NP-MRD: Showing NP-Card for 5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol (NP0296397)

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Record Information

Version

2.0

Created at

2022-09-10 05:57:16 UTC

Updated at

2022-09-10 05:57:16 UTC

NP-MRD ID

NP0296397

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol

Description

Sinensine belongs to the class of organic compounds known as phenylpyridines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyridine ring through a CC or CN bond. 5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol is found in Ganoderma sinense. Based on a literature review very few articles have been published on Sinensine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
   -3.8974    2.0204    0.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5091    1.5148    0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5014    2.3484    0.7702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2529    1.9205    0.7337 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1187    0.7148    0.2804 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5341    0.3301    0.2807 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0807   -0.2639   -0.8321 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4142   -0.6475   -0.8764 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9340   -1.2447   -2.0152 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1988   -0.4142    0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6860    0.1751    1.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5184    0.3831    2.4649 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3506    0.5391    1.3656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8597   -0.1396   -0.1787 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1723    0.2675   -0.1579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0503   -0.8041   -0.6952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1983   -2.0316   -0.4068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8163   -1.5025   -0.7292 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1799   -2.2841   -0.1543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6280    1.2005    0.2044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0058    2.8087   -0.4248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0773    2.5065    1.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7465    3.3422    1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4856   -0.4466   -1.7061 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.6777   -2.7339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2300   -0.7150    0.2031 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0131    1.2657    2.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9559    0.9968    2.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0349   -0.8445   -0.2267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0813   -0.7015   -1.7997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4827   -2.8967   -1.0114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3119   -2.2207    0.6929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7389   -1.4491   -1.8228 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3312   -3.0501   -0.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 11 13  2  0
 15  2  1  0
 13  6  1  0
 18 14  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
 16 29  1  0
 16 30  1  0
 17 31  1  0
 17 32  1  0
 18 33  1  6
 19 34  1  0
  7 24  1  0
  9 25  1  0
 10 26  1  0
 12 27  1  0
 13 28  1  0
M  END


  Mrv1652309102207572D          

 19 21  0  0  1  0            999 V2000
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8500   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    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  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 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
  6 13  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  2  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0296397

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CN=C(C2=C1CC[C@@H]2O)C1=CC(O)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H15NO3/c1-8-7-16-15(14-12(8)2-3-13(14)19)9-4-10(17)6-11(18)5-9/h4-7,13,17-19H,2-3H2,1H3/t13-/m0/s1

> <INCHI_KEY>
DSRKIBHIKLYUOK-ZDUSSCGKSA-N

> <FORMULA>
C15H15NO3

> <MOLECULAR_WEIGHT>
257.289

> <EXACT_MASS>
257.105193347

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
27.405800739233435

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-[(7S)-7-hydroxy-4-methyl-5H,6H,7H-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol

> <JCHEM_LOGP>
2.471814296666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.326513671740706

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.872176939994707

> <JCHEM_PKA_STRONGEST_BASIC>
5.043848948980673

> <JCHEM_POLAR_SURFACE_AREA>
73.58000000000001

> <JCHEM_REFRACTIVITY>
72.06500000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5-[(7S)-7-hydroxy-4-methyl-5H,6H,7H-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0       7.454   0.000   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.121  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.454  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.454  -4.620   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.788  -5.390   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.121  -5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.787  -4.620   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.453  -5.390   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.787  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.846  -1.941   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   14                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6                                                       
CONECT   14    5   15   18                                                  
CONECT   15   14    2   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   14   19                                                  
CONECT   19   18                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₅NO₃

Average Mass

257.2890 Da

Monoisotopic Mass

257.10519 Da

IUPAC Name

5-[(7S)-7-hydroxy-4-methyl-5H,6H,7H-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol

Traditional Name

5-[(7S)-7-hydroxy-4-methyl-5H,6H,7H-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol

CAS Registry Number

Not Available

SMILES

CC1=CN=C(C2=C1CC[C@@H]2O)C1=CC(O)=CC(O)=C1

InChI Identifier

InChI=1S/C15H15NO3/c1-8-7-16-15(14-12(8)2-3-13(14)19)9-4-10(17)6-11(18)5-9/h4-7,13,17-19H,2-3H2,1H3/t13-/m0/s1

InChI Key

DSRKIBHIKLYUOK-ZDUSSCGKSA-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
Ganoderma sinense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpyridines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyridine ring through a CC or CN bond.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyridines and derivatives

Sub Class

Phenylpyridines

Direct Parent

Phenylpyridines

Alternative Parents

Substituents

2-phenylpyridine
Resorcinol
Phenol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Methylpyridine
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Secondary alcohol
Azacycle
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Alcohol
Hydrocarbon derivative
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	2.47	ChemAxon
pKa (Strongest Acidic)	8.87	ChemAxon
pKa (Strongest Basic)	5.04	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	73.58 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	72.06 m³·mol⁻¹	ChemAxon
Polarizability	27.41 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

Not Available

Chemspider ID

78438597

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588492

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol (NP0296397)

MOL for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)

3D MOL for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)

3D SDF for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)

3D-SDF for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)

PDB for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)

3D PDB for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)

SMILES for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)

INCHI for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)

Structure for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)

3D Structure for NP0296397 (5-[(7s)-7-hydroxy-4-methyl-5h,6h,7h-cyclopenta[c]pyridin-1-yl]benzene-1,3-diol)