NP-MRD: Showing NP-Card for 4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione (NP0312836)

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Record Information

Version

2.0

Created at

2022-09-11 09:57:25 UTC

Updated at

2022-09-11 09:57:25 UTC

NP-MRD ID

NP0312836

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione

Description

Not Available

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112211572D          

 33 34  0  0  0  0            999 V2000
    3.2251    4.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4800    3.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2870    3.3356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9280    2.8940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1829    2.1094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6309    1.4963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8858    0.7117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6928    0.5402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3338    0.0986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5887   -0.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4847   -0.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6777   -0.8575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1257   -0.2444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3806    0.5402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6813   -0.4160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4888   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1393   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4748   -3.9898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3188   -3.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -3.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9866   -3.7311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -2.9774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1426   -2.8911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8372   -2.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1728   -1.5563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0168   -2.3962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5846   -1.5291    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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
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 32 33  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309112211572D          

 33 34  0  0  0  0            999 V2000
    3.2251    4.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4800    3.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0312836

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC(C)=CCC1(CC=C(C)C)C(=O)C(O)=C(C(=O)C2=CC=C(O)C(O)=C2)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H32O6/c1-16(2)7-6-8-18(5)12-14-27(13-11-17(3)4)25(32)22(24(31)26(27)33)23(30)19-9-10-20(28)21(29)15-19/h7,9-12,15,28-29,31H,6,8,13-14H2,1-5H3

> <INCHI_KEY>
JABJSHMLHVMIMA-UHFFFAOYSA-N

> <FORMULA>
C27H32O6

> <MOLECULAR_WEIGHT>
452.547

> <EXACT_MASS>
452.21988875

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
49.97206176779296

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione

> <JCHEM_LOGP>
6.138610762333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.972982012495728

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.7945940380242167

> <JCHEM_PKA_STRONGEST_BASIC>
-6.505900280117587

> <JCHEM_POLAR_SURFACE_AREA>
111.9

> <JCHEM_REFRACTIVITY>
132.51149999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       6.020   8.011   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.496   6.547   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002   6.226   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.466   5.402   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.941   3.938   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.911   2.793   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.387   1.329   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.893   1.008   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.356   0.184   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.832  -1.281   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.802  -2.425   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.771  -1.281   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.265  -1.601   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.235  -0.456   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.710   1.008   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.272  -0.776   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.048  -3.330   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.512  -2.854   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.572  -4.795   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.477  -6.041   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.032  -4.795   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.127  -6.041   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.753  -7.448   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.595  -5.880   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.310  -7.126   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.842  -6.965   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.468  -5.558   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -4.000  -5.397   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.563  -4.312   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -2.189  -2.905   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.031  -4.473   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.556  -3.330   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       1.091  -2.854   0.000  0.00  0.00           O+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   17   32                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   11   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   32                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   31                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   24                                                       
CONECT   32   21   11   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₂O₆

Average Mass

452.5470 Da

Monoisotopic Mass

452.21989 Da

IUPAC Name

4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione

Traditional Name

4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)=CCC1(CC=C(C)C)C(=O)C(O)=C(C(=O)C2=CC=C(O)C(O)=C2)C1=O

InChI Identifier

InChI=1S/C27H32O6/c1-16(2)7-6-8-18(5)12-14-27(13-11-17(3)4)25(32)22(24(31)26(27)33)23(30)19-9-10-20(28)21(29)15-19/h7,9-12,15,28-29,31H,6,8,13-14H2,1-5H3

InChI Key

JABJSHMLHVMIMA-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

Not Available

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	6.14	ChemAxon
pKa (Strongest Acidic)	2.79	ChemAxon
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	111.9 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	132.51 m³·mol⁻¹	ChemAxon
Polarizability	49.97 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	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-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione (NP0312836)

MOL for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)

3D MOL for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)

3D SDF for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)

3D-SDF for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)

PDB for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)

3D PDB for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)

SMILES for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)

INCHI for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)

Structure for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)

3D Structure for NP0312836 (4-(3,4-dihydroxybenzoyl)-2-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-2-(3-methylbut-2-en-1-yl)cyclopent-4-ene-1,3-dione)