NP-MRD: Showing NP-Card for (1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid (NP0232984)

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Record Information

Version

2.0

Created at

2022-09-06 14:24:28 UTC

Updated at

2022-09-06 14:24:28 UTC

NP-MRD ID

NP0232984

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid

Description

(-)-Applanatumol O belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. (1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid is found in Ganoderma applanatum. Based on a literature review very few articles have been published on (-)-applanatumol O.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
   -3.9552    0.7251   -3.0011 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2396   -0.1121   -2.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2750   -0.5981   -1.1490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6307   -1.4676   -0.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5878   -1.9317    0.7119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9031   -0.7124    1.2806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4612    0.2795    0.2629 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0067    0.6673    0.3260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9403   -0.4006    0.1044 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6165   -1.6170   -0.1271 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3611   -0.1390    0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3113   -1.1300   -0.0699 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6701   -0.9141   -0.0468 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6082   -1.9168   -0.2529 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1325    0.3631    0.1930 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007    1.3691    0.3997 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8217    1.1274    0.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0123    2.2279    0.5948 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2052    1.5384    0.5184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9964    1.9766   -0.3384 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0460    2.2520    1.6958 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8293   -0.1474   -1.1678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2544   -0.4539   -2.0474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6292   -1.8442   -0.1332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0216   -2.4866    1.5757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9196   -2.5836    0.1085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6691   -0.2775    1.9953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0765   -1.0036    1.9899 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1034    1.1973    1.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1278    1.4415   -0.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481   -2.1403   -0.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9118   -2.4054    0.6041 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1998    0.5525    0.2150 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5544    2.3711    0.5880 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3662    3.1517    0.7680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2050    3.2355    1.7896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8107    0.7524   -1.8164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1636   -0.9463   -1.4918 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 19  1  0
 19 20  2  0
  7 19  1  1
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  2  0
  3 22  1  0
  3  2  1  0
  2  1  2  0
 22  7  1  0
 17 11  1  0
 21 36  1  0
  8 29  1  0
  8 30  1  0
 12 31  1  0
 14 32  1  0
 15 33  1  0
 16 34  1  0
 18 35  1  0
  6 27  1  0
  6 28  1  0
  5 25  1  0
  5 26  1  0
  4 24  1  0
 22 37  1  0
 22 38  1  0
  2 23  1  0
M  END


  Mrv1652309062216242D          

 22 23  0  0  1  0            999 V2000
    2.3276   -4.7570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276   -3.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6131   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -3.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -2.6945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -2.2820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3683   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4441   -1.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7263   -2.5685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9744   -1.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7869   -1.3045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3172   -0.6725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1297   -0.8158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0350    0.1027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2226    0.2460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6923   -0.3860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1202   -0.2428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2414   -1.7933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1468   -0.8748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6131   -2.6945    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 19  1  6  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  7 22  1  0  0  0  0
  3 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0232984

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)[C@@]1(CC(=O)C2=CC(O)=CC=C2O)CCC=C(C1)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H16O6/c17-9-10-2-1-5-16(7-10,15(21)22)8-14(20)12-6-11(18)3-4-13(12)19/h2-4,6,9,18-19H,1,5,7-8H2,(H,21,22)/t16-/m0/s1

> <INCHI_KEY>
BIAWVSQLGIZZHL-INIZCTEOSA-N

> <FORMULA>
C16H16O6

> <MOLECULAR_WEIGHT>
304.298

> <EXACT_MASS>
304.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
29.65707521431034

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid

> <JCHEM_LOGP>
2.282122072666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.206683406632624

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.650389896406684

> <JCHEM_PKA_STRONGEST_BASIC>
-4.402696820506188

> <JCHEM_POLAR_SURFACE_AREA>
111.89999999999999

> <JCHEM_REFRACTIVITY>
78.58259999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  O   UNK     0       4.345  -8.880   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.345  -7.340   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.011  -6.570   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.677  -7.340   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.344  -6.570   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.344  -5.030   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.677  -4.260   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.688  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.829  -3.347   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.356  -4.795   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.819  -2.168   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.336  -2.435   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.325  -1.255   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -5.842  -1.523   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.799   0.192   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.282   0.459   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.292  -0.721   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.224  -0.453   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.184  -3.347   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       2.141  -1.633   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.011  -5.030   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   19   22                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17                                                            
CONECT   19    7   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22    7    3                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₆O₆

Average Mass

304.2980 Da

Monoisotopic Mass

304.09469 Da

IUPAC Name

(1S)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid

Traditional Name

(1S)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC(=O)[C@@]1(CC(=O)C2=CC(O)=CC=C2O)CCC=C(C1)C=O

InChI Identifier

InChI=1S/C16H16O6/c17-9-10-2-1-5-16(7-10,15(21)22)8-14(20)12-6-11(18)3-4-13(12)19/h2-4,6,9,18-19H,1,5,7-8H2,(H,21,22)/t16-/m0/s1

InChI Key

BIAWVSQLGIZZHL-INIZCTEOSA-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
Ganoderma applanatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Alkyl-phenylketones

Alternative Parents

Substituents

Alkyl-phenylketone
Prenylbenzoquinol
Butyrophenone
Aryl alkyl ketone
Hydroquinone
Gamma-keto acid
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Keto acid
Monocyclic benzene moiety
Vinylogous acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Aldehyde
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	2.28	ChemAxon
pKa (Strongest Acidic)	3.65	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	111.9 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	78.58 m³·mol⁻¹	ChemAxon
Polarizability	29.66 Å³	ChemAxon
Number of Rings	2	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

78441214

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586533

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid (NP0232984)

MOL for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)

3D MOL for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)

3D SDF for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)

3D-SDF for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)

PDB for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)

3D PDB for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)

SMILES for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)

INCHI for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)

Structure for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)

3D Structure for NP0232984 ((1s)-1-[2-(2,5-dihydroxyphenyl)-2-oxoethyl]-3-formylcyclohex-3-ene-1-carboxylic acid)