NP-MRD: Showing NP-Card for Schizanthine M (NP0138887)

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Record Information

Version

1.0

Created at

2022-06-29 19:21:45 UTC

Updated at

2022-06-29 19:21:45 UTC

NP-MRD ID

NP0138887

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Schizanthine M

Description

Schizanthine M belongs to the class of organic compounds known as tropane alkaloids. These are organic compounds containing the nitrogenous bicyclic alkaloid parent N-Methyl-8-azabicyclo[3.2.1]Octane. Schizanthine M is found in Schizanthus pinnatus. Based on a literature review very few articles have been published on Schizanthine M.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292221212D          

 27 28  0  0  1  0            999 V2000
   -3.8726   -4.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1582   -3.8999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4437   -4.3124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7292   -3.8999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7292   -3.0749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0147   -4.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0147   -5.1374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3003   -3.8999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4142   -4.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4142   -5.1374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1287   -3.8999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8431   -4.3124    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7815   -5.1351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3863   -5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2020   -5.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6145   -4.8588    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3131   -4.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5248   -3.8477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0504   -5.0094    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7648   -5.4219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4372   -4.9205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9020   -4.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7247   -4.3005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5440   -3.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0088   -2.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6508   -2.0706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7213   -3.4339    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  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  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
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 17 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 24 27  1  0  0  0  0
M  END

     RDKit          3D

 56 57  0  0  0  0  0  0  0  0999 V2000
    5.0686   -0.1357   -2.4370 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8100    0.3767   -1.2581 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6899    1.3616   -1.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6817    0.8121   -0.1516 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8633    0.8801    1.1002 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5130    0.2095   -0.6294 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5945   -0.2936    0.2948 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4570   -1.7924    0.1098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5954   -2.0153   -0.9546 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9920   -2.0685   -0.3709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6357   -0.8104   -0.8484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5389   -0.2490    0.0798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8518    0.0361   -0.2128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2358   -0.2290   -1.3782 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7997    0.6121    0.7236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1880    0.8665    0.2753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4612    0.9175    1.9718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4909    1.5044    2.8705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4420    0.0812   -1.1097 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7542    0.3944    0.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5688   -0.8605   -1.8319 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0847   -1.1911   -3.1255 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6296   -0.0198   -0.1207 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5683   -0.8480   -0.2906 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4384    0.4648    1.1547 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2740    0.0351    2.1988 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7278    0.3514    2.0056 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5024    0.1099   -3.3349 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8703   -0.8337   -2.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0963    2.2869   -0.6140 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2666    1.5926   -2.0772 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9753   -0.1171    1.3173 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2502   -2.3184    1.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4127   -2.1939   -0.2861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3384   -2.9025   -1.5454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5346   -2.9882   -0.6973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8812   -2.1172    0.7319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1436   -0.9826   -1.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4246    1.9548    0.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3369    0.5141   -0.7632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9445    0.3248    0.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4569    0.7447    2.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0502    2.3362    2.3784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2634    0.7149    3.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0164    1.8228    3.8288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6800    0.9635   -1.6980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3519    0.0402    1.0674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5972    1.4663    0.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7226   -2.0940   -3.1483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6056   -0.3133   -3.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2004   -1.4305   -3.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1110   -1.0617    2.4129 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9817    0.5457    3.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9728    1.3583    2.4593 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3971   -0.3708    2.4901 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0351    0.4572    0.9463 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 25  1  0
 25 23  1  0
 23 24  2  0
 23  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 11 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 20  7  1  0
 21  9  1  0
 27 54  1  0
 27 55  1  0
 27 56  1  0
 26 52  1  0
 26 53  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  7 32  1  1
  8 33  1  0
  8 34  1  0
  9 35  1  6
 10 36  1  0
 10 37  1  0
 11 38  1  6
 16 39  1  0
 16 40  1  0
 16 41  1  0
 17 42  1  0
 18 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  6
 20 47  1  0
 20 48  1  0
 22 49  1  0
 22 50  1  0
 22 51  1  0
M  END


  Mrv1652306292221212D          

 27 28  0  0  1  0            999 V2000
   -3.8726   -4.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1582   -3.8999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4437   -4.3124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7292   -3.8999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7292   -3.0749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0147   -4.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0147   -5.1374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3003   -3.8999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4142   -4.3124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4142   -5.1374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1287   -3.8999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8431   -4.3124    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7815   -5.1351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3863   -5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2020   -5.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6145   -4.8588    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3131   -4.0908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5248   -3.8477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0504   -5.0094    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7648   -5.4219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4372   -4.9205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9020   -4.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7247   -4.3005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5440   -3.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0088   -2.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6508   -2.0706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7213   -3.4339    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  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  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
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 17 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 24 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138887

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCOC(=O)C(=C)CC(=O)O[C@@H]1CC2C[C@@H](OC(=O)C(\C)=C\C)C(C1)N2C

> <INCHI_IDENTIFIER>
InChI=1S/C20H29NO6/c1-6-12(3)20(24)27-17-10-14-9-15(11-16(17)21(14)5)26-18(22)8-13(4)19(23)25-7-2/h6,14-17H,4,7-11H2,1-3,5H3/b12-6+/t14?,15-,16?,17-/m1/s1

> <INCHI_KEY>
WMFMZTXHTPOWMQ-WAMNRYJJSA-N

> <FORMULA>
C20H29NO6

> <MOLECULAR_WEIGHT>
379.453

> <EXACT_MASS>
379.199487658

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
41.04837956096

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-ethyl (3R,6R)-8-methyl-6-{[(2E)-2-methylbut-2-enoyl]oxy}-8-azabicyclo[3.2.1]octan-3-yl 2-methylidenebutanedioate

> <ALOGPS_LOGP>
2.23

> <JCHEM_LOGP>
2.552131437333333

> <ALOGPS_LOGS>
-2.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
8.17066057619373

> <JCHEM_POLAR_SURFACE_AREA>
82.14000000000001

> <JCHEM_REFRACTIVITY>
99.68189999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-ethyl (3R,6R)-8-methyl-6-{[(2E)-2-methylbut-2-enoyl]oxy}-8-azabicyclo[3.2.1]octan-3-yl 2-methylidenebutanedioate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0      -7.229  -8.050   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.895  -7.280   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.562  -8.050   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -3.228  -7.280   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -3.228  -5.740   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.894  -8.050   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.894  -9.590   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.561  -7.280   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.773  -8.050   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.773  -9.590   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       2.107  -7.280   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.441  -8.050   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.325  -9.585   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.454 -10.633   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.977 -10.403   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.747  -9.070   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.185  -7.636   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.713  -7.182   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       5.694  -9.351   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       7.028 -10.121   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.283  -9.185   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.150  -7.912   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.686  -8.028   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.482  -6.525   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.350  -5.253   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.682  -3.865   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.946  -6.410   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   12                                                       
CONECT   19   17   14   20                                                  
CONECT   20   19                                                            
CONECT   21   16   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₉NO₆

Average Mass

379.4530 Da

Monoisotopic Mass

379.19949 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

119736-78-6

SMILES

CCOC(=O)C(=C)CC(=O)O[C@@H]1CC2C[C@@H](OC(=O)C(\C)=C\C)C(C1)N2C

InChI Identifier

InChI=1S/C20H29NO6/c1-6-12(3)20(24)27-17-10-14-9-15(11-16(17)21(14)5)26-18(22)8-13(4)19(23)25-7-2/h6,14-17H,4,7-11H2,1-3,5H3/b12-6+/t14?,15-,16?,17-/m1/s1

InChI Key

WMFMZTXHTPOWMQ-WAMNRYJJSA-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
Schizanthus pinnatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tropane alkaloids. These are organic compounds containing the nitrogenous bicyclic alkaloid parent N-Methyl-8-azabicyclo[3.2.1]Octane.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Tropane alkaloids

Sub Class

Not Available

Direct Parent

Tropane alkaloids

Alternative Parents

Substituents

Tropane alkaloid
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
N-alkylpyrrolidine
Piperidine
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Pyrrolidine
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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

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

114545113

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

134715025

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Schizanthine M (NP0138887)

MOL for NP0138887 (Schizanthine M)

3D MOL for NP0138887 (Schizanthine M)

3D SDF for NP0138887 (Schizanthine M)

3D-SDF for NP0138887 (Schizanthine M)

PDB for NP0138887 (Schizanthine M)

3D PDB for NP0138887 (Schizanthine M)

SMILES for NP0138887 (Schizanthine M)

INCHI for NP0138887 (Schizanthine M)

Structure for NP0138887 (Schizanthine M)

3D Structure for NP0138887 (Schizanthine M)