NP-MRD: Showing NP-Card for 1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate (NP0322068)

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Record Information

Version

2.0

Created at

2022-09-12 00:37:54 UTC

Updated at

2022-09-12 00:37:54 UTC

NP-MRD ID

NP0322068

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate

Description

1-(Acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate is found in Anisopappus pinnatifidus. Based on a literature review very few articles have been published on 1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122202372D          

 29 29  0  0  0  0            999 V2000
    3.6585   -1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6585   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9441   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2296   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5151   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8006   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8006   -1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0862   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6283   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3428   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0572   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3394   -0.1260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269   -1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8091   -2.3085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6216   -2.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1519   -1.8197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6822   -2.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8663   -1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8697   -1.0445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3730   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0875   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8019   -0.4887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5164   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2309   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5164   -1.7262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3730    0.3363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6585    0.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9441    0.3363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6585    1.5738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  6  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
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
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 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
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 11 19  1  0  0  0  0
  2 20  1  0  0  0  0
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 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
M  END

     RDKit          3D

 71 71  0  0  0  0  0  0  0  0999 V2000
    2.9685   -0.8948    1.2083 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7338    0.0227    0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1483    1.1795   -0.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8925   -0.3798    0.7068 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2269   -0.0595    0.7354 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6873   -1.2757    1.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0900   -1.4002    1.4322 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9985   -0.5069    1.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4754   -0.7012    1.8551 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5713    0.5399    2.4749 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6622   -0.1844   -0.6150 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5155    0.7613   -1.1477 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9716    0.6307   -2.5624 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9269    1.7520   -0.4541 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.1552    2.1160    0.7943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6711   -0.2245   -0.4915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0139    0.5888    1.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1370    0.9785    2.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2169   -0.4270    3.0250 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309122202372D          

 29 29  0  0  0  0            999 V2000
    3.6585   -1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6585   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9441   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2296   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5151   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6216   -2.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6822   -2.4517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8663   -1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8697   -1.0445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3730   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0875   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8019   -0.4887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5164   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2309   -0.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5164   -1.7262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3730    0.3363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6585    0.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9441    0.3363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6585    1.5738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0322068

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCCC(=C)C(COC(C)=O)OC(C)=O)CCCC1(C)CCCC(C)(C)O1

> <INCHI_IDENTIFIER>
InChI=1S/C24H42O5/c1-18(12-9-15-24(7)16-10-14-23(5,6)29-24)11-8-13-19(2)22(28-21(4)26)17-27-20(3)25/h18,22H,2,8-17H2,1,3-7H3

> <INCHI_KEY>
MWIVNGBJWOARQO-UHFFFAOYSA-N

> <FORMULA>
C24H42O5

> <MOLECULAR_WEIGHT>
410.595

> <EXACT_MASS>
410.303224452

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
48.47773477212522

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate

> <JCHEM_LOGP>
5.201259106333331

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.202600630839344

> <JCHEM_POLAR_SURFACE_AREA>
61.830000000000005

> <JCHEM_REFRACTIVITY>
114.9144

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       6.829  -3.222   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.829  -1.682   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.496  -0.912   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.162  -1.682   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.828  -0.912   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.495  -1.682   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.495  -3.222   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.161  -0.912   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.173  -1.682   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.506  -0.912   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.840  -1.682   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.367  -0.235   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.850  -2.862   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.377  -4.309   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.894  -4.577   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.883  -3.397   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.873  -4.577   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -7.217  -2.627   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -5.357  -1.950   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.163  -0.912   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.497  -1.682   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.830  -0.912   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.164  -1.682   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.498  -0.912   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      12.164  -3.222   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.163   0.628   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.829   1.398   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.496   0.628   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.829   2.938   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    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   19                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   11                                                       
CONECT   20    2   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   20   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

View in JSmol

Synonyms

Value	Source
1-(Acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetic acid	Generator

Chemical Formula

C₂₄H₄₂O₅

Average Mass

410.5950 Da

Monoisotopic Mass

410.30322 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(CCCC(=C)C(COC(C)=O)OC(C)=O)CCCC1(C)CCCC(C)(C)O1

InChI Identifier

InChI=1S/C24H42O5/c1-18(12-9-15-24(7)16-10-14-23(5,6)29-24)11-8-13-19(2)22(28-21(4)26)17-27-20(3)25/h18,22H,2,8-17H2,1,3-7H3

InChI Key

MWIVNGBJWOARQO-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
Anisopappus pinnatifidus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Fatty alcohol ester
Dicarboxylic acid or derivatives
Oxane
Carboxylic acid ester
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Carbonyl group
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

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

14287119

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate (NP0322068)

MOL for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)

3D MOL for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)

3D SDF for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)

3D-SDF for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)

PDB for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)

3D PDB for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)

SMILES for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)

INCHI for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)

Structure for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)

3D Structure for NP0322068 (1-(acetyloxy)-7-methyl-3-methylidene-10-(2,6,6-trimethyloxan-2-yl)decan-2-yl acetate)