NP-MRD: Showing NP-Card for (1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione (NP0209254)

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Record Information

Version

2.0

Created at

2022-09-05 06:35:33 UTC

Updated at

2022-09-05 06:35:33 UTC

NP-MRD ID

NP0209254

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione

Description

(+)-9-Demethyleleutherin belongs to the class of organic compounds known as benzoisochromanequinones. These are benzo derivatives of isochromanequinones. Isochromanequinones are structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton. (1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione is found in Eleutherine bulbosa. Based on a literature review very few articles have been published on (+)-9-Demethyleleutherin.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -4.0765   -0.4997   -1.0656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7058   -0.5109   -0.4529 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9934    0.8339   -0.6690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5797    0.4758   -0.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3443   -0.2211    0.6625 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0213   -0.6591    1.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1645   -1.3219    2.0725 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1252   -0.3121    0.1400 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4206   -0.6978    0.4255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7302   -1.4163    1.5297 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4375   -0.3181   -0.4794 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1861    0.4025   -1.6030 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8937    0.7743   -1.8663 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8554    0.4253   -1.0064 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4857    0.8398   -1.3200 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2443    1.5064   -2.3570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5118   -0.5273    1.5198 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6884    0.7104    2.4146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6654   -0.8318    0.8541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9584   -0.1298   -2.1170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7878    0.1606   -0.5586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4250   -1.5478   -1.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1115   -1.2800   -1.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3992    1.5477    0.0713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1620    1.1992   -1.7018 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2359   -1.7745    2.2568 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4288   -0.6327   -0.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9522    0.6940   -2.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6718    1.3565   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2588   -1.3702    2.2169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3540    0.5002    3.4510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0782    1.5682    2.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7532    1.0564    2.3920 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 17  1  0
 17 18  1  0
 17 19  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 19  2  1  0
 14  8  1  0
 15  4  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  6
  3 24  1  0
  3 25  1  0
 17 30  1  1
 18 31  1  0
 18 32  1  0
 18 33  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
M  END


  Mrv1652309052208352D          

 19 21  0  0  1  0            999 V2000
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    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
    2.8579    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
    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 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 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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  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  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  2  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
  2 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0209254

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC2=C([C@@H](C)O1)C(=O)C1=C(O)C=CC=C1C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H14O4/c1-7-6-10-12(8(2)19-7)15(18)13-9(14(10)17)4-3-5-11(13)16/h3-5,7-8,16H,6H2,1-2H3/t7-,8+/m0/s1

> <INCHI_KEY>
PPEBHGFEKAUPBT-JGVFFNPUSA-N

> <FORMULA>
C15H14O4

> <MOLECULAR_WEIGHT>
258.273

> <EXACT_MASS>
258.089208931

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.826736457954574

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,3S)-9-hydroxy-1,3-dimethyl-1H,3H,4H,5H,10H-naphtho[2,3-c]pyran-5,10-dione

> <JCHEM_LOGP>
2.353826121

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.225843315266737

> <JCHEM_PKA_STRONGEST_BASIC>
-4.197135240784884

> <JCHEM_POLAR_SURFACE_AREA>
63.599999999999994

> <JCHEM_REFRACTIVITY>
70.51020000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3S)-9-hydroxy-1,3-dimethyl-1H,3H,4H-naphtho[2,3-c]pyran-5,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   15                                                  
CONECT    5    4    6   17                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   14                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    8   15                                                  
CONECT   15   14    4   16                                                  
CONECT   16   15                                                            
CONECT   17    5   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    2                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₄O₄

Average Mass

258.2730 Da

Monoisotopic Mass

258.08921 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1CC2=C([C@@H](C)O1)C(=O)C1=C(O)C=CC=C1C2=O

InChI Identifier

InChI=1S/C15H14O4/c1-7-6-10-12(8(2)19-7)15(18)13-9(14(10)17)4-3-5-11(13)16/h3-5,7-8,16H,6H2,1-2H3/t7-,8+/m0/s1

InChI Key

PPEBHGFEKAUPBT-JGVFFNPUSA-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
Eleutherine bulbosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoisochromanequinones. These are benzo derivatives of isochromanequinones. Isochromanequinones are structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isochromanequinones

Sub Class

Benzoisochromanequinones

Direct Parent

Benzoisochromanequinones

Alternative Parents

Substituents

Benzoisochromanequinone
Naphthopyranone
Naphthopyran
Naphthoquinone
Naphthalene
Aryl ketone
Quinone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Benzenoid
Pyran
Vinylogous acid
Ketone
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen 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

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

24646556

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46228186

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione (NP0209254)

MOL for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)

3D MOL for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)

3D SDF for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)

3D-SDF for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)

PDB for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)

3D PDB for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)

SMILES for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)

INCHI for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)

Structure for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)

3D Structure for NP0209254 ((1r,3s)-9-hydroxy-1,3-dimethyl-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione)