NP-MRD: Showing NP-Card for 3',4'-dihydro-3'-hydroxy-Xanthyletin (NP0138171)

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Record Information

Version

2.0

Created at

2022-05-31 17:01:04 UTC

Updated at

2022-05-31 17:01:04 UTC

NP-MRD ID

NP0138171

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3',4'-dihydro-3'-hydroxy-Xanthyletin

Description

Aegelinol belongs to the class of organic compounds known as linear pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) linearly fused to a coumarin moiety. Aegelinol is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Aegelinol has been detected, but not quantified in, fruits. 3',4'-dihydro-3'-hydroxy-Xanthyletin is found in Aegle marmelos, Angelica decursiva, Angelica gigas and Phlojodicarpus villosus. This could make aegelinol a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
   -3.6040    0.9930   -0.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3175    0.5451   -0.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1521    1.1581    1.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1880    0.9854   -0.8115 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0444    0.4613   -0.3794 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2163    1.0563   -0.8059 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4641    0.6009   -0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5464    1.1950   -0.8539 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7185    0.7377   -0.4745 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7370    1.3465   -0.9153 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8583   -0.3450    0.3581 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7530   -0.9894    0.8240 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -0.5001    0.4183 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3430   -1.0978    0.8469 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1066   -0.6299    0.4578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1094   -1.3210    0.9567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2445   -0.9613   -0.0019 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4434   -1.5336    0.4114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4239    0.8277    0.0296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7788    0.3962   -1.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5705    2.0838   -0.8897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7046    0.6227    2.1091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0767    1.3046    1.5524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5960    2.1894    1.2636 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589    1.9141   -1.4642 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8302   -0.6713    0.6322 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8161   -1.8464    1.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4467   -1.9509    1.5028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9746   -2.4153    1.0209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4074   -0.9438    1.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9729   -1.3371   -1.0105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9842   -1.8750   -0.3408 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11  9  1  0
  9 10  2  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
 17  2  1  0
  7 13  1  0
  6  5  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  3 22  1  0
  3 23  1  0
  3 24  1  0
 16 29  1  0
 16 30  1  0
 17 31  1  6
 18 32  1  0
 14 28  1  0
 12 27  1  0
 11 26  1  0
  6 25  1  0
M  END


  Mrv0541 05061307262D          

 18 20  0  0  0  0            999 V2000
   -0.8125    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    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
    2.8579    0.8250    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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    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   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    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
  4  3  2  0  0  0  0
  8  3  1  0  0  0  0
  8  5  2  0  0  0  0
  9  5  1  0  0  0  0
  9  6  1  0  0  0  0
 10  7  2  0  0  0  0
 10  8  1  0  0  0  0
 11  7  1  0  0  0  0
 11  9  2  0  0  0  0
 12  6  1  0  0  0  0
 13  4  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 14 12  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  2  0  0  0  0
 17 10  1  0  0  0  0
 17 13  1  0  0  0  0
 18 11  1  0  0  0  0
 18 14  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138171

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC2=C(CC1O)C=C1C=CC(=O)OC1=C2

> <INCHI_IDENTIFIER>
InChI=1S/C14H14O4/c1-14(2)12(15)6-9-5-8-3-4-13(16)17-10(8)7-11(9)18-14/h3-5,7,12,15H,6H2,1-2H3

> <INCHI_KEY>
BGXFQDFSVDZUIW-UHFFFAOYSA-N

> <FORMULA>
C14H14O4

> <MOLECULAR_WEIGHT>
246.2586

> <EXACT_MASS>
246.089208936

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
25.64278159154181

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-hydroxy-13,13-dimethyl-4,14-dioxatricyclo[8.4.0.0³,⁸]tetradeca-1(10),2,6,8-tetraen-5-one

> <ALOGPS_LOGP>
2.11

> <JCHEM_LOGP>
1.7323936069999994

> <ALOGPS_LOGS>
-2.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.82481629989488

> <JCHEM_PKA_STRONGEST_BASIC>
-3.312825350425978

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
66.3409

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.12e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-hydroxy-13,13-dimethyl-4,14-dioxatricyclo[8.4.0.0³,⁸]tetradeca-1(10),2,6,8-tetraen-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -1.517   1.273   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.527   2.987   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   1.540   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  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       6.668   2.310   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
CONECT    1   14                                                            
CONECT    2   14                                                            
CONECT    3    4    8                                                       
CONECT    4    3   13                                                       
CONECT    5    8    9                                                       
CONECT    6    9   12                                                       
CONECT    7   10   11                                                       
CONECT    8    3    5   10                                                  
CONECT    9    5    6   11                                                  
CONECT   10    7    8   17                                                  
CONECT   11    7    9   18                                                  
CONECT   12    6   14   15                                                  
CONECT   13    4   16   17                                                  
CONECT   14    1    2   12   18                                             
CONECT   15   12                                                            
CONECT   16   13                                                            
CONECT   17   10   13                                                       
CONECT   18   11   14                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

View in JSmol

Synonyms

Value	Source
Aegelinol	MeSH

Chemical Formula

C₁₄H₁₄O₄

Average Mass

246.2586 Da

Monoisotopic Mass

246.08921 Da

IUPAC Name

12-hydroxy-13,13-dimethyl-4,14-dioxatricyclo[8.4.0.0³,⁸]tetradeca-1(10),2,6,8-tetraen-5-one

Traditional Name

12-hydroxy-13,13-dimethyl-4,14-dioxatricyclo[8.4.0.0³,⁸]tetradeca-1(10),2,6,8-tetraen-5-one

CAS Registry Number

5993-18-0

SMILES

CC1(C)OC2=C(CC1O)C=C1C=CC(=O)OC1=C2

InChI Identifier

InChI=1S/C14H14O4/c1-14(2)12(15)6-9-5-8-3-4-13(16)17-10(8)7-11(9)18-14/h3-5,7,12,15H,6H2,1-2H3

InChI Key

BGXFQDFSVDZUIW-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
Aegle marmelos	LOTUS Database	35616633
Angelica decursiva	LOTUS Database	35616633
Angelica gigas	LOTUS Database	35616633
Phlojodicarpus villosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as linear pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) linearly fused to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Pyranocoumarins

Direct Parent

Linear pyranocoumarins

Alternative Parents

Substituents

Linear pyranocoumarin
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromane
Benzopyran
1-benzopyran
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Lactone
Secondary alcohol
Ether
Oxacycle
Organoheterocyclic compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	2.11	ALOGPS
logP	1.73	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	13.82	ChemAxon
pKa (Strongest Basic)	-3.3	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	0	ChemAxon
Refractivity	66.34 m³·mol⁻¹	ChemAxon
Polarizability	25.64 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

HMDB0033914

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB012112

KNApSAcK ID

Not Available

Chemspider ID

522219

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

600671

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3',4'-dihydro-3'-hydroxy-Xanthyletin (NP0138171)

MOL for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)

3D MOL for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)

3D SDF for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)

3D-SDF for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)

PDB for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)

3D PDB for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)

SMILES for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)

INCHI for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)

Structure for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)

3D Structure for NP0138171 (3',4'-dihydro-3'-hydroxy-Xanthyletin)