NP-MRD: Showing NP-Card for (1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate (NP0172060)

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Record Information

Version

2.0

Created at

2022-09-03 08:50:57 UTC

Updated at

2022-09-03 08:50:58 UTC

NP-MRD ID

NP0172060

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate

Description

Rohituka 7 belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. (1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate is found in Aphanamixis polystachya. Based on a literature review very few articles have been published on Rohituka 7.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032210502D          

 48 52  0  0  1  0            999 V2000
   -0.6307   -0.0842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0414   -1.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2371   -0.3045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3601    0.5113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0745    0.9238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0129    1.7465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8425    0.6224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0857   -0.1659    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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  8 10  1  0  0  0  0
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  2 47  1  0  0  0  0
 33 47  1  0  0  0  0
 47 48  1  1  0  0  0
M  END

     RDKit          3D

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  7 56  1  0
 12 57  1  0
 12 58  1  0
 12 59  1  0
 13 60  1  0
 13 61  1  0
 17 62  1  0
 17 63  1  0
 18 64  1  6
M  END


  Mrv1652309032210502D          

 48 52  0  0  1  0            999 V2000
   -0.6307   -0.0842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6307   -0.9092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0838   -1.3217    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7983   -0.9092    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0414   -1.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2371   -0.3045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3601    0.5113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0745    0.9238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0129    1.7465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8425    0.6224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0857   -0.1659    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6001    0.4791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9084   -0.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2663   -0.9709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8016   -1.6525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1595   -2.3958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9789   -1.5909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6209   -0.8476    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0838   -2.1467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7983   -2.5592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5127   -2.1467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2272   -2.5592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6307   -2.5592    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6307   -3.3842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0838   -3.7967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7983   -3.3842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0838   -4.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6307   -5.0342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7983   -5.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5127   -4.6217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7983   -5.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5127   -6.2717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3452   -2.1467    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4314   -2.9672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1298   -2.4017    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3847   -3.1863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8998   -3.8537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3847   -4.5212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1693   -4.2662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1693   -3.4412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6147   -1.7342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1298   -1.0668    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3847   -0.2822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1917   -0.1107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7437   -0.7238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4466    0.6740    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3452   -1.3217    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4314   -0.5013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  1  0  0  0
  4  5  1  6  0  0  0
  4  6  1  6  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  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
 18 17  1  6  0  0  0
 11 18  1  0  0  0  0
  4 18  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 23 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 36 40  2  0  0  0  0
 35 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  6  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  2  0  0  0  0
 42 47  1  0  0  0  0
  2 47  1  0  0  0  0
 33 47  1  0  0  0  0
 47 48  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0172060

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(O)C(=O)O[C@H]1[C@H](OC=O)[C@@H](C(=C)[C@@]2(O)[C@H](C[C@@H](C3=COC=C3)[C@]12C)OC(C)=O)[C@@]1(C)C=CC(=O)O[C@]2(C)COC(=O)C[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C35H44O13/c1-8-18(2)28(40)31(41)47-30-29(45-17-36)27(32(5)11-9-25(38)48-33(6)16-44-26(39)14-23(32)33)19(3)35(42)24(46-20(4)37)13-22(34(30,35)7)21-10-12-43-15-21/h9-12,15,17-18,22-24,27-30,40,42H,3,8,13-14,16H2,1-2,4-7H3/t18?,22-,23+,24-,27+,28?,29+,30-,32-,33+,34+,35+/m0/s1

> <INCHI_KEY>
ZZPUDABJUQWRTM-KIROYGDFSA-N

> <FORMULA>
C35H44O13

> <MOLECULAR_WEIGHT>
672.724

> <EXACT_MASS>
672.278191477

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
67.61229294850122

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,3aR,4R,5R,6R,7aS)-6-[(5R,5aR,9aS)-5,9a-dimethyl-2,7-dioxo-2H,5H,5aH,6H,7H,9H,9aH-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-octahydro-1H-inden-4-yl 2-hydroxy-3-methylpentanoate

> <ALOGPS_LOGP>
2.55

> <JCHEM_LOGP>
2.670062805333334

> <ALOGPS_LOGS>
-4.18

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.003860161595846

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.325650084734527

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8773265641432713

> <JCHEM_POLAR_SURFACE_AREA>
185.1

> <JCHEM_REFRACTIVITY>
164.7705

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.40e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,3aR,4R,5R,6R,7aS)-6-[(5R,5aR,9aS)-5,9a-dimethyl-2,7-dioxo-5aH,6H,9H-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.177  -0.157   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.177  -1.697   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.156  -2.467   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.490  -1.697   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.944  -3.169   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.443  -0.568   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.672   0.954   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.006   1.724   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.891   3.260   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       3.439   1.162   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.893  -0.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.853   0.894   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.429  -0.425   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.097  -1.812   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.230  -3.085   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.898  -4.472   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.694  -2.970   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.026  -1.582   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.156  -4.007   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.490  -4.777   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.824  -4.007   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.157  -4.777   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.177  -4.777   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -1.177  -6.317   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.156  -7.087   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.490  -6.317   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.156  -8.627   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.177  -9.397   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.490  -9.397   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.824  -8.627   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.490 -10.937   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.824 -11.707   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.511  -4.007   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -2.672  -5.539   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -3.976  -4.483   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -4.451  -5.948   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -3.546  -7.194   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -4.451  -8.440   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -5.916  -7.964   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -5.916  -6.424   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -4.881  -3.237   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -3.976  -1.991   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -4.451  -0.527   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -5.958  -0.207   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -6.988  -1.351   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -6.434   1.258   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -2.511  -2.467   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -2.672  -0.936   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   47                                                  
CONECT    3    2    4   19                                                  
CONECT    4    3    5    6   18                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13   18                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   11    4                                                  
CONECT   19    3   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   19   24   33                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31                                                            
CONECT   33   23   34   35   47                                             
CONECT   34   33                                                            
CONECT   35   33   36   41                                                  
CONECT   36   35   37   40                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   36                                                       
CONECT   41   35   42                                                       
CONECT   42   41   43   47                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47   42    2   33   48                                             
CONECT   48   47                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₄₄O₁₃

Average Mass

672.7240 Da

Monoisotopic Mass

672.27819 Da

IUPAC Name

(1S,3R,3aR,4R,5R,6R,7aS)-6-[(5R,5aR,9aS)-5,9a-dimethyl-2,7-dioxo-2H,5H,5aH,6H,7H,9H,9aH-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-octahydro-1H-inden-4-yl 2-hydroxy-3-methylpentanoate

Traditional Name

(1S,3R,3aR,4R,5R,6R,7aS)-6-[(5R,5aR,9aS)-5,9a-dimethyl-2,7-dioxo-5aH,6H,9H-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate

CAS Registry Number

Not Available

SMILES

CCC(C)C(O)C(=O)O[C@H]1[C@H](OC=O)[C@@H](C(=C)[C@@]2(O)[C@H](C[C@@H](C3=COC=C3)[C@]12C)OC(C)=O)[C@@]1(C)C=CC(=O)O[C@]2(C)COC(=O)C[C@H]12

InChI Identifier

InChI=1S/C35H44O13/c1-8-18(2)28(40)31(41)47-30-29(45-17-36)27(32(5)11-9-25(38)48-33(6)16-44-26(39)14-23(32)33)19(3)35(42)24(46-20(4)37)13-22(34(30,35)7)21-10-12-43-15-21/h9-12,15,17-18,22-24,27-30,40,42H,3,8,13-14,16H2,1-2,4-7H3/t18?,22-,23+,24-,27+,28?,29+,30-,32-,33+,34+,35+/m0/s1

InChI Key

ZZPUDABJUQWRTM-KIROYGDFSA-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
Aphanamixis polystachya	LOTUS Database	35616633

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
Delta_valerolactone
Fatty acid ester
Delta valerolactone
Fatty acyl
Oxane
Monosaccharide
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Furan
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	2.55	ALOGPS
logP	2.67	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	12.33	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	185.1 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	164.77 m³·mol⁻¹	ChemAxon
Polarizability	67.61 Å³	ChemAxon
Number of Rings	5	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

102274900

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate (NP0172060)

MOL for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)

3D MOL for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)

3D SDF for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)

3D-SDF for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)

PDB for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)

3D PDB for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)

SMILES for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)

INCHI for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)

Structure for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)

3D Structure for NP0172060 ((1s,3s,3ar,4r,5r,6r,7as)-6-[(5r,5ar,9as)-5,9a-dimethyl-2,7-dioxo-5ah,6h,9h-pyrano[3,4-b]oxepin-5-yl]-1-(acetyloxy)-5-(formyloxy)-3-(furan-3-yl)-7a-hydroxy-3a-methyl-7-methylidene-hexahydroinden-4-yl 2-hydroxy-3-methylpentanoate)