NP-MRD: Showing NP-Card for 2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate (NP0196364)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 14:26:45 UTC

Updated at

2022-09-04 14:26:45 UTC

NP-MRD ID

NP0196364

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate

Description

Based on a literature review very few articles have been published on 2-[(4Z,8Z,13S)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]Hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042216262D          

 26 27  0  0  1  0            999 V2000
    0.3573    1.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8882    1.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6067    0.4121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7005    1.3316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2314    0.7001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5999    0.1692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8629    1.2310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7623    0.0686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5243    0.3848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3481    0.3390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0703   -0.0597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6197    0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5481   -0.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6868   -1.5455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4589   -2.3384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9095   -2.9538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3873   -3.6264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1474   -3.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237   -3.2242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014   -2.8256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1236   -2.1530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6449   -1.5135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1977   -0.8202    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4002   -1.0312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3544   -1.8549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6611   -2.3020    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
  5  7  1  0  0  0  0
  5  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
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  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  2  0  0  0  0
 22 23  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 21 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END

     RDKit          3D

 58 59  0  0  0  0  0  0  0  0999 V2000
    5.0613   -2.0889    1.7270 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0326   -1.0424    1.3962 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2157   -0.6520    2.2529 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9564   -0.4785    0.1364 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0511    0.4924   -0.2917 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4014    0.7849   -1.7597 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1893    1.7966    0.4502 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6521   -0.0904   -0.2358 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6662    0.9175   -0.6946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1129    1.5969    0.4348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0002    2.5823   -0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4349    3.9485   -0.5547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2308    2.2882   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0569    1.4254    0.2877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7478    0.4284   -0.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3942   -0.6858    0.1050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8530   -0.6208    0.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6669   -1.7476    0.4207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2225   -1.5726    0.6399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4514   -2.8603    0.3167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0966   -2.5243   -0.2393 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2481   -1.8581   -1.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6742   -1.3515   -1.0362 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2644   -2.4559   -0.3288 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1848   -2.9329    0.4069 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2983   -3.6177    1.4748 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7670   -2.6715    2.6028 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0343   -1.5760    1.8361 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1239   -2.7701    0.8539 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1839    0.1032   -2.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5036    0.7240   -2.4078 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8055    1.8102   -1.8772 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6689    2.5862   -0.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9163    1.7431    1.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2840    2.0671    0.3572 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4357   -0.3177    0.8303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0987    0.5153   -1.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1977    1.7364   -1.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6146    2.2030    1.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6228    0.8483    1.0452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0031    4.7499   -0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6024    4.0145   -0.1791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5041    4.1553   -1.6443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6521    2.6967   -1.4732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6001    1.0060    1.1750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8926    2.0871    0.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5689    0.9814   -1.1441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0932    0.0611   -1.4248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2821   -1.6230    0.3902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9172   -0.3414    1.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3303    0.0907   -0.1960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1393   -2.7084    0.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9574   -1.2527    1.6458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8197   -0.8454   -0.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4125   -3.3809    1.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0356   -3.5530   -0.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0928   -1.5273   -2.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2572   -1.2934   -1.9687 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  5  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 23  8  1  0
 25 21  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  6 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  1
  9 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 17 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 22 57  1  0
 23 58  1  6
M  END


  Mrv1652309042216262D          

 26 27  0  0  1  0            999 V2000
    0.3573    1.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8882    1.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6067    0.4121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7005    1.3316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2314    0.7001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5999    0.1692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8629    1.2310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7623    0.0686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5243    0.3848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3481    0.3390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0703   -0.0597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6197    0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5481   -0.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6868   -1.5455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4589   -2.3384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9095   -2.9538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3873   -3.6264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1474   -3.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237   -3.2242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6014   -2.8256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1236   -2.1530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6449   -1.5135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1977   -0.8202    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4002   -1.0312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3544   -1.8549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6611   -2.3020    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
  5  7  1  0  0  0  0
  5  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
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  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  2  0  0  0  0
 22 23  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 21 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0196364

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC(C)(C)C1CC\C(C)=C/CC\C(C)=C/CCC2=C[C@@H]1OC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O4/c1-15-8-6-9-16(2)12-13-19(22(4,5)26-17(3)23)20-14-18(11-7-10-15)21(24)25-20/h9-10,14,19-20H,6-8,11-13H2,1-5H3/b15-10-,16-9-/t19?,20-/m0/s1

> <INCHI_KEY>
JRHSHBMAWLBQTD-OFVQNOMWSA-N

> <FORMULA>
C22H32O4

> <MOLECULAR_WEIGHT>
360.494

> <EXACT_MASS>
360.23005951

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.77365051545582

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(4E,8E,13S)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate

> <JCHEM_LOGP>
4.835094184999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.788570391867648

> <JCHEM_PKA_STRONGEST_BASIC>
-6.640714099783962

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
104.8603

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-[(4E,8E,13S)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       0.667   3.396   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.658   2.217   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.133   0.769   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.174   2.486   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.165   1.307   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.987   0.316   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.344   2.298   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.156   0.128   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.579   0.718   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.116   0.633   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.465  -0.111   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.490   1.038   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.357  -1.367   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.615  -2.885   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.190  -4.365   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.164  -5.514   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.056  -6.769   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.742  -6.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.204  -6.019   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.856  -5.274   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.964  -4.019   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.937  -2.825   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.102  -1.531   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.614  -1.925   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.528  -3.462   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.234  -4.297   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    7    8                                             
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    5    9   23                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22    8   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   21   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Value	Source
2-[(4Z,8Z,13S)-5,9-Dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetic acid	Generator

Chemical Formula

C₂₂H₃₂O₄

Average Mass

360.4940 Da

Monoisotopic Mass

360.23006 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OC(C)(C)C1CC\C(C)=C/CC\C(C)=C/CCC2=C[C@@H]1OC2=O

InChI Identifier

InChI=1S/C22H32O4/c1-15-8-6-9-16(2)12-13-19(22(4,5)26-17(3)23)20-14-18(11-7-10-15)21(24)25-20/h9-10,14,19-20H,6-8,11-13H2,1-5H3/b15-10-,16-9-/t19?,20-/m0/s1

InChI Key

JRHSHBMAWLBQTD-OFVQNOMWSA-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

Classification

Not classified

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	4.84	ChemAxon
pKa (Strongest Acidic)	12.79	ChemAxon
pKa (Strongest Basic)	-6.6	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	104.86 m³·mol⁻¹	ChemAxon
Polarizability	40.77 Å³	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

58134270

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162953029

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate (NP0196364)

MOL for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)

3D MOL for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)

3D SDF for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)

3D-SDF for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)

PDB for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)

3D PDB for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)

SMILES for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)

INCHI for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)

Structure for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)

3D Structure for NP0196364 (2-[(4e,8e,13s)-5,9-dimethyl-15-oxo-14-oxabicyclo[11.2.1]hexadeca-1(16),4,8-trien-12-yl]propan-2-yl acetate)