NP-MRD: Showing NP-Card for N-Methylsecoglaucine (NP0069224)

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Record Information

Version

2.0

Created at

2022-04-28 14:33:58 UTC

Updated at

2022-04-28 14:33:58 UTC

NP-MRD ID

NP0069224

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N-Methylsecoglaucine

Description

Dimethyl[2-(3,4,6,7-tetramethoxyphenanthren-1-yl)ethyl]amine belongs to the class of organic compounds known as 6,6a-secoaporphines. These are alkaloids with a structure that contains an aminoethylphenanthrene moiety. N-Methylsecoglaucine is found in Phoebe minutiflora, Phoenicanthus obliqua, Platycapnos spicata and Sarcocapnos enneaphylla. Dimethyl[2-(3,4,6,7-tetramethoxyphenanthren-1-yl)ethyl]amine is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251502502D          

 27 29  0  0  0  0            999 V2000
    0.7954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    2.0329    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079   -2.2539    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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 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
 19 22  2  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
  3 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -5.5234   -3.6571   -0.0888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5257   -2.2456   -0.0962 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2803   -1.5948   -0.0635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1259   -2.3362   -0.0257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8891   -1.7079    0.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7544   -2.4818    0.0786 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4636   -1.8780    0.1457 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5118   -0.5093    0.1357 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7649    0.0636    0.2165 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9749   -0.7777    0.2911 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1839    0.1062    0.4608 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3695   -0.7666    0.5177 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.4947   -1.3253   -0.8357 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1781   -1.8490    1.4669 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8901    1.4335    0.2183 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7745    2.2303    0.1370 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9392    3.6105    0.1422 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1851    4.2353    0.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5006    1.6612    0.0510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5132    2.5728   -0.0395 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7749    3.1381   -1.3820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6214    0.3124    0.0556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8670   -0.3087   -0.0060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9967    0.4321   -0.0384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2392   -0.2290   -0.0696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3805    0.5357   -0.1059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3045    1.9298   -0.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5192   -4.0833    0.0384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9429   -3.9598    0.8261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0059   -4.0041   -1.0168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1212   -3.4224   -0.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8349   -3.5495    0.0812 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4007   -2.4622    0.2076 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9638   -1.4755    1.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0859   -1.3935   -0.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1516    0.7186    1.3602 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3635    0.7117   -0.4758 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5650   -1.4386   -1.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0217   -0.6333   -1.5478 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9632   -2.2807   -0.8478 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1737   -2.2828    1.6789 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586   -1.5106    2.4334 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5876   -2.6878    1.0078 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8768    1.8611    0.2832 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0131    5.2968    0.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8526    3.7728    0.9535 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6587    4.1693   -0.7882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8911    3.6564   -1.7309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7057    3.6866   -1.3144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9165    2.2463   -2.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0287    1.4919    0.0069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7582    2.3352   -0.9866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8102    2.2873    0.7960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3354    2.3552   -0.1591 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 16  1  0
 16 15  2  0
 15  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
  9  8  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3 25  2  0
 25 26  1  0
 26 27  1  0
 25 24  1  0
 24 23  2  0
 23 22  1  0
 22 19  2  0
 19 20  1  0
 20 21  1  0
 19 16  1  0
 22  8  1  0
 23  5  1  0
 18 45  1  0
 18 46  1  0
 18 47  1  0
 15 44  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 13 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 14 43  1  0
  7 33  1  0
  6 32  1  0
  4 31  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 27 52  1  0
 27 53  1  0
 27 54  1  0
 24 51  1  0
 21 48  1  0
 21 49  1  0
 21 50  1  0
M  END


  Mrv1533004251502502D          

 27 29  0  0  0  0            999 V2000
    0.7954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579    2.0329    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079   -2.2539    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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 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
 19 22  2  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
  3 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0069224

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(CCN(C)C)=C2C=CC3=CC(OC)=C(OC)C=C3C2=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C22H27NO4/c1-23(2)10-9-15-12-20(26-5)22(27-6)21-16(15)8-7-14-11-18(24-3)19(25-4)13-17(14)21/h7-8,11-13H,9-10H2,1-6H3

> <INCHI_KEY>
IYAWRUZJOPTSGN-UHFFFAOYSA-N

> <FORMULA>
C22H27NO4

> <MOLECULAR_WEIGHT>
369.461

> <EXACT_MASS>
369.194008353

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.11536001854649

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
dimethyl[2-(3,4,6,7-tetramethoxyphenanthren-1-yl)ethyl]amine

> <ALOGPS_LOGP>
3.60

> <JCHEM_LOGP>
3.5515722386666657

> <ALOGPS_LOGS>
-4.81

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.316469322147183

> <JCHEM_POLAR_SURFACE_AREA>
40.160000000000004

> <JCHEM_REFRACTIVITY>
108.1089

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.66e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
dimethyl[2-(3,4,6,7-tetramethoxyphenanthren-1-yl)ethyl]amine

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       1.485  -2.874   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.255  -1.540   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.495   1.127   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.725   2.461   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      11.495   3.795   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      10.725   5.128   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.035   3.795   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      11.495  -4.207   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.725  -5.541   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.415  -4.207   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.875  -4.207   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.795  -4.207   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.255  -4.207   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   22                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    9   16                                                       
CONECT   16   15   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19    8   23                                                  
CONECT   23   22    5   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24    3   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₇NO₄

Average Mass

369.4610 Da

Monoisotopic Mass

369.19401 Da

IUPAC Name

dimethyl[2-(3,4,6,7-tetramethoxyphenanthren-1-yl)ethyl]amine

Traditional Name

dimethyl[2-(3,4,6,7-tetramethoxyphenanthren-1-yl)ethyl]amine

CAS Registry Number

Not Available

SMILES

COC1=CC(CCN(C)C)=C2C=CC3=CC(OC)=C(OC)C=C3C2=C1OC

InChI Identifier

InChI=1S/C22H27NO4/c1-23(2)10-9-15-12-20(26-5)22(27-6)21-16(15)8-7-14-11-18(24-3)19(25-4)13-17(14)21/h7-8,11-13H,9-10H2,1-6H3

InChI Key

IYAWRUZJOPTSGN-UHFFFAOYSA-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
Phoebe minutiflora	Plant	KNApSAcK
Phoenicanthus obliqua	Plant	KNApSAcK
Platycapnos spicata	Plant	KNApSAcK
Sarcocapnos enneaphylla	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 6,6a-secoaporphines. These are alkaloids with a structure that contains an aminoethylphenanthrene moiety.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

6,6a-secoaporphines

Sub Class

Not Available

Direct Parent

6,6a-secoaporphines

Alternative Parents

Substituents

6,6a-secoaporphine
Phenanthrene
Naphthalene
Phenethylamine
Anisole
Alkyl aryl ether
Aralkylamine
Benzenoid
Tertiary amine
Tertiary aliphatic amine
Ether
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Amine
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	3.6	ALOGPS
logP	3.55	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	9.32	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	40.16 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	108.11 m³·mol⁻¹	ChemAxon
Polarizability	42.12 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for N-Methylsecoglaucine (NP0069224)

MOL for NP0069224 (N-Methylsecoglaucine)

3D MOL for NP0069224 (N-Methylsecoglaucine)

3D SDF for NP0069224 (N-Methylsecoglaucine)

3D-SDF for NP0069224 (N-Methylsecoglaucine)

PDB for NP0069224 (N-Methylsecoglaucine)

3D PDB for NP0069224 (N-Methylsecoglaucine)

SMILES for NP0069224 (N-Methylsecoglaucine)

INCHI for NP0069224 (N-Methylsecoglaucine)

Structure for NP0069224 (N-Methylsecoglaucine)

3D Structure for NP0069224 (N-Methylsecoglaucine)