NP-MRD: Showing NP-Card for epi-Radulifolin A (NP0080593)

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Record Information

Version

2.0

Created at

2022-04-29 01:36:03 UTC

Updated at

2022-04-29 01:36:04 UTC

NP-MRD ID

NP0080593

Secondary Accession Numbers

None

Natural Product Identification

Common Name

epi-Radulifolin A

Description

Epi-Radulifolin A belongs to the class of organic compounds known as naphthopyranones. Naphthopyranones are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system. epi-Radulifolin A is found in Psacalium radulifolium. Based on a literature review very few articles have been published on epi-Radulifolin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
   -2.0910   -2.0452    1.0952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9593   -1.1784   -0.1322 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3201   -0.5672   -0.3770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2341    0.7769   -1.0444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5366    1.6788   -0.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1368    1.1978    0.0393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1220    2.0913    0.1433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3339    3.4525    0.2075 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1992    1.6290    0.1889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2139    2.5521    0.2929 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5114    0.2601    0.1307 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4369   -0.5864    0.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8959   -0.1495   -0.0218 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6989   -2.0614   -0.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0454   -2.3613   -0.3364 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0377   -1.6178    0.2550 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0373   -2.1148    0.8535 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9368   -0.1427    0.1901 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7076    0.2897   -1.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5541    0.3722    1.3452 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4907   -1.6686    1.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8995   -3.1261    0.8748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1461   -2.0558    1.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7500   -1.8032   -1.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9862   -1.2552   -0.9598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8519   -0.4068    0.5961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6389    0.7501   -1.9823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2538    1.1506   -1.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6650    2.7290   -0.2520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9863    1.4090    0.9887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1699    3.9621    0.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1674    2.3056    0.3242 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4285   -2.5901    0.8741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0902   -2.5504   -0.8578 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6516    0.7508   -0.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0297   -0.6005   -1.6206 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1898    1.0292   -1.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5313    0.4948    1.1486 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  1  0
  5  6  1  0
  6 13  2  0
 13 12  1  0
 12 11  2  0
 11  9  1  0
  9 10  1  0
  9  7  2  0
  7  8  1  0
 11 18  1  0
 18 19  1  0
 18 20  1  1
 18 16  1  0
 16 17  2  0
 16 15  1  0
 15 14  1  0
 13  2  1  0
 14 12  1  0
  7  6  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  6
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
 10 32  1  0
  8 31  1  0
 19 35  1  0
 19 36  1  0
 19 37  1  0
 20 38  1  0
 14 33  1  0
 14 34  1  0
M  END


  Mrv1652304292203362D          

 20 22  0  0  1  0            999 V2000
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732   -1.1265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3977   -0.7392    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  5  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
  8 18  1  0  0  0  0
 14 19  1  6  0  0  0
 14 20  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0080593

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CCCC2=C1C1=C(C(O)=C2O)[C@@](C)(O)C(=O)OC1

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O5/c1-7-4-3-5-8-10(7)9-6-20-14(18)15(2,19)11(9)13(17)12(8)16/h7,16-17,19H,3-6H2,1-2H3/t7-,15+/m0/s1

> <INCHI_KEY>
JJAZJHQERFKZAF-NZFNHWASSA-N

> <FORMULA>
C15H18O5

> <MOLECULAR_WEIGHT>
278.304

> <EXACT_MASS>
278.11542368

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
28.604980183517817

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,10S)-4,5,6-trihydroxy-4,10-dimethyl-1H,3H,4H,7H,8H,9H,10H-naphtho[1,2-c]pyran-3-one

> <ALOGPS_LOGP>
2.10

> <JCHEM_LOGP>
2.357865547

> <ALOGPS_LOGS>
-2.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.780742742003419

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.599362605936792

> <JCHEM_PKA_STRONGEST_BASIC>
-4.2711396972056805

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
72.7334

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.60e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R,10S)-4,5,6-trihydroxy-4,10-dimethyl-1H,7H,8H,9H,10H-naphtho[1,2-c]pyran-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.184  -3.231   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       2.104  -3.231   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.746   0.770   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.564   2.104   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.510  -2.103   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.742  -1.380   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   18                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10    4   12                                                  
CONECT   12   11                                                            
CONECT   13   10                                                            
CONECT   14    9   15   19   20                                             
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    8                                                       
CONECT   19   14                                                            
CONECT   20   14                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₈O₅

Average Mass

278.3040 Da

Monoisotopic Mass

278.11542 Da

IUPAC Name

(4R,10S)-4,5,6-trihydroxy-4,10-dimethyl-1H,3H,4H,7H,8H,9H,10H-naphtho[1,2-c]pyran-3-one

Traditional Name

(4R,10S)-4,5,6-trihydroxy-4,10-dimethyl-1H,7H,8H,9H,10H-naphtho[1,2-c]pyran-3-one

CAS Registry Number

Not Available

SMILES

C[C@H]1CCCC2=C1C1=C(C(O)=C2O)[C@@](C)(O)C(=O)OC1

InChI Identifier

InChI=1S/C15H18O5/c1-7-4-3-5-8-10(7)9-6-20-14(18)15(2,19)11(9)13(17)12(8)16/h7,16-17,19H,3-6H2,1-2H3/t7-,15+/m0/s1

InChI Key

JJAZJHQERFKZAF-NZFNHWASSA-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
Psacalium radulifolium	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyranones. Naphthopyranones are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Naphthopyranones

Direct Parent

Naphthopyranones

Alternative Parents

Substituents

Naphthopyranone
Benzopyran
Isochromane
2-benzopyran
Tetralin
Naphthalene
Phenol
Benzenoid
Pyran
Tertiary alcohol
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Polyol
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxygen compound
Organic oxide
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	2.1	ALOGPS
logP	2.36	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	9.6	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	72.73 m³·mol⁻¹	ChemAxon
Polarizability	28.6 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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00045896

Chemspider ID

8811657

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10636295

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for epi-Radulifolin A (NP0080593)

MOL for NP0080593 (epi-Radulifolin A)

3D MOL for NP0080593 (epi-Radulifolin A)

3D SDF for NP0080593 (epi-Radulifolin A)

3D-SDF for NP0080593 (epi-Radulifolin A)

PDB for NP0080593 (epi-Radulifolin A)

3D PDB for NP0080593 (epi-Radulifolin A)

SMILES for NP0080593 (epi-Radulifolin A)

INCHI for NP0080593 (epi-Radulifolin A)

Structure for NP0080593 (epi-Radulifolin A)

3D Structure for NP0080593 (epi-Radulifolin A)