NP-MRD: Showing NP-Card for (4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate (NP0303226)

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Record Information

Version

2.0

Created at

2022-09-10 17:24:39 UTC

Updated at

2022-09-10 17:24:39 UTC

NP-MRD ID

NP0303226

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate

Description

(4S)-4-[(3aR,7aS)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-2,3,3a,4,7,7a-hexahydro-1-benzofuran-5-yl]pentyl acetate belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate is found in Calostephane divaricata. Based on a literature review very few articles have been published on (4S)-4-[(3aR,7aS)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-2,3,3a,4,7,7a-hexahydro-1-benzofuran-5-yl]pentyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102219242D          

 25 26  0  0  1  0            999 V2000
   -0.3340   -0.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8860    0.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7065    0.3443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1190   -0.3702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0420    1.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   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
    3.5724    2.8875    0.0000 O   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
    5.0013    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 O   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  2  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
  3  5  1  0  0  0  0
  6  5  1  1  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  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  8 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25  2  1  6  0  0  0
  6 25  1  0  0  0  0
M  END

     RDKit          3D

 51 52  0  0  0  0  0  0  0  0999 V2000
   -1.5840   -4.0377   -1.5837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8966   -3.5397   -0.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0972   -3.8951    0.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8743   -4.8689    0.1837 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2388   -2.9314    1.4095 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5340   -1.8331    0.9276 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0584   -0.8171    1.8992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4991    0.2896    0.9283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9810    1.5784    1.2402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7382    2.7489    0.6257 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2515    3.9520    1.0005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216    5.2155    0.2477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0168    3.9901    2.0005 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7126   -0.1209   -0.0324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1946    0.8111   -1.0287 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2019    1.7091   -1.7298 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1687    1.3251   -1.0357 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3306    0.5965   -0.4974 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8111   -0.6052   -1.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9200   -1.1982   -0.5418 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1195   -0.6027   -0.3068 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2334   -1.2750    0.4142 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3282    0.5679   -0.7036 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3232   -1.5974   -0.1314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2432   -2.5398    0.4650 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2159   -4.7660   -2.0489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6965   -3.7519   -2.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0141   -1.4131    0.0264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8529   -0.4161    2.4981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2331   -1.2008    2.4898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9992    1.7500    2.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1429    1.4632    1.1481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5853    4.9966   -0.7698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8970    5.7731    0.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2604    5.8427    0.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0723    0.0109   -1.9271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1897    1.5013   -2.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9129    2.7745   -1.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2490    1.4682   -1.5163 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2557    2.3632   -0.5761 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4526    1.5772   -2.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1296    0.3348    0.5870 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1882    1.3211   -0.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2805   -0.2643   -2.2067 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1076   -1.3977   -1.4092 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2475   -2.3639    0.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1995   -1.0813    1.5114 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2149   -0.8846    0.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6797   -1.6455    0.3942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1518   -1.8416   -1.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8276   -3.0720    1.3738 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 15 14  1  0
 14  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2 25  1  0
 25 24  1  0
 24 14  1  0
 25  6  1  0
 16 37  1  0
 16 38  1  0
 16 39  1  0
 15 36  1  6
 17 40  1  0
 17 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 22 46  1  0
 22 47  1  0
 22 48  1  0
  9 31  1  0
  9 32  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
  7 29  1  0
  7 30  1  0
  6 28  1  6
  1 26  1  0
  1 27  1  0
 25 51  1  1
 24 49  1  0
 24 50  1  0
M  END


  Mrv1652309102219242D          

 25 26  0  0  1  0            999 V2000
   -0.3340   -0.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8860    0.4305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7065    0.3443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1190   -0.3702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0420    1.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   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
    3.5724    2.8875    0.0000 O   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
    5.0013    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 O   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  2  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
  3  5  1  0  0  0  0
  6  5  1  1  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  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  8 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25  2  1  6  0  0  0
  6 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0303226

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](CCCOC(C)=O)C1=C(COC(C)=O)C[C@@H]2OC(=O)C(=C)[C@H]2C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O6/c1-11(6-5-7-23-13(3)20)16-9-17-12(2)19(22)25-18(17)8-15(16)10-24-14(4)21/h11,17-18H,2,5-10H2,1,3-4H3/t11-,17+,18-/m0/s1

> <INCHI_KEY>
UKGBQQUROCAJPL-PDSMFRHLSA-N

> <FORMULA>
C19H26O6

> <MOLECULAR_WEIGHT>
350.411

> <EXACT_MASS>
350.172938557

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
37.846930165639904

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S)-4-[(3aR,7aS)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-2,3,3a,4,7,7a-hexahydro-1-benzofuran-5-yl]pentyl acetate

> <JCHEM_LOGP>
2.029432322000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.473122720494424

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
90.9378

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4S)-4-[(3aR,7aS)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl 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      -0.623  -0.341   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.654   0.804   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.185   0.643   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.955  -0.691   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -3.812   2.050   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334   5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.000   7.700   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.000   9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.334  10.010   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334  10.010   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.668   5.390   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.336   5.390   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.002   3.080   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   25                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    8   15   24                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   14   25                                                       
CONECT   25   24    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Value	Source
(4S)-4-[(3AR,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-2,3,3a,4,7,7a-hexahydro-1-benzofuran-5-yl]pentyl acetic acid	Generator

Chemical Formula

C₁₉H₂₆O₆

Average Mass

350.4110 Da

Monoisotopic Mass

350.17294 Da

IUPAC Name

(4S)-4-[(3aR,7aS)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-2,3,3a,4,7,7a-hexahydro-1-benzofuran-5-yl]pentyl acetate

Traditional Name

(4S)-4-[(3aR,7aS)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H](CCCOC(C)=O)C1=C(COC(C)=O)C[C@@H]2OC(=O)C(=C)[C@H]2C1

InChI Identifier

InChI=1S/C19H26O6/c1-11(6-5-7-23-13(3)20)16-9-17-12(2)19(22)25-18(17)8-15(16)10-24-14(4)21/h11,17-18H,2,5-10H2,1,3-4H3/t11-,17+,18-/m0/s1

InChI Key

UKGBQQUROCAJPL-PDSMFRHLSA-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
Calostephane divaricata	LOTUS Database	35616633

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
Benzofuran
Tricarboxylic acid or derivatives
Gamma butyrolactone
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
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
logP	2.03	ChemAxon
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.9 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	90.94 m³·mol⁻¹	ChemAxon
Polarizability	37.85 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

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

14314487

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate (NP0303226)

MOL for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)

3D MOL for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)

3D SDF for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)

3D-SDF for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)

PDB for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)

3D PDB for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)

SMILES for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)

INCHI for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)

Structure for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)

3D Structure for NP0303226 ((4s)-4-[(3ar,7as)-6-[(acetyloxy)methyl]-3-methylidene-2-oxo-3a,4,7,7a-tetrahydro-1-benzofuran-5-yl]pentyl acetate)