NP-MRD: Showing NP-Card for 14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate (NP0267975)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 12:56:33 UTC

Updated at

2022-09-08 12:56:33 UTC

NP-MRD ID

NP0267975

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate

Description

14-(Acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]Tetradeca-3(7),5-dien-8-yl 2-methylpropanoate 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. 14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate is found in Senecio mauricei. Based on a literature review very few articles have been published on 14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]Tetradeca-3(7),5-dien-8-yl 2-methylpropanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082214562D          

 28 31  0  0  0  0            999 V2000
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7859   -0.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0409   -0.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2708   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7859   -2.3174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  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
  6  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
 10 12  1  0  0  0  0
 12 13  1  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
 16 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  2  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
  5 27  1  0  0  0  0
 10 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
    4.8101   -3.1250    1.7495 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9854   -2.7449    0.5826 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7305   -3.5012   -0.3723 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4636   -1.4582    0.5559 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6682   -0.9625   -0.4817 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2632    0.2580   -1.0483 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6892    0.5956   -2.2427 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3845    0.4648   -2.3101 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2504    1.2129   -1.7527 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4737    0.2216   -0.8752 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2177   -0.7235   -1.8658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078    1.0012   -0.2002 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6251    0.1157    0.2489 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9245    0.1463   -0.2232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1862    1.0149   -1.0945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9859   -0.7576    0.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2824   -0.4544   -0.4898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6531   -2.2192   -0.0640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1106    1.8638    0.8935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5075    3.0994    1.3629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6157    3.9527    0.8619 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3580    3.3660    2.4047 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2059    2.3468    2.5322 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9458    1.4230    1.6306 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5685    0.1412    1.3524 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3327   -0.3607    2.2199 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3011   -0.5642    0.0542 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5675   -1.7220    0.4056 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2388   -2.2418    2.2506 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6934   -3.6902    1.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2838   -3.7654    2.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5540   -1.7893   -1.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    1.0981   -0.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0568   -0.4596   -2.8608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5299    1.5765   -2.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5393    2.0784   -1.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0544   -1.1954   -1.2920 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4473   -1.5365   -2.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6754   -0.1653   -2.6948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0757    1.6645   -0.9572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1649   -0.6420    1.3356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0680   -0.2685   -1.5721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9674   -1.3463   -0.4579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7575    0.4547   -0.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8031   -2.4358   -1.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3726   -2.8213    0.5335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6149   -2.4506    0.2438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2856    5.0325    0.8237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8262    3.7069   -0.2203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5266    3.8185    1.4482 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3755    4.2391    3.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1051   -1.4915    1.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 18  1  0
 16 14  1  0
 14 15  2  0
 14 13  1  0
 13 12  1  0
 12 19  1  0
 19 24  2  0
 24 23  1  0
 23 22  1  0
 22 20  2  0
 20 21  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  1  1
 27  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  6
 10 12  1  0
 20 19  1  0
 10 27  1  0
  8  6  1  0
 17 42  1  0
 17 43  1  0
 17 44  1  0
 16 41  1  0
 18 45  1  0
 18 46  1  0
 18 47  1  0
 12 40  1  6
 22 51  1  0
 21 48  1  0
 21 49  1  0
 21 50  1  0
 28 52  1  0
  5 32  1  6
  1 29  1  0
  1 30  1  0
  1 31  1  0
  6 33  1  1
  8 34  1  6
  9 35  1  0
  9 36  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
M  END


  Mrv1652309082214562D          

 28 31  0  0  0  0            999 V2000
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7859   -0.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0409   -0.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2708   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7859   -2.3174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  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
  6  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
 10 12  1  0  0  0  0
 12 13  1  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
 16 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  2  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
  5 27  1  0  0  0  0
 10 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0267975

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)OC1C2=C(OC=C2C)C(=O)C2(O)C(OC(C)=O)C3OC3CC12C

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O8/c1-8(2)18(23)28-16-12-9(3)7-25-14(12)15(22)20(24)17(26-10(4)21)13-11(27-13)6-19(16,20)5/h7-8,11,13,16-17,24H,6H2,1-5H3

> <INCHI_KEY>
QXDHYPOVZHHFNY-UHFFFAOYSA-N

> <FORMULA>
C20H24O8

> <MOLECULAR_WEIGHT>
392.404

> <EXACT_MASS>
392.147117733

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
38.46056473985

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0^{3,7}.0^{11,13}]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate

> <JCHEM_LOGP>
1.650693591000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.371906891227482

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9423436161327947

> <JCHEM_POLAR_SURFACE_AREA>
115.57000000000001

> <JCHEM_REFRACTIVITY>
93.59709999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0^{3,7}.0^{11,13}]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.667  -6.160   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       5.335  -6.160   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.800  -1.834   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.276  -0.369   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.706  -3.080   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.800  -4.326   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.336  -3.850   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.002  -6.160   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   27                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    8                                                       
CONECT    8    7    6    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12   27                                             
CONECT   11   10                                                            
CONECT   12   10   13   19                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   12   20   24                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    5   10   28                                             
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Value	Source
14-(Acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0,.0,]tetradeca-3(7),5-dien-8-yl 2-methylpropanoic acid	Generator

Chemical Formula

C₂₀H₂₄O₈

Average Mass

392.4040 Da

Monoisotopic Mass

392.14712 Da

IUPAC Name

14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0^{3,7}.0^{11,13}]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate

Traditional Name

14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0^{3,7}.0^{11,13}]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)OC1C2=C(OC=C2C)C(=O)C2(O)C(OC(C)=O)C3OC3CC12C

InChI Identifier

InChI=1S/C20H24O8/c1-8(2)18(23)28-16-12-9(3)7-25-14(12)15(22)20(24)17(26-10(4)21)13-11(27-13)6-19(16,20)5/h7-8,11,13,16-17,24H,6H2,1-5H3

InChI Key

QXDHYPOVZHHFNY-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
Senecio mauricei	LOTUS Database	35616633

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
Benzofuran
Aryl ketone
Aryl alkyl ketone
Oxepane
Dicarboxylic acid or derivatives
Cyclic alcohol
Furan
Heteroaromatic compound
Tertiary alcohol
Ketone
Carboxylic acid ester
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Hydrocarbon derivative
Organic oxide
Alcohol
Organooxygen compound
Organic oxygen compound
Carbonyl group
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	1.65	ChemAxon
pKa (Strongest Acidic)	11.37	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	115.57 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	93.6 m³·mol⁻¹	ChemAxon
Polarizability	38.46 Å³	ChemAxon
Number of Rings	4	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

163048146

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate (NP0267975)

MOL for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)

3D MOL for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)

3D SDF for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)

3D-SDF for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)

PDB for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)

3D PDB for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)

SMILES for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)

INCHI for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)

Structure for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)

3D Structure for NP0267975 (14-(acetyloxy)-1-hydroxy-6,9-dimethyl-2-oxo-4,12-dioxatetracyclo[7.5.0.0³,⁷.0¹¹,¹³]tetradeca-3(7),5-dien-8-yl 2-methylpropanoate)