NP-MRD: Showing NP-Card for (1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione (NP0292151)

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Record Information

Version

2.0

Created at

2022-09-09 23:33:16 UTC

Updated at

2022-09-09 23:33:16 UTC

NP-MRD ID

NP0292151

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione

Description

(1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione is found in Hypericum sampsonii.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102201332D          

 36 39  0  0  1  0            999 V2000
    7.1259   -4.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3659   -4.0538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7080   -4.5516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2637   -3.2351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5036   -2.9143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4014   -2.0956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119   -1.7624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0420   -2.3859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1536   -1.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8501   -0.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8685    0.8173    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    4.7237    3.1446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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 13 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309102201332D          

 36 39  0  0  1  0            999 V2000
    7.1259   -4.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.6546    0.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1119    0.2392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6838    0.6408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6295    0.2742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5914    2.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4480    2.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7237    3.1446    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
  2  4  2  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
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 15 14  1  1  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
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  6  0  0  0
 11 22  1  0  0  0  0
 22 23  2  0  0  0  0
 21 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 26 32  1  0  0  0  0
 11 32  1  0  0  0  0
 32 33  2  0  0  0  0
 26 34  1  0  0  0  0
 13 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0292151

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)[C@]12C(=O)[C@@]34CCC(C)(C)[C@H]3C[C@H](C[C@](C\C=C(\C)CCC=C(C)C)(C4=O)C1=O)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C32H46O4/c1-19(2)11-10-12-21(5)13-14-30-18-22-17-23-28(6,7)15-16-31(23,25(30)34)27(36)32(26(30)35,29(22,8)9)24(33)20(3)4/h11,13,20,22-23H,10,12,14-18H2,1-9H3/b21-13-/t22-,23-,30-,31+,32-/m1/s1

> <INCHI_KEY>
XDMXMPLDQPLYCQ-POXSQVOJSA-N

> <FORMULA>
C32H46O4

> <MOLECULAR_WEIGHT>
494.716

> <EXACT_MASS>
494.339609961

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
57.54819100158301

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,5R,7R,9S,11R)-11-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1^{7,11}.0^{1,5}]tetradecane-10,12,13-trione

> <JCHEM_LOGP>
8.848394026333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.165351589840302

> <JCHEM_PKA_STRONGEST_BASIC>
-7.3511219019259

> <JCHEM_POLAR_SURFACE_AREA>
68.28

> <JCHEM_REFRACTIVITY>
145.32599999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,5R,7R,9S,11R)-11-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1^{7,11}.0^{1,5}]tetradecane-10,12,13-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      13.302  -8.166   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.883  -7.567   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.655  -8.496   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.692  -6.039   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.273  -5.440   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.083  -3.912   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.609  -3.290   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.545  -4.454   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.753  -1.873   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.187  -0.273   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.221   1.526   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.121   3.281   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.106   4.845   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.512   4.991   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.423   3.797   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.883   4.186   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.519   5.054   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.483   5.796   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.117   2.820   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.274   1.756   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.802   2.193   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.745   0.870   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.611  -0.361   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.380   2.423   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.314   4.175   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.142   2.643   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.762   2.909   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.038   3.872   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      10.802   1.681   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.422   1.857   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.542   0.446   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.743   1.196   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      10.508   0.512   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.571   4.212   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.170   4.771   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.818   5.870   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   22   32                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   34                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   15   22   24                                             
CONECT   22   21   11   23                                                  
CONECT   23   22                                                            
CONECT   24   21   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   32   34                                             
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   26   11   33                                                  
CONECT   33   32                                                            
CONECT   34   26   13   35   36                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₆O₄

Average Mass

494.7160 Da

Monoisotopic Mass

494.33961 Da

IUPAC Name

(1S,5R,7R,9S,11R)-11-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1^{7,11}.0^{1,5}]tetradecane-10,12,13-trione

Traditional Name

(1S,5R,7R,9S,11R)-11-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1^{7,11}.0^{1,5}]tetradecane-10,12,13-trione

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)[C@]12C(=O)[C@@]34CCC(C)(C)[C@H]3C[C@H](C[C@](C\C=C(\C)CCC=C(C)C)(C4=O)C1=O)C2(C)C

InChI Identifier

InChI=1S/C32H46O4/c1-19(2)11-10-12-21(5)13-14-30-18-22-17-23-28(6,7)15-16-31(23,25(30)34)27(36)32(26(30)35,29(22,8)9)24(33)20(3)4/h11,13,20,22-23H,10,12,14-18H2,1-9H3/b21-13-/t22-,23-,30-,31+,32-/m1/s1

InChI Key

XDMXMPLDQPLYCQ-POXSQVOJSA-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
Hypericum sampsonii	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	8.85	ChemAxon
pKa (Strongest Acidic)	19.17	ChemAxon
pKa (Strongest Basic)	-7.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	68.28 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	145.33 m³·mol⁻¹	ChemAxon
Polarizability	57.55 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione (NP0292151)

MOL for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)

3D MOL for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)

3D SDF for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)

3D-SDF for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)

PDB for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)

3D PDB for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)

SMILES for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)

INCHI for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)

Structure for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)

3D Structure for NP0292151 ((1s,5r,7r,9s,11r)-11-[(2e)-3,7-dimethylocta-2,6-dien-1-yl]-4,4,8,8-tetramethyl-9-(2-methylpropanoyl)tetracyclo[7.3.1.1⁷,¹¹.0¹,⁵]tetradecane-10,12,13-trione)