NP-MRD: Showing NP-Card for (1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one (NP0145956)

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Record Information

Version

2.0

Created at

2022-09-02 01:15:43 UTC

Updated at

2022-09-02 01:15:43 UTC

NP-MRD ID

NP0145956

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one

Description

(1S,4S,7R)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]Oct-5-en-2-one belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. (1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one is found in Asarum fauriei. Based on a literature review very few articles have been published on (1S,4S,7R)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]Oct-5-en-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022203152D          

 31 33  0  0  1  0            999 V2000
   -1.9360   -1.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1222   -1.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8211   -0.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0122   -0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0958    0.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6916    1.2430    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7003    2.1341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2312    2.7985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4174    0.8507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0916    1.4505    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4405    0.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3976   -0.0916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1400   -0.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500   -0.8940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2291   -1.6696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7379   -0.4064    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8599    0.1472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8445    0.6970    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0079    0.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4861    1.2178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3110    1.2028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7365    1.9096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5613    1.8945    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9868    2.6014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3371    2.6315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7626    3.3383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5874    3.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5122    2.6465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1128    3.3684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7120    3.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0868    1.9397    0.0000 C   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  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
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 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 16  1  0  0  0  0
 16  4  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  1  0  0  0
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 22 25  2  0  0  0  0
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 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 28 31  2  0  0  0  0
 20 31  1  0  0  0  0
M  END

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
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   -1.8360   -3.2668    0.4314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9525   -2.2764   -0.6656 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.0430   -0.6886    1.2205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8061    0.7543    1.5581 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6074    0.9238    2.8952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7331    0.6121    3.6375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8666    1.6011    0.9586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3361    2.5415    1.5002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3157    1.1676   -0.4257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5725    0.7138   -0.4447 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9655   -0.3888    0.2202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2981    2.3413   -1.2260 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6871    2.1040   -2.5110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2037    0.3072   -0.9380 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8904    1.0568   -0.6881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5349    1.1092    0.7510 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5073    0.1118    1.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7966    0.2180    0.5318 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0992   -0.5474   -0.5682 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3086   -0.4564   -1.2253 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5199   -1.2762   -2.3316 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5522   -2.1880   -2.7967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2538    0.4214   -0.7815 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4723    0.5059   -1.4531 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5970   -0.2807   -1.1219 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9880    1.2144    0.3290 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9956    2.0738    0.7130 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8966    2.9353    1.7983 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7734    1.1065    0.9690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7815   -4.7748    1.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.8145   -2.5094   -1.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0872   -0.5464    0.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8998   -0.3353    1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5334   -1.3458   -0.1099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1030    1.4116   -3.1089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7607    1.7773   -2.5876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6762    3.0850   -3.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2206    0.0572   -1.9927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0072    2.0920   -1.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1132    0.5297   -1.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2787    2.1432    1.0902 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3783   -1.2691   -0.9549 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1631   -2.8413   -1.9986 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0726   -2.8415   -3.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7183   -1.6898   -3.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309022203152D          

 31 33  0  0  1  0            999 V2000
   -1.9360   -1.3778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1222   -1.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8211   -0.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0122   -0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0958    0.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6916    1.2430    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7003    2.1341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1128    3.3684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7120    3.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0868    1.9397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0145956

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C[C@H]2C[C@H]3C(CC=C)=C[C@]2(OC)C(=O)C3(OC)OC)=CC(OC)=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O7/c1-8-9-16-14-23(29-5)17(13-18(16)24(30-6,31-7)22(23)25)10-15-11-19(26-2)21(28-4)20(12-15)27-3/h8,11-12,14,17-18H,1,9-10,13H2,2-7H3/t17-,18-,23+/m0/s1

> <INCHI_KEY>
HEDWJMBFTCTVMQ-IUKKYPGJSA-N

> <FORMULA>
C24H32O7

> <MOLECULAR_WEIGHT>
432.513

> <EXACT_MASS>
432.21480337

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
46.68570560174288

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4S,7R)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one

> <ALOGPS_LOGP>
3.56

> <JCHEM_LOGP>
4.028391002666666

> <ALOGPS_LOGS>
-5.29

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7388736000142466

> <JCHEM_POLAR_SURFACE_AREA>
72.45000000000002

> <JCHEM_REFRACTIVITY>
117.43659999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.20e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,7R)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.614  -2.572   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.095  -2.319   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.533  -0.822   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.023  -0.026   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.179   1.663   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.291   2.320   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.307   3.984   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.298   5.224   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.646   1.588   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.904   2.708   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.689   0.049   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.475  -0.171   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.861  -0.995   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.080  -1.669   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.294  -3.117   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.377  -0.759   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.605   0.275   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.576   1.301   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.015   0.790   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.907   2.273   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.447   2.245   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.241   3.565   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -4.781   3.536   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -5.575   4.856   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.496   4.912   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.290   6.232   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -4.830   6.203   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.956   4.940   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -0.211   6.288   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       1.329   6.316   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.162   3.621   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    9   18                                             
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   14   16                                             
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14                                                            
CONECT   16   11    4   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17    6   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   31                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28   20                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₇

Average Mass

432.5130 Da

Monoisotopic Mass

432.21480 Da

IUPAC Name

(1S,4S,7R)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one

Traditional Name

(1S,4S,7R)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC(C[C@H]2C[C@H]3C(CC=C)=C[C@]2(OC)C(=O)C3(OC)OC)=CC(OC)=C1OC

InChI Identifier

InChI=1S/C24H32O7/c1-8-9-16-14-23(29-5)17(13-18(16)24(30-6,31-7)22(23)25)10-15-11-19(26-2)21(28-4)20(12-15)27-3/h8,11-12,14,17-18H,1,9-10,13H2,2-7H3/t17-,18-,23+/m0/s1

InChI Key

HEDWJMBFTCTVMQ-IUKKYPGJSA-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
Asarum fauriei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenoxy compound
Anisole
Methoxybenzene
Alkyl aryl ether
Ketal
Cyclohexenone
Monocyclic benzene moiety
Ketone
Acetal
Ether
Dialkyl ether
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aldehyde
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	3.56	ALOGPS
logP	4.03	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	72.45 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	117.44 m³·mol⁻¹	ChemAxon
Polarizability	46.69 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

10308101

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21722997

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one (NP0145956)

MOL for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)

3D MOL for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)

3D SDF for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)

3D-SDF for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)

PDB for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)

3D PDB for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)

SMILES for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)

INCHI for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)

Structure for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)

3D Structure for NP0145956 ((1s,4s,7r)-1,3,3-trimethoxy-5-(prop-2-en-1-yl)-7-[(3,4,5-trimethoxyphenyl)methyl]bicyclo[2.2.2]oct-5-en-2-one)