NP-MRD: Showing NP-Card for [(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate (NP0321798)

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Record Information

Version

2.0

Created at

2022-09-12 00:11:43 UTC

Updated at

2022-09-12 00:11:43 UTC

NP-MRD ID

NP0321798

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate

Description

Physacoztolide C belongs to the class of organic compounds known as withanolides and derivatives. These are c28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring. [(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate is found in Physalis coztomatl. Based on a literature review very few articles have been published on Physacoztolide C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122202112D          

 38 43  0  0  1  0            999 V2000
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M  END

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M  END


  Mrv1652309122202112D          

 38 43  0  0  1  0            999 V2000
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    6.2165    0.9666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7228    1.6179    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3741    1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0715    2.1242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2292    2.2692    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9183    3.0334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4246    3.6847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1137    4.4489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2419    3.5719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7482    4.2232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5528    2.8077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3700    2.6948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0464    2.1564    0.0000 O   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
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 14 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  9 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  1  0  0  0
 10 22  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  6  0  0  0
 27 29  1  6  0  0  0
 30 27  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 30 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0321798

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C(C)=C[C@@H](OC1=O)[C@](C)(O)[C@H]1CC[C@@]2(C)[C@@H]3C[C@H]4O[C@]44CC=CC(=O)[C@]4(C)[C@H]3CC[C@]12COC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H42O7/c1-17-14-24(37-26(34)18(17)2)29(6,35)22-10-12-27(4)21-15-25-31(38-25)11-7-8-23(33)28(31,5)20(21)9-13-30(22,27)16-36-19(3)32/h7-8,14,18,20-22,24-25,35H,9-13,15-16H2,1-6H3/t18?,20-,21+,22+,24+,25+,27-,28-,29+,30-,31+/m0/s1

> <INCHI_KEY>
HFOWXOQFYGPBMI-YEEYZRAISA-N

> <FORMULA>
C31H42O7

> <MOLECULAR_WEIGHT>
526.67

> <EXACT_MASS>
526.293053692

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
57.04650234288643

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1S,2R,7S,9R,11R,12S,15S,16S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-5,6-dihydro-2H-pyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-4-en-16-yl]methyl acetate

> <JCHEM_LOGP>
3.871061525999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.686399803679663

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.670128962946173

> <JCHEM_PKA_STRONGEST_BASIC>
-3.358778760558157

> <JCHEM_POLAR_SURFACE_AREA>
102.42999999999999

> <JCHEM_REFRACTIVITY>
141.15160000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,2R,7S,9R,11R,12S,15S,16S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-4-en-16-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       9.680   7.175   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.544   5.900   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      12.080   6.012   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       9.872   4.515   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.737   3.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.065   1.854   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.072   3.032   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.556   2.761   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.033   1.312   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.026   0.135   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.502  -1.314   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.986  -1.585   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.471  -1.856   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.994  -0.407   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.478  -0.678   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.485   0.499   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.008   1.947   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.524   2.218   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.047   3.667   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.517   1.041   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.040   2.489   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.542   0.406   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.173  -1.089   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.757  -0.539   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.032   0.325   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.604   1.804   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.549   3.020   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.765   2.075   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      11.333   3.965   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      13.494   4.236   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.914   5.662   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.859   6.878   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.279   8.305   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      15.385   6.667   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      16.330   7.883   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      15.965   5.241   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      17.491   5.030   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      15.020   4.025   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   22   26                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   20                                                  
CONECT   10    9   11   22                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12   14                                                       
CONECT   14   13   12   15   20                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    9   14   21                                             
CONECT   21   20                                                            
CONECT   22   10    6   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    6   27                                                  
CONECT   27   26   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   31   38                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   30                                                       
MASTER        0    0    0    0    0    0    0    0   38    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₄₂O₇

Average Mass

526.6700 Da

Monoisotopic Mass

526.29305 Da

IUPAC Name

[(1S,2R,7S,9R,11R,12S,15S,16S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-5,6-dihydro-2H-pyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-4-en-16-yl]methyl acetate

Traditional Name

[(1S,2R,7S,9R,11R,12S,15S,16S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0^{2,7}.0^{7,9}.0^{12,16}]octadec-4-en-16-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC1C(C)=C[C@@H](OC1=O)[C@](C)(O)[C@H]1CC[C@@]2(C)[C@@H]3C[C@H]4O[C@]44CC=CC(=O)[C@]4(C)[C@H]3CC[C@]12COC(C)=O

InChI Identifier

InChI=1S/C31H42O7/c1-17-14-24(37-26(34)18(17)2)29(6,35)22-10-12-27(4)21-15-25-31(38-25)11-7-8-23(33)28(31,5)20(21)9-13-30(22,27)16-36-19(3)32/h7-8,14,18,20-22,24-25,35H,9-13,15-16H2,1-6H3/t18?,20-,21+,22+,24+,25+,27-,28-,29+,30-,31+/m0/s1

InChI Key

HFOWXOQFYGPBMI-YEEYZRAISA-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
Physalis coztomatl	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as withanolides and derivatives. These are c28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Withanolides and derivatives

Alternative Parents

Substituents

Withanolide-skeleton
Steroid ester
14-alpha-methylsteroid
5,6-epoxysteroid
Cyclohexenone
Oxepane
Dihydropyranone
Pyran
Dicarboxylic acid or derivatives
Tertiary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	3.87	ChemAxon
pKa (Strongest Acidic)	13.67	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	102.43 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	141.15 m³·mol⁻¹	ChemAxon
Polarizability	57.05 Å³	ChemAxon
Number of Rings	6	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

C00041762

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

101403753

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate (NP0321798)

MOL for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)

3D MOL for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)

3D SDF for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)

3D-SDF for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)

PDB for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)

3D PDB for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)

SMILES for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)

INCHI for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)

Structure for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)

3D Structure for NP0321798 ([(1s,2r,7s,9r,11r,12s,15s,16s)-15-[(1r)-1-[(2r)-4,5-dimethyl-6-oxo-2,5-dihydropyran-2-yl]-1-hydroxyethyl]-2,12-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.0²,⁷.0⁷,⁹.0¹²,¹⁶]octadec-4-en-16-yl]methyl acetate)