NP-MRD: Showing NP-Card for (+)-Acetyl eburicoic acid (NP0078895)

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Record Information

Version

2.0

Created at

2022-04-28 23:59:20 UTC

Updated at

2022-04-28 23:59:20 UTC

NP-MRD ID

NP0078895

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Acetyl eburicoic acid

Description

(2R)-2-[(2S,5S,7S,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-1(10)-en-14-yl]-6-methyl-5-methylideneheptanoic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (+)-Acetyl eburicoic acid is found in Laetiporus sulphureus . Based on a literature review very few articles have been published on (2R)-2-[(2S,5S,7S,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-1(10)-en-14-yl]-6-methyl-5-methylideneheptanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292201592D          

 37 40  0  0  1  0            999 V2000
   -0.7813   -3.8908    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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  3  4  1  0  0  0  0
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  7 10  1  6  0  0  0
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  5 21  1  6  0  0  0
  4 22  1  1  0  0  0
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 26 37  1  6  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304292201592D          

 37 40  0  0  1  0            999 V2000
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   -3.4120   -1.9582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1745   -2.6727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4340   -3.4032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9213   -5.8153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0514   -6.0567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2667   -6.3117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3464   -5.7596    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1748   -4.9527    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7879   -4.4006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5725   -4.6556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7441   -5.4625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1310   -6.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6613   -6.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036   -6.8076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5287   -5.7175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7002   -6.5245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4848   -6.7794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0871   -7.0765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0033   -4.1457    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  7 10  1  6  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  5 21  1  6  0  0  0
  4 22  1  1  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 29 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 26 37  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0078895

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=C)CC[C@H]([C@H]1CC[C@@]2(C)C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](OC(C)=O)C(C)(C)[C@H]1CC3)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H52O4/c1-20(2)21(3)10-11-23(29(35)36)24-14-18-33(9)26-12-13-27-30(5,6)28(37-22(4)34)16-17-31(27,7)25(26)15-19-32(24,33)8/h20,23-24,27-28H,3,10-19H2,1-2,4-9H3,(H,35,36)/t23-,24-,27-,28+,31-,32-,33+/m1/s1

> <INCHI_KEY>
IMWCOHWUNCFQDX-NXPMFROVSA-N

> <FORMULA>
C33H52O4

> <MOLECULAR_WEIGHT>
512.775

> <EXACT_MASS>
512.386560154

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
61.258632012432656

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-2-[(2S,5S,7S,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-14-yl]-6-methyl-5-methylideneheptanoic acid

> <ALOGPS_LOGP>
7.30

> <JCHEM_LOGP>
7.4284761150000005

> <ALOGPS_LOGS>
-5.82

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.87419120337317

> <JCHEM_PKA_STRONGEST_BASIC>
-7.0037788743780505

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
148.8636

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.76e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-[(2S,5S,7S,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-14-yl]-6-methyl-5-methylideneheptanoic acid

> <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      -1.458  -7.263   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.138  -8.769   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.283  -9.800   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.747  -9.324   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.068  -7.817   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.923  -6.787   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.599  -7.656   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.225  -9.063   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.081 -10.094   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.369  -6.323   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -7.909  -6.323   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.679  -4.989   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -10.219  -4.989   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -10.989  -6.323   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -10.989  -3.655   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -12.529  -3.655   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -10.219  -2.322   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.599  -4.989   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.369  -3.655   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -4.059  -4.989   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -4.543  -6.353   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.586 -10.855   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.963 -11.306   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.498 -11.782   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.647 -10.751   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.326  -9.245   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.471  -8.215   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.935  -8.690   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.256 -10.197   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.111 -11.227   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.101 -12.407   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.687 -12.708   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.720 -10.673   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.040 -12.179   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       6.505 -12.655   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.896 -13.209   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.006  -7.739   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   26                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5    9   22                                             
CONECT    5    4    6    7   21                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4                                                       
CONECT   10    7   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   10   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21    5                                                            
CONECT   22    4                                                            
CONECT   23    3   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25    2   27   37                                             
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   33                                                  
CONECT   30   29   25   31   32                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   29   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   26                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Value	Source
(2R)-2-[(2S,5S,7S,11R,14R,15R)-5-(Acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0,.0,]heptadec-1(10)-en-14-yl]-6-methyl-5-methylideneheptanoate	Generator

Chemical Formula

C₃₃H₅₂O₄

Average Mass

512.7750 Da

Monoisotopic Mass

512.38656 Da

IUPAC Name

(2R)-2-[(2S,5S,7S,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-14-yl]-6-methyl-5-methylideneheptanoic acid

Traditional Name

(2R)-2-[(2S,5S,7S,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-14-yl]-6-methyl-5-methylideneheptanoic acid

CAS Registry Number

Not Available

SMILES

CC(C)C(=C)CC[C@H]([C@H]1CC[C@@]2(C)C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](OC(C)=O)C(C)(C)[C@H]1CC3)C(O)=O

InChI Identifier

InChI=1S/C33H52O4/c1-20(2)21(3)10-11-23(29(35)36)24-14-18-33(9)26-12-13-27-30(5,6)28(37-22(4)34)16-17-31(27,7)25(26)15-19-32(24,33)8/h20,23-24,27-28H,3,10-19H2,1-2,4-9H3,(H,35,36)/t23-,24-,27-,28+,31-,32-,33+/m1/s1

InChI Key

IMWCOHWUNCFQDX-NXPMFROVSA-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
Laetiporus sulphureus	Fungi	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Bile acid, alcohol, or derivatives
Steroid ester
Steroid acid
14-alpha-methylsteroid
Steroid
Medium-chain fatty acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid
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	7.3	ALOGPS
logP	7.43	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	4.87	ChemAxon
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	148.86 m³·mol⁻¹	ChemAxon
Polarizability	61.26 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

162842589

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Acetyl eburicoic acid (NP0078895)

MOL for NP0078895 ((+)-Acetyl eburicoic acid)

3D MOL for NP0078895 ((+)-Acetyl eburicoic acid)

3D SDF for NP0078895 ((+)-Acetyl eburicoic acid)

3D-SDF for NP0078895 ((+)-Acetyl eburicoic acid)

PDB for NP0078895 ((+)-Acetyl eburicoic acid)

3D PDB for NP0078895 ((+)-Acetyl eburicoic acid)

SMILES for NP0078895 ((+)-Acetyl eburicoic acid)

INCHI for NP0078895 ((+)-Acetyl eburicoic acid)

Structure for NP0078895 ((+)-Acetyl eburicoic acid)

3D Structure for NP0078895 ((+)-Acetyl eburicoic acid)