NP-MRD: Showing NP-Card for {3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid (NP0260072)

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Record Information

Version

2.0

Created at

2022-09-08 02:08:04 UTC

Updated at

2022-09-08 02:08:04 UTC

NP-MRD ID

NP0260072

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid

Description

Cavoxinin belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. {3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid is found in Neocucurbitaria cava. Based on a literature review very few articles have been published on Cavoxinin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 42  0  0  0  0  0  0  0  0999 V2000
   -7.2262   -0.7956   -0.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7773    0.1097    0.4327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7054   -0.5016    1.2772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4919   -0.8391    0.4853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3010   -0.3342    0.7235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1199   -0.6654   -0.0507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9170   -0.1202    0.2327 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2496   -0.4432   -0.5269 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1440   -1.2780   -1.5075 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5689    0.0908   -0.2937 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8191    0.9935    0.7239 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8496    1.4550    1.5895 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1127    1.4875    0.9166 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1378    1.0886    0.1093 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5208    1.5981    0.2927 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2501    0.7182    1.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7185   -0.2879    1.7288 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5635    1.0109    1.5279 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8639    0.1838   -0.9033 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6189   -0.3231   -1.1270 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3270   -1.2247   -2.1301 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3909   -1.6435   -2.9738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2631   -1.1681   -0.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5801   -1.6683   -0.7605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1558   -0.2147   -1.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4168    1.0983    0.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6488    0.3111    1.0883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3754    0.2891    2.0117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0911   -1.3947    1.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5926   -1.5299   -0.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2516    0.3726    1.5663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1716   -1.3495   -0.8653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9280    0.5477    1.0474 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0614    2.1037    2.3108 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3182    2.1941    1.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0663    1.6597   -0.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4799    2.6131    0.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2317    1.1603    0.7877 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6635   -0.1562   -1.5680 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0374   -2.3902   -3.7162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2512   -2.0421   -2.3961 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7688   -0.7156   -3.4694 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 18  1  0
 16 17  2  0
 14 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 20 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
 12 34  1  0
 13 35  1  0
 15 36  1  0
 15 37  1  0
 18 38  1  0
 19 39  1  0
 22 40  1  0
 22 41  1  0
 22 42  1  0
M  END


  Mrv1652309082204082D          

 22 22  0  0  0  0            999 V2000
   -2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  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
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  2  0  0  0  0
 10 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0260072

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC\C=C\C=C\C(=O)C1=C(O)C=C(CC(O)=O)C=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C17H20O5/c1-3-4-5-6-7-8-13(18)17-14(19)9-12(11-16(20)21)10-15(17)22-2/h5-10,19H,3-4,11H2,1-2H3,(H,20,21)/b6-5+,8-7+

> <INCHI_KEY>
QTMCMRWMMYEODV-BSWSSELBSA-N

> <FORMULA>
C17H20O5

> <MOLECULAR_WEIGHT>
304.342

> <EXACT_MASS>
304.131073744

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
32.79649852799925

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{3-hydroxy-5-methoxy-4-[(2E,4E)-octa-2,4-dienoyl]phenyl}acetic acid

> <JCHEM_LOGP>
3.916686041666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.206204396643241

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5469644377355283

> <JCHEM_PKA_STRONGEST_BASIC>
-4.885320403739394

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
86.05430000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
{3-hydroxy-5-methoxy-4-[(2E,4E)-octa-2,4-dienoyl]phenyl}acetic acid

> <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      -4.001  11.550   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   20                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20                                                       
CONECT   20   19   10   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₀O₅

Average Mass

304.3420 Da

Monoisotopic Mass

304.13107 Da

IUPAC Name

2-{3-hydroxy-5-methoxy-4-[(2E,4E)-octa-2,4-dienoyl]phenyl}acetic acid

Traditional Name

{3-hydroxy-5-methoxy-4-[(2E,4E)-octa-2,4-dienoyl]phenyl}acetic acid

CAS Registry Number

Not Available

SMILES

CCC\C=C\C=C\C(=O)C1=C(O)C=C(CC(O)=O)C=C1OC

InChI Identifier

InChI=1S/C17H20O5/c1-3-4-5-6-7-8-13(18)17-14(19)9-12(11-16(20)21)10-15(17)22-2/h5-10,19H,3-4,11H2,1-2H3,(H,20,21)/b6-5+,8-7+

InChI Key

QTMCMRWMMYEODV-BSWSSELBSA-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
Neocucurbitaria cava	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Aryl ketone
Phenol ether
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Monocyclic benzene moiety
Acryloyl-group
Vinylogous acid
Alpha,beta-unsaturated ketone
Enone
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Carboxylic acid
Ether
Organic oxygen compound
Organooxygen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	3.92	ChemAxon
pKa (Strongest Acidic)	3.55	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	86.05 m³·mol⁻¹	ChemAxon
Polarizability	32.8 Å³	ChemAxon
Number of Rings	1	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

4946928

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6442871

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid (NP0260072)

MOL for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)

3D MOL for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)

3D SDF for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)

3D-SDF for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)

PDB for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)

3D PDB for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)

SMILES for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)

INCHI for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)

Structure for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)

3D Structure for NP0260072 ({3-hydroxy-5-methoxy-4-[(2e,4e)-octa-2,4-dienoyl]phenyl}acetic acid)