NP-MRD: Showing NP-Card for 2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol (NP0230845)

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Record Information

Version

2.0

Created at

2022-09-06 11:25:50 UTC

Updated at

2022-09-06 11:25:50 UTC

NP-MRD ID

NP0230845

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol

Description

2-[8-Hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol belongs to the class of organic compounds known as prenylated hydroquinones. These are quinones with a structure characterized by the hydroquinone ring substituted by an prenyl side-chain. 2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol is found in Cordia alliodora and Cordia elaeagnoides. 2-[8-Hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 42  0  0  0  0  0  0  0  0999 V2000
   -4.8723   -1.3874   -0.7571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5419   -0.3764    0.2642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3005   -0.3615    0.7889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3056   -1.3383    0.3433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1079   -0.9021   -0.3772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1136   -0.0338    0.3059 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1271   -0.4530    0.4779 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2255    0.2216    1.0995 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4774    0.2178    0.2544 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4740   -0.6732    0.6019 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6654   -0.7731   -0.1059 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6605   -1.6722    0.2522 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7957    0.0755   -1.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8128    0.9682   -1.5424 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6126    1.0578   -0.8165 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6656    1.9761   -1.2294 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5060    1.3120    0.7536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9691    2.0160   -0.3847 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5621    0.5957    0.6920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0682    1.4672    1.6557 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1898   -1.2712   -1.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8539   -2.4262   -0.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8925   -1.2063   -1.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1571    0.3906    1.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0086   -1.9502    1.2631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8484   -2.0676   -0.3303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4327   -0.3541   -1.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5143   -1.7688   -0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3337   -1.4757    0.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5061   -0.3627    2.0331 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0924    1.2548    1.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3758   -1.3537    1.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3957   -1.4208    0.9013 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7162    0.0182   -1.7534 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9218    1.6434   -2.4036 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7895    2.1112   -0.7782 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4011    1.9126    1.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2136    1.2697    1.5718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5116    1.6111   -1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4465    0.0229    1.0478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9329    1.2253   -0.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6998    2.2605    1.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 19  1  0
 19 20  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6 17  1  0
 17 18  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15  9  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
 19 40  1  0
 19 41  1  0
 20 42  1  0
  3 24  1  0
  4 25  1  0
  4 26  1  0
  5 27  1  0
  5 28  1  0
 17 37  1  0
 17 38  1  0
 18 39  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
 10 32  1  0
 12 33  1  0
 13 34  1  0
 14 35  1  0
 16 36  1  0
M  END


  Mrv1533004201503262D          

 20 20  0  0  0  0            999 V2000
   -0.7145    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
    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
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   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
    0.0000    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    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  4  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  4  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  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0230845

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CO)=CCCC(CO)=CCC1=CC(O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C16H22O4/c1-12(10-17)3-2-4-13(11-18)5-6-14-9-15(19)7-8-16(14)20/h3,5,7-9,17-20H,2,4,6,10-11H2,1H3

> <INCHI_KEY>
MUMBNEKSWRFQTG-UHFFFAOYSA-N

> <FORMULA>
C16H22O4

> <MOLECULAR_WEIGHT>
278.348

> <EXACT_MASS>
278.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
31.294635215703313

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol

> <ALOGPS_LOGP>
2.04

> <JCHEM_LOGP>
2.1928541336666667

> <ALOGPS_LOGS>
-3.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.417233945612667

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.533339665881876

> <JCHEM_PKA_STRONGEST_BASIC>
-2.0797068168715134

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
81.61459999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      -1.334  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  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -4.001  11.550   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -5.335  10.780   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    9   16                                                  
CONECT   16   15                                                            
CONECT   17    6   18                                                       
CONECT   18   17                                                            
CONECT   19    2   20                                                       
CONECT   20   19                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₂O₄

Average Mass

278.3480 Da

Monoisotopic Mass

278.15181 Da

IUPAC Name

2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol

Traditional Name

2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol

CAS Registry Number

Not Available

SMILES

CC(CO)=CCCC(CO)=CCC1=CC(O)=CC=C1O

InChI Identifier

InChI=1S/C16H22O4/c1-12(10-17)3-2-4-13(11-18)5-6-14-9-15(19)7-8-16(14)20/h3,5,7-9,17-20H,2,4,6,10-11H2,1H3

InChI Key

MUMBNEKSWRFQTG-UHFFFAOYSA-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
Cordia alliodora	LOTUS Database	35616633
Cordia elaeagnoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prenylated hydroquinones. These are quinones with a structure characterized by the hydroquinone ring substituted by an prenyl side-chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Quinone and hydroquinone lipids

Direct Parent

Prenylated hydroquinones

Alternative Parents

Substituents

Prenylbenzoquinol
Aromatic monoterpenoid
Monocyclic monoterpenoid
Monoterpenoid
Fatty alcohol
Hydroquinone
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Primary alcohol
Organooxygen compound
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	2.04	ALOGPS
logP	2.19	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	9.53	ChemAxon
pKa (Strongest Basic)	-2.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	81.61 m³·mol⁻¹	ChemAxon
Polarizability	31.29 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

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

579894

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol (NP0230845)

MOL for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)

3D MOL for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)

3D SDF for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)

3D-SDF for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)

PDB for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)

3D PDB for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)

SMILES for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)

INCHI for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)

Structure for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)

3D Structure for NP0230845 (2-[8-hydroxy-3-(hydroxymethyl)-7-methylocta-2,6-dien-1-yl]benzene-1,4-diol)