NP-MRD: Showing NP-Card for (1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate (NP0200341)

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Record Information

Version

2.0

Created at

2022-09-04 19:09:48 UTC

Updated at

2022-09-04 19:09:48 UTC

NP-MRD ID

NP0200341

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate

Description

121480-72-6 Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate is found in Ajuga nipponensis. Based on a literature review very few articles have been published on 121480-72-6.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042221092D          

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  8 40  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309042221092D          

 40 42  0  0  1  0            999 V2000
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    9.2881    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2881    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8592   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3322   -0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8625   -1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0501   -1.7435    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5198   -1.1115    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7679   -2.5188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2292   -3.2027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7213   -3.8528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9487   -4.6459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9461   -3.5707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9749   -2.7462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  1  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  1  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 34 39  1  0  0  0  0
 40 29  1  1  0  0  0
  8 40  1  0  0  0  0
 18 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0200341

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)C(=O)O[C@@H]1CC[C@](O)(COC(C)=O)[C@]2(COC(C)=O)[C@@H](O)C[C@@H](C)[C@](C)(C[C@H](O)C3=CC(=O)OC3)[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C29H44O11/c1-7-16(2)26(35)40-22-8-9-28(36,14-38-18(4)30)29(15-39-19(5)31)23(33)10-17(3)27(6,25(22)29)12-21(32)20-11-24(34)37-13-20/h11,16-17,21-23,25,32-33,36H,7-10,12-15H2,1-6H3/t16-,17+,21-,22+,23-,25+,27-,28-,29+/m0/s1

> <INCHI_KEY>
PCXVVBLCDMHQIP-PVHCJARNSA-N

> <FORMULA>
C29H44O11

> <MOLECULAR_WEIGHT>
568.66

> <EXACT_MASS>
568.288362237

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
59.3378797208238

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,4R,4aR,5S,7R,8S,8aR)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2S)-2-hydroxy-2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-7,8-dimethyl-decahydronaphthalen-1-yl (2S)-2-methylbutanoate

> <JCHEM_LOGP>
1.1204095686666662

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.374708298981485

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.766976817383378

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0101499076535694

> <JCHEM_POLAR_SURFACE_AREA>
165.89000000000001

> <JCHEM_REFRACTIVITY>
141.23010000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R,4aR,5S,7R,8S,8aR)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2S)-2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1H-naphthalen-1-yl (2S)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336   0.770   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      10.669   0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      12.003   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.337   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.670   2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      16.187   2.043   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      15.197   3.757   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      14.207   4.937   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      12.691   4.669   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.164   3.222   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      11.701   5.849   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      14.670   0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.004   1.540   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      16.004   3.080   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      17.338   3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.338   5.390   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      18.672   3.080   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      16.004   0.000   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      17.338   0.770   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      16.004  -1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.670  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.670  -3.850   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.337  -1.540   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.820  -1.273   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.810  -2.987   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      11.293  -3.255   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      10.304  -2.075   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      10.767  -4.702   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.628  -5.978   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.680  -7.192   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      11.104  -8.672   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       9.233  -6.665   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       9.286  -5.126   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   40                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   18                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   11   19   24   40                                             
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   18   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31   40                                             
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   34                                                       
CONECT   40   29    8   18                                                  
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₄O₁₁

Average Mass

568.6600 Da

Monoisotopic Mass

568.28836 Da

IUPAC Name

(1R,4R,4aR,5S,7R,8S,8aR)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2S)-2-hydroxy-2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl]-7,8-dimethyl-decahydronaphthalen-1-yl (2S)-2-methylbutanoate

Traditional Name

(1R,4R,4aR,5S,7R,8S,8aR)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2S)-2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1H-naphthalen-1-yl (2S)-2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC[C@H](C)C(=O)O[C@@H]1CC[C@](O)(COC(C)=O)[C@]2(COC(C)=O)[C@@H](O)C[C@@H](C)[C@](C)(C[C@H](O)C3=CC(=O)OC3)[C@@H]12

InChI Identifier

InChI=1S/C29H44O11/c1-7-16(2)26(35)40-22-8-9-28(36,14-38-18(4)30)29(15-39-19(5)31)23(33)10-17(3)27(6,25(22)29)12-21(32)20-11-24(34)37-13-20/h11,16-17,21-23,25,32-33,36H,7-10,12-15H2,1-6H3/t16-,17+,21-,22+,23-,25+,27-,28-,29+/m0/s1

InChI Key

PCXVVBLCDMHQIP-PVHCJARNSA-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
Ajuga nipponensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Tetracarboxylic acid or derivatives
Fatty acid ester
2-furanone
Fatty acyl
Cyclic alcohol
Dihydrofuran
Tertiary alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Lactone
Carboxylic acid ester
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
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	1.12	ChemAxon
pKa (Strongest Acidic)	5.77	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	165.89 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	141.23 m³·mol⁻¹	ChemAxon
Polarizability	59.34 Å³	ChemAxon
Number of Rings	3	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

156696

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

180057

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate (NP0200341)

MOL for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)

3D MOL for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)

3D SDF for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)

3D-SDF for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)

PDB for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)

3D PDB for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)

SMILES for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)

INCHI for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)

Structure for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)

3D Structure for NP0200341 ((1r,4r,4ar,5s,7r,8s,8ar)-4,4a-bis[(acetyloxy)methyl]-4,5-dihydroxy-8-[(2s)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2s)-2-methylbutanoate)