NP-MRD: Showing NP-Card for 15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate (NP0233408)

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Record Information

Version

2.0

Created at

2022-09-06 14:59:46 UTC

Updated at

2022-09-06 14:59:46 UTC

NP-MRD ID

NP0233408

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate

Description

15-[1-(Acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]Octadecan-17-yl 2-methylbut-2-enoate belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. 15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate is found in Swietenia mahagoni. 15-[1-(Acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]Octadecan-17-yl 2-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231519212D          

 46 51  0  0  0  0            999 V2000
    1.0408   -4.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8377   -2.7104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5865   -2.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2383   -2.0364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6368   -2.7588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2104   -3.4651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4616   -2.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9849   -1.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1533004231519212D          

 46 51  0  0  0  0            999 V2000
    1.0408   -4.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6145   -3.4490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0129   -2.7265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8377   -2.7104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2383   -2.0364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2104   -3.4651    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5156   -0.5762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1039   -1.1211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1130   -0.0418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9697    0.1484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5637    0.8666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2612    0.8742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6672    1.5924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6803    0.1635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5052    0.1711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9242   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2743   -0.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8311    0.1638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8048    0.9884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7014    0.2037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5129    0.3050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2086   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7646   -1.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2098   -1.9837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0396   -1.9993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4558   -1.2840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8608   -2.0028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0559   -0.5624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4809    0.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3057    0.1302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7307    0.8373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7056   -0.5914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2806   -1.2985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6805   -2.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4994   -2.1208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6567   -2.9306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9351   -3.3305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3318   -2.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8688   -1.3102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8847   -2.1350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8584   -0.5895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6832   -0.5686    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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  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  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  4  0  0  0
 18 21  1  0  0  0  0
 14 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
 25 26  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  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 30 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 38 42  1  0  0  0  0
 27 43  1  0  0  0  0
 10 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 22 45  1  0  0  0  0
 45 46  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0233408

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(OC(C)=O)C1C(C)(C)C(OC(=O)C(C)=CC)C2(O)C3OC33C(CCC4(C)C3CC(=O)OC4C3=COC=C3)C1(C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H42O12/c1-9-16(2)25(37)45-28-30(4,5)23(22(26(38)41-8)43-17(3)35)32(7)19-10-12-31(6)20(34(19)29(46-34)33(28,40)27(32)39)14-21(36)44-24(31)18-11-13-42-15-18/h9,11,13,15,19-20,22-24,28-29,40H,10,12,14H2,1-8H3

> <INCHI_KEY>
CYIZQHWSHNNMLB-UHFFFAOYSA-N

> <FORMULA>
C34H42O12

> <MOLECULAR_WEIGHT>
642.698

> <EXACT_MASS>
642.267626792

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
64.89460154962721

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate

> <ALOGPS_LOGP>
3.60

> <JCHEM_LOGP>
3.839314507333334

> <ALOGPS_LOGS>
-4.15

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.110540935006151

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8704617088328277

> <JCHEM_POLAR_SURFACE_AREA>
168.17000000000002

> <JCHEM_REFRACTIVITY>
156.94789999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.59e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       1.943  -7.756   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.147  -6.438   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.891  -5.090   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.430  -5.059   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.095  -3.771   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.445  -3.801   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.189  -5.150   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.393  -6.468   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.728  -5.180   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.839  -2.423   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.962  -1.076   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.194  -2.093   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.211  -0.078   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.810   0.277   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.052   1.618   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.488   1.632   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.245   2.972   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.270   0.305   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.810   0.319   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.592  -1.007   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.512  -1.035   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.418   0.306   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.369   1.845   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.043   0.380   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.557   0.569   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.989  -0.921   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.161  -2.358   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.992  -3.703   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.541  -3.732   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.317  -2.397   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.073  -3.739   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.571  -1.050   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.364   0.270   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.904   0.243   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      10.697   1.563   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      10.650  -1.104   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       9.857  -2.424   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      10.604  -3.771   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      12.132  -3.959   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      12.426  -5.471   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      11.079  -6.217   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       9.953  -5.167   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       3.488  -2.446   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       3.518  -3.985   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.469  -1.100   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       5.009  -1.061   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    5   11   43                                                  
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18                                                            
CONECT   22   14   23   24   45                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24   26                                                       
CONECT   26   25   24   27   32                                             
CONECT   27   26   28   43                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32   37                                             
CONECT   31   30                                                            
CONECT   32   30   26   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   30   38                                                  
CONECT   38   37   39   42                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   38                                                       
CONECT   43   27   10   44   45                                             
CONECT   44   43                                                            
CONECT   45   43   22   46                                                  
CONECT   46   45                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  102    0
END

View in JSmol

Synonyms

Value	Source
15-[1-(Acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0,.0,.0,]octadecan-17-yl 2-methylbut-2-enoic acid	Generator
15-[1-(Acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₃₄H₄₂O₁₂

Average Mass

642.6980 Da

Monoisotopic Mass

642.26763 Da

IUPAC Name

15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate

Traditional Name

15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

COC(=O)C(OC(C)=O)C1C(C)(C)C(OC(=O)C(C)=CC)C2(O)C3OC33C(CCC4(C)C3CC(=O)OC4C3=COC=C3)C1(C)C2=O

InChI Identifier

InChI=1S/C34H42O12/c1-9-16(2)25(37)45-28-30(4,5)23(22(26(38)41-8)43-17(3)35)32(7)19-10-12-31(6)20(34(19)29(46-34)33(28,40)27(32)39)14-21(36)44-24(31)18-11-13-42-15-18/h9,11,13,15,19-20,22-24,28-29,40H,10,12,14H2,1-8H3

InChI Key

CYIZQHWSHNNMLB-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
Swietenia mahagoni	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
Mexicanolide
Naphthopyran
Tetracarboxylic acid or derivatives
Naphthalene
Delta valerolactone
Fatty acid ester
Delta_valerolactone
Oxepane
Fatty acyl
Oxane
Pyran
Cyclic alcohol
Furan
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tertiary alcohol
Lactone
Ketone
Carboxylic acid ester
Ether
Oxirane
Dialkyl ether
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Alcohol
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	3.6	ALOGPS
logP	3.84	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	11.11	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	168.17 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	156.95 m³·mol⁻¹	ChemAxon
Polarizability	64.89 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	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

72783834

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate (NP0233408)

MOL for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)

3D MOL for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)

3D SDF for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)

3D-SDF for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)

PDB for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)

3D PDB for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)

SMILES for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)

INCHI for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)

Structure for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)

3D Structure for NP0233408 (15-[1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-1-hydroxy-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate)