NP-MRD: Showing NP-Card for 5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate (NP0255322)

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Record Information

Version

2.0

Created at

2022-09-07 19:46:40 UTC

Updated at

2022-09-07 19:46:40 UTC

NP-MRD ID

NP0255322

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate

Description

5A-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-decahydro-2H-spiro[naphtho[1,2-b]furan-9,2'-oxirane]-6-yl 2-(hydroxymethyl)prop-2-enoate belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton. 5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate is found in Dimerostemma brasilianum. 5A-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-decahydro-2H-spiro[naphtho[1,2-b]furan-9,2'-oxirane]-6-yl 2-(hydroxymethyl)prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241504242D          

 31 34  0  0  0  0            999 V2000
    4.5364    2.7327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1464    2.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5810    1.3045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3218    1.9800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8872    2.6812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9318    1.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3664    0.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1910    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0156    0.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4502   -0.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8849   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4949   -1.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6703   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6960   -2.3766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9690   -1.9866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2357   -0.8508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4111   -0.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8784   -1.5066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1147   -1.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4134   -1.6293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1752   -0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5452    0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9765   -0.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8402    0.6290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6648    0.6548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0994   -0.0465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0548    1.3818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6202    2.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8794    1.4075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3140    0.7063    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  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  2  0  0  0  0
 22 24  1  0  0  0  0
  7 24  1  0  0  0  0
 18 24  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  1  0  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
 30 31  1  0  0  0  0
M  END

     RDKit          3D

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   -1.2183    3.2492   -2.8826 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0912    2.6414   -3.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1644    2.3069   -2.1699 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0690   -3.7519    0.7252 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1605   -3.7865    1.5761 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6368   -4.7825    2.2155 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7301   -2.4132    1.6364 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7454   -2.1017    2.4159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9153   -1.6555    0.6781 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5829   -0.2556    0.9949 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7370    0.5709    0.7806 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2310    1.4504    1.7234 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5876    1.4927    2.8269 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4059    2.3121    1.5437 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6702    1.5189    1.2454 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6428    3.1347    2.7822 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9132   -4.9174    0.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8461   -2.2067    1.7615 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1378   -1.1058    2.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2317   -2.8108    3.0676 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3010   -1.7686   -0.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2264   -0.1045    2.0060 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2689    3.0386    0.7013 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4953    2.2244    0.9903 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5175    0.7946    0.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9817    0.9446    2.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6971    3.5775    3.1815 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6631    1.2974    0.1161 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004241504242D          

 31 34  0  0  0  0            999 V2000
    4.5364    2.7327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1464    2.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5810    1.3045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3218    1.9800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8872    2.6812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9318    1.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3664    0.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1910    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0156    0.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4502   -0.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4949   -1.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8402    0.6290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0994   -0.0465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0548    1.3818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6202    2.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8794    1.4075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0255322

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)OC1CC2(C)C(CCC3(CO3)C2C2OC(=O)C(=C)C12)OC(=O)C(=C)CO

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O8/c1-11(2)19(25)29-14-8-22(5)15(30-20(26)12(3)9-24)6-7-23(10-28-23)18(22)17-16(14)13(4)21(27)31-17/h11,14-18,24H,3-4,6-10H2,1-2,5H3

> <INCHI_KEY>
DWVUSVRIEQYQMH-UHFFFAOYSA-N

> <FORMULA>
C23H30O8

> <MOLECULAR_WEIGHT>
434.485

> <EXACT_MASS>
434.194067926

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
45.432489567878775

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-decahydro-2H-spiro[naphtho[1,2-b]furan-9,2'-oxirane]-6-yl 2-(hydroxymethyl)prop-2-enoate

> <ALOGPS_LOGP>
1.53

> <JCHEM_LOGP>
2.200969992666667

> <ALOGPS_LOGS>
-3.18

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.89640622480848

> <JCHEM_PKA_STRONGEST_BASIC>
-2.844111917268771

> <JCHEM_POLAR_SURFACE_AREA>
111.66000000000001

> <JCHEM_REFRACTIVITY>
107.40689999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.84e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxirane]-6-yl 2-(hydroxymethyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       8.468   5.101   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.740   3.744   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.551   2.435   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.201   3.696   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.389   5.005   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       5.473   2.339   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.284   1.030   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.823   1.078   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.635  -0.231   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.363   1.126   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.174  -0.183   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.985  -1.492   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.257  -2.849   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.718  -2.897   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.766  -4.436   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.409  -3.708   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.907  -1.588   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.367  -1.636   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.373  -2.812   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.947  -2.230   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.638  -3.041   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.060  -0.694   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.884   0.300   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.556  -0.327   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.902   1.174   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      12.441   1.222   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      13.252  -0.087   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      13.169   2.579   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.358   3.888   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.708   2.627   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      15.520   1.318   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   24                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11   17                                             
CONECT   10    9                                                            
CONECT   11    9   12   25                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14   16                                                       
CONECT   16   15   14                                                       
CONECT   17   14    9   18                                                  
CONECT   18   17   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    7   18                                                  
CONECT   25   11   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Value	Source
5a-Methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-decahydro-2H-spiro[naphtho[1,2-b]furan-9,2'-oxirane]-6-yl 2-(hydroxymethyl)prop-2-enoic acid	Generator

Chemical Formula

C₂₃H₃₀O₈

Average Mass

434.4850 Da

Monoisotopic Mass

434.19407 Da

IUPAC Name

5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-decahydro-2H-spiro[naphtho[1,2-b]furan-9,2'-oxirane]-6-yl 2-(hydroxymethyl)prop-2-enoate

Traditional Name

5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxirane]-6-yl 2-(hydroxymethyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)OC1CC2(C)C(CCC3(CO3)C2C2OC(=O)C(=C)C12)OC(=O)C(=C)CO

InChI Identifier

InChI=1S/C23H30O8/c1-11(2)19(25)29-14-8-22(5)15(30-20(26)12(3)9-24)6-7-23(10-28-23)18(22)17-16(14)13(4)21(27)31-17/h11,14-18,24H,3-4,6-10H2,1-2,5H3

InChI Key

DWVUSVRIEQYQMH-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
Dimerostemma brasilianum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmanolides, secoeudesmanolides, and derivatives. These are terpenoids with a structure based on the eudesmanolide (a 3,5a,9-trimethyl-naphtho[1,2-b]furan-2-one derivative) or secoeudesmanolide (a 3,6-dimethyl-5-(pentan-2-yl)-1-benzofuran-2-one derivative) skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Eudesmanolides, secoeudesmanolides, and derivatives

Alternative Parents

Substituents

Eudesmanolide
Sesquiterpenoid
Naphthofuran
Tricarboxylic acid or derivatives
Beta-hydroxy acid
Gamma butyrolactone
Hydroxy acid
Alpha,beta-unsaturated carboxylic ester
Tetrahydrofuran
Enoate ester
Lactone
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
Organic oxygen compound
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	1.53	ALOGPS
logP	2.2	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	14.9	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	111.66 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	107.41 m³·mol⁻¹	ChemAxon
Polarizability	45.43 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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 5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate (NP0255322)

MOL for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)

3D MOL for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)

3D SDF for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)

3D-SDF for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)

PDB for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)

3D PDB for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)

SMILES for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)

INCHI for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)

Structure for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)

3D Structure for NP0255322 (5a-methyl-3-methylidene-4-[(2-methylpropanoyl)oxy]-2-oxo-octahydrospiro[naphtho[1,2-b]furan-9,2'-oxiran]-6-yl 2-(hydroxymethyl)prop-2-enoate)