NP-MRD: Showing NP-Card for 6-hydroxyprotopine (NP0209764)

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Record Information

Version

2.0

Created at

2022-09-05 07:18:32 UTC

Updated at

2022-09-05 07:18:32 UTC

NP-MRD ID

NP0209764

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-hydroxyprotopine

Description

6-Hydroxyprotopine belongs to the class of organic compounds known as protopine alkaloids. These are alkaloids with a structure based on a tricyclic protopine formed by oxidative ring fission of protoberberine N-metho salts. 6-hydroxyprotopine is found in Apis cerana. 6-Hydroxyprotopine is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251516412D          

 27 31  0  0  0  0            999 V2000
    1.2459   -0.7858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0828    0.0229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3009    0.2860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1378    1.0947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7566    1.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5385    1.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1574    1.9228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9943    2.7315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9393    1.6597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5581    2.2053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3400    1.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5031    1.1334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8843    0.5878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1024    0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4835    0.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7016    0.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0450    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3226    1.0386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6661    1.7887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0588    2.3471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5935    2.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1884    2.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8072    2.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6441    1.3579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3629    0.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9702    1.5113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6267    2.2614    0.0000 O   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  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
  4 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  1  0  0  0  0
M  END

     RDKit          3D

 46 50  0  0  0  0  0  0  0  0999 V2000
   -1.5674    3.1238   -0.7380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1564    1.7654   -0.4501 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8531    0.7890   -1.2182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2848   -0.4036   -0.4225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5594   -1.5715   -0.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0766   -2.5973    0.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2654   -2.5088    1.1118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9760   -1.3420    1.0243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4954   -0.3039    0.2694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4021    0.7356    0.3578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6338    0.2332    0.8377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1882   -0.9130    1.5705 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2838   -1.7712   -1.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8715   -2.0531   -0.1534 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8958   -3.2143    0.3911 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9824   -1.1893    0.1687 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2766   -1.7378    0.0694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4180   -1.0282    0.3358 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3525    0.2776    0.7205 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0999    0.8421    0.8279 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9234    0.1261    0.5582 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6784    0.9081    0.7648 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2781    1.6703   -0.4655 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8380    2.9562   -0.4859 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6422    0.7609    0.9263 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5449   -0.1631    0.3500 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7792   -1.3580    0.3042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4355    3.0360   -1.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8699    3.6699    0.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7695    3.7228   -1.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2722    0.5455   -2.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7879    1.2849   -1.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5064   -3.5219    0.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6340   -3.3478    1.7098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3465   -0.0169    0.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0676    0.9225    1.6095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4104   -2.7320   -1.6332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0522   -1.0295   -1.8187 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4343   -2.7792   -0.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0571    1.8777    1.1336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1235    0.2955    1.2172 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8651    1.7073    1.5441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6779    1.1659   -1.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1276    3.2294    0.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7969    0.2056   -0.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4778   -0.2691    0.9207 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 25  1  0
 25 26  1  0
 26 27  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 23  2  1  0
 12  8  1  0
  9  4  1  0
 21 16  1  0
 27 18  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
 13 37  1  0
 13 38  1  0
 17 39  1  0
 26 45  1  0
 26 46  1  0
 20 40  1  0
 22 41  1  0
 22 42  1  0
 23 43  1  6
 24 44  1  0
  6 33  1  0
  7 34  1  0
 11 35  1  0
 11 36  1  0
M  END


  Mrv1533004251516412D          

 27 31  0  0  0  0            999 V2000
    1.2459   -0.7858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0828    0.0229    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3009    0.2860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1378    1.0947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7566    1.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5385    1.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1574    1.9228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9943    2.7315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9393    1.6597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5581    2.2053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3400    1.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5031    1.1334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8843    0.5878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1024    0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4835    0.3054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7016    0.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0450    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3226    1.0386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6661    1.7887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0588    2.3471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5935    2.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1884    2.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8072    2.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6441    1.3579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3629    0.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9702    1.5113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6267    2.2614    0.0000 O   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  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 11 20  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
  4 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0209764

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1CC2=C(CC(=O)C3=CC4=C(OCO4)C=C3CC1O)C=CC1=C2OCO1

> <INCHI_IDENTIFIER>
InChI=1S/C20H19NO6/c1-21-8-14-11(2-3-16-20(14)27-10-24-16)4-15(22)13-7-18-17(25-9-26-18)5-12(13)6-19(21)23/h2-3,5,7,19,23H,4,6,8-10H2,1H3

> <INCHI_KEY>
QRZCXUNTBXMAPR-UHFFFAOYSA-N

> <FORMULA>
C20H19NO6

> <MOLECULAR_WEIGHT>
369.373

> <EXACT_MASS>
369.121237336

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
37.43157722736189

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14-hydroxy-15-methyl-7,9,19,21-tetraoxa-15-azapentacyclo[15.7.0.0⁴,¹².0⁶,¹⁰.0¹⁸,²²]tetracosa-1(17),4,6(10),11,18(22),23-hexaen-3-one

> <ALOGPS_LOGP>
1.20

> <JCHEM_LOGP>
2.0000599553333327

> <ALOGPS_LOGS>
-2.86

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.824608338010016

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.41188996559293

> <JCHEM_PKA_STRONGEST_BASIC>
3.3084515943523725

> <JCHEM_POLAR_SURFACE_AREA>
77.46000000000002

> <JCHEM_REFRACTIVITY>
95.70910000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.15e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxyprotopine

> <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       2.326  -1.467   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       2.021   0.043   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       0.562   0.534   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.257   2.044   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.412   3.062   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.872   2.571   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.027   3.589   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.723   5.099   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.487   3.098   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.642   4.116   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.101   3.625   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.406   2.116   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.251   1.097   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.791   1.588   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.636   0.570   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.176   1.061   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.817   2.461   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       9.936   1.939   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.577   3.339   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.443   4.381   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.108   4.572   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.352   5.063   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.507   4.044   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.202   2.535   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.544   1.779   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -3.678   2.821   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -3.037   4.221   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   16                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   24                                                  
CONECT    5    4    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   20                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15    2   17                                                  
CONECT   17   16                                                            
CONECT   18   12   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   11                                                       
CONECT   21    5   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23    4   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   23                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Value	Source
10-Hydroxyprotopine	ChEBI
8-Hydroxy-7-methyl-6,8,9,16-tetrahydrobis[1,3]benzodioxolo[4,5-c:5',6'-g]azecin-15(7H)-one	ChEBI

Chemical Formula

C₂₀H₁₉NO₆

Average Mass

369.3730 Da

Monoisotopic Mass

369.12124 Da

IUPAC Name

14-hydroxy-15-methyl-7,9,19,21-tetraoxa-15-azapentacyclo[15.7.0.0⁴,¹².0⁶,¹⁰.0¹⁸,²²]tetracosa-1(17),4,6(10),11,18(22),23-hexaen-3-one

Traditional Name

6-hydroxyprotopine

CAS Registry Number

Not Available

SMILES

CN1CC2=C(CC(=O)C3=CC4=C(OCO4)C=C3CC1O)C=CC1=C2OCO1

InChI Identifier

InChI=1S/C20H19NO6/c1-21-8-14-11(2-3-16-20(14)27-10-24-16)4-15(22)13-7-18-17(25-9-26-18)5-12(13)6-19(21)23/h2-3,5,7,19,23H,4,6,8-10H2,1H3

InChI Key

QRZCXUNTBXMAPR-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, 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
Apis cerana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as protopine alkaloids. These are alkaloids with a structure based on a tricyclic protopine formed by oxidative ring fission of protoberberine N-metho salts.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Protopine alkaloids

Sub Class

Not Available

Direct Parent

Protopine alkaloids

Alternative Parents

Substituents

Protopine skeleton
Benzodioxole
Aryl ketone
Aryl alkyl ketone
Benzenoid
Hemiaminal
Ketone
Organoheterocyclic compound
Alkanolamine
Acetal
Azacycle
Oxacycle
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

tertiary amino compound (CHEBI:17104 )
hemiaminal (CHEBI:17104 )
dibenzazecine alkaloid (CHEBI:17104 )
Isoquinoline alkaloids (C05190 )

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	1.2	ALOGPS
logP	2	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	13.41	ChemAxon
pKa (Strongest Basic)	3.31	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	77.46 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	95.71 m³·mol⁻¹	ChemAxon
Polarizability	37.43 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

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C05190

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

440587

PDB ID

Not Available

ChEBI ID

17104

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-hydroxyprotopine (NP0209764)

MOL for NP0209764 (6-hydroxyprotopine)

3D MOL for NP0209764 (6-hydroxyprotopine)

3D SDF for NP0209764 (6-hydroxyprotopine)

3D-SDF for NP0209764 (6-hydroxyprotopine)

PDB for NP0209764 (6-hydroxyprotopine)

3D PDB for NP0209764 (6-hydroxyprotopine)

SMILES for NP0209764 (6-hydroxyprotopine)

INCHI for NP0209764 (6-hydroxyprotopine)

Structure for NP0209764 (6-hydroxyprotopine)

3D Structure for NP0209764 (6-hydroxyprotopine)