.869   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.695  -6.535   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.664  -7.679   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.258  -7.053   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.249  -7.373   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.019  -6.040   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -3.550  -5.879   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.988  -4.895   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.234  -3.990   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.218  -3.561   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.322  -3.561   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.419  -5.521   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.925  -5.201   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       3.725  -5.391   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      14.468  -5.247   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      15.802  -6.017   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      15.802  -7.557   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      17.135  -5.247   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      17.135  -3.707   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      18.469  -6.017   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      19.803  -5.247   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      18.469  -7.557   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   24                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   23                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   22   23                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   21                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   17   13   22                                                  
CONECT   22   21   11                                                       
CONECT   23   11    8                                                       
CONECT   24    2   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
7-[6-(Hydroxymethyl)-6-methyl-5-oxo-tetrahydro-3H-spiro[furo[3,2-b]furan-2,2'-oxolane]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoic acid	Generator

Chemical Formula

C₂₃H₃₄O₈

Average Mass

438.5170 Da

Monoisotopic Mass

438.22537 Da

IUPAC Name

7-[6-(hydroxymethyl)-6-methyl-5-oxo-tetrahydro-3H-spiro[furo[3,2-b]furan-2,2'-oxolane]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate

Traditional Name

7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3H-spiro[furo[3,2-b]furan-2,2'-oxolane]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC(CC=CC=CC1CCC2(CC3OC(=O)C(C)(CO)C3O2)O1)OC(=O)C(C)C(C)O

InChI Identifier

InChI=1S/C23H34O8/c1-14(28-20(26)15(2)16(3)25)8-6-5-7-9-17-10-11-23(30-17)12-18-19(31-23)22(4,13-24)21(27)29-18/h5-7,9,14-19,24-25H,8,10-13H2,1-4H3

InChI Key

NQHCVEOIXCDKGY-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 furofurans. These are organic compounds containing a two furan rings fused to each other. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Furofurans

Sub Class

Not Available

Direct Parent

Furofurans

Alternative Parents

Substituents

Furofuran
Beta-hydroxy acid
Ketal
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Gamma butyrolactone
Hydroxy acid
Monosaccharide
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Lactone
Oxacycle
Acetal
Carboxylic acid derivative
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Primary alcohol
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	2.49	ChemAxon
pKa (Strongest Acidic)	14.6	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	111.52 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	113.13 m³·mol⁻¹	ChemAxon
Polarizability	46.6 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

74000358

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate (NP0248036)

MOL for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)

3D MOL for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)

3D SDF for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)

3D-SDF for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)

PDB for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)

3D PDB for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)

SMILES for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)

INCHI for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)

Structure for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)

3D Structure for NP0248036 (7-[6-(hydroxymethyl)-6-methyl-5-oxo-dihydro-3h-spiro[furo[3,2-b]furan-2,2'-oxolan]-5'-yl]hepta-4,6-dien-2-yl 3-hydroxy-2-methylbutanoate)