NP-MRD: Showing NP-Card for (1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate (NP0270615)

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Record Information

Version

2.0

Created at

2022-09-08 16:37:28 UTC

Updated at

2022-09-08 16:37:29 UTC

NP-MRD ID

NP0270615

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate

Description

Arteminolide A belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. (1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate is found in Artemisia argyi. (1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate was first documented in 2002 (PMID: 12398488). Based on a literature review very few articles have been published on Arteminolide A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082218372D          

 43 49  0  0  1  0            999 V2000
    1.8926    3.1106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3242    2.1629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2588    1.8777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0594    0.8251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9385    0.9571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1659    1.7501    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6876    2.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2603    1.7486    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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 40 42  1  0  0  0  0
 35 43  1  0  0  0  0
 43 24  1  1  0  0  0
 19 43  1  0  0  0  0
M  END

     RDKit          2D

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M  END


  Mrv1652309082218372D          

 43 49  0  0  1  0            999 V2000
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    0.8093    2.3644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2603    1.7486    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5383    1.2185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2206    2.5781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3995    0.9354    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2155    0.1312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8199   -0.4303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6084   -0.1876    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7558   -0.9743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1221    0.5373    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7925    0.6166    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1880    1.1781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0596    1.3972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2290    2.3896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8845    1.3843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1272    0.5958    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9189    0.3640    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5486    0.8970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6977    1.7434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2501    0.4629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0541   -0.3384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6841   -0.9190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2313   -0.3996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8291   -1.1199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3154   -1.8329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0152   -1.2546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4024   -0.7021    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7690   -1.5393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6427   -2.4028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8516   -2.6369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2531   -2.9822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8389   -3.7278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2632   -4.4353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0140   -3.7415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4523    0.1213    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  2  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  6  0  0  0
 10 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 18 16  1  1  0  0  0
  6 18  1  0  0  0  0
 13 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  6  0  0  0
 13 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 24 23  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  1  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  2  0  0  0  0
 29 31  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 35 43  1  0  0  0  0
 43 24  1  1  0  0  0
 19 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270615

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC(=O)O[C@H]1CC(C)=C2[C@@H]([C@H]3OC(=O)[C@@]4(C[C@@]56C=C[C@@]4(C)[C@@H]5[C@H]4OC(=O)C(=C)[C@@H]4CC[C@@]6(C)O)[C@H]13)C(C)=CC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H42O8/c1-16(2)12-23(37)41-22-14-18(4)24-21(36)13-17(3)25(24)28-26(22)35(31(39)43-28)15-34-11-10-32(35,6)29(34)27-20(8-9-33(34,7)40)19(5)30(38)42-27/h10-11,13,16,20,22,25-29,40H,5,8-9,12,14-15H2,1-4,6-7H3/t20-,22-,25-,26+,27-,28+,29-,32-,33+,34-,35+/m0/s1

> <INCHI_KEY>
RAKYLPJLLBOHHN-PAIAVIFNSA-N

> <FORMULA>
C35H42O8

> <MOLECULAR_WEIGHT>
590.713

> <EXACT_MASS>
590.287968312

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
58.635213440040765

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'R,2'R,3S,3aR,4S,5'S,9'S,9aS,9bR,10'S,11'S)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-3a,4,5,7,9a,9b-hexahydro-2H-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0^{1,10}.0^{5,9}]pentadecan]-14'-en-4-yl 3-methylbutanoate

> <JCHEM_LOGP>
4.060946780666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.09112634721778

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.365709186191264

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0212361670736607

> <JCHEM_POLAR_SURFACE_AREA>
116.20000000000002

> <JCHEM_REFRACTIVITY>
158.39690000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,2'R,3S,3aR,4S,5'S,9'S,9aS,9bR,10'S,11'S)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3aH-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0^{1,10}.0^{5,9}]pentadecan]-14'-en-4-yl 3-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       3.533   5.806   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.472   4.037   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.451   2.987   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.483   3.505   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       1.978   1.540   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.619   1.787   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.043   3.267   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.150   4.522   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.511   4.414   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.486   3.264   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.005   2.274   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.412   4.812   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.746   1.746   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.402   0.245   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.530  -0.803   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.002  -0.350   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.277  -1.819   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.095   1.003   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.346   1.151   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.218   2.199   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.845   2.608   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.161   4.461   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       5.384   2.584   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.837   1.112   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.315   0.679   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.491   1.674   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.769   3.254   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.800   0.864   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.434  -0.632   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.610  -1.715   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.899  -0.746   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.148  -2.090   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.055  -3.421   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.628  -2.342   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.485  -1.311   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.302  -2.873   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       3.066  -4.485   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       1.590  -4.922   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       4.206  -5.567   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.433  -6.959   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.225  -8.279   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       1.893  -6.984   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.578   0.227   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14   18   20                                             
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16    6   13                                                  
CONECT   19   16   20   21   43                                             
CONECT   20   19   13                                                       
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   43                                                  
CONECT   25   24   26   31                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   25   32                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   43                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   35   24   19                                                  
MASTER        0    0    0    0    0    0    0    0   43    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₄₂O₈

Average Mass

590.7130 Da

Monoisotopic Mass

590.28797 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)O[C@H]1CC(C)=C2[C@@H]([C@H]3OC(=O)[C@@]4(C[C@@]56C=C[C@@]4(C)[C@@H]5[C@H]4OC(=O)C(=C)[C@@H]4CC[C@@]6(C)O)[C@H]13)C(C)=CC2=O

InChI Identifier

InChI=1S/C35H42O8/c1-16(2)12-23(37)41-22-14-18(4)24-21(36)13-17(3)25(24)28-26(22)35(31(39)43-28)15-34-11-10-32(35,6)29(34)27-20(8-9-33(34,7)40)19(5)30(38)42-27/h10-11,13,16,20,22,25-29,40H,5,8-9,12,14-15H2,1-4,6-7H3/t20-,22-,25-,26+,27-,28+,29-,32-,33+,34-,35+/m0/s1

InChI Key

RAKYLPJLLBOHHN-PAIAVIFNSA-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
Artemisia argyi	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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

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

8802605

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15968984

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lee SH, Kim HK, Seo JM, Kang HM, Kim JH, Son KH, Lee H, Kwon BM, Shin J, Seo Y: Arteminolides B, C, and D, new inhibitors of farnesyl protein transferase from Artemisia argyi. J Org Chem. 2002 Nov 1;67(22):7670-5. doi: 10.1021/jo020299z. [PubMed:12398488 ]
LOTUS database [Link]

Showing NP-Card for (1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate (NP0270615)

MOL for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)

3D MOL for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)

3D SDF for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)

3D-SDF for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)

PDB for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)

3D PDB for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)

SMILES for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)

INCHI for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)

Structure for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)

3D Structure for NP0270615 ((1'r,2'r,3s,3ar,4s,5's,9's,9as,9br,10's,11's)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxo-4,5,9a,9b-tetrahydro-3ah-8'-oxaspiro[azuleno[4,5-b]furan-3,12'-tetracyclo[9.2.2.0¹,¹⁰.0⁵,⁹]pentadecan]-14'-en-4-yl 3-methylbutanoate)