NP-MRD: Showing NP-Card for (-)-Isonorargemonine (NP0067605)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 12:27:44 UTC

Updated at

2022-04-28 12:27:44 UTC

NP-MRD ID

NP0067605

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Isonorargemonine

Description

(?)-Isonorargemonine belongs to the class of organic compounds known as pavine alkaloids. These are alkaloids with a structure based on the pavine skeleton. (-)-Isonorargemonine is found in Argemone gracilenta Greene, Argemone munita, Argemone munita Dur.and Hilg subsp.argentea G.B.Ownb., Eschscholtzia californica Cham, Eschscholtzia douglasii Walp., Eschscholtzia glauca Greene, Thalictrum flavum and Thalictrum revolutum DC.. Based on a literature review very few articles have been published on (?)-Isonorargemonine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214272D          

 25 28  0  0  1  0            999 V2000
   -0.9280   -1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9280   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2135    0.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5009   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5009   -1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2135   -1.6219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843   -1.7928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9093   -1.7928    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4927   -1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4927   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9093    0.1990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843    0.1990    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2478   -0.9000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4456   -0.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2071    0.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9216   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9216   -1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2071   -1.6219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6361   -1.6219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6361   -2.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6361    0.0281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6361    0.8531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6425    0.0281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6425    0.8531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6425   -1.6219    0.0000 O   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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  1  0  0  0
  8 13  1  1  0  0  0
 13 14  1  0  0  0  0
 10 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
  9 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 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
M  END

     RDKit          3D

 48 51  0  0  0  0  0  0  0  0999 V2000
    5.3373   -3.0122   -0.1674 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2424   -1.7011   -0.6896 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1197   -0.9042   -0.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9788   -1.3435    0.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8873   -0.5266    0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9278    0.7265   -0.2950 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0637    1.1782   -0.9817 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1558    0.3569   -1.1025 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2963    0.7968   -1.7862 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7607    1.6107   -0.1750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1809    1.2519    0.9152 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4475    0.7753    0.3125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5190    1.6044    0.1368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7088    1.1372   -0.4296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7514    2.0055   -0.5841 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6347    3.3507   -0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7973   -0.1940   -0.8185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0063   -0.6240   -1.3820 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1018   -1.9609   -1.7751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7330   -1.0270   -0.6466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5489   -0.5356   -0.0760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4080   -1.4540    0.0972 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6787   -0.9846    0.9891 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2572    0.1693    1.7782 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2838    0.5830    2.6973 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8480   -3.0324    0.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4286   -3.2333    0.0194 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9067   -3.7599   -0.8660 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9522   -2.3190    0.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1015    2.1657   -1.4225 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3089    1.7142   -2.1859 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2458    1.6309   -1.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0974    2.6852   -0.0587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3651    2.1255    1.5825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4734    2.6246    0.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6600    3.8175   -0.2520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9079    3.8876   -0.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3251    3.3495    0.8845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4223   -2.1774   -2.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1030   -2.2620   -2.0904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7790   -2.6113   -0.9289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8147   -2.0615   -0.9537 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0270   -1.6668   -0.9134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7966   -2.4243    0.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9470   -1.7615    1.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8930    0.4603    3.7291 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5534    1.6406    2.4854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1856   -0.0709    2.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 17  1  0
 17 20  2  0
 20 21  1  0
 21 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 12 11  1  0
 11 10  1  0
 10  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8  3  2  0
  3  2  1  0
  2  1  1  0
  3  4  1  0
  4  5  2  0
  5 23  1  0
 23 22  1  0
 23 24  1  0
 24 25  1  0
 14 17  1  0
 24 11  1  0
 22 21  1  0
  5  6  1  0
 19 39  1  0
 19 40  1  0
 19 41  1  0
 20 42  1  0
 13 35  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 11 34  1  1
 10 32  1  0
 10 33  1  0
  7 30  1  0
  9 31  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
 23 45  1  1
 22 43  1  0
 22 44  1  0
 25 46  1  0
 25 47  1  0
 25 48  1  0
M  END


  Mrv1652304282214272D          

 25 28  0  0  1  0            999 V2000
   -0.9280   -1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9280   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2135    0.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5009   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5009   -1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2135   -1.6219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843   -1.7928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9093   -1.7928    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4927   -1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4927   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9093    0.1990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843    0.1990    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2478   -0.9000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4456   -0.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2071    0.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9216   -0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9216   -1.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2071   -1.6219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6361   -1.6219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6361   -2.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6361    0.0281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6361    0.8531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6425    0.0281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6425    0.8531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6425   -1.6219    0.0000 O   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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  1  0  0  0
  8 13  1  1  0  0  0
 13 14  1  0  0  0  0
 10 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
  9 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 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
M  END
> <DATABASE_ID>
NP0067605

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=C1OC)[C@@H]1CC3=CC(O)=C(OC)C=C3[C@H](C2)N1C

> <INCHI_IDENTIFIER>
InChI=1S/C20H23NO4/c1-21-15-5-11-7-17(22)18(23-2)9-13(11)16(21)6-12-8-19(24-3)20(25-4)10-14(12)15/h7-10,15-16,22H,5-6H2,1-4H3/t15-,16-/m0/s1

> <INCHI_KEY>
WVHCKSAXAXNGBF-HOTGVXAUSA-N

> <FORMULA>
C20H23NO4

> <MOLECULAR_WEIGHT>
341.407

> <EXACT_MASS>
341.162708225

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
37.16187820823224

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,9S)-4,12,13-trimethoxy-17-methyl-17-azatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadeca-2,4,6,10(15),11,13-hexaen-5-ol

> <ALOGPS_LOGP>
2.84

> <JCHEM_LOGP>
3.061847734333333

> <ALOGPS_LOGS>
-3.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.96268463914378

> <JCHEM_PKA_STRONGEST_BASIC>
6.689120437808983

> <JCHEM_POLAR_SURFACE_AREA>
51.160000000000004

> <JCHEM_REFRACTIVITY>
96.54339999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.63e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,9S)-4,12,13-trimethoxy-17-methyl-17-azatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadeca-2,4,6,10(15),11,13-hexaen-5-ol

> <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      -1.732  -2.258   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.732  -0.718   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.399   0.052   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.935  -0.718   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.935  -2.258   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.399  -3.028   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.024  -3.346   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.564  -3.346   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.653  -2.258   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.653  -0.718   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.564   0.371   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.024   0.371   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       2.329  -1.680   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       0.832  -1.321   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.987   0.052   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.320  -0.718   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.320  -2.258   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.987  -3.028   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.654  -3.028   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.654  -4.568   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.654   0.052   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.654   1.592   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.066   0.052   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -3.066   1.592   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -3.066  -3.028   0.000  0.00  0.00           O+0
CONECT    1    2    6   25                                                  
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   12                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10   18                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11    4   13                                                  
CONECT   13   12    8   14                                                  
CONECT   14   13                                                            
CONECT   15   10   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17    9                                                       
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   16   22                                                       
CONECT   22   21                                                            
CONECT   23    2   24                                                       
CONECT   24   23                                                            
CONECT   25    1                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₃NO₄

Average Mass

341.4070 Da

Monoisotopic Mass

341.16271 Da

IUPAC Name

(1S,9S)-4,12,13-trimethoxy-17-methyl-17-azatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadeca-2,4,6,10(15),11,13-hexaen-5-ol

Traditional Name

(1S,9S)-4,12,13-trimethoxy-17-methyl-17-azatetracyclo[7.7.1.0^{2,7}.0^{10,15}]heptadeca-2,4,6,10(15),11,13-hexaen-5-ol

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1OC)[C@@H]1CC3=CC(O)=C(OC)C=C3[C@H](C2)N1C

InChI Identifier

InChI=1S/C20H23NO4/c1-21-15-5-11-7-17(22)18(23-2)9-13(11)16(21)6-12-8-19(24-3)20(25-4)10-14(12)15/h7-10,15-16,22H,5-6H2,1-4H3/t15-,16-/m0/s1

InChI Key

WVHCKSAXAXNGBF-HOTGVXAUSA-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, 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
Argemone gracilenta Greene	Plant	KNApSAcK
Argemone munita	LOTUS Database	35616633
Argemone munita Dur.and Hilg subsp.argentea G.B.Ownb.	Plant	KNApSAcK
Eschscholtzia californica Cham	Plant	KNApSAcK
Eschscholtzia douglasii Walp.	Plant	KNApSAcK
Eschscholtzia glauca Greene	Plant	KNApSAcK
Thalictrum flavum	Plant	KNApSAcK
Thalictrum revolutum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pavine alkaloids. These are alkaloids with a structure based on the pavine skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Pavine alkaloids

Sub Class

Not Available

Direct Parent

Pavine alkaloids

Alternative Parents

Substituents

Pavine skeleton
Tetrahydroisoquinoline
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Benzenoid
Tertiary aliphatic amine
Tertiary amine
Ether
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Amine
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	2.84	ALOGPS
logP	3.06	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	9.96	ChemAxon
pKa (Strongest Basic)	6.69	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	51.16 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	96.54 m³·mol⁻¹	ChemAxon
Polarizability	37.16 Å³	ChemAxon
Number of Rings	4	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

C00025400

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Bracket

METLIN ID

Not Available

PubChem Compound

12311125

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (-)-Isonorargemonine (NP0067605)

MOL for NP0067605 ((-)-Isonorargemonine)

3D MOL for NP0067605 ((-)-Isonorargemonine)

3D SDF for NP0067605 ((-)-Isonorargemonine)

3D-SDF for NP0067605 ((-)-Isonorargemonine)

PDB for NP0067605 ((-)-Isonorargemonine)

3D PDB for NP0067605 ((-)-Isonorargemonine)

SMILES for NP0067605 ((-)-Isonorargemonine)

INCHI for NP0067605 ((-)-Isonorargemonine)

Structure for NP0067605 ((-)-Isonorargemonine)

3D Structure for NP0067605 ((-)-Isonorargemonine)