NP-MRD: Showing NP-Card for (1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate (NP0281197)

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Record Information

Version

2.0

Created at

2022-09-09 07:23:56 UTC

Updated at

2022-09-09 07:23:57 UTC

NP-MRD ID

NP0281197

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate

Description

(1R,2S,4R,6R,9S,10S,11S,12S,14R,15R,18R)-14-hydroxy-6-[(2S)-2-hydroxy-5-oxo-2,5-dihydrofuran-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]Octadec-7-en-12-yl 3-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. (1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate is found in Azadirachta indica. Based on a literature review very few articles have been published on (1R,2S,4R,6R,9S,10S,11S,12S,14R,15R,18R)-14-hydroxy-6-[(2S)-2-hydroxy-5-oxo-2,5-dihydrofuran-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]Octadec-7-en-12-yl 3-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092209232D          

 42 47  0  0  1  0            999 V2000
    5.1893    3.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4019    3.6286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8612    1.2134    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1246    1.9952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6825    1.2908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3016    1.8361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2242    2.6575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0115    1.4159    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7688    1.7433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9491    2.5484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7704    2.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1906    3.3357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 42 24  1  1  0  0  0
 27 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309092209232D          

 42 47  0  0  1  0            999 V2000
    5.1893    3.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4019    3.6286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2541    1.7720    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8612    1.2134    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1246    1.9952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6825    1.2908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3016    1.8361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2242    2.6575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0115    1.4159    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7688    1.7433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9491    2.5484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7704    2.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1906    3.3357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0978    1.8685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4788    1.3231    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5561    0.5017    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8313    0.6108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0099    0.5335    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3909   -0.0119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6809    0.4083    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8936    0.1619    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5499   -0.5881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7304   -0.4930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5676    0.3158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8950   -0.1619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8577    0.7360    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1388    0.3313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8666    1.5610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5855    1.9657    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5650    2.7904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2690    3.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9935    2.8259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2485    4.0453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5241    4.4399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8200    4.0098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5036    5.2647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4668    1.5256    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5326    2.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2865    0.7205    0.0000 C   0  0  1  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
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  6  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  1  0  0  0
 23 22  1  6  0  0  0
  7 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  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  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 32 40  1  0  0  0  0
  6 40  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 42 24  1  1  0  0  0
 27 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281197

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@@H]1[C@]2(C)[C@H](O[C@@H]3C[C@H](C(C)=C23)C2=CC(=O)O[C@@H]2O)[C@@H]2OC[C@@]3(C)[C@H]2[C@@]1(C)[C@H](C[C@H]3O)OC(=O)C=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C32H42O10/c1-14(2)8-23(35)41-21-12-20(33)30(4)13-39-26-27(30)31(21,5)19(11-22(34)38-7)32(6)25-15(3)16(9-18(25)40-28(26)32)17-10-24(36)42-29(17)37/h8,10,16,18-21,26-29,33,37H,9,11-13H2,1-7H3/t16-,18-,19+,20-,21+,26-,27+,28-,29+,30-,31-,32+/m1/s1

> <INCHI_KEY>
LWHAGFHXOKLHEU-QAJJQNCFSA-N

> <FORMULA>
C32H42O10

> <MOLECULAR_WEIGHT>
586.678

> <EXACT_MASS>
586.277797552

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
61.95822089412659

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,4R,6R,9S,10S,11S,12S,14R,15R,18R)-14-hydroxy-6-[(2S)-2-hydroxy-5-oxo-2,5-dihydrofuran-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0^{2,9}.0^{4,8}.0^{15,18}]octadec-7-en-12-yl 3-methylbut-2-enoate

> <JCHEM_LOGP>
2.1533668303333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.775722058151349

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.755313824436019

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9995708796707863

> <JCHEM_POLAR_SURFACE_AREA>
137.82000000000002

> <JCHEM_REFRACTIVITY>
149.8068

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4R,6R,9S,10S,11S,12S,14R,15R,18R)-14-hydroxy-6-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0^{2,9}.0^{4,8}.0^{15,18}]octadec-7-en-12-yl 3-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       9.687   7.233   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.217   6.773   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.880   5.271   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       9.014   4.228   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.411   4.811   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.074   3.308   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.208   2.265   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.699   3.724   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.741   2.409   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.896   3.427   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.752   4.961   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.222   2.643   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.635   3.254   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.972   4.757   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.505   4.901   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      15.289   6.227   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      15.116   3.488   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      13.960   2.470   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      14.105   0.937   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.885   1.140   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.352   0.996   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.196  -0.022   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.871   0.762   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.401   0.302   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.760  -1.098   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.230  -0.920   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.926   0.589   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.671  -0.302   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.601   1.374   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.259   0.618   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.618   2.914   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.960   3.669   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.921   5.209   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.236   6.012   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.588   5.275   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       4.197   7.551   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.845   8.288   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       1.531   7.485   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.807   9.827   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       4.605   2.848   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.728   4.383   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.268   1.345   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                                                       
CONECT    6    5    7   40                                                  
CONECT    7    6    8    9   23                                             
CONECT    8    7                                                            
CONECT    9    7   10   21                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   20                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   13   19                                                  
CONECT   19   18                                                            
CONECT   20   12   21                                                       
CONECT   21   20    9   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22    7   24                                                  
CONECT   24   23   25   42                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   42                                             
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   40                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37                                                            
CONECT   40   32    6   41   42                                             
CONECT   41   40                                                            
CONECT   42   40   24   27                                                  
MASTER        0    0    0    0    0    0    0    0   42    0   94    0
END

View in JSmol

Synonyms

Value	Source
(1R,2S,4R,6R,9S,10S,11S,12S,14R,15R,18R)-14-Hydroxy-6-[(2S)-2-hydroxy-5-oxo-2,5-dihydrofuran-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0,.0,.0,]octadec-7-en-12-yl 3-methylbut-2-enoic acid	Generator

Chemical Formula

C₃₂H₄₂O₁₀

Average Mass

586.6780 Da

Monoisotopic Mass

586.27780 Da

IUPAC Name

Traditional Name

(1R,2S,4R,6R,9S,10S,11S,12S,14R,15R,18R)-14-hydroxy-6-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0^{2,9}.0^{4,8}.0^{15,18}]octadec-7-en-12-yl 3-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@@H]1[C@]2(C)[C@H](O[C@@H]3C[C@H](C(C)=C23)C2=CC(=O)O[C@@H]2O)[C@@H]2OC[C@@]3(C)[C@H]2[C@@]1(C)[C@H](C[C@H]3O)OC(=O)C=C(C)C

InChI Identifier

InChI=1S/C32H42O10/c1-14(2)8-23(35)41-21-12-20(33)30(4)13-39-26-27(30)31(21,5)19(11-22(34)38-7)32(6)25-15(3)16(9-18(25)40-28(26)32)17-10-24(36)42-29(17)37/h8,10,16,18-21,26-29,33,37H,9,11-13H2,1-7H3/t16-,18-,19+,20-,21+,26-,27+,28-,29+,30-,31-,32+/m1/s1

InChI Key

LWHAGFHXOKLHEU-QAJJQNCFSA-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
Azadirachta indica	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
Naphthofuran
Tricarboxylic acid or derivatives
Fatty acid ester
2-furanone
Fatty acyl
Cyclic alcohol
Dihydrofuran
Tetrahydrofuran
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Hemiacetal
Secondary alcohol
Carboxylic acid ester
Oxacycle
Ether
Dialkyl ether
Organoheterocyclic compound
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
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	2.15	ChemAxon
pKa (Strongest Acidic)	6.76	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	137.82 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	149.81 m³·mol⁻¹	ChemAxon
Polarizability	61.96 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

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BiGG ID

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Wikipedia Link

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METLIN ID

Not Available

PubChem Compound

162951523

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate (NP0281197)

MOL for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)

3D MOL for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)

3D SDF for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)

3D-SDF for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)

PDB for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)

3D PDB for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)

SMILES for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)

INCHI for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)

Structure for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)

3D Structure for NP0281197 ((1r,2s,4r,6r,9s,10s,11s,12s,14r,15r,18r)-14-hydroxy-6-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl 3-methylbut-2-enoate)