NP-MRD: Showing NP-Card for 10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one (NP0163529)

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Record Information

Version

2.0

Created at

2022-09-02 22:12:09 UTC

Updated at

2022-09-02 22:12:10 UTC

NP-MRD ID

NP0163529

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one

Description

Hypecoumine belongs to the class of organic compounds known as phthalide isoquinolines. These are organic compounds with a structure characterized by an isoquinoline moiety linked to phthalide. 10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one is found in Corydalis decumbens. Hypecoumine is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261516532D          

 26 31  0  0  0  0            999 V2000
    0.5315   -4.4120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7615   -2.9599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0964   -2.9599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9034   -2.7884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4554   -3.4015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2004   -4.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6129   -4.9006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0609   -5.5137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3072   -5.1781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3935   -4.3576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   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
    1.4289    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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -0.1576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8419   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -1.4924    0.0000 O   0  0  0  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   -1.6500    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
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
  2 13  1  0  0  0  0
  5 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 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
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 14 26  2  0  0  0  0
 18 26  1  0  0  0  0
M  END

     RDKit          3D

 37 42  0  0  0  0  0  0  0  0999 V2000
    2.4647    1.3392   -3.2277 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9148    1.0590   -2.1148 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5908    1.0555   -1.7820 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4005    0.6922   -0.4641 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4546   -0.5063   -0.2949 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0925   -1.7272   -0.3147 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6177   -2.8506   -0.1404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9668   -2.7741    0.0694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5874   -1.5411    0.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9427   -1.4470    0.3020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5468   -0.2092    0.3214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8215    0.9483    0.1413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4509    0.8334   -0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8086   -0.3838   -0.0880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6606    2.0484    0.2047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9462    1.5757    0.6329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8872    0.1567    0.5057 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7662    0.4413    0.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2134    0.0478    1.3491 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5679   -0.1049    1.5549 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4947    0.1182    0.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0295    0.5048   -0.6889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6563    0.6674   -0.9251 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1100    0.6787   -1.5586 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2756    0.6985   -0.7391 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8814    0.0454    0.4695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0228    1.6084    0.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1033   -3.8199   -0.1688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5794   -3.6485    0.2149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4998   -2.3624    0.4415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8592    1.7308   -0.2177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0717    1.8849    1.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7531    1.9135   -0.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4883   -0.1302    2.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9607   -0.4082    2.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5607    1.7322   -0.4457 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1120    0.1330   -1.1840 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 26  1  0
 26 25  1  0
 25 24  1  0
 24 22  1  0
 22 23  2  0
  4  5  1  0
  5 14  1  0
 14 13  2  0
 13 12  1  0
 12 15  1  0
 15 16  1  0
 16 17  1  0
 17 11  1  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
 23  2  1  0
  6  5  2  0
 23 18  1  0
  9 14  1  0
 22 21  1  0
 11 12  2  0
  4 27  1  1
 19 34  1  0
 20 35  1  0
 25 36  1  0
 25 37  1  0
 13 31  1  0
 16 32  1  0
 16 33  1  0
 10 30  1  0
  8 29  1  0
  7 28  1  0
M  END


  Mrv1533004261516532D          

 26 31  0  0  0  0            999 V2000
    0.5315   -4.4120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7615   -2.9599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0964   -2.9599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9034   -2.7884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4554   -3.4015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2004   -4.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6129   -4.9006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0609   -5.5137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3072   -5.1781    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3935   -4.3576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 N   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
    1.4289    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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -0.1576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8419   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -1.4924    0.0000 O   0  0  0  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   -1.6500    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
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
  2 13  1  0  0  0  0
  5 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 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
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 14 26  2  0  0  0  0
 18 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0163529

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C1OC(C2=CC=C3OCOC3=C12)C1=C2C=C3OCOC3=CC2=CC=N1

> <INCHI_IDENTIFIER>
InChI=1S/C19H11NO6/c21-19-15-10(1-2-12-18(15)25-8-22-12)17(26-19)16-11-6-14-13(23-7-24-14)5-9(11)3-4-20-16/h1-6,17H,7-8H2

> <INCHI_KEY>
PMPWZNJOVFBHJT-UHFFFAOYSA-N

> <FORMULA>
C19H11NO6

> <MOLECULAR_WEIGHT>
349.298

> <EXACT_MASS>
349.058637078

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
34.073642556451276

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-{2H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one

> <ALOGPS_LOGP>
2.52

> <JCHEM_LOGP>
2.5641226416666667

> <ALOGPS_LOGS>
-3.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.3232544148042

> <JCHEM_PKA_STRONGEST_BASIC>
4.322450135714663

> <JCHEM_POLAR_SURFACE_AREA>
76.11000000000001

> <JCHEM_REFRACTIVITY>
86.3007

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.65e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-{2H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  O   UNK     0       0.992  -8.236   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.897  -6.990   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.421  -5.525   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.913  -5.525   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.420  -5.205   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.450  -6.349   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.974  -7.814   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.744  -9.148   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.714 -10.292   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.307  -9.666   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.468  -8.134   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.437  -6.990   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       1.334  -2.310   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.133  -0.294   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.038  -1.540   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.133  -2.786   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   14                                                  
CONECT    5    4    6   13                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    8   13                                                  
CONECT   13   12    2    5                                                  
CONECT   14    4   15   26                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   14   18                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₁NO₆

Average Mass

349.2980 Da

Monoisotopic Mass

349.05864 Da

IUPAC Name

10-{2H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one

Traditional Name

10-{2H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one

CAS Registry Number

Not Available

SMILES

O=C1OC(C2=CC=C3OCOC3=C12)C1=C2C=C3OCOC3=CC2=CC=N1

InChI Identifier

InChI=1S/C19H11NO6/c21-19-15-10(1-2-12-18(15)25-8-22-12)17(26-19)16-11-6-14-13(23-7-24-14)5-9(11)3-4-20-16/h1-6,17H,7-8H2

InChI Key

PMPWZNJOVFBHJT-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, 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
Corydalis decumbens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phthalide isoquinolines. These are organic compounds with a structure characterized by an isoquinoline moiety linked to phthalide.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Phthalide isoquinolines

Sub Class

Not Available

Direct Parent

Phthalide isoquinolines

Alternative Parents

Substituents

Phthalide isoquinoline
Benzofuranone
Isoquinoline
Isobenzofuranone
Phthalide
Benzodioxole
Isocoumaran
Pyridine
Benzenoid
Heteroaromatic compound
Carboxylic acid ester
Lactone
Azacycle
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Acetal
Organopnictogen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
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	2.52	ALOGPS
logP	2.56	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	12.32	ChemAxon
pKa (Strongest Basic)	4.32	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	76.11 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	86.3 m³·mol⁻¹	ChemAxon
Polarizability	34.07 Å³	ChemAxon
Number of Rings	6	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

127491

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one (NP0163529)

MOL for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)

3D MOL for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)

3D SDF for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)

3D-SDF for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)

PDB for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)

3D PDB for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)

SMILES for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)

INCHI for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)

Structure for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)

3D Structure for NP0163529 (10-{2h-[1,3]dioxolo[4,5-g]isoquinolin-5-yl}-3,5,11-trioxatricyclo[7.3.0.0²,⁶]dodeca-1,6,8-trien-12-one)