NP-MRD: Showing NP-Card for n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid (NP0321291)

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Record Information

Version

2.0

Created at

2022-09-11 23:25:33 UTC

Updated at

2022-09-11 23:25:33 UTC

NP-MRD ID

NP0321291

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid

Description

N-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]Tetradeca-1,3(7),8-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid is found in Aglaia edulis. N-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]Tetradeca-1,3(7),8-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161502062D          

 49 54  0  0  0  0            999 V2000
   -3.6019   -4.0628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7784   -4.0134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4094   -3.2756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8639   -2.5870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5859   -3.2262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1314   -3.9147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2168   -2.4884    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3933   -2.4390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1307   -3.0763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -2.7749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8493   -1.9513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0508   -1.7438    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2506   -0.9758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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 25 70  1  0
 25 71  1  0
 34 74  1  0
 34 75  1  0
 34 76  1  0
 36 77  1  0
 37 78  1  0
 40 79  1  0
 40 80  1  0
 40 81  1  0
 41 82  1  0
 42 83  1  0
M  END


  Mrv1533004161502062D          

 49 54  0  0  0  0            999 V2000
   -3.6019   -4.0628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7784   -4.0134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4094   -3.2756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8639   -2.5870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5859   -3.2262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1314   -3.9147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2168   -2.4884    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3933   -2.4390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1307   -3.0763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -2.7749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8493   -1.9513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0508   -1.7438    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2506   -0.9758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0644   -1.1110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2638   -0.3308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0942    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8788    0.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0503   -0.6494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8349   -0.9043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4480   -0.3523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2765    0.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4919    0.7096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2638    1.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0681    1.3394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7131    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4276    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267    1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4116    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4276   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4276   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7131    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0681   -0.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2517   -1.3187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4873    1.4970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0348    2.1142    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1584    1.0171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9095    1.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0983    1.9640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6844    2.2248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8499    3.0331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2327    3.5805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3981    4.3887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2191    4.9362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5500    3.3197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7155    2.5115    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
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 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
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  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
 27 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  2  0  0  0  0
 25 35  1  0  0  0  0
 35 36  1  0  0  0  0
 15 36  1  0  0  0  0
 36 37  2  0  0  0  0
 23 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 23 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 45 48  1  0  0  0  0
 48 49  2  0  0  0  0
 42 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0321291

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)NC1CCCN1C(=O)C1C(C2=CC=CC=C2)C(OC2=CC3=C(OCO3)C(OC)=C2C1=O)(C(=O)OC)C1=CC=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C37H40N2O10/c1-6-21(2)34(41)38-27-13-10-18-39(27)35(42)29-30(22-11-8-7-9-12-22)37(36(43)46-5,23-14-16-24(44-3)17-15-23)49-25-19-26-32(48-20-47-26)33(45-4)28(25)31(29)40/h7-9,11-12,14-17,19,21,27,29-30H,6,10,13,18,20H2,1-5H3,(H,38,41)

> <INCHI_KEY>
OCAUDZRWYYOTLH-UHFFFAOYSA-N

> <FORMULA>
C37H40N2O10

> <MOLECULAR_WEIGHT>
672.731

> <EXACT_MASS>
672.268295496

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
69.84430012243092

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-methoxy-11-(4-methoxyphenyl)-13-[2-(2-methylbutanamido)pyrrolidine-1-carbonyl]-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1,3(7),8-triene-11-carboxylate

> <ALOGPS_LOGP>
3.85

> <JCHEM_LOGP>
4.6311735196666675

> <ALOGPS_LOGS>
-5.29

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.20756169440116

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.246162254338515

> <JCHEM_PKA_STRONGEST_BASIC>
-1.059904035623524

> <JCHEM_POLAR_SURFACE_AREA>
138.92999999999998

> <JCHEM_REFRACTIVITY>
175.7478

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.43e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-methoxy-11-(4-methoxyphenyl)-13-[2-(2-methylbutanamido)pyrrolidine-1-carbonyl]-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1,3(7),8-triene-11-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -6.724  -7.584   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.186  -7.492   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.498  -6.114   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.346  -4.829   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.960  -6.022   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.112  -7.308   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0      -2.271  -4.645   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      -0.734  -4.553   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.244  -5.742   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.677  -5.180   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.585  -3.643   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       0.095  -3.255   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      -0.468  -1.822   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.987  -2.074   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.492  -0.617   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.176   0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.640   0.294   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.961  -1.212   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.425  -1.688   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.570  -0.658   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.249   0.849   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.785   1.325   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.492   2.157   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.994   2.500   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.198   1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.532   2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.865   1.540   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.330   2.016   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.235   0.770   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.330  -0.476   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       5.865   0.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.532  -0.770   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.532  -2.310   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.865  -3.080   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.198   0.000   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.994  -0.960   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.337  -2.462   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.910   2.794   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -1.932   3.946   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -2.162   1.899   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -3.564   2.535   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.184   3.666   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -1.278   4.153   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -1.586   5.662   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -0.434   6.684   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -0.743   8.192   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       0.409   9.214   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       1.027   6.197   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       1.336   4.688   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   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    8   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   36                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   16   24   38   42                                             
CONECT   24   23   25                                                       
CONECT   25   24   26   35                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   31                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   27   32                                                  
CONECT   32   31   33   35                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   32   25   36                                                  
CONECT   36   35   15   37                                                  
CONECT   37   36                                                            
CONECT   38   23   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40                                                            
CONECT   42   23   43   49                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46   48                                                  
CONECT   46   45   47                                                       
CONECT   47   46                                                            
CONECT   48   45   49                                                       
CONECT   49   48   42                                                       
MASTER        0    0    0    0    0    0    0    0   49    0  108    0
END

View in JSmol

Synonyms

Value	Source
N-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0,]tetradeca-1,3(7),8-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidate	Generator
N-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1,3(7),8-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidate	Generator

Chemical Formula

C₃₇H₄₀N₂O₁₀

Average Mass

672.7310 Da

Monoisotopic Mass

672.26830 Da

IUPAC Name

methyl 2-methoxy-11-(4-methoxyphenyl)-13-[2-(2-methylbutanamido)pyrrolidine-1-carbonyl]-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1,3(7),8-triene-11-carboxylate

Traditional Name

methyl 2-methoxy-11-(4-methoxyphenyl)-13-[2-(2-methylbutanamido)pyrrolidine-1-carbonyl]-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1,3(7),8-triene-11-carboxylate

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)NC1CCCN1C(=O)C1C(C2=CC=CC=C2)C(OC2=CC3=C(OCO3)C(OC)=C2C1=O)(C(=O)OC)C1=CC=C(OC)C=C1

InChI Identifier

InChI=1S/C37H40N2O10/c1-6-21(2)34(41)38-27-13-10-18-39(27)35(42)29-30(22-11-8-7-9-12-22)37(36(43)46-5,23-14-16-24(44-3)17-15-23)49-25-19-26-32(48-20-47-26)33(45-4)28(25)31(29)40/h7-9,11-12,14-17,19,21,27,29-30H,6,10,13,18,20H2,1-5H3,(H,38,41)

InChI Key

OCAUDZRWYYOTLH-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
Aglaia edulis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
Benzoxepine
Benzodioxole
Phenol ether
Aryl ketone
Aryl alkyl ketone
N-acylpyrrolidine
Methoxybenzene
Phenoxy compound
Anisole
Alkyl aryl ether
Fatty acyl
1,3-dicarbonyl compound
N-acyl-amine
Fatty amide
Benzenoid
Monocyclic benzene moiety
Methyl ester
Pyrrolidine
Tertiary carboxylic acid amide
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid ester
Ketone
Acetal
Carboxylic acid derivative
Ether
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Azacycle
Organooxygen compound
Carbonyl group
Organic oxygen compound
Organonitrogen compound
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
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	3.85	ALOGPS
logP	4.63	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	12.25	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	138.93 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	175.75 m³·mol⁻¹	ChemAxon
Polarizability	69.84 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

85286435

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid (NP0321291)

MOL for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)

3D MOL for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)

3D SDF for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)

3D-SDF for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)

PDB for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)

3D PDB for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)

SMILES for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)

INCHI for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)

Structure for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)

3D Structure for NP0321291 (n-{1-[2-methoxy-11-(methoxycarbonyl)-11-(4-methoxyphenyl)-14-oxo-12-phenyl-4,6,10-trioxatricyclo[7.5.0.0³,⁷]tetradeca-1(9),2,7-triene-13-carbonyl]pyrrolidin-2-yl}-2-methylbutanimidic acid)