NP-MRD: Showing NP-Card for (3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate (NP0230620)

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Record Information

Version

2.0

Created at

2022-09-06 11:07:33 UTC

Updated at

2022-09-06 11:07:33 UTC

NP-MRD ID

NP0230620

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate

Description

Eupachifolin D belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative. (3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate is found in Eupatorium chinense. (3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate was first documented in 2004 (PMID: 15387644). Based on a literature review very few articles have been published on Eupachifolin D (PMID: 15104494).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062213072D          

 31 33  0  0  1  0            999 V2000
   -0.1007   -1.8172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5878   -1.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6248   -0.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0202   -0.0242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4201   -0.3191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8746   -1.0076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6996   -1.0076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1541   -0.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8642    0.4533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9493   -0.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9864   -1.3627    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6749   -1.8172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4127   -1.4482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1013   -1.9027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4621   -0.6247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2140   -1.6526    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0304   -2.4569    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8554   -2.4569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2140   -3.2612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6092   -3.8224    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.2871   -2.8149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5438   -2.4569    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8988   -2.9713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0217   -3.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7897   -4.0885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3767   -4.3015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3912   -4.0001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4997   -5.1173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2677   -5.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3906   -6.2344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3602   -1.6526    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 16 11  1  1  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  6  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 22 31  1  0  0  0  0
 31  2  1  1  0  0  0
  6 31  1  0  0  0  0
M  END


  Mrv1652309062213072D          

 31 33  0  0  1  0            999 V2000
   -0.1007   -1.8172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5878   -1.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6248   -0.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0202   -0.0242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4201   -0.3191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8746   -1.0076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6996   -1.0076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1541   -0.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8642    0.4533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9493   -0.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9864   -1.3627    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6749   -1.8172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4127   -1.4482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1013   -1.9027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4621   -0.6247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2140   -1.6526    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0304   -2.4569    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8554   -2.4569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2140   -3.2612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6092   -3.8224    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.2871   -2.8149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5438   -2.4569    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8988   -2.9713    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0217   -3.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7897   -4.0885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3767   -4.3015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3912   -4.0001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4997   -5.1173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2677   -5.4187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3906   -6.2344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3602   -1.6526    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 16 11  1  1  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  6  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 22 31  1  0  0  0  0
 31  2  1  1  0  0  0
  6 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0230620

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C=C(C)[C@@H]2[C@H]3OC(=O)C(=C)[C@@H]3[C@@H](C[C@@](O)(CCl)[C@H]12)OC(=O)C(\C)=C/CO

> <INCHI_IDENTIFIER>
InChI=1S/C22H27ClO8/c1-10(5-6-24)20(26)30-15-8-22(28,9-23)18-14(29-13(4)25)7-11(2)16(18)19-17(15)12(3)21(27)31-19/h5,7,14-19,24,28H,3,6,8-9H2,1-2,4H3/b10-5-/t14-,15-,16+,17-,18-,19-,22-/m1/s1

> <INCHI_KEY>
ROLUXMBDEQQZQJ-SDNFJHMKSA-N

> <FORMULA>
C22H27ClO8

> <MOLECULAR_WEIGHT>
454.9

> <EXACT_MASS>
454.1394455

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
44.4948997280005

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,4R,6S,6aS,7R,9aR,9bR)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl (2Z)-4-hydroxy-2-methylbut-2-enoate

> <JCHEM_LOGP>
1.1235233646666678

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.56852844601488

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.59927873708574

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5521985968748453

> <JCHEM_POLAR_SURFACE_AREA>
119.36

> <JCHEM_REFRACTIVITY>
111.24299999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,4R,6S,6aS,7R,9aR,9bR)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3aH,4H,5H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl (2Z)-4-hydroxy-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.188  -3.392   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.097  -2.544   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.166  -1.005   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.038  -0.045   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       2.651  -0.596   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.499  -1.881   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.039  -1.881   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.888  -0.596   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.346   0.846   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.372  -1.005   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.441  -2.544   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.726  -3.392   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.104  -2.703   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.389  -3.552   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.196  -1.166   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.999  -3.085   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.657  -4.586   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.197  -4.586   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.999  -6.088   0.000  0.00  0.00           C+0
HETATM   20 Cl   UNK     0       4.871  -7.135   0.000  0.00  0.00          Cl+0
HETATM   21  C   UNK     0       4.269  -5.254   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.882  -4.586   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.678  -5.546   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.907  -7.069   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.341  -7.632   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.703  -8.029   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.730  -7.467   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.933  -9.552   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.366 -10.115   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.596 -11.638   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.539  -3.085   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   31                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   11    7   17                                                  
CONECT   17   16   18   19   21                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   17   22                                                       
CONECT   22   21   23   31                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   22    2    6                                                  
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₇ClO₈

Average Mass

454.9000 Da

Monoisotopic Mass

454.13945 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C=C(C)[C@@H]2[C@H]3OC(=O)C(=C)[C@@H]3[C@@H](C[C@@](O)(CCl)[C@H]12)OC(=O)C(\C)=C/CO

InChI Identifier

InChI=1S/C22H27ClO8/c1-10(5-6-24)20(26)30-15-8-22(28,9-23)18-14(29-13(4)25)7-11(2)16(18)19-17(15)12(3)21(27)31-19/h5,7,14-19,24,28H,3,6,8-9H2,1-2,4H3/b10-5-/t14-,15-,16+,17-,18-,19-,22-/m1/s1

InChI Key

ROLUXMBDEQQZQJ-SDNFJHMKSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Eupatorium chinense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Guaianolides and derivatives

Alternative Parents

Substituents

Guaianolide-skeleton
Sesquiterpenoid
Guaiane sesquiterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Lactone
Halohydrin
Chlorohydrin
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organochloride
Organohalogen compound
Carbonyl group
Alkyl halide
Alkyl chloride
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00020439

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

101277293

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Huo J, Yang SP, Ding J, Yue JM: Cytotoxic sesquiterpene lactones from Eupatorium lindleyanum. J Nat Prod. 2004 Sep;67(9):1470-5. doi: 10.1021/np040023h. [PubMed:15387644 ]
Yang SP, Huo J, Wang Y, Lou LG, Yue JM: Cytotoxic sesquiterpenoids from Eupatorium chinense. J Nat Prod. 2004 Apr;67(4):638-43. doi: 10.1021/np0304159. [PubMed:15104494 ]
LOTUS database [Link]

Showing NP-Card for (3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate (NP0230620)

MOL for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)

3D MOL for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)

3D SDF for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)

3D-SDF for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)

PDB for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)

3D PDB for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)

SMILES for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)

INCHI for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)

Structure for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)

3D Structure for NP0230620 ((3ar,4r,6s,6as,7r,9ar,9br)-7-(acetyloxy)-6-(chloromethyl)-6-hydroxy-9-methyl-3-methylidene-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl (2z)-4-hydroxy-2-methylbut-2-enoate)