NP-MRD: Showing NP-Card for (1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0189832)

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Record Information

Version

2.0

Created at

2022-09-04 06:23:18 UTC

Updated at

2022-09-04 06:23:18 UTC

NP-MRD ID

NP0189832

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Description

(1S,2R,4S)-4,7,7-trimethylbicyclo[2.2.1]Heptan-2-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. (1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate is found in Cleistopholis staudtii. Based on a literature review very few articles have been published on (1S,2R,4S)-4,7,7-trimethylbicyclo[2.2.1]Heptan-2-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 50 52  0  0  0  0  0  0  0  0999 V2000
    5.3234    2.8528   -0.2987 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1429    1.7145   -0.3128 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6248    0.4219   -0.2969 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2484    0.2432   -0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6697   -1.0121   -0.2491 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2207   -1.1021   -0.2170 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5782   -2.2552   -0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1226   -2.3031   -0.1669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4806   -3.3956   -0.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6425   -1.1480   -0.1541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0369   -1.1284   -0.1236 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6376   -0.4005   -1.3290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5214    0.6935   -0.7562 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6439    1.0972   -1.5943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6030    1.7936   -0.2949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8278    1.0981    0.8260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4696   -0.2470    1.0207 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9104    0.0610    0.5794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7019   -1.1892    0.4165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5325    1.0544    1.5097 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5292   -2.0837   -0.2643 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9168   -1.9033   -0.2953 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4718   -0.6540   -0.3118 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8500   -0.4866   -0.3426 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4943    2.8020   -1.0180 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9598    3.0990    0.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9751    3.7202   -0.5735 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6064    1.1102   -0.2551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6407   -0.1599   -0.2076 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1401   -3.1646   -0.2082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4967   -2.1278   -0.1100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8353    0.1014   -1.9207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2227   -1.0704   -1.9694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5720    0.5020   -1.3512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9259    2.1577   -1.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4510    0.8772   -2.6738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1337    2.6865    0.0620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9378    2.0594   -1.1416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7637    1.7065    1.7321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7895    0.8988    0.4337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3994   -0.6739    1.9990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6813   -1.6208   -0.6016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7566   -1.0474    0.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2565   -1.9558    1.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7941    1.7461    1.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3676    1.5583    0.9818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9633    0.4895    2.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1088   -3.0756   -0.2516 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5068   -2.7901   -0.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2252    0.4501   -0.3541 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
  5 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23  3  1  0
 17 11  1  0
 18 13  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  6 29  1  0
  7 30  1  0
 11 31  1  1
 12 32  1  0
 12 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 17 41  1  1
 19 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
 20 47  1  0
 21 48  1  0
 22 49  1  0
 24 50  1  0
M  END


  Mrv1652309042208232D          

 24 26  0  0  1  0            999 V2000
   -3.6471    5.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875    5.6521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7865    4.8333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0269    4.5114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9258    3.6926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1662    3.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0652    2.5519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3056    2.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3530    2.7269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1998    1.3727    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2733    0.5639    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2543   -0.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8472   -0.6569    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1127   -1.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5709   -0.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5899    0.5639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8850    0.9927    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6599    0.1726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2793    0.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3152    0.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5844    3.1957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3440    3.5176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4450    4.3364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2046    4.6583    0.0000 O   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  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
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  1  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
  5 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0189832

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\C(=O)O[C@@H]2C[C@]3(C)CC[C@H]2C3(C)C)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O4/c1-19(2)14-9-10-20(19,3)12-17(14)24-18(22)8-6-13-5-7-15(21)16(11-13)23-4/h5-8,11,14,17,21H,9-10,12H2,1-4H3/b8-6+/t14-,17-,20+/m1/s1

> <INCHI_KEY>
DDKIZPUZACBOPC-ILUDWHBUSA-N

> <FORMULA>
C20H26O4

> <MOLECULAR_WEIGHT>
330.424

> <EXACT_MASS>
330.183109317

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
37.279698357766925

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,4S)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
4.484158285000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.867762515555388

> <JCHEM_PKA_STRONGEST_BASIC>
-4.888809926222042

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
93.40310000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4S)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.808  11.151   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -5.390  10.551   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.201   9.022   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.783   8.421   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.595   6.893   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.177   6.292   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.988   4.764   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.570   4.163   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.659   5.090   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -0.373   2.562   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.510   1.053   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.475  -0.487   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.581  -1.226   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.077  -2.761   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.932  -0.487   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.968   1.053   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.652   1.853   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.232   0.322   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.521   0.637   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.588   0.121   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.824   5.965   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.242   6.566   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -6.431   8.095   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -7.849   8.696   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15   18                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17   13   19   20                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21    5   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    3   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,4S)-4,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₆O₄

Average Mass

330.4240 Da

Monoisotopic Mass

330.18311 Da

IUPAC Name

(1S,2R,4S)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Traditional Name

(1S,2R,4S)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\C(=O)O[C@@H]2C[C@]3(C)CC[C@H]2C3(C)C)=CC=C1O

InChI Identifier

InChI=1S/C20H26O4/c1-19(2)14-9-10-20(19,3)12-17(14)24-18(22)8-6-13-5-7-15(21)16(11-13)23-4/h5-8,11,14,17,21H,9-10,12H2,1-4H3/b8-6+/t14-,17-,20+/m1/s1

InChI Key

DDKIZPUZACBOPC-ILUDWHBUSA-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
Cleistopholis staudtii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acids and derivatives

Alternative Parents

Substituents

Coumaric acid or derivatives
Cinnamic acid ester
Bicyclic monoterpenoid
Methoxyphenol
Bornane monoterpenoid
Monoterpenoid
Norbornane monoterpenoid
Aromatic monoterpenoid
Styrene
Phenol ether
Methoxybenzene
Phenoxy compound
Anisole
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acid ester
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
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	4.48	ChemAxon
pKa (Strongest Acidic)	9.87	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	93.4 m³·mol⁻¹	ChemAxon
Polarizability	37.28 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	No	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

163192917

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0189832)

MOL for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D MOL for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D SDF for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D-SDF for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

PDB for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D PDB for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

SMILES for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

INCHI for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

Structure for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D Structure for NP0189832 ((1s,2r,4s)-4,7,7-trimethylbicyclo[2.2.1]heptan-2-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)