NP-MRD: Showing NP-Card for 5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate (NP0325418)

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Record Information

Version

2.0

Created at

2022-09-12 06:10:01 UTC

Updated at

2022-09-12 06:10:02 UTC

NP-MRD ID

NP0325418

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate

Description

5'-(Furan-3-yl)-8-methyl-2',3-dioxo-1,3,5,6,6a,8,9,10-octahydrospiro[naphtho[4,4a-c]furan-7,3'-oxolane]-5-yl 2-methylbut-2-enoate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate is found in Baccharis nitida. 5'-(Furan-3-yl)-8-methyl-2',3-dioxo-1,3,5,6,6a,8,9,10-octahydrospiro[naphtho[4,4a-c]furan-7,3'-oxolane]-5-yl 2-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241518262D          

 32 36  0  0  0  0            999 V2000
    3.1897    6.4683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9990    5.6657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    5.4295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6088    5.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0178    4.6269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2273    4.3907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6175    4.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4268    3.2577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0265    2.6912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8358    1.8886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0453    1.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9770    0.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4543    0.2833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2448    0.5194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8446   -0.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4356    1.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7091    2.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5339    2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7700    1.2902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0912    0.8214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3274    0.0309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0346    2.7364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7985    3.5269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4773    3.9957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1330    3.4950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8594    2.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6919    0.9070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8737    1.0128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7215    1.8236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0240    2.1770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4456    2.2189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6363    3.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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
 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
 14 16  1  0  0  0  0
 10 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
 19 20  1  0  0  0  0
 16 20  1  0  0  0  0
 20 21  2  0  0  0  0
 18 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 22 26  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 11 31  1  0  0  0  0
 31 32  2  0  0  0  0
  8 32  1  0  0  0  0
M  END

     RDKit          3D

 60 64  0  0  0  0  0  0  0  0999 V2000
   -5.7842    3.8512   -0.0219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7805    2.7733   -0.0761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7908    1.8197    0.8204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8204    1.8391    1.8850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8258    0.7203    0.8215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8950   -0.1587    1.7166 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8333    0.5719   -0.0949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8680   -0.4988   -0.1169 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1337   -1.4336   -1.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2045   -2.1040   -1.7500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1855   -3.1068   -2.8526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2245   -3.6394   -3.3657 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1375   -3.3330   -3.1932 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8230   -2.1781   -2.7403 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2007   -1.9984   -1.3490 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5236   -3.2093   -0.5259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0094   -2.8642    0.8531 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2666   -2.0283    0.6460 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3939   -2.8401    0.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9360   -0.7594   -0.0377 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1776    0.3519    0.9737 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4009    1.6035    0.1980 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5329    2.4152    0.7050 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8836    2.1333    0.7208 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5499    3.2190    1.3058 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6424    4.0891    1.6164 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4238    3.6650    1.2822 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7895    1.0770   -1.0775 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0414   -0.3081   -0.9640 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9586   -0.9539   -1.5099 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6010   -0.6954   -0.7195 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4818   -0.0001    0.0371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5709    4.6780   -0.7243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7649    3.3919   -0.3010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8542    4.1928    1.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0395    2.7739   -0.8545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5715    2.5339    2.7067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9824    0.8456    2.3547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8160    2.1624    1.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1890   -1.0930    0.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1585   -1.5407   -1.5452 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9016   -2.3043   -2.7004 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5443   -1.2977   -3.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3376   -3.9035   -0.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3214   -3.8102   -1.0121 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2860   -3.8082    1.3660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3098   -2.2726    1.4517 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6064   -1.8593    1.7199 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3836   -2.3783    0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4162   -3.7877    0.7011 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3324   -3.1228   -0.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5560    0.3829    1.8348 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2131    0.0972    1.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5225    2.2610    0.1120 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3180    1.2238    0.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6286    3.2437    1.4358 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5501    4.2725    1.4720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7677   -0.0392   -1.6103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5446    1.1081   -0.2006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2930    0.0300    1.1514 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8 32  1  0
 32 31  1  0
 31 15  1  0
 15 14  1  6
 14 13  1  0
 13 11  1  0
 11 12  2  0
 11 10  1  0
 10  9  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 28  1  0
 28 29  1  0
 29 30  2  0
 22 23  1  0
 23 27  2  0
 27 26  1  0
 26 25  1  0
 25 24  2  0
  9  8  1  0
 20 29  1  6
 24 23  1  0
 20 31  1  0
 10 15  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  4 37  1  0
  4 38  1  0
  4 39  1  0
  8 40  1  1
 32 59  1  0
 32 60  1  0
 31 58  1  6
 14 42  1  0
 14 43  1  0
  9 41  1  0
 16 44  1  0
 16 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  1
 19 49  1  0
 19 50  1  0
 19 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  6
 27 57  1  0
 25 56  1  0
 24 55  1  0
M  END


  Mrv1533004241518262D          

 32 36  0  0  0  0            999 V2000
    3.1897    6.4683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9990    5.6657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    5.4295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6088    5.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0178    4.6269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2273    4.3907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6175    4.0604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4268    3.2577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0265    2.6912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8358    1.8886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0453    1.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9770    0.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4543    0.2833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2448    0.5194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8446   -0.0471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4356    1.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7091    2.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5339    2.0807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7700    1.2902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0912    0.8214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3274    0.0309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0346    2.7364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7985    3.5269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4773    3.9957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1330    3.4950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8594    2.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6919    0.9070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8737    1.0128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7215    1.8236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0240    2.1770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4456    2.2189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6363    3.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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
 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
 14 16  1  0  0  0  0
 10 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
 19 20  1  0  0  0  0
 16 20  1  0  0  0  0
 20 21  2  0  0  0  0
 18 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 22 26  1  0  0  0  0
 11 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 11 31  1  0  0  0  0
 31 32  2  0  0  0  0
  8 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325418

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1CC2C3(COC(=O)C3=C1)CCC(C)C21CC(OC1=O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O7/c1-4-14(2)21(26)31-17-9-18-22(27)30-13-24(18)7-5-15(3)25(20(24)10-17)11-19(32-23(25)28)16-6-8-29-12-16/h4,6,8-9,12,15,17,19-20H,5,7,10-11,13H2,1-3H3

> <INCHI_KEY>
DLLARZGQLPQITN-UHFFFAOYSA-N

> <FORMULA>
C25H28O7

> <MOLECULAR_WEIGHT>
440.492

> <EXACT_MASS>
440.183503242

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
45.23184424541036

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5'-(furan-3-yl)-8-methyl-2',3-dioxo-1,3,5,6,6a,8,9,10-octahydrospiro[naphtho[4,4a-c]furan-7,3'-oxolane]-5-yl 2-methylbut-2-enoate

> <ALOGPS_LOGP>
3.61

> <JCHEM_LOGP>
4.3018252053333335

> <ALOGPS_LOGS>
-4.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8885253499295973

> <JCHEM_POLAR_SURFACE_AREA>
92.04000000000002

> <JCHEM_REFRACTIVITY>
114.44489999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.62e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1H-spiro[naphtho[4,4a-c]furan-7,3'-oxolane]-5-yl 2-methylbut-2-enoate

> <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       5.954  12.074   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.598  10.576   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.123  10.135   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.003  11.193   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.767   8.637   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.291   8.196   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       4.886   7.579   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.530   6.081   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.650   5.024   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.294   3.525   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.818   3.085   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.690   1.215   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.581   0.529   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.057   0.970   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.177  -0.088   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.413   2.468   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.924   3.921   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.463   3.884   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.904   2.408   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.637   1.533   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.078   0.058   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.398   5.108   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.957   6.583   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.224   7.459   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.448   6.524   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.938   5.071   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.158   1.693   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.631   1.890   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.347   3.404   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.045   4.064   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.698   4.142   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.054   5.640   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   32                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12   27   31                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   10   17   20                                             
CONECT   17   16   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   16   21                                                  
CONECT   21   20                                                            
CONECT   22   18   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   22                                                       
CONECT   27   11   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   11   32                                                  
CONECT   32   31    8                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Value	Source
5'-(Furan-3-yl)-8-methyl-2',3-dioxo-1,3,5,6,6a,8,9,10-octahydrospiro[naphtho[4,4a-c]furan-7,3'-oxolane]-5-yl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₅H₂₈O₇

Average Mass

440.4920 Da

Monoisotopic Mass

440.18350 Da

IUPAC Name

5'-(furan-3-yl)-8-methyl-2',3-dioxo-1,3,5,6,6a,8,9,10-octahydrospiro[naphtho[4,4a-c]furan-7,3'-oxolane]-5-yl 2-methylbut-2-enoate

Traditional Name

5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1H-spiro[naphtho[4,4a-c]furan-7,3'-oxolane]-5-yl 2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1CC2C3(COC(=O)C3=C1)CCC(C)C21CC(OC1=O)C1=COC=C1

InChI Identifier

InChI=1S/C25H28O7/c1-4-14(2)21(26)31-17-9-18-22(27)30-13-24(18)7-5-15(3)25(20(24)10-17)11-19(32-23(25)28)16-6-8-29-12-16/h4,6,8-9,12,15,17,19-20H,5,7,10-11,13H2,1-3H3

InChI Key

DLLARZGQLPQITN-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
Baccharis nitida	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Naphthofuran
Tricarboxylic acid or derivatives
Fatty acid ester
Gamma butyrolactone
Fatty acyl
Enoate ester
Tetrahydrofuran
Heteroaromatic compound
Furan
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	3.61	ALOGPS
logP	4.3	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	92.04 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	114.44 m³·mol⁻¹	ChemAxon
Polarizability	45.23 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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 5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate (NP0325418)

MOL for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)

3D MOL for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)

3D SDF for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)

3D-SDF for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)

PDB for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)

3D PDB for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)

SMILES for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)

INCHI for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)

Structure for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)

3D Structure for NP0325418 (5'-(furan-3-yl)-8-methyl-2',3-dioxo-5,6,6a,8,9,10-hexahydro-1h-spiro[naphtho[1,8a-c]furan-7,3'-oxolan]-5-yl 2-methylbut-2-enoate)