NP-MRD: Showing NP-Card for 1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate (NP0260748)

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Record Information

Version

2.0

Created at

2022-09-08 03:00:01 UTC

Updated at

2022-09-08 03:00:01 UTC

NP-MRD ID

NP0260748

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate

Description

Incarvillateine C belongs to the class of organic compounds known as 1-hydroxy-2-unsubstituted benzenoids. These are phenols that are unsubstituted at the 2-position. 1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate is found in Incarvillea sinensis. Based on a literature review a small amount of articles have been published on Incarvillateine C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082205002D          

 48 54  0  0  1  0            999 V2000
    2.9939   -8.6628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2489   -7.8782    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7639   -7.2107    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9389   -7.2107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5264   -6.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9389   -5.7818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7014   -6.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181   -7.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181   -7.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8326   -8.3171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8326   -9.1421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4653   -6.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7973   -6.1943    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5118   -6.6068    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -5.2263   -6.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2263   -5.3693    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9407   -4.9568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4624   -6.7982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4624   -7.6232    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1769   -8.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0335   -7.6232    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  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  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
  8 16  1  0  0  0  0
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 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 20 19  1  6  0  0  0
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 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 29 28  1  1  0  0  0
 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  6  0  0  0
 16 32  1  0  0  0  0
  7 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 33 39  1  0  0  0  0
  3 40  1  0  0  0  0
 41 40  1  1  0  0  0
 41 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 48 47  1  1  0  0  0
 41 48  1  0  0  0  0
  2 48  1  0  0  0  0
M  END

     RDKit          3D

102108  0  0  0  0  0  0  0  0999 V2000
    5.1068   -1.6090   -2.1122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6541   -1.2474   -0.7721 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5625   -1.2797    0.2990 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4657   -0.5043   -0.1479 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8181    1.5340    1.3937 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2115    0.4340   -0.0343 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3565    0.7616    0.7250 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0862   -0.4402    1.2396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3939   -0.4778    0.5267 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.5869   -0.4935    1.4422 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -8.8190   -0.5713    0.5983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8692    0.3756   -0.4621 N   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3250   -0.1399   -1.7139 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.4337    0.5929   -0.5092 C   0  0  1  0  0  0  0  0  0  0  0  0
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 23 22  1  0
  1 49  1  0
  1 50  1  0
  1 51  1  0
  2 52  1  1
  3 53  1  1
 40 88  1  0
 40 89  1  0
 41 90  1  6
 48102  1  6
 47100  1  0
 47101  1  0
 46 97  1  0
 46 98  1  0
 46 99  1  0
 44 95  1  0
 44 96  1  0
 42 91  1  1
 43 92  1  0
 43 93  1  0
 43 94  1  0
  7 54  1  6
 32 82  1  6
 16 61  1  6
  8 55  1  1
 10 56  1  0
 11 57  1  0
 13 58  1  0
 14 59  1  0
 15 60  1  0
 20 62  1  1
 21 63  1  0
 21 64  1  0
 22 65  1  6
 29 77  1  6
 28 75  1  0
 28 76  1  0
 27 72  1  0
 27 73  1  0
 27 74  1  0
 25 70  1  0
 25 71  1  0
 23 66  1  1
 24 67  1  0
 24 68  1  0
 24 69  1  0
 30 78  1  1
 31 79  1  0
 31 80  1  0
 31 81  1  0
 34 83  1  0
 35 84  1  0
 37 85  1  0
 38 86  1  0
 39 87  1  0
M  END


  Mrv1652309082205002D          

 48 54  0  0  1  0            999 V2000
    2.9939   -8.6628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2489   -7.8782    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7639   -7.2107    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9389   -7.2107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5264   -6.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9389   -5.7818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7014   -6.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181   -7.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181   -7.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8326   -8.3171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8326   -9.1421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181   -9.5546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181  -10.3796    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5964   -9.1421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5964   -8.3171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4653   -6.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2903   -6.4962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7028   -7.2107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7028   -5.7818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5278   -5.7818    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0127   -6.4492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7973   -6.1943    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5118   -6.6068    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5118   -7.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2263   -6.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2263   -5.3693    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9407   -4.9568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5118   -4.9568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7973   -5.3693    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0127   -5.1143    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7578   -4.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181   -5.9129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181   -5.0879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5964   -4.6754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5964   -3.8504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181   -3.4379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1181   -2.6129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8326   -3.8504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8326   -4.6754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2489   -6.5433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0335   -6.7982    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7480   -6.3857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7480   -5.5607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4624   -6.7982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4624   -7.6232    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1769   -8.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7480   -8.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0335   -7.6232    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  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  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 20 19  1  6  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 29 28  1  1  0  0  0
 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  6  0  0  0
 16 32  1  0  0  0  0
  7 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 33 39  1  0  0  0  0
  3 40  1  0  0  0  0
 41 40  1  1  0  0  0
 41 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 48 47  1  1  0  0  0
 41 48  1  0  0  0  0
  2 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0260748

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H](C[C@@H]2[C@H]1CN(C)C[C@@H]2C)OC(=O)C1C(C(C1C1=CC=C(O)C=C1)C(=O)O[C@@H]1C[C@@H]2[C@@H](CN(C)C[C@@H]2C)[C@@H]1C)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C40H54N2O6/c1-21-17-41(5)19-31-23(3)33(15-29(21)31)47-39(45)37-35(25-7-11-27(43)12-8-25)38(36(37)26-9-13-28(44)14-10-26)40(46)48-34-16-30-22(2)18-42(6)20-32(30)24(34)4/h7-14,21-24,29-38,43-44H,15-20H2,1-6H3/t21-,22-,23-,24-,29-,30-,31-,32-,33+,34+,35?,36?,37?,38?/m0/s1

> <INCHI_KEY>
WIWBHTSWIXPGLX-IBRMZUEBSA-N

> <FORMULA>
C40H54N2O6

> <MOLECULAR_WEIGHT>
658.88

> <EXACT_MASS>
658.398187467

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
102

> <JCHEM_AVERAGE_POLARIZABILITY>
75.5761711729684

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,3-bis[(4R,4aS,6R,7S,7aR)-2,4,7-trimethyl-octahydro-1H-cyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate

> <JCHEM_LOGP>
4.192674415327368

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
9.924770680146093

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.068365102301938

> <JCHEM_PKA_STRONGEST_BASIC>
10.385144484090336

> <JCHEM_POLAR_SURFACE_AREA>
99.53999999999999

> <JCHEM_REFRACTIVITY>
186.272

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
1,3-bis[(4R,4aS,6R,7S,7aR)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       5.589 -16.171   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.065 -14.706   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.159 -13.460   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.619 -13.460   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.849 -12.126   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.619 -10.793   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.309 -12.126   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.220 -13.215   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.220 -14.755   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.554 -15.525   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.554 -17.065   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.220 -17.835   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.220 -19.375   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.113 -17.065   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.113 -15.525   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.869 -12.126   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.409 -12.126   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.179 -13.460   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -3.179 -10.793   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.719 -10.793   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.624 -12.039   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -7.088 -11.563   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -8.422 -12.333   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.422 -13.873   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -9.756 -11.563   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0      -9.756 -10.023   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0     -11.089  -9.253   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -8.422  -9.253   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -7.088 -10.023   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -5.624  -9.547   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -5.148  -8.082   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.220 -11.037   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.220  -9.497   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.113  -8.727   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.113  -7.187   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.220  -6.417   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       0.220  -4.877   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.554  -7.187   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.554  -8.727   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.065 -12.214   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.529 -12.690   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       8.863 -11.920   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       8.863 -10.380   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      10.197 -12.690   0.000  0.00  0.00           C+0
HETATM   45  N   UNK     0      10.197 -14.230   0.000  0.00  0.00           N+0
HETATM   46  C   UNK     0      11.530 -15.000   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.863 -15.000   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       7.529 -14.230   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   48                                                  
CONECT    3    2    4   40                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   32                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    9                                                       
CONECT   16    8   17   32                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   30                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   22   30                                                  
CONECT   30   29   20   31                                                  
CONECT   31   30                                                            
CONECT   32   16    7   33                                                  
CONECT   33   32   34   39                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   33                                                       
CONECT   40    3   41                                                       
CONECT   41   40   42   48                                                  
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48                                                       
CONECT   48   47   41    2                                                  
MASTER        0    0    0    0    0    0    0    0   48    0  108    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₅₄N₂O₆

Average Mass

658.8800 Da

Monoisotopic Mass

658.39819 Da

IUPAC Name

1,3-bis[(4R,4aS,6R,7S,7aR)-2,4,7-trimethyl-octahydro-1H-cyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate

Traditional Name

1,3-bis[(4R,4aS,6R,7S,7aR)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H](C[C@@H]2[C@H]1CN(C)C[C@@H]2C)OC(=O)C1C(C(C1C1=CC=C(O)C=C1)C(=O)O[C@@H]1C[C@@H]2[C@@H](CN(C)C[C@@H]2C)[C@@H]1C)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C40H54N2O6/c1-21-17-41(5)19-31-23(3)33(15-29(21)31)47-39(45)37-35(25-7-11-27(43)12-8-25)38(36(37)26-9-13-28(44)14-10-26)40(46)48-34-16-30-22(2)18-42(6)20-32(30)24(34)4/h7-14,21-24,29-38,43-44H,15-20H2,1-6H3/t21-,22-,23-,24-,29-,30-,31-,32-,33+,34+,35?,36?,37?,38?/m0/s1

InChI Key

WIWBHTSWIXPGLX-IBRMZUEBSA-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
Incarvillea sinensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-hydroxy-2-unsubstituted benzenoids. These are phenols that are unsubstituted at the 2-position.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenols

Sub Class

1-hydroxy-2-unsubstituted benzenoids

Direct Parent

1-hydroxy-2-unsubstituted benzenoids

Alternative Parents

Substituents

1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Piperidine
Amino acid or derivatives
Carboxylic acid ester
Tertiary amine
Tertiary aliphatic amine
Carboxylic acid derivative
Azacycle
Organoheterocyclic compound
Organooxygen compound
Organonitrogen compound
Organic oxide
Organopnictogen compound
Amine
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organic nitrogen 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	4.19	ChemAxon
pKa (Strongest Acidic)	9.07	ChemAxon
pKa (Strongest Basic)	10.39	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	99.54 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	186.27 m³·mol⁻¹	ChemAxon
Polarizability	75.58 Å³	ChemAxon
Number of Rings	7	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

C00039409

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

15488887

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate (NP0260748)

MOL for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)

3D MOL for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)

3D SDF for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)

3D-SDF for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)

PDB for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)

3D PDB for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)

SMILES for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)

INCHI for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)

Structure for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)

3D Structure for NP0260748 (1,3-bis[(4r,4as,6r,7s,7ar)-2,4,7-trimethyl-octahydrocyclopenta[c]pyridin-6-yl] 2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylate)