NP-MRD: Showing NP-Card for 6-hydroxy-5-methoxy-n-methylphthalimide (NP0027652)

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Record Information

Version

2.0

Created at

2021-06-19 19:45:01 UTC

Updated at

2021-06-29 23:53:53 UTC

NP-MRD ID

NP0027652

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-hydroxy-5-methoxy-n-methylphthalimide

Provided By

JEOL Database JEOL Logo

Description

6-hydroxy-5-methoxy-n-methylphthalimide is found in Menispermum dauricum. 6-hydroxy-5-methoxy-n-methylphthalimide was first documented in 2004 (Zhang, X., et al.). Based on a literature review very few articles have been published on 5-hydroxy-6-methoxy-2-methyl-2,3-dihydro-1H-isoindole-1,3-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192121453D          

 24 25  0  0  0  0            999 V2000
    1.1941   -3.6858    1.6000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1848   -3.1485    0.7507 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2997   -1.8210    0.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3129   -0.9595    0.8476 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2497    0.3510    0.4042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2385    0.8117   -0.4230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7759   -0.0114   -0.8601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7272   -1.3328   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7211   -2.1779   -0.8397 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4920    2.2276   -0.6835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2108    2.9365   -1.3772 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6363    2.5466   -0.0042 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2203    3.8648   -0.0105 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1474    1.4738    0.6706 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401    1.3959    1.3683 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1950   -3.1871    2.5748 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1791   -3.6301    1.1251 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9628   -4.7423    1.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1276   -1.2636    1.4936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5675    0.3480   -1.5073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5150   -3.0437   -0.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4510    4.1426   -1.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1284    3.8955    0.5965 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4862    4.5769    0.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  5  6  1  0  0  0  0
  3  8  2  0  0  0  0
  5  4  2  0  0  0  0
  4  3  1  0  0  0  0
  3  2  1  0  0  0  0
  6 10  1  0  0  0  0
 10 12  1  0  0  0  0
 12 14  1  0  0  0  0
 14  5  1  0  0  0  0
  8  7  1  0  0  0  0
 10 11  2  0  0  0  0
  8  9  1  0  0  0  0
 14 15  2  0  0  0  0
  7  6  2  0  0  0  0
 12 13  1  0  0  0  0
  7 20  1  0  0  0  0
  4 19  1  0  0  0  0
  9 21  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
 13 22  1  0  0  0  0
 13 23  1  0  0  0  0
 13 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0027652

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(OC([H])([H])[H])C([H])=C2C(=O)N(C(=O)C2=C1[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C10H9NO4/c1-11-9(13)5-3-7(12)8(15-2)4-6(5)10(11)14/h3-4,12H,1-2H3

> <INCHI_KEY>
STQUCJZSEVAMPY-UHFFFAOYSA-N

> <FORMULA>
C10H9NO4

> <MOLECULAR_WEIGHT>
207.185

> <EXACT_MASS>
207.053157774

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
24

> <JCHEM_AVERAGE_POLARIZABILITY>
20.05091674333145

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-6-methoxy-2-methyl-2,3-dihydro-1H-isoindole-1,3-dione

> <ALOGPS_LOGP>
0.71

> <JCHEM_LOGP>
0.4558625166666667

> <ALOGPS_LOGS>
-1.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.271501901361333

> <JCHEM_PKA_STRONGEST_BASIC>
-4.908761869811713

> <JCHEM_POLAR_SURFACE_AREA>
66.84

> <JCHEM_REFRACTIVITY>
52.65560000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.12e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-6-methoxy-2-methylisoindole-1,3-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       1.194  -3.686   1.600  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.185  -3.148   0.751  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.300  -1.821   0.423  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.313  -0.960   0.848  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.250   0.351   0.404  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.239   0.812  -0.423  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.776  -0.011  -0.860  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.727  -1.333  -0.423  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.721  -2.178  -0.840  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.492   2.228  -0.684  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.211   2.937  -1.377  0.00  0.00           O+0
HETATM   12  N   UNK     0       1.636   2.547  -0.004  0.00  0.00           N+0
HETATM   13  C   UNK     0       2.220   3.865  -0.011  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.147   1.474   0.671  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.140   1.396   1.368  0.00  0.00           O+0
HETATM   16  H   UNK     0       1.195  -3.187   2.575  0.00  0.00           H+0
HETATM   17  H   UNK     0       2.179  -3.630   1.125  0.00  0.00           H+0
HETATM   18  H   UNK     0       0.963  -4.742   1.766  0.00  0.00           H+0
HETATM   19  H   UNK     0       2.128  -1.264   1.494  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.567   0.348  -1.507  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.515  -3.044  -0.435  0.00  0.00           H+0
HETATM   22  H   UNK     0       2.451   4.143  -1.043  0.00  0.00           H+0
HETATM   23  H   UNK     0       3.128   3.896   0.597  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.486   4.577   0.378  0.00  0.00           H+0
CONECT    1    2   16   17   18                                             
CONECT    2    1    3                                                       
CONECT    3    8    4    2                                                  
CONECT    4    5    3   19                                                  
CONECT    5    6    4   14                                                  
CONECT    6    5   10    7                                                  
CONECT    7    8    6   20                                                  
CONECT    8    3    7    9                                                  
CONECT    9    8   21                                                       
CONECT   10    6   12   11                                                  
CONECT   11   10                                                            
CONECT   12   10   14   13                                                  
CONECT   13   12   22   23   24                                             
CONECT   14   12    5   15                                                  
CONECT   15   14                                                            
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    4                                                            
CONECT   20    7                                                            
CONECT   21    9                                                            
CONECT   22   13                                                            
CONECT   23   13                                                            
CONECT   24   13                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₀H₉NO₄

Average Mass

207.1850 Da

Monoisotopic Mass

207.05316 Da

IUPAC Name

5-hydroxy-6-methoxy-2-methyl-2,3-dihydro-1H-isoindole-1,3-dione

Traditional Name

5-hydroxy-6-methoxy-2-methylisoindole-1,3-dione

CAS Registry Number

Not Available

SMILES

[H]OC1=C(OC([H])([H])[H])C([H])=C2C(=O)N(C(=O)C2=C1[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C10H9NO4/c1-11-9(13)5-3-7(12)8(15-2)4-6(5)10(11)14/h3-4,12H,1-2H3

InChI Key

STQUCJZSEVAMPY-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃+CD₃OD (1:1), simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Menispermum dauricum	JEOL database	Zhang, X., et al, Phytochemistry 65, 929 (2004)

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Isoindolines

Direct Parent

Phthalimides

Alternative Parents

Substituents

Phthalimide
Isoindole
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Carboxylic acid imide, n-substituted
Carboxylic acid imide
Carboxylic acid derivative
Ether
Azacycle
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
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
logP	0.71	ALOGPS
logP	0.46	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	8.27	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	66.84 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	52.66 m³·mol⁻¹	ChemAxon
Polarizability	20.05 Å³	ChemAxon
Number of Rings	2	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

557035

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

641801

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang, X., et al. (2004). Zhang, X., et al, Phytochemistry 65, 929 (2004). Phytochem..

Showing NP-Card for 6-hydroxy-5-methoxy-n-methylphthalimide (NP0027652)

MOL for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)

3D MOL for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)

3D SDF for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)

3D-SDF for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)

PDB for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)

3D PDB for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)

SMILES for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)

INCHI for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)

Structure for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)

3D Structure for NP0027652 (6-hydroxy-5-methoxy-n-methylphthalimide)