NP-MRD: Showing NP-Card for Cephasamine (NP0067949)

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Record Information

Version

2.0

Created at

2022-04-28 12:47:22 UTC

Updated at

2022-04-28 12:47:22 UTC

NP-MRD ID

NP0067949

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cephasamine

Description

Cephasamine belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic. Cephasamine is found in Stephania cephalantha and Stephania cepharantha Hayata . Based on a literature review very few articles have been published on Cephasamine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214472D          

 26 30  0  0  1  0            999 V2000
   -0.8959   -0.5703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0075   -1.4636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2807   -1.8282    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2423   -1.2103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3637   -0.4326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0464    0.0527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8310    0.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1323    0.9628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9781    1.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4970    0.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1804   -0.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3555   -0.4436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0632   -1.1913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2961    1.8186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1143    1.9239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4192    1.4019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2426    0.8903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0589    1.0791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6347    0.4889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3250   -0.2663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8415   -0.9096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4446    0.6462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9858    0.0236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2910    1.8708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0927    2.0656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1154   -2.6364    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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  2  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  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
  4 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
  8 16  1  0  0  0  0
 17 16  1  1  0  0  0
  6 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
  5 20  1  1  0  0  0
 20 21  2  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 26  1  0  0  0  0
M  END

     RDKit          3D

 49 53  0  0  0  0  0  0  0  0999 V2000
    4.6477    1.1004   -0.8923 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3211    1.2112   -1.3971 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3238    0.6603   -0.5714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8233    1.3740    0.4403 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3399    2.6514    0.6112 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1742    3.6832   -0.3289 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7918    0.9097    1.3579 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3908    1.7430    1.3316 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2080    1.2787    0.3051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2179    1.8162   -0.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5902    3.1236   -0.3017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5895    3.7745   -1.0349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8357    1.0275   -1.4546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4483   -0.2940   -1.6315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4527   -0.8314   -0.8528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8855   -0.0153    0.0752 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1863   -0.4122    1.0084 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3881   -1.1120    2.2158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0306   -2.4066    1.8585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1565   -3.2237    1.0417 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046   -4.5173    0.7903 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2446   -2.5251   -0.1702 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9677   -2.2164   -0.9681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0755   -1.3587    0.2587 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8201   -0.6852   -0.7982 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0349   -1.2423   -1.8985 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7397    1.6219    0.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3954    1.4982   -1.5829 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8757    0.0302   -0.6987 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5960    3.4535   -1.3228 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0832    3.9246   -0.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6866    4.5793    0.0628 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1863    0.8950    2.3854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5869    3.7356   -0.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3080    4.8651   -1.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6973    3.4402   -2.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6235    1.4017   -2.0924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9065   -0.9414   -2.3757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1920   -0.4252    2.6131 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3828   -1.2807    2.9749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1865   -2.9795    2.8112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0448   -2.2922    1.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2488   -5.2274    1.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3253   -4.8639   -0.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7958   -4.5727    0.7770 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8704   -3.2645   -0.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7975   -2.8944   -0.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8400   -2.4625   -2.0649 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8198   -1.7539    1.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 10  1  0
 10 13  2  0
 13 14  1  0
 14 15  2  0
 15 23  1  0
 23 22  1  0
 22 24  1  0
 24 25  1  0
 25 26  2  0
 25  3  1  0
  3  2  1  0
  2  1  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  4  7  1  0
  7  8  1  0
  8  9  1  0
  9 16  2  0
 16 17  1  0
 17 18  1  1
 18 19  1  0
 19 20  1  0
 20 21  1  0
  9 10  1  0
 16 15  1  0
 20 22  1  0
 17 24  1  0
 17  7  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  0
 14 38  1  0
 23 47  1  0
 23 48  1  0
 22 46  1  6
 24 49  1  1
  1 27  1  0
  1 28  1  0
  1 29  1  0
  6 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  1
 18 39  1  0
 18 40  1  0
 19 41  1  0
 19 42  1  0
 21 43  1  0
 21 44  1  0
 21 45  1  0
M  END


  Mrv1652304282214472D          

 26 30  0  0  1  0            999 V2000
   -0.8959   -0.5703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0075   -1.4636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2807   -1.8282    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2423   -1.2103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3637   -0.4326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0464    0.0527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8310    0.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1323    0.9628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9781    1.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4970    0.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1804   -0.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3555   -0.4436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0632   -1.1913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2961    1.8186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1143    1.9239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4192    1.4019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2426    0.8903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0589    1.0791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6347    0.4889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3250   -0.2663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8415   -0.9096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4446    0.6462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9858    0.0236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2910    1.8708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0927    2.0656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1154   -2.6364    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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  2  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  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
  4 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
  8 16  1  0  0  0  0
 17 16  1  1  0  0  0
  6 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
  5 20  1  1  0  0  0
 20 21  2  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067949

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C[C@H]3[C@H]4C(=O)C(OC)=C(OC)[C@H]5OC1=C2[C@@]45CCN3C

> <INCHI_IDENTIFIER>
InChI=1S/C20H23NO5/c1-21-8-7-20-13-10-5-6-12(23-2)16(13)26-19(20)18(25-4)17(24-3)15(22)14(20)11(21)9-10/h5-6,11,14,19H,7-9H2,1-4H3/t11-,14-,19+,20-/m0/s1

> <INCHI_KEY>
MCTHALKBVQHAHJ-MKXBKGISSA-N

> <FORMULA>
C20H23NO5

> <MOLECULAR_WEIGHT>
357.406

> <EXACT_MASS>
357.157622845

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
37.06223408819637

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,5S,13S,17S)-10,14,15-trimethoxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0^{1,13}.0^{5,17}.0^{7,18}]octadeca-7,9,11(18),14-tetraen-16-one

> <ALOGPS_LOGP>
1.90

> <JCHEM_LOGP>
0.968453421333333

> <ALOGPS_LOGS>
-2.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.33408413064868

> <JCHEM_PKA_STRONGEST_BASIC>
8.131723086502657

> <JCHEM_POLAR_SURFACE_AREA>
57.230000000000004

> <JCHEM_REFRACTIVITY>
97.17229999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.11e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,5S,13S,17S)-10,14,15-trimethoxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0^{1,13}.0^{5,17}.0^{7,18}]octadeca-7,9,11(18),14-tetraen-16-one

> <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      -1.672  -1.065   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.881  -2.732   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -0.524  -3.413   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       0.452  -2.259   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.679  -0.807   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.087   0.098   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.551   0.365   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.114   1.797   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.692   1.974   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.661   0.747   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.070  -0.671   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.530  -0.828   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.985  -2.224   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.286   3.395   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.813   3.591   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.782   2.617   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.453   1.662   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.977   2.014   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.052   0.913   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.473  -0.497   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -3.437  -1.698   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -4.563   1.206   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -5.573   0.044   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.410   3.492   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -3.906   3.856   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.215  -4.921   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   26                                                  
CONECT    4    3    5   13                                                  
CONECT    5    4    6   20                                                  
CONECT    6    5    1    7   17                                             
CONECT    7    6    8   12                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    7   13                                                  
CONECT   13   12    4                                                       
CONECT   14    9   15                                                       
CONECT   15   14                                                            
CONECT   16    8   17                                                       
CONECT   17   16    6   18                                                  
CONECT   18   17   19   24                                                  
CONECT   19   18   20   22                                                  
CONECT   20   19    5   21                                                  
CONECT   21   20                                                            
CONECT   22   19   23                                                       
CONECT   23   22                                                            
CONECT   24   18   25                                                       
CONECT   25   24                                                            
CONECT   26    3                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₃NO₅

Average Mass

357.4060 Da

Monoisotopic Mass

357.15762 Da

IUPAC Name

(1R,5S,13S,17S)-10,14,15-trimethoxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0^{1,13}.0^{5,17}.0^{7,18}]octadeca-7,9,11(18),14-tetraen-16-one

Traditional Name

(1R,5S,13S,17S)-10,14,15-trimethoxy-4-methyl-12-oxa-4-azapentacyclo[9.6.1.0^{1,13}.0^{5,17}.0^{7,18}]octadeca-7,9,11(18),14-tetraen-16-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C2C[C@H]3[C@H]4C(=O)C(OC)=C(OC)[C@H]5OC1=C2[C@@]45CCN3C

InChI Identifier

InChI=1S/C20H23NO5/c1-21-8-7-20-13-10-5-6-12(23-2)16(13)26-19(20)18(25-4)17(24-3)15(22)14(20)11(21)9-10/h5-6,11,14,19H,7-9H2,1-4H3/t11-,14-,19+,20-/m0/s1

InChI Key

MCTHALKBVQHAHJ-MKXBKGISSA-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
Stephania cephalantha	LOTUS Database	35616633
Stephania cepharantha Hayata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Morphinans

Sub Class

Not Available

Direct Parent

Morphinans

Alternative Parents

Substituents

Morphinan
Phenanthrene
Azaphilone
Tetralin
Coumaran
Anisole
Phenol ether
Cyclohexenone
Aralkylamine
Alkyl aryl ether
Piperidine
Benzenoid
Vinylogous ester
Tertiary aliphatic amine
Tertiary amine
Ketone
Organoheterocyclic compound
Azacycle
Ether
Oxacycle
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Carbonyl group
Amine
Organic oxide
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	1.9	ALOGPS
logP	0.97	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	16.33	ChemAxon
pKa (Strongest Basic)	8.13	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.23 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	97.17 m³·mol⁻¹	ChemAxon
Polarizability	37.06 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

C00025792

Chemspider ID

9967334

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11792660

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Cephasamine (NP0067949)

MOL for NP0067949 (Cephasamine)

3D MOL for NP0067949 (Cephasamine)

3D SDF for NP0067949 (Cephasamine)

3D-SDF for NP0067949 (Cephasamine)

PDB for NP0067949 (Cephasamine)

3D PDB for NP0067949 (Cephasamine)

SMILES for NP0067949 (Cephasamine)

INCHI for NP0067949 (Cephasamine)

Structure for NP0067949 (Cephasamine)

3D Structure for NP0067949 (Cephasamine)