NP-MRD: Showing NP-Card for 1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one (NP0291668)

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Record Information

Version

1.0

Created at

2022-09-09 22:50:59 UTC

Updated at

2022-09-09 22:51:00 UTC

NP-MRD ID

NP0291668

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one

Description

1-[2,3-Dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated. 1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one is found in Magallana gigas and Meretrix petechialis. 1-[2,3-Dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201501552D          

 44 45  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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 29 80  1  0
 31 81  1  0
 31 82  1  0
 31 83  1  0
 36 84  1  0
 36 85  1  0
 36 86  1  0
 37 87  1  0
 37 88  1  0
 38 89  1  6
 39 90  1  0
 40 91  1  0
 40 92  1  0
 42 93  1  0
 42 94  1  0
 42 95  1  0
 43 96  1  0
 43 97  1  0
 43 98  1  0
M  END


  Mrv1533004201501552D          

 44 45  0  0  0  0            999 V2000
   -6.7979  -12.9271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0132  -13.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7583  -13.9667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9333  -13.9667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4484  -14.6341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6279  -14.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2923  -13.7942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1430  -15.2153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6784  -13.1820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3458  -12.6971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9408  -11.9784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7508  -11.9784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3308  -11.2683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5059  -11.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7358  -10.5495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3159   -9.8394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7209   -9.1206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3009   -8.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7059   -7.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2860   -6.9817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6909   -6.2629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2710   -5.5528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6760   -4.8341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2560   -4.1239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4311   -4.1326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6610   -3.4052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2411   -2.6951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6461   -1.9763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2261   -1.2662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4011   -1.2749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6311   -0.5475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0361    0.1713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4411    0.8900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2660    0.8987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6860    0.1886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6710    1.6174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2511    2.3275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6561    3.0463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4261    2.3189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0211    1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2887    1.9798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2968    1.2052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5309   -7.6831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5608  -10.5409    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  4  0  0  0
 23 24  2  0  0  0  0
 24 25  1  4  0  0  0
 26 24  1  4  0  0  0
 26 27  2  0  0  0  0
 28 27  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  3  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 33 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 19 43  1  0  0  0  0
 15 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0291668

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(CC(C)=O)OC1(C)CC(=O)C(C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C)C#CC1=C(C)CC(O)CC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C40H54O4/c1-28(17-13-18-30(3)21-22-37-32(5)23-35(42)26-39(37,8)9)15-11-12-16-29(2)19-14-20-31(4)38(43)27-40(10)33(6)24-36(44-40)25-34(7)41/h11-20,33,35-36,42H,23-27H2,1-10H3

> <INCHI_KEY>
KFNGKYUGHHQDEE-UHFFFAOYSA-N

> <FORMULA>
C40H54O4

> <MOLECULAR_WEIGHT>
598.868

> <EXACT_MASS>
598.402210219

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
72.80730071370641

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one

> <ALOGPS_LOGP>
7.48

> <JCHEM_LOGP>
7.930071345000001

> <ALOGPS_LOGS>
-5.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.722741218451727

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.568773875998673

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1699260967336005

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
192.64880000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.63e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0     -12.689 -24.131   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -11.225 -24.606   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -10.749 -26.071   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.209 -26.071   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.304 -27.317   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.772 -27.156   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -6.146 -25.749   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -5.867 -28.402   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -8.733 -24.606   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -9.979 -23.701   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.223 -22.360   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -10.735 -22.360   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -9.951 -21.034   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -8.411 -21.050   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0     -10.707 -19.692   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -9.923 -18.367   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -10.679 -17.025   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -9.895 -15.700   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -10.651 -14.358   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -9.867 -13.032   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -10.623 -11.691   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -9.839 -10.365   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -10.595  -9.024   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -9.811  -7.698   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -8.271  -7.714   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -10.567  -6.356   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -9.783  -5.031   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -10.539  -3.689   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -9.755  -2.364   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.215  -2.380   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -10.511  -1.022   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -11.267   0.320   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -12.023   1.661   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -13.563   1.678   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -14.347   0.352   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -14.319   3.019   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -13.535   4.345   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0     -14.291   5.686   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0     -11.995   4.329   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -11.239   2.987   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -9.872   3.696   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -9.887   2.250   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0     -12.191 -14.342   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -12.247 -19.676   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10                                                       
CONECT   10    9    2   11   12                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   44                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   43                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   40                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   33   41   42                                             
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   19                                                            
CONECT   44   15                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₅₄O₄

Average Mass

598.8680 Da

Monoisotopic Mass

598.40221 Da

IUPAC Name

1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one

Traditional Name

1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one

CAS Registry Number

Not Available

SMILES

CC1CC(CC(C)=O)OC1(C)CC(=O)C(C)=CC=CC(C)=CC=CC=C(C)C=CC=C(C)C#CC1=C(C)CC(O)CC1(C)C

InChI Identifier

InChI=1S/C40H54O4/c1-28(17-13-18-30(3)21-22-37-32(5)23-35(42)26-39(37,8)9)15-11-12-16-29(2)19-14-20-31(4)38(43)27-40(10)33(6)24-36(44-40)25-34(7)41/h11-20,33,35-36,42H,23-27H2,1-10H3

InChI Key

KFNGKYUGHHQDEE-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Magallana gigas	LOTUS Database	35616633
Meretrix petechialis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Diterpene glycosides

Alternative Parents

Substituents

Diterpene glycoside
Diterpenoid
Alpha-branched alpha,beta-unsaturated-ketone
Acryloyl-group
Enone
Alpha,beta-unsaturated ketone
Oxolane
Ketone
Secondary alcohol
Dialkyl ether
Oxacycle
Ether
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	7.48	ALOGPS
logP	7.93	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	18.57	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	192.65 m³·mol⁻¹	ChemAxon
Polarizability	72.81 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

74052708

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one (NP0291668)

MOL for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)

3D MOL for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)

3D SDF for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)

3D-SDF for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)

PDB for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)

3D PDB for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)

SMILES for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)

INCHI for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)

Structure for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)

3D Structure for NP0291668 (1-[2,3-dimethyl-5-(2-oxopropyl)oxolan-2-yl]-18-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-3,5,7,9,11,13,15-heptaen-17-yn-2-one)