NP-MRD: Showing NP-Card for Dehydrocycloguanandin (NP0051688)

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Record Information

Version

2.0

Created at

2022-04-27 22:57:45 UTC

Updated at

2022-04-27 22:57:45 UTC

NP-MRD ID

NP0051688

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Dehydrocycloguanandin

Description

Dehydrocycloguanandin belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system. Dehydrocycloguanandin is found in Calophyllum brasilience, Calophyllum brasiliense , Calophyllum caledonicum, Calophyllum inophyllum and Mesua ferrea . Dehydrocycloguanandin is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 39  0  0  0  0  0  0  0  0999 V2000
    3.7052    1.6275    1.3774 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1958    0.7868    0.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7135    1.5048   -1.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8321   -0.5388    0.1908 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1232   -1.6361    0.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6752   -1.5852    0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9350   -2.7738    0.1058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4443   -2.6774    0.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1318   -1.4746    0.1109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5136   -1.4389    0.0954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1195   -2.5298    0.0634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1649   -0.2221    0.1154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5404   -0.1267    0.1013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3493   -1.2057    0.0672 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1258    1.1415    0.1233 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3085    2.2332    0.1578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9501    2.1395    0.1717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3328    0.8847    0.1504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0135    0.8068    0.1642 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3659   -0.3296    0.1460 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0165   -0.3827    0.1611 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7942    0.7534    0.1962 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4778    2.3394    1.0894 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8840    2.1913    1.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0865    0.9041    2.1293 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021    2.5667   -0.8996 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1927    1.0515   -1.9030 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7925    1.2638   -1.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9329   -0.6262    0.2018 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6053   -2.6351    0.1404 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4532   -3.7118    0.0905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0368   -3.5785    0.0642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1666   -2.1395    0.0482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1976    1.1798    0.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8140    3.2134    0.1741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3424    3.0244    0.1990 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2 22  1  0
 22 21  1  0
 21  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 20  2  0
 20 19  1  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  2  0
 15 13  1  0
 13 14  1  0
 13 12  2  0
 12 10  1  0
 10 11  2  0
  6  5  1  0
  5  4  2  0
  4  2  1  0
 20 21  1  0
 12 18  1  0
 10  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  7 31  1  0
  8 32  1  0
 17 36  1  0
 16 35  1  0
 15 34  1  0
 14 33  1  0
  5 30  1  0
  4 29  1  0
M  END


  Mrv1533004191513512D          

 22 25  0  0  0  0            999 V2000
    3.5965   -3.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3023   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5944   -3.2656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124   -2.6861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8424   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0323   -1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7622   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1124   -0.5034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9226   -0.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4627   -0.9711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2728   -0.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5428   -0.0357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8129   -1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6230   -1.2829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -0.5034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1631   -1.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8931   -2.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0829   -2.8421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5428   -2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7327   -2.3743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1926   -1.7507    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  6  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
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 22  1  0  0  0  0
 11 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0051688

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC2=C(C=CC3=C2OC2=CC=CC(O)=C2C3=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H14O4/c1-18(2)9-8-10-6-7-11-15(20)14-12(19)4-3-5-13(14)21-17(11)16(10)22-18/h3-9,19H,1-2H3

> <INCHI_KEY>
WTSFSOWKXDTLJX-UHFFFAOYSA-N

> <FORMULA>
C18H14O4

> <MOLECULAR_WEIGHT>
294.306

> <EXACT_MASS>
294.089208931

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
30.866314892810422

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-hydroxy-2,2-dimethyl-2,7-dihydro-1,12-dioxatetraphen-7-one

> <ALOGPS_LOGP>
4.14

> <JCHEM_LOGP>
4.206698300666666

> <ALOGPS_LOGS>
-4.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.410076117822129

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7764683018900596

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
83.19060000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.15e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
dehydrocycloguanandin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       6.714  -6.744   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.164  -5.305   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.843  -6.096   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.677  -5.014   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.181  -3.559   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.172  -2.395   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.660  -2.686   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.156  -4.141   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.677  -0.940   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.189  -0.649   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.197  -1.813   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.709  -1.522   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.213  -0.067   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      12.717  -2.686   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.230  -2.395   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      14.734  -0.940   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      15.238  -3.559   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.734  -5.014   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.221  -5.305   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.213  -4.141   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.701  -4.432   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.693  -3.268   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    8                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7    2                                                       
CONECT    9    6   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   22                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   20                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   14   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21    5   11                                                  
MASTER        0    0    0    0    0    0    0    0   22    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₄O₄

Average Mass

294.3060 Da

Monoisotopic Mass

294.08921 Da

IUPAC Name

8-hydroxy-2,2-dimethyl-2,7-dihydro-1,12-dioxatetraphen-7-one

Traditional Name

dehydrocycloguanandin

CAS Registry Number

Not Available

SMILES

CC1(C)OC2=C(C=CC3=C2OC2=CC=CC(O)=C2C3=O)C=C1

InChI Identifier

InChI=1S/C18H14O4/c1-18(2)9-8-10-6-7-11-15(20)14-12(19)4-3-5-13(14)21-17(11)16(10)22-18/h3-9,19H,1-2H3

InChI Key

WTSFSOWKXDTLJX-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Calophyllum brasilience	Plant	KNApSAcK
Calophyllum brasiliense	Plant	KNApSAcK
Calophyllum caledonicum	Plant	KNApSAcK
Calophyllum inophyllum	Plant	KNApSAcK
Mesua ferrea	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranoxanthones

Alternative Parents

Substituents

Pyranoxanthone
2,2-dimethyl-1-benzopyran
Chromone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Ether
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

pyranoxanthones (CHEBI:4360 )
xanthenes (C10055 )

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	4.14	ALOGPS
logP	4.21	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	8.41	ChemAxon
pKa (Strongest Basic)	-3.8	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	83.19 m³·mol⁻¹	ChemAxon
Polarizability	30.87 Å³	ChemAxon
Number of Rings	4	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

C00002945

Chemspider ID

Not Available

KEGG Compound ID

C10055

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5281625

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Dehydrocycloguanandin (NP0051688)

MOL for NP0051688 (Dehydrocycloguanandin)

3D MOL for NP0051688 (Dehydrocycloguanandin)

3D SDF for NP0051688 (Dehydrocycloguanandin)

3D-SDF for NP0051688 (Dehydrocycloguanandin)

PDB for NP0051688 (Dehydrocycloguanandin)

3D PDB for NP0051688 (Dehydrocycloguanandin)

SMILES for NP0051688 (Dehydrocycloguanandin)

INCHI for NP0051688 (Dehydrocycloguanandin)

Structure for NP0051688 (Dehydrocycloguanandin)

3D Structure for NP0051688 (Dehydrocycloguanandin)