NP-MRD: Showing NP-Card for 1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate (NP0251083)

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Record Information

Version

2.0

Created at

2022-09-07 14:09:15 UTC

Updated at

2022-09-07 14:09:16 UTC

NP-MRD ID

NP0251083

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate

Description

CHEMBL3234604 belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. 1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate is found in Lagopsis supina. Based on a literature review very few articles have been published on CHEMBL3234604.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072216092D          

 27 28  0  0  1  0            999 V2000
    1.7309   -0.5230    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
    2.9684   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809   -0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809   -1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -2.6664    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3809   -3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0129   -2.8506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0129   -3.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309   -3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.6664    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1146   -1.8419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4438   -2.2293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4726   -1.4048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7153   -2.6166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0157   -2.1794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7127   -2.5667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8275   -3.3837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6400   -3.5269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0273   -2.7985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4542   -2.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
 10  5  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 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
 10 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  6  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  2  0  0  0  0
M  END

     RDKit          3D

 59 60  0  0  0  0  0  0  0  0999 V2000
   -4.4194   -3.1795   -0.4562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7906   -1.8731   -0.8771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3910   -1.7362   -0.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9480   -2.6619    0.2400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5713   -0.5654   -0.6606 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3635    0.3856   -1.3611 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1455    0.8386   -2.6276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0935    1.8396   -3.1837 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1640    0.3884   -3.2478 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8386    0.1113    0.4359 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6483    0.6541    1.5818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9718   -0.2967    2.6769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9548    1.2717    1.1108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8964    1.8374    2.1917 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5780    1.7377    2.1506 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9673    0.2884    2.0883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5125   -0.3436    0.7626 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8268   -1.7820    0.9191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4897    0.1944   -0.2552 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0437    0.8895   -1.1408 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9358   -0.0845   -0.2179 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6303    0.5964   -1.3600 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0830    0.3256   -1.3361 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0563    1.0509   -0.7054 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2633    0.4414   -0.9463 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0222   -0.6070   -1.6913 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7270   -0.7199   -1.9529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2076   -2.9383    0.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8917   -3.7333   -1.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6588   -3.7827    0.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8455   -1.8784   -2.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4202   -1.0102   -0.5902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7575   -0.7998   -1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1217    1.4105   -3.0012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0758    2.7867   -2.6004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9852    1.9925   -4.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6084    1.1298   -0.0850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5835   -1.3097    2.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7423    0.1554    3.6912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0940   -0.4503    2.7639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2685    1.9406    1.9755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8369    1.9689    0.2722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7686    0.5533    1.0502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1841    2.8002    1.6997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2172    1.9804    3.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9978    2.1368    3.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0581    2.3460    1.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5075   -0.2163    2.9599 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0651    0.1844    2.2228 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3291   -2.3637    1.6652 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7139   -2.2795   -0.0660 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9385   -1.9201    1.1253 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1028   -1.1909   -0.3758 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4338    0.2563    0.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1870    0.3346   -2.3446 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5218    1.7157   -1.2860 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9096    1.9392   -0.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2330    0.7620   -0.5904 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3303   -1.5216   -2.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  5 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  6
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 27  2  0
 27 26  1  0
 26 25  1  0
 25 24  2  0
 17 10  1  0
 24 23  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  5 33  1  6
  8 34  1  0
  8 35  1  0
  8 36  1  0
 10 37  1  6
 12 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 18 50  1  0
 18 51  1  0
 18 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 27 59  1  0
 25 58  1  0
 24 57  1  0
M  END


  Mrv1652309072216092D          

 27 28  0  0  1  0            999 V2000
    1.7309   -0.5230    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
    2.9684   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809   -0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809   -1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -1.9520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -2.6664    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3809   -3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0129   -2.8506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0129   -3.9112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309   -3.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.6664    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1146   -1.8419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4438   -2.2293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4726   -1.4048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7153   -2.6166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0157   -2.1794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7127   -2.5667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8275   -3.3837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6400   -3.5269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0273   -2.7985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4542   -2.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
 10  5  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 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
 10 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  6  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0251083

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=O)C(OC(C)=O)[C@H]1C(C)(C)CCC[C@]1(C)C(=O)CCC1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O5/c1-6-17(24)19(27-15(2)23)20-21(3,4)11-7-12-22(20,5)18(25)9-8-16-10-13-26-14-16/h10,13-14,19-20H,6-9,11-12H2,1-5H3/t19?,20-,22+/m0/s1

> <INCHI_KEY>
WRGBXVVSPJQVPJ-VDZZXDNDSA-N

> <FORMULA>
C22H32O5

> <MOLECULAR_WEIGHT>
376.493

> <EXACT_MASS>
376.22497413

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
41.354257872815325

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[(1S,2S)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate

> <JCHEM_LOGP>
4.8715371350000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.448518593589785

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.163345246422114

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8759620016855574

> <JCHEM_POLAR_SURFACE_AREA>
73.58000000000001

> <JCHEM_REFRACTIVITY>
102.31769999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-[(1S,2S)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       3.231  -0.976   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.541  -2.310   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.311  -0.976   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.311  -3.644   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.851  -3.644   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.621  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.161  -2.310   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.851  -0.976   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.541  -4.977   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.311  -6.311   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.491  -5.321   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.491  -7.301   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.541  -7.645   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -7.645   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.231  -6.311   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -4.977   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.947  -3.438   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.695  -4.161   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.749  -2.622   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.335  -4.884   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.029  -4.068   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.330  -4.791   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.545  -6.316   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.061  -6.584   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.784  -5.224   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.715  -4.116   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    5   11   17                                                  
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   10   18   19                                             
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   23                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₂O₅

Average Mass

376.4930 Da

Monoisotopic Mass

376.22497 Da

IUPAC Name

1-[(1S,2S)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate

Traditional Name

1-[(1S,2S)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate

CAS Registry Number

Not Available

SMILES

CCC(=O)C(OC(C)=O)[C@H]1C(C)(C)CCC[C@]1(C)C(=O)CCC1=COC=C1

InChI Identifier

InChI=1S/C22H32O5/c1-6-17(24)19(27-15(2)23)20-21(3,4)11-7-12-22(20,5)18(25)9-8-16-10-13-26-14-16/h10,13-14,19-20H,6-9,11-12H2,1-5H3/t19?,20-,22+/m0/s1

InChI Key

WRGBXVVSPJQVPJ-VDZZXDNDSA-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
Lagopsis supina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Aromatic monoterpenoids

Alternative Parents

Substituents

Aromatic monoterpenoid
Monocyclic monoterpenoid
Alpha-acyloxy ketone
Furan
Heteroaromatic compound
Carboxylic acid ester
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	4.87	ChemAxon
pKa (Strongest Acidic)	17.16	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	73.58 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	102.32 m³·mol⁻¹	ChemAxon
Polarizability	41.35 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

34237778

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90670466

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate (NP0251083)

MOL for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)

3D MOL for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)

3D SDF for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)

3D-SDF for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)

PDB for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)

3D PDB for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)

SMILES for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)

INCHI for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)

Structure for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)

3D Structure for NP0251083 (1-[(1s,2s)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl acetate)