NP-MRD: Showing NP-Card for (7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate (NP0308284)

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Record Information

Version

2.0

Created at

2022-09-11 01:58:00 UTC

Updated at

2022-09-11 01:58:00 UTC

NP-MRD ID

NP0308284

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate

Description

Papracinine belongs to the class of organic compounds known as tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives. (7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate is found in Fumaria indica. Based on a literature review very few articles have been published on Papracinine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112203582D          

 26 30  0  0  1  0            999 V2000
    7.8154    1.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1510    0.8612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3952    1.1920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3039    2.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5482    2.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8838    1.8538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9751    1.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7308    0.7030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8221   -0.1169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1280    2.1847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1331    1.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3501    1.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0192    0.3442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1993    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7102    0.9174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0411    1.6731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8611    1.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3418    2.4348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4246    2.2213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7127    1.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8892    0.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0367    3.0047    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    3.2451    2.7724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6705    3.7439    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    4.7012    3.4937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4569    3.1628    0.0000 C   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  2  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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 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
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 10 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 15 21  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
  5 26  1  0  0  0  0
M  CHG  2  22   1  24  -1
M  END

     RDKit          3D

 47 51  0  0  0  0  0  0  0  0999 V2000
    6.0755    0.5010    1.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9751    1.3178    2.1503 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7317    0.9681    1.6363 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5470   -0.1275    0.8051 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3273   -0.4832    0.2919 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2321    0.3024    0.6306 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3677    1.4023    1.4540 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6324    1.7336    1.9591 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7538    2.8407    2.7851 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0564   -0.1276    0.0406 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6903   -1.3104    0.7081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1605   -1.1296    0.3871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2188   -2.0119    0.3115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4897   -1.5944   -0.0114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7363   -0.2621   -0.2706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6501    0.6181   -0.1888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3993    0.1921    0.1315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1141    0.9211    0.2940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1854    1.8847   -0.4962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5922    1.8620   -0.3384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8552    0.4777   -0.6135 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1785   -0.3021   -1.3722 N   0  0  1  0  0  4  0  0  0  0  0  0
   -0.9932   -0.5877   -2.1583 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5889    0.9444   -1.7992 O   0  0  0  0  0  1  0  0  0  0  0  0
    1.1888   -1.2492   -1.6874 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1229   -1.6464   -0.5986 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0408    0.9525    2.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9619   -0.5359    2.1573 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1830    0.4150    0.6757 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3994   -0.7408    0.5404 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5580    2.0522    1.7449 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9559    3.4110    3.0301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4438   -2.2886    0.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5714   -1.1895    1.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0158   -3.0690    0.5187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3164   -2.3013   -0.0677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0230    1.8147   -0.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0810    1.1301    1.4106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0829    2.5044   -1.0931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9044    2.1072    0.6946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4890   -1.5304   -1.9414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6656    0.2934   -2.2446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5984   -0.7131   -3.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8222   -0.8030   -2.5136 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7279   -2.1433   -2.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8590   -2.5683   -0.0467 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1035   -1.9313   -1.1051 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  7  1  0
  7  8  2  0
  8  9  1  0
  6 10  1  0
 10 11  1  1
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 21  1  0
 21 20  1  0
 20 19  1  0
 19 16  1  0
 16 17  2  0
 17 18  1  0
 10 22  1  0
 22 23  1  0
 22 24  1  6
 22 25  1  0
 25 26  1  0
  8  3  1  0
 18 10  1  0
 26  5  1  0
 17 12  1  0
 16 15  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  7 31  1  0
  9 32  1  0
 11 33  1  0
 11 34  1  0
 13 35  1  0
 14 36  1  0
 20 39  1  0
 20 40  1  0
 18 37  1  0
 18 38  1  0
 23 41  1  0
 23 42  1  0
 23 43  1  0
 25 44  1  0
 25 45  1  0
 26 46  1  0
 26 47  1  0
M  CHG  2  22   1  24  -1
M  END


  Mrv1652309112203582D          

 26 30  0  0  1  0            999 V2000
    7.8154    1.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1510    0.8612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3952    1.1920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3039    2.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5482    2.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8838    1.8538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9751    1.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7308    0.7030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8221   -0.1169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1280    2.1847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1331    1.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3501    1.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0192    0.3442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1993    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7102    0.9174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0411    1.6731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8611    1.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3418    2.4348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4246    2.2213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7127    1.8044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8892    0.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0367    3.0047    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    3.2451    2.7724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6705    3.7439    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    4.7012    3.4937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4569    3.1628    0.0000 C   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  2  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
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 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
 12 17  1  0  0  0  0
 17 18  1  0  0  0  0
 10 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 15 21  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
  5 26  1  0  0  0  0
M  CHG  2  22   1  24  -1
M  END
> <DATABASE_ID>
NP0308284

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=C1O)[C@]1(CC3=CC=C4OCOC4=C3C1)[N+](C)([O-])CC2

> <INCHI_IDENTIFIER>
InChI=1S/C20H21NO5/c1-21(23)6-5-12-7-18(24-2)16(22)8-15(12)20(21)9-13-3-4-17-19(14(13)10-20)26-11-25-17/h3-4,7-8,22H,5-6,9-11H2,1-2H3/t20-,21?/m1/s1

> <INCHI_KEY>
JNIPFMUGTLRRJS-VQCQRNETSA-N

> <FORMULA>
C20H21NO5

> <MOLECULAR_WEIGHT>
355.39

> <EXACT_MASS>
355.14197278

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
37.57253958805109

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(7R)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2H,2'H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate

> <JCHEM_LOGP>
2.0287113986666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.810014815497526

> <JCHEM_PKA_STRONGEST_BASIC>
3.363074512728118

> <JCHEM_POLAR_SURFACE_AREA>
70.98

> <JCHEM_REFRACTIVITY>
96.40319999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(7R)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      14.589   2.520   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      13.348   1.607   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.938   2.225   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.767   3.756   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.357   4.373   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.116   3.460   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.287   1.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.697   1.312   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.868  -0.218   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.706   4.078   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.715   2.538   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.254   2.053   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.636   0.643   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.105   0.472   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.192   1.712   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.810   3.123   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.341   3.294   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.238   4.545   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.659   4.146   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.330   3.368   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.660   1.864   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0       7.535   5.609   0.000  0.00  0.00           N+1
HETATM   23  C   UNK     0       6.058   5.175   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.852   6.989   0.000  0.00  0.00           O-1
HETATM   25  C   UNK     0       8.775   6.522   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.186   5.904   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   26                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    6   11   18   22                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16   12   18                                                  
CONECT   18   17   10                                                       
CONECT   19   16   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   15                                                       
CONECT   22   10   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26                                                       
CONECT   26   25    5                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₁NO₅

Average Mass

355.3900 Da

Monoisotopic Mass

355.14197 Da

IUPAC Name

(7R)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2H,2'H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate

Traditional Name

(7R)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1O)[C@]1(CC3=CC=C4OCOC4=C3C1)[N+](C)([O-])CC2

InChI Identifier

InChI=1S/C20H21NO5/c1-21(23)6-5-12-7-18(24-2)16(22)8-15(12)20(21)9-13-3-4-17-19(14(13)10-20)26-11-25-17/h3-4,7-8,22H,5-6,9-11H2,1-2H3/t20-,21?/m1/s1

InChI Key

JNIPFMUGTLRRJS-VQCQRNETSA-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
Fumaria indica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydroisoquinolines

Sub Class

Not Available

Direct Parent

Tetrahydroisoquinolines

Alternative Parents

Substituents

Tetrahydroisoquinoline
Benzodioxole
Indane
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Trialkyl amine oxide
Acetal
N-oxide
Ether
Trisubstituted n-oxide
Oxacycle
Azacycle
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic nitrogen compound
Hydrocarbon derivative
Organic oxygen compound
Organic zwitterion
Organic salt
Organopnictogen 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	2.03	ChemAxon
pKa (Strongest Acidic)	9.81	ChemAxon
pKa (Strongest Basic)	3.36	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	70.98 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	96.4 m³·mol⁻¹	ChemAxon
Polarizability	37.57 Å³	ChemAxon
Number of Rings	5	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

101630423

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate (NP0308284)

MOL for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)

3D MOL for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)

3D SDF for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)

3D-SDF for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)

PDB for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)

3D PDB for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)

SMILES for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)

INCHI for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)

Structure for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)

3D Structure for NP0308284 ((7r)-7'-hydroxy-6'-methoxy-2'-methyl-3',4',6,8-tetrahydro-2h-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-2'-ium-2'-olate)