NP-MRD: Showing NP-Card for methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate (NP0273834)

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Record Information

Version

2.0

Created at

2022-09-08 21:00:10 UTC

Updated at

2022-09-08 21:00:11 UTC

NP-MRD ID

NP0273834

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate

Description

Methyl (2E,6E)-7-[(2R)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate is found in Isolona hexaloba. Based on a literature review very few articles have been published on methyl (2E,6E)-7-[(2R)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 45  0  0  0  0  0  0  0  0999 V2000
    6.9377    2.3977    0.2933 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5512    2.1953    0.4462 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9692    0.9189    0.4406 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7506   -0.0297    0.2922 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5274    0.8173    0.6060 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9320   -0.3575    0.6083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7946   -1.5534    0.4363 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4481   -0.4940    0.7782 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9017   -1.1660   -0.4350 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5724   -1.3557   -0.3803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3528   -0.8118   -1.2930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6766   -0.0057   -2.3690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8184   -0.9154   -1.3621 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4586   -1.7154   -0.2962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6704   -0.6588    0.7909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9716    0.5378   -0.0889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6052    1.8349    0.5986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4814    0.5074   -0.3638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3352    0.3713   -1.2877 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4265    2.6333    1.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0649    3.3210   -0.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4494    1.5892   -0.2392 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9196    1.6897    0.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2696   -1.6116   -0.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4903   -1.7107    1.2846 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1076   -2.4485    0.4665 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3270   -1.1732    1.6728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9736    0.4468    1.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2368   -0.6340   -1.3212 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3339   -2.1946   -0.4930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0529   -1.9374    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3991    0.5270   -3.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0144   -0.6299   -2.9826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1115    0.8099   -1.8290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0727   -1.3631   -2.3581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4982   -1.9765   -0.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9440   -2.5978    0.0472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7124   -0.4517    1.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4917   -0.9129    1.4600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5597    1.6816    1.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3864    2.6049    0.3347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6288    2.1525    0.2255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9235    1.4728    0.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6908    0.4966   -1.4534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9831   -0.3007    0.1751 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  2  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 16 19  1  0
 19 13  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  5 23  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
  9 30  1  0
 10 31  1  0
 12 32  1  0
 12 33  1  0
 12 34  1  0
 13 35  1  6
 14 36  1  0
 14 37  1  0
 15 38  1  0
 15 39  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  0
 18 44  1  0
 18 45  1  0
M  END


  Mrv1652309082223002D          

 19 19  0  0  1  0            999 V2000
    2.0626   -6.5072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5777   -5.8397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9133   -5.0860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7338   -4.9998    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4284   -4.4186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7639   -3.6649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5844   -3.5787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2790   -2.9975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6145   -2.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1296   -1.5764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2857   -0.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0157    1.7274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1198    1.7274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 13 11  1  1  0  0  0
 13 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
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 13 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0273834

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)\C=C(/C)CC\C=C(/C)[C@H]1CCC(C)(C)O1

> <INCHI_IDENTIFIER>
InChI=1S/C16H26O3/c1-12(11-15(17)18-5)7-6-8-13(2)14-9-10-16(3,4)19-14/h8,11,14H,6-7,9-10H2,1-5H3/b12-11+,13-8+/t14-/m1/s1

> <INCHI_KEY>
DDRPTKPVVFJQRF-GDFAELGLSA-N

> <FORMULA>
C16H26O3

> <MOLECULAR_WEIGHT>
266.381

> <EXACT_MASS>
266.188194697

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
31.657815252398553

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2E,6E)-7-[(2R)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate

> <JCHEM_LOGP>
3.7269567999999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.212283112092114

> <JCHEM_POLAR_SURFACE_AREA>
35.53

> <JCHEM_REFRACTIVITY>
78.61270000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2E,6E)-7-[(2R)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       3.850 -12.147   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.945 -10.901   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.571  -9.494   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.103  -9.333   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.666  -8.248   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.293  -6.841   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.824  -6.680   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.387  -5.595   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.014  -4.188   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.109  -2.943   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.735  -1.536   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.267  -1.375   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.029   3.224   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.090   3.224   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.306   1.175   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   13                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   38    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2E,6E)-7-[(2R)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoic acid	Generator

Chemical Formula

C₁₆H₂₆O₃

Average Mass

266.3810 Da

Monoisotopic Mass

266.18819 Da

IUPAC Name

methyl (2E,6E)-7-[(2R)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate

Traditional Name

methyl (2E,6E)-7-[(2R)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate

CAS Registry Number

Not Available

SMILES

COC(=O)\C=C(/C)CC\C=C(/C)[C@H]1CCC(C)(C)O1

InChI Identifier

InChI=1S/C16H26O3/c1-12(11-15(17)18-5)7-6-8-13(2)14-9-10-16(3,4)19-14/h8,11,14H,6-7,9-10H2,1-5H3/b12-11+,13-8+/t14-/m1/s1

InChI Key

DDRPTKPVVFJQRF-GDFAELGLSA-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
Isolona hexaloba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Monocyclic monoterpenoid
Monoterpenoid
Fatty acid ester
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tetrahydrofuran
Carboxylic acid ester
Carboxylic acid derivative
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
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	3.73	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	35.53 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	78.61 m³·mol⁻¹	ChemAxon
Polarizability	31.66 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

162922478

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate (NP0273834)

MOL for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)

3D MOL for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)

3D SDF for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)

3D-SDF for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)

PDB for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)

3D PDB for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)

SMILES for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)

INCHI for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)

Structure for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)

3D Structure for NP0273834 (methyl (2e,6e)-7-[(2r)-5,5-dimethyloxolan-2-yl]-3-methylocta-2,6-dienoate)