NP-MRD: Showing NP-Card for 8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate (NP0322532)

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Record Information

Version

2.0

Created at

2022-09-12 01:21:14 UTC

Updated at

2022-09-12 01:21:14 UTC

NP-MRD ID

NP0322532

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate

Description

8-(Acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl}-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-4-yl 2-methylbutanoate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. 8-(Acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl}-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-4-yl 2-methylbutanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004251511392D          

 44 47  0  0  0  0            999 V2000
    3.2436   -1.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5258   -0.6019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9955    0.0301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2777    0.8053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1830   -0.1132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9009   -0.8884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6527    0.5188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8403    0.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5581   -0.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2544   -0.5430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7847    0.0890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4166   -0.4413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    0.3712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5025    0.8643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2440    1.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9280    0.7646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6695    1.1262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7270    1.9492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3534    0.6649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0328    1.4963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7506    2.2715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0618    2.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3440    3.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5921    1.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224    2.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3066    1.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0211    1.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7356    1.3703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4500    1.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4500    2.6078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1645    1.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8790    1.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1645    0.5453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0211    2.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3536    3.0927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6086    3.8773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1237    4.5448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4336    3.8773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6885    3.0927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3100    1.0075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8453    1.3530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3756    1.9850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1171    2.3466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0934    2.7602    0.0000 C   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
  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  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 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
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  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
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 27 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 34 39  1  0  0  0  0
 24 40  1  0  0  0  0
  8 40  1  0  0  0  0
 14 40  1  0  0  0  0
 20 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
M  END


  Mrv1533004251511392D          

 44 47  0  0  0  0            999 V2000
    3.2436   -1.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5258   -0.6019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9955    0.0301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2777    0.8053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1830   -0.1132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9009   -0.8884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6527    0.5188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8403    0.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5581   -0.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2544   -0.5430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7847    0.0890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4166   -0.4413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5599    0.3712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5025    0.8643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2440    1.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9280    0.7646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6695    1.1262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7270    1.9492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3534    0.6649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0328    1.4963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7506    2.2715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0618    2.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3440    3.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5921    1.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1224    2.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3066    1.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0211    1.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7356    1.3703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4500    1.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4500    2.6078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1645    1.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8790    1.7828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1645    0.5453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0211    2.6078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3536    3.0927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6086    3.8773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1237    4.5448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4336    3.8773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6885    3.0927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3100    1.0075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8453    1.3530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3756    1.9850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1171    2.3466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0934    2.7602    0.0000 C   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
  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  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 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
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  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
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 27 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 34 39  1  0  0  0  0
 24 40  1  0  0  0  0
  8 40  1  0  0  0  0
 14 40  1  0  0  0  0
 20 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322532

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)OC1CCC2(CO2)C2(COC(C)=O)C(CC(C)C(C)(CC(OC(=O)C(C)C)C3=CC(=O)OC3)C12)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H48O11/c1-9-19(4)30(38)43-24-10-11-32(16-41-32)33(17-40-21(6)34)26(42-22(7)35)12-20(5)31(8,28(24)33)14-25(44-29(37)18(2)3)23-13-27(36)39-15-23/h13,18-20,24-26,28H,9-12,14-17H2,1-8H3

> <INCHI_KEY>
CUISVSYCDKXXAJ-UHFFFAOYSA-N

> <FORMULA>
C33H48O11

> <MOLECULAR_WEIGHT>
620.736

> <EXACT_MASS>
620.319662366

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
65.70407040310133

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl}-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-4-yl 2-methylbutanoate

> <ALOGPS_LOGP>
3.40

> <JCHEM_LOGP>
3.9667606766666634

> <ALOGPS_LOGS>
-5.47

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.593879031097253

> <JCHEM_PKA_STRONGEST_BASIC>
-4.204449139462975

> <JCHEM_POLAR_SURFACE_AREA>
144.03

> <JCHEM_REFRACTIVITY>
156.07290000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.11e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2H-furan-3-yl)ethyl}-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-4-yl 2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       6.055  -2.571   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.582  -1.124   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.592   0.056   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.118   1.503   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.075  -0.211   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.548  -1.658   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       3.085   0.968   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.569   0.701   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.042  -0.746   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.475  -1.014   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.465   0.166   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.644  -0.824   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.912   0.693   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.938   1.613   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.322   2.288   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -3.599   1.427   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -4.983   2.102   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -5.090   3.639   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -6.260   1.241   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.928   2.793   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.401   4.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.115   4.508   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.642   5.955   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.105   3.328   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.095   4.508   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.439   2.558   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.773   3.328   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.106   2.558   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.440   3.328   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.440   4.868   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.774   2.558   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.107   3.328   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.774   1.018   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.773   4.868   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.527   5.773   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.003   7.238   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.097   8.484   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       4.543   7.238   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       5.019   5.773   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.579   1.881   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -3.444   2.526   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -4.434   3.705   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -5.819   4.380   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -3.908   5.152   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   40                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   14                                             
CONECT   12   11   13                                                       
CONECT   13   12   11                                                       
CONECT   14   11   15   20   40                                             
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   14   21   41                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26   40                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   34                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   27   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   34                                                       
CONECT   40   24    8   14                                                  
CONECT   41   20   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   94    0
END

View in JSmol

Synonyms

Value	Source
8-(Acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl}-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-4-yl 2-methylbutanoic acid	Generator

Chemical Formula

C₃₃H₄₈O₁₁

Average Mass

620.7360 Da

Monoisotopic Mass

620.31966 Da

IUPAC Name

8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2,5-dihydrofuran-3-yl)ethyl}-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-4-yl 2-methylbutanoate

Traditional Name

8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2H-furan-3-yl)ethyl}-hexahydro-2H-spiro[naphthalene-1,2'-oxirane]-4-yl 2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)OC1CCC2(CO2)C2(COC(C)=O)C(CC(C)C(C)(CC(OC(=O)C(C)C)C3=CC(=O)OC3)C12)OC(C)=O

InChI Identifier

InChI=1S/C33H48O11/c1-9-19(4)30(38)43-24-10-11-32(16-41-32)33(17-40-21(6)34)26(42-22(7)35)12-20(5)31(8,28(24)33)14-25(44-29(37)18(2)3)23-13-27(36)39-15-23/h13,18-20,24-26,28H,9-12,14-17H2,1-8H3

InChI Key

CUISVSYCDKXXAJ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Fatty acid ester
2-furanone
Fatty acyl
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Ether
Oxirane
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
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	3.4	ALOGPS
logP	3.97	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	5.59	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	144.03 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	156.07 m³·mol⁻¹	ChemAxon
Polarizability	65.7 Å³	ChemAxon
Number of Rings	4	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

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 8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate (NP0322532)

MOL for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)

3D MOL for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)

3D SDF for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)

3D-SDF for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)

PDB for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)

3D PDB for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)

SMILES for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)

INCHI for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)

Structure for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)

3D Structure for NP0322532 (8-(acetyloxy)-8a-[(acetyloxy)methyl]-5,6-dimethyl-5-{2-[(2-methylpropanoyl)oxy]-2-(5-oxo-2h-furan-3-yl)ethyl}-hexahydro-2h-spiro[naphthalene-1,2'-oxiran]-4-yl 2-methylbutanoate)