NP-MRD: Showing NP-Card for (E)-omega-Oxoferulenol (NP0063220)

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Record Information

Version

2.0

Created at

2022-04-28 07:41:02 UTC

Updated at

2022-04-28 07:41:03 UTC

NP-MRD ID

NP0063220

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(E)-omega-Oxoferulenol

Description

4-Hydroxy-3-[(2E,6E,10E)-12-oxo-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl]-2H-1-benzopyran-2-one belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (E)-omega-Oxoferulenol is found in Ferula communis . Based on a literature review very few articles have been published on 4-Hydroxy-3-[(2E,6E,10E)-12-oxo-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl]-2H-1-benzopyran-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282209412D          

 28 29  0  0  0  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   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   -1.6500    0.0000 O   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
    2.8579   -0.0000    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    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    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
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  4 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  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
 17 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
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 18 26  1  0  0  0  0
 14 27  1  0  0  0  0
  7 28  1  0  0  0  0
M  END

     RDKit          3D

 56 57  0  0  0  0  0  0  0  0999 V2000
    8.1438    0.1006   -0.6921 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6238   -1.3081   -0.5773 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3912   -2.4412   -1.0289 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5335   -2.3570   -1.5451 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4312   -1.5081   -0.0481 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5618   -0.4292    0.4451 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2643   -0.4916   -0.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3019    0.5613    0.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6059    1.9962   -0.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1024    0.1580    0.5438 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1627    1.1974    0.9538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1268    1.2904    0.2112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9864    0.0791    0.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5688   -1.2141   -0.3142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2092    0.1443    0.8147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1641   -0.9582    0.9326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4773   -0.6774    0.3079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3843    0.1505    0.9303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1042    0.7357    2.1356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6235    0.4300    0.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5640    1.2466    0.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7736    1.4688    0.3095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0576    0.8766   -0.9088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1120    0.0623   -1.4767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8842   -0.1701   -0.8450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0179   -0.9550   -1.4293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8215   -1.2314   -0.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0422   -1.9993   -1.5232 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1989    0.0698   -1.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0143    0.6520    0.2615 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5524    0.5888   -1.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9871   -3.4360   -0.9313 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0613   -2.5206    0.0323 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3226   -0.5449    1.5242 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9752    0.5698    0.3096 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8271   -1.5027   -0.2400 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4870   -0.3739   -1.4369 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8620    2.5537   -0.5988 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6914    2.4894    0.9687 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5835    2.1575   -0.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9005   -0.9045    0.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6307    2.2115    0.9889 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8719    1.0005    2.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6917    2.1835    0.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0499    1.5331   -0.8613 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2736   -1.1137   -1.0371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4433   -1.7144   -0.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2480   -1.8879    0.4834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4754    1.1434    1.2063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7701   -1.9436    0.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3764   -1.0744    2.0467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2817    0.6497    2.6837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3778    1.7188    1.8819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5305    2.1090    0.7447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9870    1.0424   -1.4031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3124   -0.4132   -2.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  2  2  0
  2  1  1  0
  2  3  1  0
  3  4  2  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 27 17  1  0
 25 20  1  0
  9 38  1  0
  9 39  1  0
  9 40  1  0
  7 36  1  0
  7 37  1  0
  6 34  1  0
  6 35  1  0
  5 33  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
 10 41  1  0
 11 42  1  0
 11 43  1  0
 12 44  1  0
 12 45  1  0
 14 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 16 50  1  0
 16 51  1  0
 19 52  1  0
 21 53  1  0
 22 54  1  0
 23 55  1  0
 24 56  1  0
M  END


  Mrv1652304282209412D          

 28 29  0  0  0  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   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   -1.6500    0.0000 O   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
    2.8579   -0.0000    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    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    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
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  4 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  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
 17 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
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 18 26  1  0  0  0  0
 14 27  1  0  0  0  0
  7 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0063220

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(CC\C=C(/C)C=O)=C/CC\C(C)=C\CC1=C(O)C2=CC=CC=C2OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O4/c1-17(9-7-11-19(3)16-25)8-6-10-18(2)14-15-21-23(26)20-12-4-5-13-22(20)28-24(21)27/h4-5,8,11-14,16,26H,6-7,9-10,15H2,1-3H3/b17-8+,18-14+,19-11+

> <INCHI_KEY>
BRIDRHNPTZTJFO-QTUSMQKXSA-N

> <FORMULA>
C24H28O4

> <MOLECULAR_WEIGHT>
380.484

> <EXACT_MASS>
380.198759382

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
43.20098815800234

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,6E,10E)-12-(4-hydroxy-2-oxo-2H-chromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trienal

> <ALOGPS_LOGP>
5.86

> <JCHEM_LOGP>
4.993013712333334

> <ALOGPS_LOGS>
-5.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.613932028389276

> <JCHEM_PKA_STRONGEST_BASIC>
-4.1727274721108945

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
115.39659999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.68e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,6E,10E)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trienal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336   8.470   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.669   9.240   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.669  10.780   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.003  11.550   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.337  10.780   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.003  13.090   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.669  13.860   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   28                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    4                                                       
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   18                                                            
CONECT   27   14                                                            
CONECT   28    7                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₈O₄

Average Mass

380.4840 Da

Monoisotopic Mass

380.19876 Da

IUPAC Name

(2E,6E,10E)-12-(4-hydroxy-2-oxo-2H-chromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trienal

Traditional Name

(2E,6E,10E)-12-(4-hydroxy-2-oxochromen-3-yl)-2,6,10-trimethyldodeca-2,6,10-trienal

CAS Registry Number

Not Available

SMILES

C\C(CC\C=C(/C)C=O)=C/CC\C(C)=C\CC1=C(O)C2=CC=CC=C2OC1=O

InChI Identifier

InChI=1S/C24H28O4/c1-17(9-7-11-19(3)16-25)8-6-10-18(2)14-15-21-23(26)20-12-4-5-13-22(20)28-24(21)27/h4-5,8,11-14,16,26H,6-7,9-10,15H2,1-3H3/b17-8+,18-14+,19-11+

InChI Key

BRIDRHNPTZTJFO-QTUSMQKXSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Ferula communis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
Farsesane sesquiterpenoid
4-hydroxycoumarin
Hydroxycoumarin
Coumarin
Benzopyran
1-benzopyran
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Enal
Alpha,beta-unsaturated aldehyde
Vinylogous acid
Lactone
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Aldehyde
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	5.86	ALOGPS
logP	4.99	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	5.61	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	115.4 m³·mol⁻¹	ChemAxon
Polarizability	43.2 Å³	ChemAxon
Number of Rings	2	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

C00019991

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

101826532

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (E)-omega-Oxoferulenol (NP0063220)

MOL for NP0063220 ((E)-omega-Oxoferulenol)

3D MOL for NP0063220 ((E)-omega-Oxoferulenol)

3D SDF for NP0063220 ((E)-omega-Oxoferulenol)

3D-SDF for NP0063220 ((E)-omega-Oxoferulenol)

PDB for NP0063220 ((E)-omega-Oxoferulenol)

3D PDB for NP0063220 ((E)-omega-Oxoferulenol)

SMILES for NP0063220 ((E)-omega-Oxoferulenol)

INCHI for NP0063220 ((E)-omega-Oxoferulenol)

Structure for NP0063220 ((E)-omega-Oxoferulenol)

3D Structure for NP0063220 ((E)-omega-Oxoferulenol)