NP-MRD: Showing NP-Card for (1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione (NP0196166)

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Record Information

Version

2.0

Created at

2022-09-04 14:11:43 UTC

Updated at

2022-09-04 14:11:43 UTC

NP-MRD ID

NP0196166

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione

Description

PAPUAFORIN E belongs to the class of organic compounds known as monoterpenoids. Monoterpenoids are compounds containing a chain of two isoprene units. (1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione is found in Hypericum papuanum. Based on a literature review very few articles have been published on PAPUAFORIN E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042216112D          

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M  END

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M  END


  Mrv1652309042216112D          

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  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 20 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 16 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  2  0  0  0  0
 28 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0196166

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)[C@@]12C(=O)C3=C(OC(C)(C)C=C3)[C@](C)(C[C@@H](CC=C(C)C)[C@]1(C)CCC=C(C)C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H44O4/c1-19(2)12-11-16-30(10)22(14-13-20(3)4)18-29(9)26-23(15-17-28(7,8)35-26)25(33)31(30,27(29)34)24(32)21(5)6/h12-13,15,17,21-22H,11,14,16,18H2,1-10H3/t22-,29+,30+,31+/m1/s1

> <INCHI_KEY>
FJWIFMCUHVVWDK-LSPALGPYSA-N

> <FORMULA>
C31H44O4

> <MOLECULAR_WEIGHT>
480.689

> <EXACT_MASS>
480.323959897

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
72.83498995257362

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,9S,10S,11R)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0^{2,7}]trideca-2(7),5-diene-8,13-dione

> <JCHEM_LOGP>
7.811068018666668

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.09074012492201

> <JCHEM_PKA_STRONGEST_BASIC>
-4.880794760972376

> <JCHEM_POLAR_SURFACE_AREA>
60.44

> <JCHEM_REFRACTIVITY>
145.91949999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,9S,10S,11R)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0^{2,7}]trideca-2(7),5-diene-8,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      13.579  -1.429   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.063  -1.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.539  -3.148   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.070  -0.523   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.593   0.926   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.601   2.103   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.085   1.832   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.739   0.438   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.215   3.366   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.683   3.833   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.012   5.337   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.875   6.375   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.204   7.879   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.407   5.908   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.222   4.544   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.688   4.674   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.221   6.142   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.777   2.909   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.239   2.424   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.907   0.839   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.374  -0.628   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.878  -0.958   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.336  -1.766   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.803  -3.234   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.832  -1.436   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.373   0.970   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.665  -0.398   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.380   2.147   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.511   3.682   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.247   4.562   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.853   3.908   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.451   5.394   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.319   3.770   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.722   2.373   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.986   1.493   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   20                                             
CONECT    8    7                                                            
CONECT    9    7   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    9   16                                                       
CONECT   16   15   17   18   29                                             
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    7   21   26                                             
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   20   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   35                                                  
CONECT   29   28   16   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31   35                                                       
CONECT   35   34   28                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₄₄O₄

Average Mass

480.6890 Da

Monoisotopic Mass

480.32396 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)[C@@]12C(=O)C3=C(OC(C)(C)C=C3)[C@](C)(C[C@@H](CC=C(C)C)[C@]1(C)CCC=C(C)C)C2=O

InChI Identifier

InChI=1S/C31H44O4/c1-19(2)12-11-16-30(10)22(14-13-20(3)4)18-29(9)26-23(15-17-28(7,8)35-26)25(33)31(30,27(29)34)24(32)21(5)6/h12-13,15,17,21-22H,11,14,16,18H2,1-10H3/t22-,29+,30+,31+/m1/s1

InChI Key

FJWIFMCUHVVWDK-LSPALGPYSA-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 papuanum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monoterpenoids. Monoterpenoids are compounds containing a chain of two isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Monoterpenoids

Alternative Parents

Substituents

Monoterpenoid
Cyclohexenone
Pyran
Vinylogous ester
Ketone
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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

C00046277

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

101117449

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione (NP0196166)

MOL for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)

3D MOL for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)

3D SDF for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)

3D-SDF for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)

PDB for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)

3D PDB for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)

SMILES for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)

INCHI for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)

Structure for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)

3D Structure for NP0196166 ((1s,9s,10s,11r)-1,4,4,10-tetramethyl-11-(3-methylbut-2-en-1-yl)-10-(4-methylpent-3-en-1-yl)-9-(2-methylpropanoyl)-3-oxatricyclo[7.3.1.0²,⁷]trideca-2(7),5-diene-8,13-dione)