NP-MRD: Showing NP-Card for (+)-argemonine (NP0207538)

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Record Information

Version

2.0

Created at

2022-09-05 04:11:06 UTC

Updated at

2022-09-05 04:11:06 UTC

NP-MRD ID

NP0207538

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-argemonine

Description

(+)-Argemonine belongs to the class of organic compounds known as pavine alkaloids. These are alkaloids with a structure based on the pavine skeleton. (+)-argemonine is found in Argemone platyceras. Based on a literature review very few articles have been published on (+)-argemonine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052206112D          

 26 29  0  0  1  0            999 V2000
   -1.6425    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
   -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
   -0.9280   -1.2094    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
   -1.6425   -2.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843   -1.7928    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9093   -1.7928    0.0000 C   0  0  0  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
    3.2071   -1.6219    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
    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
    3.9216   -0.3844    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
    3.2071    0.0281    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  1  0  0  0  0  0  0  0  0  0
    1.0843    0.1990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2478   -0.6938    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8168    0.0097    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
  9 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  5 24  1  0  0  0  0
 23 25  1  1  0  0  0
 11 25  1  1  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 51 54  0  0  0  0  0  0  0  0999 V2000
    5.1214   -2.1951   -1.7948 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0904   -0.8391   -1.4071 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9333   -0.3215   -0.8025 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8267   -1.1460   -0.5896 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6758   -0.6693    0.0012 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6735    0.6522    0.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7431    1.4732    0.1688 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8952    0.9843   -0.4258 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9491    1.8511   -0.6060 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8924    3.1998   -0.2101 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4454    1.1858    1.0064 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5523    1.4803   -0.0773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7452    0.6253   -0.0733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8987    1.0942   -0.7252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0170    0.2893   -0.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1774    0.7161   -1.3663 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2981    1.9442   -2.0188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0104   -0.9446   -0.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1636   -1.7483   -0.1402 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1594   -3.0146    0.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8554   -1.3740    0.5141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7210   -0.5970    0.5417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4713   -1.0219    1.2212 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4995   -1.5549    0.2244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0426    0.1914    1.8955 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6914   -0.0194    3.0790 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1645   -2.4330   -2.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4425   -2.3012   -2.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8040   -2.8508   -0.9449 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8740   -2.1741   -0.8931 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7080    2.5278    0.4747 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5895    3.2564    0.8574 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8828    3.6691   -0.3892 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0902    3.6969   -0.8004 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6732    2.0919    1.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8285    2.5747   -0.0811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0844    1.3523   -1.1048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9091    2.0623   -1.2087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2470    1.9125   -2.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3935    2.7851   -1.3069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4925    2.1189   -2.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6568   -3.7385   -0.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2307   -3.3147    0.5875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6919   -2.9639    1.4811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8078   -2.3390    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6883   -1.7557    2.0349 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0416   -1.7590   -0.7704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8782   -2.5416    0.5900 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3128    0.7018    3.8616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7694    0.2027    2.9848 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4752   -1.0223    3.4866 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
  9 10  1  0
  6 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  2  0
 18 19  1  0
 19 20  1  0
 18 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
  8  3  1  0
 25 11  1  0
 24  5  1  0
 22 13  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  7 31  1  0
 10 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  1
 12 36  1  0
 12 37  1  0
 14 38  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 20 42  1  0
 20 43  1  0
 20 44  1  0
 21 45  1  0
 23 46  1  1
 24 47  1  0
 24 48  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
M  END


  Mrv1652309052206112D          

 26 29  0  0  1  0            999 V2000
   -1.6425    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
   -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
   -0.9280   -1.2094    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
   -1.6425   -2.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0843   -1.7928    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9093   -1.7928    0.0000 C   0  0  0  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
    3.2071   -1.6219    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
    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
    3.9216   -0.3844    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
    3.2071    0.0281    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  1  0  0  0  0  0  0  0  0  0
    1.0843    0.1990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2478   -0.6938    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8168    0.0097    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
  9 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 13 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  5 24  1  0  0  0  0
 23 25  1  1  0  0  0
 11 25  1  1  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207538

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C21H25NO4/c1-22-16-6-12-8-18(23-2)20(25-4)10-14(12)17(22)7-13-9-19(24-3)21(26-5)11-15(13)16/h8-11,16-17H,6-7H2,1-5H3/t16-,17-/m1/s1

> <INCHI_KEY>
QEOWCPFWLCIQSL-IAGOWNOFSA-N

> <FORMULA>
C21H25NO4

> <MOLECULAR_WEIGHT>
355.434

> <EXACT_MASS>
355.178358289

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
39.57331677638777

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <JCHEM_LOGP>
3.2077417903333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
6.678565640864285

> <JCHEM_POLAR_SURFACE_AREA>
40.160000000000004

> <JCHEM_REFRACTIVITY>
101.02569999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.066   1.592   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.066   0.052   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.732  -0.718   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.399   0.052   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.935  -0.718   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.935  -2.258   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.399  -3.028   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.732  -2.258   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.066  -3.028   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -3.066  -4.568   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.024  -3.346   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.564  -3.346   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.653  -2.258   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.987  -3.028   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.320  -2.258   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.654  -3.028   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.654  -4.568   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.320  -0.718   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.654   0.052   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.654   1.592   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.987   0.052   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.653  -0.718   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.564   0.371   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.024   0.371   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       2.329  -1.295   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       1.525   0.018   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   24                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    6   12   25                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22                                                       
CONECT   22   21   13   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23    5                                                       
CONECT   25   23   11   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Value	Source
(R,R)-Argemonine	ChEBI
(R,R)-N-Methylpavine	ChEBI

Chemical Formula

C₂₁H₂₅NO₄

Average Mass

355.4340 Da

Monoisotopic Mass

355.17836 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C21H25NO4/c1-22-16-6-12-8-18(23-2)20(25-4)10-14(12)17(22)7-13-9-19(24-3)21(26-5)11-15(13)16/h8-11,16-17H,6-7H2,1-5H3/t16-,17-/m1/s1

InChI Key

QEOWCPFWLCIQSL-IAGOWNOFSA-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
Argemone platyceras	LOTUS Database	35616633

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
Aralkylamine
Benzenoid
Tertiary aliphatic amine
Tertiary amine
Organoheterocyclic compound
Ether
Azacycle
Amine
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

2,3,8,9-tetramethoxy-13-methyl-5,6,11,12-tetrahydro-5,11-epiminodibenzo[a,e][8]annulene (CHEBI:77059 )

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	3.21	ChemAxon
pKa (Strongest Basic)	6.68	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	40.16 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	101.03 m³·mol⁻¹	ChemAxon
Polarizability	39.57 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

Not Available

Chemspider ID

1267917

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

1551634

PDB ID

Not Available

ChEBI ID

77059

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (+)-argemonine (NP0207538)

MOL for NP0207538 ((+)-argemonine)

3D MOL for NP0207538 ((+)-argemonine)

3D SDF for NP0207538 ((+)-argemonine)

3D-SDF for NP0207538 ((+)-argemonine)

PDB for NP0207538 ((+)-argemonine)

3D PDB for NP0207538 ((+)-argemonine)

SMILES for NP0207538 ((+)-argemonine)

INCHI for NP0207538 ((+)-argemonine)

Structure for NP0207538 ((+)-argemonine)

3D Structure for NP0207538 ((+)-argemonine)