NP-MRD: Showing NP-Card for (-)-Esulatin E (NP0082164)

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Record Information

Version

2.0

Created at

2022-04-29 03:13:02 UTC

Updated at

2022-04-29 03:13:02 UTC

NP-MRD ID

NP0082164

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Esulatin E

Description

(1R,2R,3aR,5R,13R,13aS)-1,2,13-tris(acetyloxy)-2,5,8,8-tetramethyl-12-methylidene-4,9-dioxo-1H,2H,3H,3aH,4H,5H,8H,9H,12H,13H,13aH-cyclopenta[12]annulen-3a-yl acetate belongs to the class of organic compounds known as jatrophane and cyclojatrophane diterpenoids. These are diterpenoids with a structure based on the jatrophane or the 9,13-jatrophane skeleton. Jatrophane can be derived from casbane by 6,10-cyclization and opening of the cyclopropane. Cyclojatrophane diterpenoids are based on the 9,13-cyclization of the jatrophane skeleton yields the 9,13-cyclojatrophane skeleton. (-)-Esulatin E is found in Euphorbia esula. Based on a literature review very few articles have been published on (1R,2R,3aR,5R,13R,13aS)-1,2,13-tris(acetyloxy)-2,5,8,8-tetramethyl-12-methylidene-4,9-dioxo-1H,2H,3H,3aH,4H,5H,8H,9H,12H,13H,13aH-cyclopenta[12]annulen-3a-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292205132D          

 38 39  0  0  1  0            999 V2000
    1.9453    0.7150    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1622    0.4556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9952   -0.3524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5459    1.0041    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7128    1.8120    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4960    2.0715    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6629    2.8794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4868    3.6854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4460    3.1388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0623    2.5903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8954    1.7824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6785    2.0418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5116    1.2338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  1 15  1  0  0  0  0
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  6 18  1  6  0  0  0
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 19 21  1  0  0  0  0
  5 22  1  0  0  0  0
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  4 24  1  0  0  0  0
 23 25  1  6  0  0  0
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  4 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
  1 38  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304292205132D          

 38 39  0  0  1  0            999 V2000
    1.9453    0.7150    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -1.0660    0.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1122    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  1 15  1  0  0  0  0
 13 16  1  0  0  0  0
 13 17  1  0  0  0  0
  6 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  5 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  4 24  1  0  0  0  0
 23 25  1  6  0  0  0
 23 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 22 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
  4 34  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
  1 38  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0082164

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1\C=C/C(C)(C)C(=O)\C=C/C(=C)[C@H](OC(C)=O)[C@H]2[C@@H](OC(C)=O)[C@@](C)(C[C@]2(OC(C)=O)C1=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H36O10/c1-15-10-11-21(33)26(7,8)13-12-16(2)24(34)28(38-20(6)32)14-27(9,37-19(5)31)25(36-18(4)30)22(28)23(15)35-17(3)29/h10-13,16,22-23,25H,1,14H2,2-9H3/b11-10-,13-12-/t16-,22+,23+,25-,27-,28-/m1/s1

> <INCHI_KEY>
UXVRDUFFNLUIPX-CGRRHHLWSA-N

> <FORMULA>
C28H36O10

> <MOLECULAR_WEIGHT>
532.586

> <EXACT_MASS>
532.230847359

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
53.48417656531133

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3aR,5R,13R,13aS)-2,3a,13-tris(acetyloxy)-2,5,8,8-tetramethyl-12-methylidene-4,9-dioxo-1H,2H,3H,3aH,4H,5H,8H,9H,12H,13H,13aH-cyclopenta[12]annulen-1-yl acetate

> <ALOGPS_LOGP>
1.85

> <JCHEM_LOGP>
2.7616067710000016

> <ALOGPS_LOGS>
-5.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.001534076755963

> <JCHEM_PKA_STRONGEST_BASIC>
-5.025052084967467

> <JCHEM_POLAR_SURFACE_AREA>
139.34000000000003

> <JCHEM_REFRACTIVITY>
135.3672

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.18e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3aR,5R,13R,13aS)-2,3a,13-tris(acetyloxy)-2,5,8,8-tetramethyl-12-methylidene-4,9-dioxo-1H,3H,5H,13H,13aH-cyclopenta[12]annulen-1-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       3.631   1.335   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.169   0.850   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.858  -0.658   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       1.019   1.874   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.331   3.382   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.792   3.867   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.104   5.375   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.775   6.879   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.566   5.859   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.716   4.835   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.405   3.327   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.867   3.811   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.555   2.303   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.243   0.795   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.782   0.311   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.073   2.044   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.618   3.417   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.642   4.891   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.954   6.399   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.803   7.423   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.852   7.650   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.007   4.145   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.146   3.108   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.512   1.705   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.307   4.120   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.613   2.639   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.940   1.134   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.801   0.098   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -4.407   0.665   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.177   5.675   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.588   6.294   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -2.828   5.381   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -1.757   7.824   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       0.552   0.407   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -0.953   0.078   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -1.420  -1.389   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -1.990   1.217   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.943   2.843   0.000  0.00  0.00           C+0
CONECT    1    2   15   38                                                  
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   24   34                                             
CONECT    5    4    6   22                                                  
CONECT    6    5    7   18                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   16   17                                             
CONECT   14   13   15                                                       
CONECT   15   14    1                                                       
CONECT   16   13                                                            
CONECT   17   13                                                            
CONECT   18    6   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22    5   23   30                                                  
CONECT   23   22   24   25   26                                             
CONECT   24   23    4                                                       
CONECT   25   23                                                            
CONECT   26   23   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   22   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34    4   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38    1                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   78    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,3AR,5R,13R,13as)-1,2,13-tris(acetyloxy)-2,5,8,8-tetramethyl-12-methylidene-4,9-dioxo-1H,2H,3H,3ah,4H,5H,8H,9H,12H,13H,13ah-cyclopenta[12]annulen-3a-yl acetic acid	Generator

Chemical Formula

C₂₈H₃₆O₁₀

Average Mass

532.5860 Da

Monoisotopic Mass

532.23085 Da

IUPAC Name

(1R,2R,3aR,5R,13R,13aS)-2,3a,13-tris(acetyloxy)-2,5,8,8-tetramethyl-12-methylidene-4,9-dioxo-1H,2H,3H,3aH,4H,5H,8H,9H,12H,13H,13aH-cyclopenta[12]annulen-1-yl acetate

Traditional Name

(1R,2R,3aR,5R,13R,13aS)-2,3a,13-tris(acetyloxy)-2,5,8,8-tetramethyl-12-methylidene-4,9-dioxo-1H,3H,5H,13H,13aH-cyclopenta[12]annulen-1-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1\C=C/C(C)(C)C(=O)\C=C/C(=C)[C@H](OC(C)=O)[C@H]2[C@@H](OC(C)=O)[C@@](C)(C[C@]2(OC(C)=O)C1=O)OC(C)=O

InChI Identifier

InChI=1S/C28H36O10/c1-15-10-11-21(33)26(7,8)13-12-16(2)24(34)28(38-20(6)32)14-27(9,37-19(5)31)25(36-18(4)30)22(28)23(15)35-17(3)29/h10-13,16,22-23,25H,1,14H2,2-9H3/b11-10-,13-12-/t16-,22+,23+,25-,27-,28-/m1/s1

InChI Key

UXVRDUFFNLUIPX-CGRRHHLWSA-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
Euphorbia esula	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as jatrophane and cyclojatrophane diterpenoids. These are diterpenoids with a structure based on the jatrophane or the 9,13-jatrophane skeleton. Jatrophane can be derived from casbane by 6,10-cyclization and opening of the cyclopropane. Cyclojatrophane diterpenoids are based on the 9,13-cyclization of the jatrophane skeleton yields the 9,13-cyclojatrophane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Jatrophane and cyclojatrophane diterpenoids

Alternative Parents

Substituents

Jatrophane diterpenoid
Tetracarboxylic acid or derivatives
Alpha-acyloxy ketone
Cyclic ketone
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	1.85	ALOGPS
logP	2.76	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	15	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	139.34 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	135.37 m³·mol⁻¹	ChemAxon
Polarizability	53.48 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

58134886

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163005323

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (-)-Esulatin E (NP0082164)

MOL for NP0082164 ((-)-Esulatin E)

3D MOL for NP0082164 ((-)-Esulatin E)

3D SDF for NP0082164 ((-)-Esulatin E)

3D-SDF for NP0082164 ((-)-Esulatin E)

PDB for NP0082164 ((-)-Esulatin E)

3D PDB for NP0082164 ((-)-Esulatin E)

SMILES for NP0082164 ((-)-Esulatin E)

INCHI for NP0082164 ((-)-Esulatin E)

Structure for NP0082164 ((-)-Esulatin E)

3D Structure for NP0082164 ((-)-Esulatin E)