NP-MRD: Showing NP-Card for 16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one (NP0289865)

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Record Information

Version

2.0

Created at

2022-09-09 20:15:40 UTC

Updated at

2022-09-09 20:15:40 UTC

NP-MRD ID

NP0289865

Secondary Accession Numbers

None

Natural Product Identification

Common Name

16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one

Description

ZINC34645716 belongs to the class of organic compounds known as isoquinolones and derivatives. These are aromatic polycyclic compounds containing a ketone bearing isoquinoline moiety. 16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one is found in Coptis japonica, Coptis trifolia and Nandina domestica. Based on a literature review very few articles have been published on ZINC34645716.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092222152D          

 24 28  0  0  0  0            999 V2000
   -0.1991   -1.8461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6258   -1.8587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0274   -2.5793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8523   -2.5919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2538   -3.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0788   -3.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021   -2.6170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3270   -2.6295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7503   -1.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5752   -1.9340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9768   -2.6546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5535   -3.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7286   -3.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3052   -4.0583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4803   -4.0458    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0570   -4.7539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2321   -4.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8305   -4.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0056   -4.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6040   -3.2875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2209   -3.2749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0961   -3.9842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8548   -3.6601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7811   -2.8384    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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  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
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  2  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 24  1  0  0  0  0
M  END

     RDKit          3D

 39 43  0  0  0  0  0  0  0  0999 V2000
    4.4665    2.8811   -0.3881 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6293    1.7789    0.4966 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8889    0.6380    0.2491 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5488    0.7256    0.1740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6992   -0.4413   -0.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3745   -0.2787   -0.1476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2619    1.0124    0.0315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5824    1.0812   -0.0451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2500    2.2863    0.1171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6069    2.4206    0.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3696    1.3184   -0.1911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7466    0.0984   -0.3588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3619   -0.0391   -0.2897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8251   -1.2409   -0.4601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4023   -1.4269   -0.3967 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0861   -2.7521   -0.5892 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5410   -2.9604   -0.5350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3099   -1.7434   -0.2699 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6512   -1.8276   -0.1941 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4809   -0.6685    0.0626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7347   -0.7535    0.1323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7370   -0.8536   -0.5887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0014   -0.3092   -0.2848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7380    1.0796   -0.3238 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7317    2.6238   -1.4334 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1589    3.6974   -0.0722 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4248    3.2572   -0.4031 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0979    1.6815    0.3093 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2582    1.9272    0.2234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6619    3.1972    0.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1193    3.3768    0.1791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4611   -2.0935   -0.6491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3823   -3.3611    0.2501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3268   -3.1609   -1.5572 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8027   -3.7641    0.2211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8825   -3.3947   -1.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1343   -2.7843   -0.3273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3014   -0.6218    0.7359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7661   -0.6060   -1.0386 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 22  1  0
 22 23  1  0
 23 24  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 20  3  1  0
 18  5  1  0
 15  6  1  0
 13  8  1  0
 24 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  7 29  1  0
  9 30  1  0
 10 31  1  0
 23 38  1  0
 23 39  1  0
 14 32  1  0
 16 33  1  0
 16 34  1  0
 17 35  1  0
 17 36  1  0
 19 37  1  0
M  END


  Mrv1652309092222152D          

 24 28  0  0  0  0            999 V2000
   -0.1991   -1.8461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6258   -1.8587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0274   -2.5793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8523   -2.5919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2538   -3.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0788   -3.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5021   -2.6170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3270   -2.6295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7503   -1.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5752   -1.9340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9768   -2.6546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5535   -3.3627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7286   -3.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3052   -4.0583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4803   -4.0458    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0570   -4.7539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2321   -4.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8305   -4.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0056   -4.0081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6040   -3.2875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2209   -3.2749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0961   -3.9842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8548   -3.6601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7811   -2.8384    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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  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
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  2  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0289865

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3C=C4C=CC5=C(OCO5)C4=CN3CCC2=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C19H15NO4/c1-22-18-8-13-12(7-16(18)21)4-5-20-9-14-11(6-15(13)20)2-3-17-19(14)24-10-23-17/h2-3,6-9H,4-5,10H2,1H3

> <INCHI_KEY>
PGIOBGCIEGZHJH-UHFFFAOYSA-N

> <FORMULA>
C19H15NO4

> <MOLECULAR_WEIGHT>
321.332

> <EXACT_MASS>
321.100107967

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
34.17141790050748

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one

> <JCHEM_LOGP>
-0.2420623859999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.216249808231808

> <JCHEM_PKA_STRONGEST_BASIC>
4.765624136635202

> <JCHEM_POLAR_SURFACE_AREA>
48.0

> <JCHEM_REFRACTIVITY>
96.32629999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.372  -3.446   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.168  -3.470   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.918  -4.815   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.458  -4.838   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.207  -6.183   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.747  -6.207   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.537  -4.885   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.077  -4.908   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.867  -3.587   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.407  -3.610   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.157  -4.955   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.366  -6.277   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.827  -6.254   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.036  -7.575   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       6.497  -7.552   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       5.706  -8.874   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.167  -8.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.417  -7.505   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.877  -7.482   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.128  -6.137   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.412  -6.113   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      11.379  -7.437   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      12.796  -6.832   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.658  -5.298   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   18                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   24                                                  
CONECT   12   11   13   22                                                  
CONECT   13   12    8   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14    6   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    5   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19    3   21                                                  
CONECT   21   20                                                            
CONECT   22   12   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   11                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₅NO₄

Average Mass

321.3320 Da

Monoisotopic Mass

321.10011 Da

IUPAC Name

16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one

Traditional Name

16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0^{3,11}.0^{4,8}.0^{14,19}]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3C=C4C=CC5=C(OCO5)C4=CN3CCC2=CC1=O

InChI Identifier

InChI=1S/C19H15NO4/c1-22-18-8-13-12(7-16(18)21)4-5-20-9-14-11(6-15(13)20)2-3-17-19(14)24-10-23-17/h2-3,6-9H,4-5,10H2,1H3

InChI Key

PGIOBGCIEGZHJH-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
Coptis japonica	LOTUS Database	35616633
Coptis trifolia	LOTUS Database	35616633
Nandina domestica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoquinolones and derivatives. These are aromatic polycyclic compounds containing a ketone bearing isoquinoline moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoquinolines and derivatives

Sub Class

Isoquinolones and derivatives

Direct Parent

Isoquinolones and derivatives

Alternative Parents

Substituents

Isoquinolone
Dihydroisoquinoline
Benzodioxole
Tetrahydropyridine
Benzenoid
Ketone
Tertiary amine
Tertiary aliphatic amine
Cyclic ketone
Acetal
Enamine
Azacycle
Oxacycle
Amine
Organic oxide
Aldehyde
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
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	-0.24	ChemAxon
pKa (Strongest Acidic)	17.22	ChemAxon
pKa (Strongest Basic)	4.77	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	48 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	96.33 m³·mol⁻¹	ChemAxon
Polarizability	34.17 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

9898295

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11723579

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one (NP0289865)

MOL for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)

3D MOL for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)

3D SDF for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)

3D-SDF for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)

PDB for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)

3D PDB for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)

SMILES for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)

INCHI for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)

Structure for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)

3D Structure for NP0289865 (16-methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.0³,¹¹.0⁴,⁸.0¹⁴,¹⁹]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one)