NP-MRD: Showing NP-Card for 4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate (NP0165726)

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Record Information

Version

2.0

Created at

2022-09-03 00:56:34 UTC

Updated at

2022-09-03 00:56:34 UTC

NP-MRD ID

NP0165726

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate

Description

4,5-Dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. 4,5-Dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171523032D          

 42 44  0  0  0  0            999 V2000
    2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  6 11  1  0  0  0  0
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 17 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004171523032D          

 42 44  0  0  0  0            999 V2000
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    1.4289   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -11.5500    0.0000 O   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
  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
  6 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 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
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  4  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 28 33  1  0  0  0  0
 33 34  2  0  0  0  0
 31 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 24 38  1  0  0  0  0
 20 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 17 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0165726

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCCC1=CCC(CC1)C(C)=C)COC1OCC(OC(=O)C(C)=CCCC2=CCC(CC2=O)C(C)=C)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C35H52O7/c1-22(2)27-15-13-26(14-16-27)11-7-9-24(5)20-40-35-33(38)32(37)31(21-41-35)42-34(39)25(6)10-8-12-28-17-18-29(23(3)4)19-30(28)36/h10,13,17,24,27,29,31-33,35,37-38H,1,3,7-9,11-12,14-16,18-21H2,2,4-6H3

> <INCHI_KEY>
ZOAZAXICYHOXKH-UHFFFAOYSA-N

> <FORMULA>
C35H52O7

> <MOLECULAR_WEIGHT>
584.794

> <EXACT_MASS>
584.371304014

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
68.673178485302

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate

> <ALOGPS_LOGP>
5.37

> <JCHEM_LOGP>
7.08762144

> <ALOGPS_LOGS>
-5.37

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.889988882245046

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.275487288905587

> <JCHEM_PKA_STRONGEST_BASIC>
-3.68772551133727

> <JCHEM_POLAR_SURFACE_AREA>
102.29

> <JCHEM_REFRACTIVITY>
166.9365

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.48e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       5.335 -16.940   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335 -18.480   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001 -19.250   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667 -18.480   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334 -19.250   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000 -18.480   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334 -19.250   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667 -18.480   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334 -16.170   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000 -16.940   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.335 -16.940   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668 -19.250   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.002 -18.480   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.336 -19.250   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.669 -18.480   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      12.003 -19.250   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.003 -20.790   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      13.337 -21.560   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      13.337 -23.100   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      12.003 -23.870   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      14.670 -23.870   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      14.670 -25.410   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.004 -26.180   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      17.338 -25.410   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      18.672 -26.180   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      20.005 -25.410   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      21.339 -26.180   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      21.339 -27.720   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      20.005 -28.490   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      18.672 -27.720   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      17.338 -28.490   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      22.673 -28.490   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      24.006 -27.720   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      22.673 -30.030   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      16.004 -23.100   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.669 -21.560   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      10.669 -23.100   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       9.336 -20.790   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       8.002 -21.560   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    6                                                       
CONECT   12    9   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    2   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   41                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   39                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   38                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   35                                                  
CONECT   32   31   33                                                       
CONECT   33   32   28   34                                                  
CONECT   34   33                                                            
CONECT   35   31   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   24                                                            
CONECT   39   20   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   17   42                                                  
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

View in JSmol

Synonyms

Value	Source
4,5-Dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoic acid	Generator

Chemical Formula

C₃₅H₅₂O₇

Average Mass

584.7940 Da

Monoisotopic Mass

584.37130 Da

IUPAC Name

4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate

Traditional Name

4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate

CAS Registry Number

Not Available

SMILES

CC(CCCC1=CCC(CC1)C(C)=C)COC1OCC(OC(=O)C(C)=CCCC2=CCC(CC2=O)C(C)=C)C(O)C1O

InChI Identifier

InChI=1S/C35H52O7/c1-22(2)27-15-13-26(14-16-27)11-7-9-24(5)20-40-35-33(38)32(37)31(21-41-35)42-34(39)25(6)10-8-12-28-17-18-29(23(3)4)19-30(28)36/h10,13,17,24,27,29,31-33,35,37-38H,1,3,7-9,11-12,14-16,18-21H2,2,4-6H3

InChI Key

ZOAZAXICYHOXKH-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

O-glycosyl compound
Monocyclic monoterpenoid
Monoterpenoid
P-menthane monoterpenoid
Fatty acid ester
Cyclohexenone
Monosaccharide
Fatty acyl
Oxane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
1,2-diol
Ketone
Carboxylic acid ester
Secondary alcohol
Cyclic ketone
Acetal
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
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	5.37	ALOGPS
logP	7.09	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	12.28	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	102.29 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	166.94 m³·mol⁻¹	ChemAxon
Polarizability	68.67 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate (NP0165726)

MOL for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)

3D MOL for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)

3D SDF for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)

3D-SDF for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)

PDB for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)

3D PDB for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)

SMILES for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)

INCHI for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)

Structure for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)

3D Structure for NP0165726 (4,5-dihydroxy-6-({2-methyl-5-[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pentyl}oxy)oxan-3-yl 2-methyl-5-[6-oxo-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]pent-2-enoate)