NP-MRD: Showing NP-Card for Dehydroglaucine (NP0069779)

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Record Information

Version

2.0

Created at

2022-04-28 15:07:19 UTC

Updated at

2022-04-28 15:07:19 UTC

NP-MRD ID

NP0069779

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Dehydroglaucine

Description

4,5,15,16-Tetramethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]Heptadeca-1,3,5,7,9(17),11,13,15-octaene belongs to the class of organic compounds known as aporphines. These are quinoline alkaloids containing the dibenzo[de,g]quinoline ring system or a dehydrogenated derivative thereof. Dehydroglaucine is found in Glaucium flavum, Glaucium flavum Crantz. , Liriodendron tulipifera , Platycapnos spicata, Sarcocapnos enneaphylla, Sarcocapnos saetabensis, Thalictrum ichengense and Xylopia aromatica . 4,5,15,16-Tetramethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]Heptadeca-1,3,5,7,9(17),11,13,15-octaene is a moderately basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261500132D          

 26 29  0  0  0  0            999 V2000
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  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
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 20 21  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
  3 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 26  1  0  0  0  0
  7 26  1  0  0  0  0
 12 26  2  0  0  0  0
M  END

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
    5.2215   -2.3358    0.2756 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8143   -0.9851    0.2216 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4638   -0.7190    0.1788 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5218   -1.7186    0.1868 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809   -1.3838    0.1409 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2319   -2.3884    0.1976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0949   -2.0525    0.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5319   -0.7470    0.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8901   -0.4723    0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3096    0.8374    0.0956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4139    1.8684    0.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7481    3.1997   -0.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0475    3.7037   -0.0310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0336    1.5688    0.0140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1993    2.6653   -0.0738 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0269    3.2578   -1.3898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5752    0.2900    0.0747 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7750   -0.0461    0.0815 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7191    0.9498    0.0788 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0682    0.6002    0.1267 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9918    1.6351    0.1196 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6247    2.9909    0.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9057   -1.5272    0.2204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4671   -2.7736    0.2735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0644   -3.0772    0.2647 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6225   -4.4403    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2931   -2.4494    0.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6374   -2.7919    1.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9792   -2.9124   -0.6215 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8085   -2.7670    0.2284 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5407   -3.4311    0.2406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3567    1.0571    0.1059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8171    3.0293    0.3487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0488    4.6202    0.6075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3139    4.0525   -1.0502 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8504    3.9567   -1.2584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9042    3.6744   -1.7907 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3646    2.4105   -2.0169 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5257    1.9751    0.0958 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0634    3.1145   -0.9051 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9110    3.2497    0.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4715    3.6731    0.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9642   -1.2984    0.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1752   -3.5715    0.3241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2434   -4.8335   -0.6402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8719   -4.5869    1.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4864   -5.0712    0.6136 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 11  1  0
 11 10  2  0
 10  9  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 20  2  0
 20 21  1  0
 21 22  1  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 14  2  0
 14 15  1  0
 15 16  1  0
  7 25  1  0
 25 26  1  0
 25 24  1  0
 24 23  2  0
 14 11  1  0
 23  9  1  0
 17  8  1  0
 18  5  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 10 32  1  0
  6 31  1  0
  4 30  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
 22 40  1  0
 22 41  1  0
 22 42  1  0
 19 39  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 26 45  1  0
 26 46  1  0
 26 47  1  0
 24 44  1  0
 23 43  1  0
M  END


  Mrv1533004261500132D          

 26 29  0  0  0  0            999 V2000
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  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
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 20 21  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
  3 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 26  1  0  0  0  0
  7 26  1  0  0  0  0
 12 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0069779

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3C(=CC4=CC(OC)=C(OC)C=C4C3=C1OC)N(C)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C21H21NO4/c1-22-7-6-12-9-18(25-4)21(26-5)20-14-11-17(24-3)16(23-2)10-13(14)8-15(22)19(12)20/h6-11H,1-5H3

> <INCHI_KEY>
XTZOEAMYNLFKGH-UHFFFAOYSA-N

> <FORMULA>
C21H21NO4

> <MOLECULAR_WEIGHT>
351.402

> <EXACT_MASS>
351.14705816

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
38.73736299100207

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,5,15,16-tetramethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(16),2,4,6,8,11,13(17),14-octaene

> <ALOGPS_LOGP>
3.72

> <JCHEM_LOGP>
3.5641256766666656

> <ALOGPS_LOGS>
-5.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
1.4076825887441489

> <JCHEM_POLAR_SURFACE_AREA>
40.160000000000004

> <JCHEM_REFRACTIVITY>
102.6425

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.45e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5,15,16-tetramethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(16),2,4,6,8,11,13(17),14-octaene

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       2.667  -3.080   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.669   0.000   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   26                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   26                                                  
CONECT   21   20    5   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22    3   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   20    7   12                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₁NO₄

Average Mass

351.4020 Da

Monoisotopic Mass

351.14706 Da

IUPAC Name

4,5,15,16-tetramethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(16),2,4,6,8,11,13(17),14-octaene

Traditional Name

4,5,15,16-tetramethoxy-10-methyl-10-azatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadeca-1(16),2,4,6,8,11,13(17),14-octaene

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3C(=CC4=CC(OC)=C(OC)C=C4C3=C1OC)N(C)C=C2

InChI Identifier

InChI=1S/C21H21NO4/c1-22-7-6-12-9-18(25-4)21(26-5)20-14-11-17(24-3)16(23-2)10-13(14)8-15(22)19(12)20/h6-11H,1-5H3

InChI Key

XTZOEAMYNLFKGH-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
Glaucium flavum	LOTUS Database	35616633
Glaucium flavum Crantz.	Plant	KNApSAcK
Liriodendron tulipifera	Plant	KNApSAcK
Platycapnos spicata	Plant	KNApSAcK
Sarcocapnos enneaphylla	Plant	KNApSAcK
Sarcocapnos saetabensis	Plant	KNApSAcK
Thalictrum ichangense	Plant	KNApSAcK
Xylopia aromatica	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aporphines. These are quinoline alkaloids containing the dibenzo[de,g]quinoline ring system or a dehydrogenated derivative thereof.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aporphines

Sub Class

Not Available

Direct Parent

Aporphines

Alternative Parents

Substituents

Aporphine
Benzoquinoline
Phenanthrene
Isoquinoline
Quinoline
Naphthalene
Anisole
Phenol ether
Alkyl aryl ether
Benzenoid
Pyridine
Heteroaromatic compound
Azacycle
Ether
Organoheterocyclic compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
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	3.72	ALOGPS
logP	3.56	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Basic)	1.41	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	102.64 m³·mol⁻¹	ChemAxon
Polarizability	38.74 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

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

13857125

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Dehydroglaucine (NP0069779)

MOL for NP0069779 (Dehydroglaucine)

3D MOL for NP0069779 (Dehydroglaucine)

3D SDF for NP0069779 (Dehydroglaucine)

3D-SDF for NP0069779 (Dehydroglaucine)

PDB for NP0069779 (Dehydroglaucine)

3D PDB for NP0069779 (Dehydroglaucine)

SMILES for NP0069779 (Dehydroglaucine)

INCHI for NP0069779 (Dehydroglaucine)

Structure for NP0069779 (Dehydroglaucine)

3D Structure for NP0069779 (Dehydroglaucine)