NP-MRD: Showing NP-Card for 4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate (NP0248470)

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Record Information

Version

2.0

Created at

2022-09-07 10:44:46 UTC

Updated at

2022-09-07 10:44:46 UTC

NP-MRD ID

NP0248470

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate

Description

4A,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-2H,3H,3aH,4H,4aH,5H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate belongs to the class of organic compounds known as sesquiterpene lactones. These are sesquiterpenoids containing a lactone ring. 4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate is found in Tetraneuris ivesiana. 4A,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-2H,3H,3aH,4H,4aH,5H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161522492D          

 32 34  0  0  0  0            999 V2000
    4.9574    3.7283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9574    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2429    2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2429    1.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9574    1.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    1.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    0.4283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2717    0.0703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4553   -0.7340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2770   -0.8079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6013   -0.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4056    0.1343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9800    0.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3042    1.2521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9409   -1.3790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2989   -2.1223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8342   -2.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0115   -2.7423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1921   -3.5472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7274   -4.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0853   -4.9722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9047   -4.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1159   -1.3790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7580   -2.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6016   -0.7340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7799   -0.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4556   -0.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0769    0.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0030    1.3152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7851    0.0703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8222    0.8945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
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  9 14  1  0  0  0  0
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 10 16  1  0  0  0  0
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 17 18  1  0  0  0  0
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 21 23  1  0  0  0  0
 16 24  1  0  0  0  0
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 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
  8 31  1  0  0  0  0
 26 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END

     RDKit          3D

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   -1.1879    1.6520    0.4813 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -2.7095   -0.3570   -2.3806 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0251    1.0718    1.8343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3501    1.5089    1.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3192    3.0085    1.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7510    2.4704   -0.2284 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3726    2.2334   -0.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8543    4.2569    0.5987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7754    4.1347    2.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7540    3.6320   -0.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2979    2.3082   -1.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1268    2.6270    0.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0246    0.2334   -1.0168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6480   -1.3751   -3.5134 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004161522492D          

 32 34  0  0  0  0            999 V2000
    4.9574    3.7283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9574    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2429    2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    2.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2429    1.6658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9574    1.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    1.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284    0.4283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2717    0.0703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4553   -0.7340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2770   -0.8079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.4056    0.1343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0853   -4.9722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9047   -4.1672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1159   -1.3790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7580   -2.1223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7799   -0.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4556   -0.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0769    0.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0030    1.3152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7851    0.0703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8222    0.8945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  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
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 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0248470

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1C2C(OC(=O)C2=C)C(OC(=O)C=C(C)C)C(C)C2C=CC(=O)C12C

> <INCHI_IDENTIFIER>
InChI=1S/C25H30O7/c1-8-13(4)23(28)32-22-19-15(6)24(29)31-21(19)20(30-18(27)11-12(2)3)14(5)16-9-10-17(26)25(16,22)7/h8-11,14,16,19-22H,6H2,1-5,7H3

> <INCHI_KEY>
FWQMAPNSBVFNPC-UHFFFAOYSA-N

> <FORMULA>
C25H30O7

> <MOLECULAR_WEIGHT>
442.508

> <EXACT_MASS>
442.199153306

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
46.46958817988214

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-2H,3H,3aH,4H,4aH,5H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate

> <ALOGPS_LOGP>
2.29

> <JCHEM_LOGP>
5.123642296000001

> <ALOGPS_LOGS>
-4.87

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.024648999842537

> <JCHEM_PKA_STRONGEST_BASIC>
-5.111400802932471

> <JCHEM_POLAR_SURFACE_AREA>
95.97

> <JCHEM_REFRACTIVITY>
118.49210000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.03e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3aH,4H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       9.254   6.959   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.254   5.419   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.920   4.649   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.586   5.419   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.920   3.109   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       9.254   2.339   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       6.586   2.339   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.586   0.799   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.974   0.131   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.317  -1.370   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.850  -1.508   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.456  -0.092   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.957   0.251   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.296   0.921   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.901   2.337   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.356  -2.574   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.025  -3.962   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.157  -5.234   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.621  -5.119   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.825  -6.622   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.958  -7.894   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.626  -9.281   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.422  -7.779   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.816  -2.574   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.148  -3.962   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.856  -1.370   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.322  -1.508   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.717  -0.092   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.877   0.921   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.739   2.455   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.199   0.131   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.268   1.670   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   31                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    9   15                                                  
CONECT   15   14                                                            
CONECT   16   10   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   16   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    8   26   32                                             
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
4a,8-Dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-2H,3H,3ah,4H,4ah,5H,7ah,8H,9H,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₅H₃₀O₇

Average Mass

442.5080 Da

Monoisotopic Mass

442.19915 Da

IUPAC Name

4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-2H,3H,3aH,4H,4aH,5H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate

Traditional Name

4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3aH,4H,7aH,8H,9H,9aH-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1C2C(OC(=O)C2=C)C(OC(=O)C=C(C)C)C(C)C2C=CC(=O)C12C

InChI Identifier

InChI=1S/C25H30O7/c1-8-13(4)23(28)32-22-19-15(6)24(29)31-21(19)20(30-18(27)11-12(2)3)14(5)16-9-10-17(26)25(16,22)7/h8-11,14,16,19-22H,6H2,1-5,7H3

InChI Key

FWQMAPNSBVFNPC-UHFFFAOYSA-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
Tetraneuris ivesiana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpene lactones. These are sesquiterpenoids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Sesquiterpene lactones

Alternative Parents

Substituents

Helenalin-skeleton
Ambrosanolide
Pseudoguaiane sesquiterpenoid
Sesquiterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Ketone
Lactone
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Carbonyl group
Organic oxygen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
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	2.29	ALOGPS
logP	5.12	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	15.02	ChemAxon
pKa (Strongest Basic)	-5.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	95.97 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	118.49 m³·mol⁻¹	ChemAxon
Polarizability	46.47 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate (NP0248470)

MOL for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)

3D MOL for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)

3D SDF for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)

3D-SDF for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)

PDB for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)

3D PDB for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)

SMILES for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)

INCHI for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)

Structure for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)

3D Structure for NP0248470 (4a,8-dimethyl-4-[(2-methylbut-2-enoyl)oxy]-3-methylidene-2,5-dioxo-3ah,4h,7ah,8h,9h,9ah-azuleno[6,5-b]furan-9-yl 3-methylbut-2-enoate)