NP-MRD: Showing NP-Card for [3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid (NP0058408)

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Record Information

Version

2.0

Created at

2022-04-28 03:46:25 UTC

Updated at

2022-04-28 03:46:25 UTC

NP-MRD ID

NP0058408

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid

Description

(2E)-3-{[(3aR,4R,9R,11aS)-9-(acetyloxy)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety. [3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid is found in Liatris cylindracea. Based on a literature review very few articles have been published on (2E)-3-{[(3aR,4R,9R,11aS)-9-(acetyloxy)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282205462D          

 36 37  0  0  1  0            999 V2000
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M  END

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  Mrv1652304282205462D          

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  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  9 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
  8 26  1  6  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
  7 30  1  6  0  0  0
  5 31  1  0  0  0  0
  4 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
  1 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0058408

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/CO)C(=O)OC\C(=C/C)C(=O)O[C@@H]1C\C(C)=C\C[C@@H](OC(C)=O)\C(C)=C/[C@@H]2OC(=O)C(=C)[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O9/c1-7-19(13-28)26(31)33-14-20(8-2)27(32)36-22-11-15(3)9-10-21(34-18(6)29)16(4)12-23-24(22)17(5)25(30)35-23/h7-9,12,21-24,28H,5,10-11,13-14H2,1-4,6H3/b15-9+,16-12-,19-7+,20-8+/t21-,22-,23+,24-/m1/s1

> <INCHI_KEY>
GBKBPIXSSQJOPJ-RURDHMKASA-N

> <FORMULA>
C27H34O9

> <MOLECULAR_WEIGHT>
502.56

> <EXACT_MASS>
502.220282675

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
52.46092760354382

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-3-{[(3aR,4R,9R,11aS)-9-(acetyloxy)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate

> <ALOGPS_LOGP>
3.16

> <JCHEM_LOGP>
3.5456513459999996

> <ALOGPS_LOGS>
-4.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.886246127014672

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8485559440437687

> <JCHEM_POLAR_SURFACE_AREA>
125.43

> <JCHEM_REFRACTIVITY>
133.39309999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.49e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-{[(3aR,4R,9R,11aS)-9-(acetyloxy)-6,10-dimethyl-3-methylidene-2-oxo-3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      10.105   2.114   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.580   1.672   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.615   0.133   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.738  -1.134   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.285  -1.643   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.810  -1.201   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.877   0.024   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.841   1.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.718   2.830   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.171   3.339   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.785   4.055   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.379   5.476   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.906   5.672   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.445   6.701   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.918   6.505   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.984   7.730   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.039   8.122   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.106   9.346   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.700  10.767   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.228  10.963   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.767  11.992   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.361  13.413   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.427  14.638   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.239  11.796   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.306  13.021   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.366   2.006   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.857   3.460   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.490   0.740   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.950   0.705   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       5.423  -0.485   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       9.320  -3.182   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      11.672  -2.359   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      11.078  -3.779   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      12.011  -5.004   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       9.550  -3.975   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.228   0.848   0.000  0.00  0.00           C+0
CONECT    1    2   10   36                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   32                                                  
CONECT    5    4    6   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   30                                                  
CONECT    8    7    9   26                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    1                                                       
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25                                                       
CONECT   25   24                                                            
CONECT   26    8   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    7                                                       
CONECT   31    5                                                            
CONECT   32    4   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36    1                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   74    0
END

View in JSmol

Synonyms

Value	Source
(2E)-3-{[(3ar,4R,9R,11as)-9-(acetyloxy)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3ah,4H,5H,8H,9H,11ah-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoic acid	Generator

Chemical Formula

C₂₇H₃₄O₉

Average Mass

502.5600 Da

Monoisotopic Mass

502.22028 Da

IUPAC Name

(2E)-3-{[(3aR,4R,9R,11aS)-9-(acetyloxy)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate

Traditional Name

(2E)-3-{[(3aR,4R,9R,11aS)-9-(acetyloxy)-6,10-dimethyl-3-methylidene-2-oxo-3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(/CO)C(=O)OC\C(=C/C)C(=O)O[C@@H]1C\C(C)=C\C[C@@H](OC(C)=O)\C(C)=C/[C@@H]2OC(=O)C(=C)[C@H]12

InChI Identifier

InChI=1S/C27H34O9/c1-7-19(13-28)26(31)33-14-20(8-2)27(32)36-22-11-15(3)9-10-21(34-18(6)29)16(4)12-23-24(22)17(5)25(30)35-23/h7-9,12,21-24,28H,5,10-11,13-14H2,1-4,6H3/b15-9+,16-12-,19-7+,20-8+/t21-,22-,23+,24-/m1/s1

InChI Key

GBKBPIXSSQJOPJ-RURDHMKASA-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
Liatris cylindracea	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Germacranolides and derivatives

Alternative Parents

Substituents

Germacranolide
Sesquiterpenoid
Germacrane sesquiterpenoid
Tetracarboxylic acid or derivatives
Fatty acid ester
Beta-hydroxy acid
Fatty acyl
Hydroxy acid
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
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	3.16	ALOGPS
logP	3.55	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	14.89	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	125.43 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	133.39 m³·mol⁻¹	ChemAxon
Polarizability	52.46 Å³	ChemAxon
Number of Rings	2	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

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

163025423

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for [3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid (NP0058408)

MOL for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D MOL for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D SDF for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D-SDF for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

PDB for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D PDB for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

SMILES for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

INCHI for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

Structure for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D Structure for NP0058408 ([3aR-[3aR*,4R*[E(E)],6E,9S*,10Z,11aR*]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

Showing NP-Card for [3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid (NP0058408)

MOL for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D MOL for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D SDF for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D-SDF for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

PDB for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D PDB for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

SMILES for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

INCHI for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

Structure for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)

3D Structure for NP0058408 ([3aR-[3aR,4R[E(E)],6E,9S,10Z,11aR]]-2-[[[9-(acetyloxy)-2,3,3a,4,5,8,9,11a-octahydro-6,10-dimethyl-3-methylene-2-oxocyclodeca[b]furan-4-yl]oxy]carbonyl]-2-butenyl ester 2-(hydroxymethyl)-2-Butenoic acid)