NP-MRD: Showing NP-Card for 4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate (NP0229675)

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Record Information

Version

2.0

Created at

2022-09-06 09:50:43 UTC

Updated at

2022-09-06 09:50:43 UTC

NP-MRD ID

NP0229675

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate

Description

4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate is found in Euglena gracilis.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062211502D          

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M  END

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  Mrv1652309062211502D          

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   20.0052  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -14.0250    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  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
 12 13  1  0  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
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 21 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
 32 34  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0229675

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC\C(C)=C\CC1=CC(OC)=C(C)C(C)=C1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H52O3/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25(2)22-23-29-24-30(33-6)26(3)27(4)31(29)34-28(5)32/h22,24H,7-21,23H2,1-6H3/b25-22+

> <INCHI_KEY>
JACGZFDJBGVEDW-YYDJUVGSSA-N

> <FORMULA>
C31H52O3

> <MOLECULAR_WEIGHT>
472.754

> <EXACT_MASS>
472.391645534

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
61.87239748930035

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-methoxy-2,3-dimethyl-6-[(2E)-3-methylnonadec-2-en-1-yl]phenyl acetate

> <JCHEM_LOGP>
10.846775277666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.813413856549301

> <JCHEM_POLAR_SURFACE_AREA>
35.53

> <JCHEM_REFRACTIVITY>
146.9938

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-methoxy-2,3-dimethyl-6-[(2E)-3-methylnonadec-2-en-1-yl]phenyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      12.003 -20.790   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.337 -21.560   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.670 -20.790   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.004 -21.560   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.338 -20.790   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.672 -21.560   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.005 -20.790   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.339 -21.560   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      22.673 -20.790   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.006 -21.560   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      25.340 -20.790   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      26.674 -21.560   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      28.007 -20.790   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      29.341 -21.560   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      30.675 -20.790   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      32.008 -21.560   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      33.342 -20.790   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      33.342 -19.250   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      34.676 -21.560   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      36.009 -20.790   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      37.343 -21.560   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      38.677 -20.790   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      40.010 -21.560   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      41.344 -20.790   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      41.344 -19.250   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      40.010 -23.100   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      41.344 -23.870   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      38.677 -23.870   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      38.677 -25.410   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      37.343 -23.100   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      36.009 -23.870   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      36.009 -25.410   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      37.343 -26.180   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      34.676 -26.180   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   30                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   21   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₅₂O₃

Average Mass

472.7540 Da

Monoisotopic Mass

472.39165 Da

IUPAC Name

4-methoxy-2,3-dimethyl-6-[(2E)-3-methylnonadec-2-en-1-yl]phenyl acetate

Traditional Name

4-methoxy-2,3-dimethyl-6-[(2E)-3-methylnonadec-2-en-1-yl]phenyl acetate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC\C(C)=C\CC1=CC(OC)=C(C)C(C)=C1OC(C)=O

InChI Identifier

InChI=1S/C31H52O3/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25(2)22-23-29-24-30(33-6)26(3)27(4)31(29)34-28(5)32/h22,24H,7-21,23H2,1-6H3/b25-22+

InChI Key

JACGZFDJBGVEDW-YYDJUVGSSA-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
Euglena gracilis	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	10.85	ChemAxon
pKa (Strongest Basic)	-4.8	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	20	ChemAxon
Refractivity	146.99 m³·mol⁻¹	ChemAxon
Polarizability	61.87 Å³	ChemAxon
Number of Rings	1	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate (NP0229675)

MOL for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)

3D MOL for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)

3D SDF for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)

3D-SDF for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)

PDB for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)

3D PDB for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)

SMILES for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)

INCHI for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)

Structure for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)

3D Structure for NP0229675 (4-methoxy-2,3-dimethyl-6-[(2e)-3-methylnonadec-2-en-1-yl]phenyl acetate)