NP-MRD: Showing NP-Card for 2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid (NP0158686)

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Record Information

Version

1.0

Created at

2022-09-02 16:19:14 UTC

Updated at

2022-09-02 16:19:14 UTC

NP-MRD ID

NP0158686

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid

Description

2-Methyl-4-oxo-6-[(1R,3R,5R,10S,14R,15R,18R)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]Octadec-11-en-15-yl]heptanoic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid is found in Ganoderma applanatum. Based on a literature review very few articles have been published on 2-methyl-4-oxo-6-[(1R,3R,5R,10S,14R,15R,18R)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]Octadec-11-en-15-yl]heptanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022218192D          

 37 41  0  0  1  0            999 V2000
    4.7744   -1.6527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2 35  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309022218192D          

 37 41  0  0  1  0            999 V2000
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   -0.4139   -8.4184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7110   -7.0206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2189   -7.6708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4394   -6.6333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4560   -6.2360    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0081   -5.6229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7531   -4.8383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4982   -4.0537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0539   -4.6668    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4888   -2.8902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2033   -2.4777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4888   -3.7152    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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  7  1  6  0  0  0
  9 10  1  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  1  0  0  0
 13 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
 21 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 34 33  1  1  0  0  0
 20 34  1  0  0  0  0
 32 34  1  0  0  0  0
 13 34  1  0  0  0  0
  2 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0158686

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CC(=O)CC(C)C(O)=O)[C@H]1CC(=O)[C@@]2(C)[C@@]34O[C@@H]3C[C@H]3C(C)(C)C(=O)CC[C@]3(C)C4=CC(=O)[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H40O7/c1-15(10-17(31)11-16(2)25(35)36)18-12-23(34)29(7)28(18,6)22(33)13-20-27(5)9-8-21(32)26(3,4)19(27)14-24-30(20,29)37-24/h13,15-16,18-19,24H,8-12,14H2,1-7H3,(H,35,36)/t15?,16?,18-,19+,24-,27+,28+,29-,30+/m1/s1

> <INCHI_KEY>
KSNKHYBQEAKBLD-UGUXJHLISA-N

> <FORMULA>
C30H40O7

> <MOLECULAR_WEIGHT>
512.643

> <EXACT_MASS>
512.277403628

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
55.86863066845846

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-methyl-4-oxo-6-[(1R,3R,5R,10S,14R,15R,18R)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0^{1,3}.0^{5,10}.0^{14,18}]octadec-11-en-15-yl]heptanoic acid

> <ALOGPS_LOGP>
3.94

> <JCHEM_LOGP>
4.584531308333334

> <ALOGPS_LOGS>
-5.26

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.865277352674173

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.0935311050391086

> <JCHEM_PKA_STRONGEST_BASIC>
-4.263047686337436

> <JCHEM_POLAR_SURFACE_AREA>
118.11

> <JCHEM_REFRACTIVITY>
136.0603

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.83e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-methyl-4-oxo-6-[(1R,3R,5R,10S,14R,15R,18R)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0^{1,3}.0^{5,10}.0^{14,18}]octadec-11-en-15-yl]heptanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       8.912  -3.085   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.912  -4.625   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.578  -5.395   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.245  -4.625   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.245  -3.085   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.911  -5.395   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.577  -4.625   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.577  -3.085   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.244  -5.395   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.837  -4.769   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.194  -5.913   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.725  -5.752   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.576  -7.247   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.930  -6.927   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.083  -6.927   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.547  -6.451   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.113  -8.071   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.620  -7.751   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.637  -9.536   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.131  -9.856   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.655 -11.320   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.161 -11.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.686 -12.465   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.210 -13.929   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.297 -14.250   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.773 -15.714   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.327 -13.105   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.275 -14.319   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.687 -12.382   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.851 -11.641   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.882 -10.496   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.406  -9.032   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.930  -7.567   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       0.101  -8.711   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.246  -5.395   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      11.579  -4.625   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      10.246  -6.935   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   35                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   34                                             
CONECT   14   13                                                            
CONECT   15   13    9   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   34                                                  
CONECT   21   20   22   23   30                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   21   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32   34                                                       
CONECT   34   33   20   32   13                                             
CONECT   35    2   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Value	Source
2-Methyl-4-oxo-6-[(1R,3R,5R,10S,14R,15R,18R)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0,.0,.0,]octadec-11-en-15-yl]heptanoate	Generator

Chemical Formula

C₃₀H₄₀O₇

Average Mass

512.6430 Da

Monoisotopic Mass

512.27740 Da

IUPAC Name

2-methyl-4-oxo-6-[(1R,3R,5R,10S,14R,15R,18R)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0^{1,3}.0^{5,10}.0^{14,18}]octadec-11-en-15-yl]heptanoic acid

Traditional Name

2-methyl-4-oxo-6-[(1R,3R,5R,10S,14R,15R,18R)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0^{1,3}.0^{5,10}.0^{14,18}]octadec-11-en-15-yl]heptanoic acid

CAS Registry Number

Not Available

SMILES

CC(CC(=O)CC(C)C(O)=O)[C@H]1CC(=O)[C@@]2(C)[C@@]34O[C@@H]3C[C@H]3C(C)(C)C(=O)CC[C@]3(C)C4=CC(=O)[C@]12C

InChI Identifier

InChI=1S/C30H40O7/c1-15(10-17(31)11-16(2)25(35)36)18-12-23(34)29(7)28(18,6)22(33)13-20-27(5)9-8-21(32)26(3,4)19(27)14-24-30(20,29)37-24/h13,15-16,18-19,24H,8-12,14H2,1-7H3,(H,35,36)/t15?,16?,18-,19+,24-,27+,28+,29-,30+/m1/s1

InChI Key

KSNKHYBQEAKBLD-UGUXJHLISA-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
Ganoderma applanatum	LOTUS Database	35616633

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
Cholane-skeleton
Bile acid, alcohol, or derivatives
Medium-chain keto acid
Gamma-keto acid
Cyclohexenone
Oxepane
Keto acid
Ketone
Cyclic ketone
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Oxirane
Ether
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organooxygen compound
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
logP	3.94	ALOGPS
logP	4.58	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	4.09	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	118.11 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	136.06 m³·mol⁻¹	ChemAxon
Polarizability	55.87 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	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

78442692

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586894

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid (NP0158686)

MOL for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)

3D MOL for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)

3D SDF for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)

3D-SDF for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)

PDB for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)

3D PDB for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)

SMILES for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)

INCHI for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)

Structure for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)

3D Structure for NP0158686 (2-methyl-4-oxo-6-[(1r,3r,5r,10s,14r,15r,18r)-6,6,10,14,18-pentamethyl-7,13,17-trioxo-2-oxapentacyclo[9.7.0.0¹,³.0⁵,¹⁰.0¹⁴,¹⁸]octadec-11-en-15-yl]heptanoic acid)