NP-MRD: Showing NP-Card for (1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate (NP0321930)

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Record Information

Version

2.0

Created at

2022-09-12 00:24:23 UTC

Updated at

2022-09-12 00:24:23 UTC

NP-MRD ID

NP0321930

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

Description

CASEARLUCIN E belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations. (1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate is found in Casearia lucida. Based on a literature review very few articles have been published on CASEARLUCIN E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122202242D          

 38 40  0  0  1  0            999 V2000
    3.5207    0.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0074   -0.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1750   -0.1622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2024    0.6624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4169   -0.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5924   -0.2774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3353   -0.3216    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0200   -1.1135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8905   -0.9319    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7473   -1.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6966   -0.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9365   -0.2034    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    1.8420    3.0062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5839    3.7898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6544    2.8371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3583    1.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0292    3.1601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7272    0.6468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.8401   -1.0984    0.0000 O   0  0  0  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
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
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 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
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 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 18 26  1  0  0  0  0
 27 26  1  6  0  0  0
  7 27  1  0  0  0  0
 15 27  1  0  0  0  0
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 33 34  1  0  0  0  0
 15 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
M  END

     RDKit          3D

 82 84  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309122202242D          

 38 40  0  0  1  0            999 V2000
    3.5207    0.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0074   -0.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2039    3.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0311    1.0745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5863    0.4643    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4682    1.4301    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9746    2.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7923    2.3699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3583    1.7696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0292    3.1601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7272    0.6468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0623    0.1585    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3975   -0.7763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0578   -1.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8935   -2.1688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8401   -1.0984    0.0000 O   0  0  0  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
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 18 26  1  0  0  0  0
 27 26  1  6  0  0  0
  7 27  1  0  0  0  0
 15 27  1  0  0  0  0
 16 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 15 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0321930

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)O[C@@H]1C[C@H]2[C@]3([C@@H](OC(C)=O)O[C@@H](OC(C)=O)C3=C1)[C@@H](C[C@H](C)[C@]2(C)CCC(=C)C=C)OC

> <INCHI_IDENTIFIER>
InChI=1S/C30H44O8/c1-10-17(3)12-13-29(8)19(5)14-25(34-9)30-23(27(35-20(6)31)38-28(30)36-21(7)32)15-22(16-24(29)30)37-26(33)18(4)11-2/h10,15,18-19,22,24-25,27-28H,1,3,11-14,16H2,2,4-9H3/t18?,19-,22-,24+,25+,27+,28-,29-,30-/m0/s1

> <INCHI_KEY>
PRXYABXGJNKXKE-ITLUKHRWSA-N

> <FORMULA>
C30H44O8

> <MOLECULAR_WEIGHT>
532.674

> <EXACT_MASS>
532.303618377

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
58.864889745770924

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3S,5R,6aR,7S,8S,10R,10aR)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

> <JCHEM_LOGP>
5.200778383333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9901845671091887

> <JCHEM_POLAR_SURFACE_AREA>
97.36000000000001

> <JCHEM_REFRACTIVITY>
141.4614

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S,5R,6aR,7S,8S,10R,10aR)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1H,3H,5H,6H,6aH,8H,9H,10H-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

> <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       6.572   0.672   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.614  -0.534   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.060  -0.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.111   1.236   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.645  -1.058   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.106  -0.518   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.626  -0.600   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.037  -2.078   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.662  -1.740   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.395  -3.373   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.167  -1.412   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.615  -0.380   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -5.447  -0.125   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -6.856  -1.019   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.599   1.195   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.067   2.662   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.031   3.801   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.526   3.473   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.365   4.846   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.907   5.296   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.422   3.834   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.438   5.612   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.957   7.074   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.955   5.296   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.981   6.444   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.058   2.006   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.094   0.867   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.607   2.670   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -5.553   4.062   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -7.079   4.424   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -8.136   3.303   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -7.521   5.899   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      -5.091   1.207   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -3.850   0.296   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -4.475  -1.449   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -5.708  -2.539   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -5.401  -4.048   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -7.168  -2.050   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   27                                             
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   27   34                                             
CONECT   16   15   17   28                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   18   27                                                       
CONECT   27   26    7   15                                                  
CONECT   28   16   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   28   34                                                       
CONECT   34   33   15   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₄O₈

Average Mass

532.6740 Da

Monoisotopic Mass

532.30362 Da

IUPAC Name

(1R,3S,5R,6aR,7S,8S,10R,10aR)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

Traditional Name

(1R,3S,5R,6aR,7S,8S,10R,10aR)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1H,3H,5H,6H,6aH,8H,9H,10H-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)O[C@@H]1C[C@H]2[C@]3([C@@H](OC(C)=O)O[C@@H](OC(C)=O)C3=C1)[C@@H](C[C@H](C)[C@]2(C)CCC(=C)C=C)OC

InChI Identifier

InChI=1S/C30H44O8/c1-10-17(3)12-13-29(8)19(5)14-25(34-9)30-23(27(35-20(6)31)38-28(30)36-21(7)32)15-22(16-24(29)30)37-26(33)18(4)11-2/h10,15,18-19,22,24-25,27-28H,1,3,11-14,16H2,2,4-9H3/t18?,19-,22-,24+,25+,27+,28-,29-,30-/m0/s1

InChI Key

PRXYABXGJNKXKE-ITLUKHRWSA-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
Casearia lucida	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Substituents

Clerodane diterpenoid
Naphthofuran
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Tetrahydrofuran
Carboxylic acid ester
Acetal
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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	5.2	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	97.36 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	141.46 m³·mol⁻¹	ChemAxon
Polarizability	58.86 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

C00045723

Chemspider ID

24690658

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44584142

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate (NP0321930)

MOL for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D MOL for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D SDF for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D-SDF for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

PDB for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D PDB for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

SMILES for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

INCHI for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

Structure for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)

3D Structure for NP0321930 ((1r,3s,5r,6ar,7s,8s,10r,10ar)-1,3-bis(acetyloxy)-10-methoxy-7,8-dimethyl-7-(3-methylidenepent-4-en-1-yl)-1h,3h,5h,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-5-yl 2-methylbutanoate)