NP-MRD: Showing NP-Card for N-Formyldehydroovigerine (NP0069333)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 14:41:39 UTC

Updated at

2022-04-28 14:41:40 UTC

NP-MRD ID

NP0069333

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N-Formyldehydroovigerine

Description

4,6,19,21-Tetraoxa-13-azahexacyclo[10.10.1.0²,¹⁰.0³,⁷.0¹⁶,²³.0¹⁸,²²]Tricosa-1,3(7),8,10,12(23),16,18(22)-heptaene-13-carbaldehyde 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. N-Formyldehydroovigerine is found in Hernandia sonora. 4,6,19,21-Tetraoxa-13-azahexacyclo[10.10.1.0²,¹⁰.0³,⁷.0¹⁶,²³.0¹⁸,²²]Tricosa-1,3(7),8,10,12(23),16,18(22)-heptaene-13-carbaldehyde is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251515342D          

 25 30  0  0  0  0            999 V2000
   -2.0194    2.1623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2136    1.9852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9640    1.1989    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5202    0.5896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2707   -0.1968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4649   -0.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2154   -1.1602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5904   -1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9980   -2.0545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8061   -1.8885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8980   -1.0687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1466   -0.7280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971    0.0584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0913    0.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1582    1.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3980    1.6311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2037    1.4540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7600    2.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5657    1.8863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8153    1.0999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5667    0.7592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4748   -0.0606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6667   -0.2266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2591    0.4906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4533    0.6677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  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
  8  9  1  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
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
  6 14  2  0  0  0  0
 14 15  1  0  0  0  0
  3 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 13 25  1  0  0  0  0
 17 25  1  0  0  0  0
M  END

     RDKit          3D

 38 43  0  0  0  0  0  0  0  0999 V2000
    5.2859   -0.7146   -1.5003 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0502   -0.9158   -1.4460 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2795   -0.2348   -0.4985 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8017    0.7263    0.4698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0189    1.9950    0.3088 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5742    1.7247    0.4056 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7309    2.7264    0.8767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6059    2.5201    0.9523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1884    1.3049    0.5641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3485    0.3234    0.1015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0279    0.5275    0.0213 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8633   -0.4691   -0.4362 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3452   -1.6736   -0.8197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0116   -1.8795   -0.7433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5394   -3.1071   -1.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8917   -3.3360   -1.0666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7592   -2.3646   -0.6133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2409   -1.1209   -0.2156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8842   -0.9056   -0.2886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3621   -0.4189    0.1670 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4118   -1.3257    0.5303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1484   -2.3427   -0.4495 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5143    1.4784    0.7799 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8695    2.7595    1.2000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6045    3.3759    1.3865 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5994   -1.6040   -2.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6864    0.3486    1.5117 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8675    0.8828    0.2236 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2096    2.3624   -0.7373 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3580    2.7563    1.0528 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1879    3.6575    1.1728 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0173   -2.4547   -1.1815 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1727   -3.8502   -1.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2916   -4.2978   -1.3743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1805   -1.6906    1.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3925   -0.8684    0.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3408    3.3089    0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4906    2.7960    2.1060 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 22  1  0
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  1  0
 19 10  2  0
 10  9  1  0
  9 23  1  0
 23 24  1  0
 24 25  1  0
 25  8  1  0
  8  7  1  0
 12  3  1  0
 19 14  1  0
  8  9  2  0
  7  6  2  0
 10 11  1  0
 18 17  2  0
  2 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
 13 32  1  0
 15 33  1  0
 16 34  1  0
 21 35  1  0
 21 36  1  0
 24 37  1  0
 24 38  1  0
  7 31  1  0
M  END


  Mrv1533004251515342D          

 25 30  0  0  0  0            999 V2000
   -2.0194    2.1623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2136    1.9852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9640    1.1989    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5202    0.5896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2707   -0.1968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4649   -0.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2154   -1.1602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5904   -1.3373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9980   -2.0545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8061   -1.8885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8980   -1.0687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1466   -0.7280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971    0.0584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0913    0.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1582    1.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3980    1.6311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2037    1.4540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7600    2.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5657    1.8863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8153    1.0999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5667    0.7592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4748   -0.0606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6667   -0.2266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2591    0.4906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4533    0.6677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  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
  8  9  1  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
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
  6 14  2  0  0  0  0
 14 15  1  0  0  0  0
  3 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 13 25  1  0  0  0  0
 17 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0069333

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=CN1CCC2=C3C1=CC1=CC=C4OCOC4=C1C3=C1OCOC1=C2

> <INCHI_IDENTIFIER>
InChI=1S/C19H13NO5/c21-7-20-4-3-11-6-14-19(25-9-23-14)17-15(11)12(20)5-10-1-2-13-18(16(10)17)24-8-22-13/h1-2,5-7H,3-4,8-9H2

> <INCHI_KEY>
PUYUAWYAHPMAMP-UHFFFAOYSA-N

> <FORMULA>
C19H13NO5

> <MOLECULAR_WEIGHT>
335.315

> <EXACT_MASS>
335.079372523

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
33.959055580997074

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,6,19,21-tetraoxa-13-azahexacyclo[10.10.1.0²,¹⁰.0³,⁷.0¹⁶,²³.0¹⁸,²²]tricosa-1(22),2,7,9,11,16(23),17-heptaene-13-carbaldehyde

> <ALOGPS_LOGP>
1.85

> <JCHEM_LOGP>
2.2916324990000003

> <ALOGPS_LOGS>
-3.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6191591290558605

> <JCHEM_POLAR_SURFACE_AREA>
57.230000000000004

> <JCHEM_REFRACTIVITY>
87.2902

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.05e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,6,19,21-tetraoxa-13-azahexacyclo[10.10.1.0²,¹⁰.0³,⁷.0¹⁶,²³.0¹⁸,²²]tricosa-1(22),2,7,9,11,16(23),17-heptaene-13-carbaldehyde

> <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  O   UNK     0      -3.769   4.036   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -2.265   3.706   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -1.800   2.238   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -2.838   1.100   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.372  -0.367   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.868  -0.698   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.402  -2.166   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.102  -2.496   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.863  -3.835   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.371  -3.525   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.543  -1.995   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.140  -1.359   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.675   0.109   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.170   0.440   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.295   1.907   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.743   3.045   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.247   2.714   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.285   3.852   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.789   3.521   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.255   2.053   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.658   1.417   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.486  -0.113   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.978  -0.423   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.217   0.916   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.713   1.246   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   15                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    8   13                                                  
CONECT   13   12   14   25                                                  
CONECT   14   13    6   15                                                  
CONECT   15   14    3   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20   25                                                  
CONECT   25   24   13   17                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₃NO₅

Average Mass

335.3150 Da

Monoisotopic Mass

335.07937 Da

IUPAC Name

4,6,19,21-tetraoxa-13-azahexacyclo[10.10.1.0²,¹⁰.0³,⁷.0¹⁶,²³.0¹⁸,²²]tricosa-1(22),2,7,9,11,16(23),17-heptaene-13-carbaldehyde

Traditional Name

4,6,19,21-tetraoxa-13-azahexacyclo[10.10.1.0²,¹⁰.0³,⁷.0¹⁶,²³.0¹⁸,²²]tricosa-1(22),2,7,9,11,16(23),17-heptaene-13-carbaldehyde

CAS Registry Number

Not Available

SMILES

O=CN1CCC2=C3C1=CC1=CC=C4OCOC4=C1C3=C1OCOC1=C2

InChI Identifier

InChI=1S/C19H13NO5/c21-7-20-4-3-11-6-14-19(25-9-23-14)17-15(11)12(20)5-10-1-2-13-18(16(10)17)24-8-22-13/h1-2,5-7H,3-4,8-9H2

InChI Key

PUYUAWYAHPMAMP-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
Hernandia sonora	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
Naphthalene
Quinoline
Benzodioxole
Benzenoid
Tertiary carboxylic acid amide
Carboxamide group
Acetal
Carboxylic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Organopnictogen 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	1.85	ALOGPS
logP	2.29	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.23 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	87.29 m³·mol⁻¹	ChemAxon
Polarizability	33.96 Å³	ChemAxon
Number of Rings	6	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

9997062

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for N-Formyldehydroovigerine (NP0069333)

MOL for NP0069333 (N-Formyldehydroovigerine)

3D MOL for NP0069333 (N-Formyldehydroovigerine)

3D SDF for NP0069333 (N-Formyldehydroovigerine)

3D-SDF for NP0069333 (N-Formyldehydroovigerine)

PDB for NP0069333 (N-Formyldehydroovigerine)

3D PDB for NP0069333 (N-Formyldehydroovigerine)

SMILES for NP0069333 (N-Formyldehydroovigerine)

INCHI for NP0069333 (N-Formyldehydroovigerine)

Structure for NP0069333 (N-Formyldehydroovigerine)

3D Structure for NP0069333 (N-Formyldehydroovigerine)