NP-MRD: Showing NP-Card for (2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate (NP0190629)

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Record Information

Version

2.0

Created at

2022-09-04 07:20:31 UTC

Updated at

2022-09-04 07:20:31 UTC

NP-MRD ID

NP0190629

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate

Description

(2R,3R,4S,5R,6S)-6-{[(1aS,1bS,2R,4aS,5S,7aR)-1,1,2,5-tetramethyl-decahydro-1H-cyclopropa[e]azulen-5-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2Z)-2-methylbut-2-enoate belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone. (2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate is found in Pittosporum tobira. Based on a literature review very few articles have been published on (2R,3R,4S,5R,6S)-6-{[(1aS,1bS,2R,4aS,5S,7aR)-1,1,2,5-tetramethyl-decahydro-1H-cyclopropa[e]azulen-5-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2Z)-2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042209202D          

 35 38  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309042209202D          

 35 38  0  0  1  0            999 V2000
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    2.5251   -1.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4596   -0.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6095   -1.3508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2732   -0.6761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9813    2.2196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6410    2.7149    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3999    2.3913    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  1  0  0  0
 18 17  1  1  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 23 22  1  1  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  6  0  0  0
 23 30  1  0  0  0  0
 22 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 16 33  1  0  0  0  0
 33 34  1  0  0  0  0
  8 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0190629

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)O[C@H]1[C@@H](C)O[C@@H](O[C@@]2(C)CC[C@@H]3[C@H]([C@@H]4[C@H](C)CC[C@H]24)C3(C)C)[C@H](OC(C)=O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C28H44O7/c1-9-14(2)25(31)34-23-16(4)32-26(24(22(23)30)33-17(5)29)35-28(8)13-12-19-21(27(19,6)7)20-15(3)10-11-18(20)28/h9,15-16,18-24,26,30H,10-13H2,1-8H3/b14-9-/t15-,16-,18+,19-,20-,21-,22+,23+,24-,26+,28+/m1/s1

> <INCHI_KEY>
SKAKJPNQCVOEEY-KTFFIBKXSA-N

> <FORMULA>
C28H44O7

> <MOLECULAR_WEIGHT>
492.653

> <EXACT_MASS>
492.308703757

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
54.989107431813615

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5R,6S)-6-{[(1aR,4S,4aS,7R,7aS,7bS)-1,1,4,7-tetramethyl-decahydro-1H-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
5.108639385

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.92500814664638

> <JCHEM_PKA_STRONGEST_BASIC>
-3.706401436656873

> <JCHEM_POLAR_SURFACE_AREA>
91.29000000000002

> <JCHEM_REFRACTIVITY>
130.4509

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5R,6S)-6-{[(1aR,4S,4aS,7R,7aS,7bS)-1,1,4,7-tetramethyl-octahydro-1aH-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2Z)-2-methylbut-2-enoate

> <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      10.756   9.975   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.173   9.371   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.358   7.842   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.774   7.238   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.126   6.917   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.311   5.388   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       9.710   7.521   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.478   6.597   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.062   7.201   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.877   8.730   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.830   6.276   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.414   6.880   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.229   8.409   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.460   9.334   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.812   9.014   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.015   4.747   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.784   3.823   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.969   2.294   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.437   2.454   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.418   2.815   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.729   2.006   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.914   0.477   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.834  -0.621   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.302  -0.461   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.472   0.836   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.982   0.448   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.891  -1.090   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.325  -1.651   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.713  -3.141   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.325  -1.007   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.604  -2.521   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.843  -1.262   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.432   4.143   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.663   5.068   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.080   4.464   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   34                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   11   17   33                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20   25                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   30                                                  
CONECT   23   22   24   30                                                  
CONECT   24   23   25   28                                                  
CONECT   25   24   18   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   24   29                                                  
CONECT   29   28                                                            
CONECT   30   23   22   31   32                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   16   34                                                       
CONECT   34   33    8   35                                                  
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Value	Source
(2R,3R,4S,5R,6S)-6-{[(1as,1BS,2R,4as,5S,7ar)-1,1,2,5-tetramethyl-decahydro-1H-cyclopropa[e]azulen-5-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2Z)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₈H₄₄O₇

Average Mass

492.6530 Da

Monoisotopic Mass

492.30870 Da

IUPAC Name

(2R,3R,4S,5R,6S)-6-{[(1aR,4S,4aS,7R,7aS,7bS)-1,1,4,7-tetramethyl-decahydro-1H-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2Z)-2-methylbut-2-enoate

Traditional Name

(2R,3R,4S,5R,6S)-6-{[(1aR,4S,4aS,7R,7aS,7bS)-1,1,4,7-tetramethyl-octahydro-1aH-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2Z)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)O[C@H]1[C@@H](C)O[C@@H](O[C@@]2(C)CC[C@@H]3[C@H]([C@@H]4[C@H](C)CC[C@H]24)C3(C)C)[C@H](OC(C)=O)[C@H]1O

InChI Identifier

InChI=1S/C28H44O7/c1-9-14(2)25(31)34-23-16(4)32-26(24(22(23)30)33-17(5)29)35-28(8)13-12-19-21(27(19,6)7)20-15(3)10-11-18(20)28/h9,15-16,18-24,26,30H,10-13H2,1-8H3/b14-9-/t15-,16-,18+,19-,20-,21-,22+,23+,24-,26+,28+/m1/s1

InChI Key

SKAKJPNQCVOEEY-KTFFIBKXSA-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
Pittosporum tobira	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene glycosides. These are prenol lipids containing a carbohydrate moiety glycosidically bound to a terpene backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Terpene glycosides

Alternative Parents

Substituents

Terpene glycoside
Aromadendrane sesquiterpenoid
Guaiane sesquiterpenoid
5,10-cycloaromadendrane sesquiterpenoid
Sesquiterpenoid
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Monosaccharide
Oxane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Alcohol
Hydrocarbon derivative
Organic oxide
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	5.11	ChemAxon
pKa (Strongest Acidic)	12.93	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	91.29 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	130.45 m³·mol⁻¹	ChemAxon
Polarizability	54.99 Å³	ChemAxon
Number of Rings	4	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

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

162960775

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate (NP0190629)

MOL for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)

PDB for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)

Structure for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0190629 ((2r,3r,4s,5r,6s)-6-{[(1ar,4s,4as,7r,7as,7bs)-1,1,4,7-tetramethyl-octahydro-1ah-cyclopropa[e]azulen-4-yl]oxy}-5-(acetyloxy)-4-hydroxy-2-methyloxan-3-yl (2z)-2-methylbut-2-enoate)