NP-MRD: Showing NP-Card for {4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate (NP0286719)

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Record Information

Version

2.0

Created at

2022-09-09 15:25:21 UTC

Updated at

2022-09-09 15:25:21 UTC

NP-MRD ID

NP0286719

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate

Description

{4,5,6-Trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]Pentadeca-2,7-dien-7-yl}methyl octanoate belongs to the class of organic compounds known as tigliane and ingenane diterpenoids. These are diterpenoids containing the tigliane or ingenane carbon skeleton. The tigliane skeleton is a tetracyclic ring that consists of the 4/7/6/3 ring junction. It is derived from casbane by 6,10- and 5,14-cyclizations and is a framework of phorbol. The ingenane skeleton is derived by rearrangement of tigliane. {4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate is found in Euphorbia peplus. {4,5,6-Trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]Pentadeca-2,7-dien-7-yl}methyl octanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241510402D          

 34 37  0  0  0  0            999 V2000
    3.1392   -6.7533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8537   -6.3408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2826   -6.3408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9971   -6.7533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7116   -6.3408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4260   -6.7533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1405   -6.3408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 16 32  1  0  0  0  0
 15 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
M  END

     RDKit          3D

 76 79  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004241510402D          

 34 37  0  0  0  0            999 V2000
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  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 12 28  1  0  0  0  0
 28 29  1  0  0  0  0
 20 30  1  0  0  0  0
 14 30  1  0  0  0  0
 30 31  2  0  0  0  0
 16 32  1  0  0  0  0
 15 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0286719

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC(=O)OCC1=CC2C3C(CC(C)C4(C=C(C)C(O)C4(O)C1O)C2=O)C3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C28H42O6/c1-6-7-8-9-10-11-21(29)34-15-18-13-19-22-20(26(22,4)5)12-17(3)27(25(19)32)14-16(2)23(30)28(27,33)24(18)31/h13-14,17,19-20,22-24,30-31,33H,6-12,15H2,1-5H3

> <INCHI_KEY>
OKKFGJXSFAIADD-UHFFFAOYSA-N

> <FORMULA>
C28H42O6

> <MOLECULAR_WEIGHT>
474.638

> <EXACT_MASS>
474.298139072

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
54.16246499290802

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate

> <ALOGPS_LOGP>
3.60

> <JCHEM_LOGP>
3.657172608666667

> <ALOGPS_LOGS>
-4.54

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.446576613207117

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.109538674247888

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5333303031381718

> <JCHEM_POLAR_SURFACE_AREA>
104.06

> <JCHEM_REFRACTIVITY>
130.81029999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.36e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       5.860 -12.606   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.194 -11.836   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.527 -12.606   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.861 -11.836   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.195 -12.606   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.528 -11.836   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.862 -12.606   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.196 -11.836   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      15.196 -10.296   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      16.529 -12.606   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      17.863 -11.836   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      19.197 -12.606   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.510 -11.750   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      22.060 -12.167   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      23.629 -11.848   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      24.878 -12.749   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      24.917 -14.339   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.625 -15.273   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.005 -16.765   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.970 -15.061   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      22.290 -16.635   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      21.028 -17.533   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.006 -19.073   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      19.799 -16.605   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      18.320 -17.034   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      20.339 -15.165   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      18.852 -15.564   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      19.112 -14.159   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      17.703 -14.779   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      22.026 -13.641   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      23.565 -13.689   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      25.034 -11.217   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      26.489 -10.711   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      25.056  -9.677   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   28                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   30                                                  
CONECT   15   14   16   32                                                  
CONECT   16   15   17   32                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   26   30                                             
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   20   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   12   29                                                  
CONECT   29   28                                                            
CONECT   30   20   14   31                                                  
CONECT   31   30                                                            
CONECT   32   16   15   33   34                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Value	Source
{4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0,.0,]pentadeca-2,7-dien-7-yl}methyl octanoic acid	Generator
{4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoic acid	Generator

Chemical Formula

C₂₈H₄₂O₆

Average Mass

474.6380 Da

Monoisotopic Mass

474.29814 Da

IUPAC Name

{4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate

Traditional Name

{4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCC(=O)OCC1=CC2C3C(CC(C)C4(C=C(C)C(O)C4(O)C1O)C2=O)C3(C)C

InChI Identifier

InChI=1S/C28H42O6/c1-6-7-8-9-10-11-21(29)34-15-18-13-19-22-20(26(22,4)5)12-17(3)27(25(19)32)14-16(2)23(30)28(27,33)24(18)31/h13-14,17,19-20,22-24,30-31,33H,6-12,15H2,1-5H3

InChI Key

OKKFGJXSFAIADD-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
Euphorbia peplus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tigliane and ingenane diterpenoids. These are diterpenoids containing the tigliane or ingenane carbon skeleton. The tigliane skeleton is a tetracyclic ring that consists of the 4/7/6/3 ring junction. It is derived from casbane by 6,10- and 5,14-cyclizations and is a framework of phorbol. The ingenane skeleton is derived by rearrangement of tigliane.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Tigliane and ingenane diterpenoids

Alternative Parents

Substituents

Ingenane diterpenoid
Fatty acid ester
Fatty acyl
Tertiary alcohol
Carboxylic acid ester
Ketone
Secondary alcohol
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organooxygen compound
Organic oxygen compound
Alcohol
Carbonyl group
Organic oxide
Hydrocarbon derivative
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	3.6	ALOGPS
logP	3.66	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	12.11	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	130.81 m³·mol⁻¹	ChemAxon
Polarizability	54.16 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate (NP0286719)

MOL for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)

3D MOL for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)

3D SDF for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)

3D-SDF for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)

PDB for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)

3D PDB for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)

SMILES for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)

INCHI for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)

Structure for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)

3D Structure for NP0286719 ({4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxotetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-7-yl}methyl octanoate)