NP-MRD: Showing NP-Card for 11-Acetyltorilolone (NP0084736)

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Record Information

Version

2.0

Created at

2022-04-29 05:24:18 UTC

Updated at

2022-04-29 05:24:18 UTC

NP-MRD ID

NP0084736

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-Acetyltorilolone

Description

11-Acetoxytorilolone belongs to the class of organic compounds known as guaianes. These are sesquiterpenoids with a structure based on the guaiane skeleton. Guaiane is a bicyclic compound consisting of a decahydroazulene moiety, substituted with two methyl groups and a 1-methylethyl group at the 1-, 4-, and 7-position, respectively. 11-Acetyltorilolone is found in Daucus carota . Based on a literature review very few articles have been published on 11-Acetoxytorilolone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 48  0  0  0  0  0  0  0  0999 V2000
    4.6268   -0.2722   -1.5524 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4085    0.4010   -0.9922 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8449    1.2932   -1.6211 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9502    0.0176    0.1922 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9231    0.3184    1.0288 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1929   -0.5571    2.2896 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9571    1.7504    1.5568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5677   -0.0162    0.4935 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1967    0.8008   -0.6950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3347    0.7962   -0.7008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0753    1.8728   -0.6026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6065    3.2888   -0.4664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4887    1.5178   -0.6430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5072    2.2399   -0.5561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5577    0.0451   -0.8178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1125   -0.4414   -0.8215 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9610   -1.4013    0.3012 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1861   -2.3170    0.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6926   -2.2003    0.3169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5621   -1.4740    0.0415 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9816   -1.5326   -1.2782 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4770    0.1060   -0.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5812   -1.3615   -1.4750 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8252    0.0528   -2.5815 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8299    0.0453    2.9588 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2525   -0.7710    2.7876 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7766   -1.4556    2.0117 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2261    1.7951    2.3902 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6923    2.4983    0.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9625    1.8792    2.0060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2238    0.1254    1.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4689    1.8500   -0.6803 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4804    0.2687   -1.6510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3921    3.9175    0.0104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3994    3.7122   -1.4741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7048    3.3567    0.1564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1264   -0.3550    0.0662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0910   -0.1652   -1.7468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9752   -0.9244   -1.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0077   -0.8304    1.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7698   -2.2359   -0.6279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8641   -3.3764    0.4853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8485   -2.0606    1.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8226   -2.9953   -0.4774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6083   -2.7788    1.2621 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3812   -1.9741    0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1907   -2.4529   -1.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 13  1  0
 13 14  2  0
 13 11  1  0
 11 12  1  0
 11 10  2  0
 10  9  1  0
  9  8  1  0
  8 20  1  0
 20 21  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  0
  8  5  1  0
  5  6  1  0
  5  7  1  0
  5  4  1  6
  4  2  1  0
  2  1  1  0
  2  3  2  0
 10 16  1  0
 17 16  1  0
 16 39  1  6
 15 37  1  0
 15 38  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
  9 32  1  0
  9 33  1  0
  8 31  1  1
 20 46  1  1
 21 47  1  0
 19 44  1  0
 19 45  1  0
 17 40  1  1
 18 41  1  0
 18 42  1  0
 18 43  1  0
  6 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  7 30  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
M  END


  Mrv1652304292207242D          

 22 23  0  0  1  0            999 V2000
   -0.5033   -2.1531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2483   -1.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7333   -0.7011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2483   -0.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5583   -0.7011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5363   -1.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5363   -0.2886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2796   -0.6465    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1813    0.2258    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9977    1.0301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9856    0.0422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3436   -0.7011    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1686   -0.7011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9856   -1.4444    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5000   -2.0894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0144   -2.7344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7130   -3.5024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2273   -4.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8972   -3.6253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8550   -2.6038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1450   -1.5750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1813   -1.6280    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
  3  5  2  0  0  0  0
  2  6  2  0  0  0  0
  6  7  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  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
 15 20  1  0  0  0  0
 15 21  1  0  0  0  0
 14 22  1  0  0  0  0
  6 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0084736

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12CC(=O)C(C)=C1C[C@@H]([C@H](O)C[C@@H]2C)C(C)(C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H26O4/c1-9-6-16(20)14(17(4,5)21-11(3)18)7-13-10(2)15(19)8-12(9)13/h9,12,14,16,20H,6-8H2,1-5H3/t9-,12+,14-,16+/m0/s1

> <INCHI_KEY>
PSVQRRSHJWNFPZ-UODBANLJSA-N

> <FORMULA>
C17H26O4

> <MOLECULAR_WEIGHT>
294.391

> <EXACT_MASS>
294.183109317

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
32.60804069074857

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(5S,6R,8S,8aR)-6-hydroxy-3,8-dimethyl-2-oxo-1,2,4,5,6,7,8,8a-octahydroazulen-5-yl]propan-2-yl acetate

> <ALOGPS_LOGP>
1.96

> <JCHEM_LOGP>
1.8457886483333323

> <ALOGPS_LOGS>
-3.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.840044206165032

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8687646642234146

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
80.65630000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.85e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(5S,6R,8S,8aR)-6-hydroxy-3,8-dimethyl-2-oxo-4,5,6,7,8,8a-hexahydro-1H-azulen-5-yl]propan-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      -0.939  -4.019   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.464  -2.555   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.369  -1.309   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.464  -0.063   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.909  -1.309   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.001  -2.079   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.001  -0.539   0.000  0.00  0.00           C+0
HETATM    8  H   UNK     0       2.389  -1.207   0.000  0.00  0.00           H+0
HETATM    9  C   UNK     0       2.205   0.421   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.862   1.923   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.706   0.079   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.375  -1.309   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.915  -1.309   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.706  -2.696   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.667  -3.900   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.627  -5.104   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.064  -6.538   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.024  -7.742   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.541  -6.767   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.463  -4.860   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.871  -2.940   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.205  -3.039   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3    7                                                       
CONECT    5    3                                                            
CONECT    6    2    7   22                                                  
CONECT    7    6    4    8    9                                             
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   22                                                  
CONECT   15   14   16   20   21                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15                                                            
CONECT   21   15                                                            
CONECT   22   14    6                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₆O₄

Average Mass

294.3910 Da

Monoisotopic Mass

294.18311 Da

IUPAC Name

2-[(5S,6R,8S,8aR)-6-hydroxy-3,8-dimethyl-2-oxo-1,2,4,5,6,7,8,8a-octahydroazulen-5-yl]propan-2-yl acetate

Traditional Name

2-[(5S,6R,8S,8aR)-6-hydroxy-3,8-dimethyl-2-oxo-4,5,6,7,8,8a-hexahydro-1H-azulen-5-yl]propan-2-yl acetate

CAS Registry Number

Not Available

SMILES

[H][C@]12CC(=O)C(C)=C1C[C@@H]([C@H](O)C[C@@H]2C)C(C)(C)OC(C)=O

InChI Identifier

InChI=1S/C17H26O4/c1-9-6-16(20)14(17(4,5)21-11(3)18)7-13-10(2)15(19)8-12(9)13/h9,12,14,16,20H,6-8H2,1-5H3/t9-,12+,14-,16+/m0/s1

InChI Key

PSVQRRSHJWNFPZ-UODBANLJSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Daucus carota	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guaianes. These are sesquiterpenoids with a structure based on the guaiane skeleton. Guaiane is a bicyclic compound consisting of a decahydroazulene moiety, substituted with two methyl groups and a 1-methylethyl group at the 1-, 4-, and 7-position, respectively.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Guaianes

Alternative Parents

Substituents

Guaiane sesquiterpenoid
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	1.96	ALOGPS
logP	1.85	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	14.84	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	80.66 m³·mol⁻¹	ChemAxon
Polarizability	32.61 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00054305

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

45102165

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 11-Acetyltorilolone (NP0084736)

MOL for NP0084736 (11-Acetyltorilolone)

3D MOL for NP0084736 (11-Acetyltorilolone)

3D SDF for NP0084736 (11-Acetyltorilolone)

3D-SDF for NP0084736 (11-Acetyltorilolone)

PDB for NP0084736 (11-Acetyltorilolone)

3D PDB for NP0084736 (11-Acetyltorilolone)

SMILES for NP0084736 (11-Acetyltorilolone)

INCHI for NP0084736 (11-Acetyltorilolone)

Structure for NP0084736 (11-Acetyltorilolone)

3D Structure for NP0084736 (11-Acetyltorilolone)