NP-MRD: Showing NP-Card for Thalprzewalskiinone (NP0069271)

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Record Information

Version

2.0

Created at

2022-04-28 14:37:27 UTC

Updated at

2022-04-28 14:37:27 UTC

NP-MRD ID

NP0069271

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Thalprzewalskiinone

Description

1-(3-Hydroxy-4-methoxybenzoyl)-2-methyl-6,7-dimethoxyisoquinolinium belongs to the class of organic compounds known as benzylisoquinolines. These are organic compounds containing an isoquinoline to which a benzyl group is attached. Thalprzewalskiinone is found in Thalictrum przewalskii. Based on a literature review very few articles have been published on 1-(3-Hydroxy-4-methoxybenzoyl)-2-methyl-6,7-dimethoxyisoquinolinium.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282216372D          

 26 28  0  0  0  0            999 V2000
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   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
    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 N   0  3  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
    1.4289   -1.6500    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
    1.4289    0.8250    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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   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    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    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
   -1.4289    0.0000    0.0000 O   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
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  0  0  0  0
  1 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  CHG  1   8   1
M  END

     RDKit          3D

 46 48  0  0  0  0  0  0  0  0999 V2000
    6.7650   -1.0403   -0.8153 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6743   -0.1928   -0.9949 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4075   -0.4262   -0.5084 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0803   -1.5436    0.2210 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7864   -1.7460    0.6971 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7761   -0.8125    0.4451 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4166   -1.0161    0.9264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0692   -2.1469    1.1435 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4175    0.1540    1.1636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6366    0.2052    0.4916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0901   -0.7818   -0.3539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3031   -0.7288   -1.0279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184   -1.7576   -1.8752 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8462   -2.8625   -2.0175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0902    0.3820   -0.8313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2988    0.4258   -1.5079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1514    1.5207   -1.3594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6548    1.3890    0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4523    1.3234    0.6751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0072    2.3213    1.5136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7870    2.2178    2.1554 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0006    1.1421    1.9811 N   0  0  0  0  0  4  0  0  0  0  0  0
    1.2742    1.0077    2.6627 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1565    0.2890   -0.2900 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4179    0.5048   -0.7645 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7470    1.6368   -1.5026 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7287   -1.8701   -1.5738 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7982   -1.4286    0.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7170   -0.4905   -1.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8451   -2.2786    0.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5775   -2.6376    1.2645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4833   -1.6521   -0.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6845   -3.2561   -0.9771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8597   -2.4833   -2.3556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2664   -3.6493   -2.6662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8231    2.3752   -2.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1693    1.2410   -1.7567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2240    1.9185   -0.3469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2769    2.2580    0.1647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6546    3.1948    1.6507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4337    2.9995    2.8147 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6398   -0.0267    2.7372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0991    1.3122    3.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0729    1.6430    2.2340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3596    1.0171   -0.4840 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0581    2.3490   -1.7169 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6 24  1  0
 24 25  2  0
 25 26  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 22  2  0
 22 23  1  0
 22 21  1  0
 21 20  2  0
 20 19  1  0
 19 18  2  0
 18 15  1  0
 15 16  1  0
 16 17  1  0
 15 12  2  0
 12 13  1  0
 13 14  1  0
 12 11  1  0
 11 10  2  0
 25  3  1  0
 10  9  1  0
 10 19  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
 24 45  1  0
 26 46  1  0
 23 42  1  0
 23 43  1  0
 23 44  1  0
 21 41  1  0
 20 40  1  0
 18 39  1  0
 17 36  1  0
 17 37  1  0
 17 38  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 11 32  1  0
M  CHG  1  22   1
M  END


  Mrv1652304282216372D          

 26 28  0  0  0  0            999 V2000
   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   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
    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 N   0  3  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
    1.4289   -1.6500    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
    1.4289    0.8250    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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   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    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    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
   -1.4289    0.0000    0.0000 O   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
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  0  0  0  0
  1 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  CHG  1   8   1
M  END
> <DATABASE_ID>
NP0069271

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1O)C(=O)C1=[N+](C)C=CC2=CC(OC)=C(OC)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H19NO5/c1-21-8-7-12-10-17(25-3)18(26-4)11-14(12)19(21)20(23)13-5-6-16(24-2)15(22)9-13/h5-11H,1-4H3/p+1

> <INCHI_KEY>
PHPIFKHJYINVDM-UHFFFAOYSA-O

> <FORMULA>
C20H20NO5

> <MOLECULAR_WEIGHT>
354.381

> <EXACT_MASS>
354.133599168

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
37.20291299278183

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(3-hydroxy-4-methoxybenzoyl)-6,7-dimethoxy-2-methylisoquinolin-2-ium

> <ALOGPS_LOGP>
0.54

> <JCHEM_LOGP>
-1.5955431718050797

> <ALOGPS_LOGS>
-5.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.209130260896117

> <JCHEM_PKA_STRONGEST_BASIC>
-4.43600225869849

> <JCHEM_POLAR_SURFACE_AREA>
68.87

> <JCHEM_REFRACTIVITY>
98.33019999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.86e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(3-hydroxy-4-methoxybenzoyl)-6,7-dimethoxy-2-methylisoquinolin-2-ium

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       4.001  -0.770   0.000  0.00  0.00           N+1
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668   3.850   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  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.002   1.540   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       8.002   4.620   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
CONECT    1    2    6   25                                                  
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   12                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8                                                            
CONECT   12    7   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   21                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   14                                                       
CONECT   20   18                                                            
CONECT   21   17   22                                                       
CONECT   22   21                                                            
CONECT   23    2   24                                                       
CONECT   24   23                                                            
CONECT   25    1   26                                                       
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₀NO₅

Average Mass

354.3810 Da

Monoisotopic Mass

354.13360 Da

IUPAC Name

1-(3-hydroxy-4-methoxybenzoyl)-6,7-dimethoxy-2-methylisoquinolin-2-ium

Traditional Name

1-(3-hydroxy-4-methoxybenzoyl)-6,7-dimethoxy-2-methylisoquinolin-2-ium

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1O)C(=O)C1=[N+](C)C=CC2=CC(OC)=C(OC)C=C12

InChI Identifier

InChI=1S/C20H19NO5/c1-21-8-7-12-10-17(25-3)18(26-4)11-14(12)19(21)20(23)13-5-6-16(24-2)15(22)9-13/h5-11H,1-4H3/p+1

InChI Key

PHPIFKHJYINVDM-UHFFFAOYSA-O

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
Thalictrum przewalskii	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzylisoquinolines. These are organic compounds containing an isoquinoline to which a benzyl group is attached.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoquinolines and derivatives

Sub Class

Benzylisoquinolines

Direct Parent

Benzylisoquinolines

Alternative Parents

Substituents

Benzylisoquinoline
Aryl-phenylketone
Methoxyphenol
Pyridine carboxylic acid or derivatives
Phenoxy compound
Anisole
Benzoyl
Methoxybenzene
Aryl ketone
Phenol ether
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Pyridinium
Pyridine
Heteroaromatic compound
Ketone
Azacycle
Ether
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic cation
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	0.54	ALOGPS
logP	-1.6	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	9.21	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	68.87 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	98.33 m³·mol⁻¹	ChemAxon
Polarizability	37.2 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

C00027495

Chemspider ID

9071402

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10896139

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Thalprzewalskiinone (NP0069271)

MOL for NP0069271 (Thalprzewalskiinone)

3D MOL for NP0069271 (Thalprzewalskiinone)

3D SDF for NP0069271 (Thalprzewalskiinone)

3D-SDF for NP0069271 (Thalprzewalskiinone)

PDB for NP0069271 (Thalprzewalskiinone)

3D PDB for NP0069271 (Thalprzewalskiinone)

SMILES for NP0069271 (Thalprzewalskiinone)

INCHI for NP0069271 (Thalprzewalskiinone)

Structure for NP0069271 (Thalprzewalskiinone)

3D Structure for NP0069271 (Thalprzewalskiinone)