NP-MRD: Showing NP-Card for 4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate (NP0296495)

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Record Information

Version

2.0

Created at

2022-09-10 06:06:23 UTC

Updated at

2022-09-10 06:06:23 UTC

NP-MRD ID

NP0296495

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate

Description

4,8,12,16-Tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]Octadeca-4,10,16-trien-13-yl acetate belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals. 4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate is found in Briareum asbestinum. Based on a literature review very few articles have been published on 4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]Octadeca-4,10,16-trien-13-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102208062D          

 28 31  0  0  0  0            999 V2000
    3.8332   -1.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4386   -0.3022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8689    0.4018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6139   -0.2815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2194    0.4430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3796    0.3334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6216    0.7701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7106    1.5466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5537    2.2737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2558    1.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1948    1.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363    0.4865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0841    2.9912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5364    3.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2414    4.4581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3320    3.4731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9781    3.9861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3606    2.6526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2080    2.5580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7765    1.9148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4951    2.3199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5037    3.1448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2053    1.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9240    2.3051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1968    1.0751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4781    0.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7679    1.0898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9049    0.2763    0.0000 C   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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
  9 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  2  0  0  0  0
  9 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
  5 27  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -3.9500   -3.2316    0.7026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6104   -2.5458    0.6612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7950   -2.6768    1.5849 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2832   -1.7635   -0.4123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0304   -1.0638   -0.5546 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2656   -1.6440   -1.6645 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1618   -2.0180   -1.4018 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1317   -1.1241   -1.6973 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5594   -0.4838   -0.5458 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9197   -1.2508    0.5706 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4140   -2.3418    0.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1318   -3.6709    0.6235 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9259   -0.5497   -0.2834 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3530    0.6798    0.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4765    1.0138    0.6333 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2393    1.5975   -0.0596 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2363    3.0838    0.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2242    0.9315   -0.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9011    1.3704   -1.0609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1590    1.1437   -0.0017 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4325    2.4816    0.6162 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0250    2.5433    2.0810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8568    2.8635    0.6222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3021    4.0244    0.4282 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7885    1.7770    0.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5310    0.6245    0.3102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3473    0.4102   -0.5639 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7478    0.9629   -1.8967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2777   -3.4136    1.7435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9364   -4.1725    0.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6886   -2.5659    0.2024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4927   -1.3268    0.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7606   -2.6661   -1.8660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3912   -1.1775   -2.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3825   -2.9461   -2.0100 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8585   -1.0207    1.6132 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1475   -3.6376    1.7274 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1730   -4.0879    0.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9483   -4.3889    0.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5929    3.5950   -0.5855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9055    3.3224    1.1966 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2846    3.4051    0.0693 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5845    0.8265   -1.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8967    2.4442   -1.3638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2347    0.5042    0.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1085    3.3053    0.1067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8439    2.4263    2.7622 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5416    3.4765    2.3060 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7427    1.7087    2.2065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6768    1.9257    1.5218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2359   -0.2253    0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8560    0.8506   -2.0623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2524    0.6154   -2.7768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5895    2.0800   -1.8395 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 16  2  0
 16 17  1  0
 16 14  1  0
 14 15  2  0
 14 13  1  0
  9 13  1  1
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 27  1  0
 27 28  1  6
 27 26  1  0
 26 25  2  0
 25 23  1  0
 23 24  2  0
  7 11  1  0
 11 12  1  0
 11 10  2  0
 23 21  1  0
 27 20  1  0
  9 18  1  0
 10  9  1  0
 22 47  1  0
 22 48  1  0
 22 49  1  0
 21 46  1  6
 20 45  1  1
 19 43  1  0
 19 44  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
  7 35  1  6
  6 33  1  0
  6 34  1  0
  5 32  1  1
  1 29  1  0
  1 30  1  0
  1 31  1  0
 28 52  1  0
 28 53  1  0
 28 54  1  0
 26 51  1  0
 25 50  1  0
 12 37  1  0
 12 38  1  0
 12 39  1  0
 10 36  1  0
M  END


  Mrv1652309102208062D          

 28 31  0  0  0  0            999 V2000
    3.8332   -1.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4386   -0.3022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8689    0.4018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6139   -0.2815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2194    0.4430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3796    0.3334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6216    0.7701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7106    1.5466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5537    2.2737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2558    1.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1948    1.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363    0.4865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0841    2.9912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5364    3.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2414    4.4581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3320    3.4731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9781    3.9861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3606    2.6526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2080    2.5580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7765    1.9148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4951    2.3199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5037    3.1448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2053    1.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9240    2.3051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1968    1.0751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4781    0.6700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7679    1.0898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9049    0.2763    0.0000 C   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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
  9 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  2  0  0  0  0
  9 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
  5 27  1  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0296495

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2CC3=C(C)C(=O)OC33OC(CC(OC(C)=O)C2(C)C=CC1=O)C(C)=C3

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O6/c1-11-10-22-16(13(3)20(25)28-22)8-15-12(2)17(24)6-7-21(15,5)19(26-14(4)23)9-18(11)27-22/h6-7,10,12,15,18-19H,8-9H2,1-5H3

> <INCHI_KEY>
AUOMMFOGAUIRHO-UHFFFAOYSA-N

> <FORMULA>
C22H26O6

> <MOLECULAR_WEIGHT>
386.444

> <EXACT_MASS>
386.172938557

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
39.903002681188994

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0^{1,5}.0^{7,12}]octadeca-4,10,16-trien-13-yl acetate

> <JCHEM_LOGP>
3.4509068503333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.362789313136114

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
102.65409999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0^{1,5}.0^{7,12}]octadeca-4,10,16-trien-13-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       7.155  -1.917   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.419  -0.564   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.222   0.750   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       4.879  -0.526   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.143   0.827   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.575   0.622   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.160   1.438   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.326   2.887   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.034   4.244   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.477   3.507   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.364   1.877   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.561   0.908   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.157   5.583   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.001   6.884   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.451   8.322   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.486   6.483   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.692   7.441   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.540   4.951   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.122   4.775   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.183   3.574   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.524   4.330   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.540   5.870   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.850   3.547   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.191   4.303   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.834   2.007   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.492   1.251   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.167   2.034   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.422   0.516   0.000  0.00  0.00           C+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                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   13   18                                             
CONECT   10    9   11                                                       
CONECT   11   10    7   12                                                  
CONECT   12   11                                                            
CONECT   13    9   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    9   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   27                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26    5   20   28                                             
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Value	Source
4,8,12,16-Tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0,.0,]octadeca-4,10,16-trien-13-yl acetic acid	Generator

Chemical Formula

C₂₂H₂₆O₆

Average Mass

386.4440 Da

Monoisotopic Mass

386.17294 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1C2CC3=C(C)C(=O)OC33OC(CC(OC(C)=O)C2(C)C=CC1=O)C(C)=C3

InChI Identifier

InChI=1S/C22H26O6/c1-11-10-22-16(13(3)20(25)28-22)8-15-12(2)17(24)6-7-21(15,5)19(26-14(4)23)9-18(11)27-22/h6-7,10,12,15,18-19H,8-9H2,1-5H3

InChI Key

AUOMMFOGAUIRHO-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
Briareum asbestinum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Ketals

Alternative Parents

Substituents

Ketal
Cyclohexenone
2-furanone
Dicarboxylic acid or derivatives
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Ketone
Lactone
Cyclic ketone
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
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

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

73818036

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate (NP0296495)

MOL for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)

3D MOL for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)

3D SDF for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)

3D-SDF for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)

PDB for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)

3D PDB for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)

SMILES for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)

INCHI for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)

Structure for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)

3D Structure for NP0296495 (4,8,12,16-tetramethyl-3,9-dioxo-2,18-dioxatetracyclo[13.2.1.0¹,⁵.0⁷,¹²]octadeca-4,10,16-trien-13-yl acetate)