NP-MRD: Showing NP-Card for heptaphyllone A (NP0040470)

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Record Information

Version

2.0

Created at

2021-06-20 22:37:31 UTC

Updated at

2021-06-30 00:14:24 UTC

NP-MRD ID

NP0040470

Secondary Accession Numbers

None

Natural Product Identification

Common Name

heptaphyllone A

Provided By

JEOL Database JEOL Logo

Description

Heptaohyllone A belongs to the class of organic compounds known as hydroquinolones. Hydroquinolones are compounds containing a hydrogenated quinoline bearing a ketone group. heptaphyllone A is found in Raputia heptaphylla. heptaphyllone A was first documented in 2011 (Barrera, C. A. C., et al.). Based on a literature review very few articles have been published on Heptaohyllone A.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100373D          

 32 34  0  0  0  0            999 V2000
    1.7786    2.1196    0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7747    1.1431   -0.2034 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0731    0.5036    0.7028 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0662    0.8220    2.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9579    1.5056    2.6733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0959    1.2919    4.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0918    1.9580    4.7614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9434    2.8468    4.1062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7960    3.0747    2.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7999    2.4095    2.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656   -0.4330    0.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1110   -0.7973   -1.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9278   -1.6466   -1.4049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2479   -0.1024   -2.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3782   -0.4205   -3.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4213    0.2191   -4.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3446    1.1708   -3.9259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4716    1.4847   -2.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6798    0.8563   -1.5884 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8103    2.2489    1.3109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7839    1.8020   -0.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5650    3.1065   -0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    0.6018    4.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2028    1.7844    5.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7199    3.3657    4.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4554    3.7736    2.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6901    2.6133    0.9588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5990   -0.9428    1.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1025   -1.1660   -3.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240   -0.0242   -5.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9725    1.6746   -4.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    2.2368   -2.3003 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  8  2  0  0  0  0
 11 12  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
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  3  4  1  0  0  0  0
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 19 14  2  0  0  0  0
  4  5  1  0  0  0  0
 14 15  1  0  0  0  0
 19  2  1  0  0  0  0
 15 16  2  0  0  0  0
  5  6  2  0  0  0  0
 16 17  1  0  0  0  0
  2  3  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  6  7  1  0  0  0  0
  2  1  1  0  0  0  0
  3 11  2  0  0  0  0
 12 13  2  0  0  0  0
 11 28  1  0  0  0  0
  6 23  1  0  0  0  0
  7 24  1  0  0  0  0
  8 25  1  0  0  0  0
  9 26  1  0  0  0  0
 10 27  1  0  0  0  0
 15 29  1  0  0  0  0
 16 30  1  0  0  0  0
 17 31  1  0  0  0  0
 18 32  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
M  END

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
    1.7786    2.1196    0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7747    1.1431   -0.2034 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0731    0.5036    0.7028 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0662    0.8220    2.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9579    1.5056    2.6733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0959    1.2919    4.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0918    1.9580    4.7614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9434    2.8468    4.1062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7960    3.0747    2.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7999    2.4095    2.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656   -0.4330    0.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1110   -0.7973   -1.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9278   -1.6466   -1.4049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2479   -0.1024   -2.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3782   -0.4205   -3.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4213    0.2191   -4.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3446    1.1708   -3.9259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4716    1.4847   -2.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6798    0.8563   -1.5884 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8103    2.2489    1.3109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7839    1.8020   -0.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5650    3.1065   -0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    0.6018    4.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2028    1.7844    5.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7199    3.3657    4.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4554    3.7736    2.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6901    2.6133    0.9588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5990   -0.9428    1.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1025   -1.1660   -3.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240   -0.0242   -5.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9725    1.6746   -4.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    2.2368   -2.3003 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  8  2  0
 11 12  1  0
  8  9  1  0
  9 10  2  0
 10  5  1  0
  3  4  1  0
 14 12  1  0
 19 14  2  0
  4  5  1  0
 14 15  1  0
 19  2  1  0
 15 16  2  0
  5  6  2  0
 16 17  1  0
  2  3  1  0
 17 18  2  0
 18 19  1  0
  6  7  1  0
  2  1  1  0
  3 11  2  0
 12 13  2  0
 11 28  1  0
  6 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 15 29  1  0
 16 30  1  0
 17 31  1  0
 18 32  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END


  Mrv1652306212100373D          

 32 34  0  0  0  0            999 V2000
    1.7786    2.1196    0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7747    1.1431   -0.2034 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0731    0.5036    0.7028 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0662    0.8220    2.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9579    1.5056    2.6733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0959    1.2919    4.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0918    1.9580    4.7614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9434    2.8468    4.1062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7960    3.0747    2.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7999    2.4095    2.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656   -0.4330    0.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1110   -0.7973   -1.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9278   -1.6466   -1.4049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2479   -0.1024   -2.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3782   -0.4205   -3.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4213    0.2191   -4.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3446    1.1708   -3.9259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4716    1.4847   -2.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6798    0.8563   -1.5884 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8103    2.2489    1.3109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7839    1.8020   -0.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5650    3.1065   -0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    0.6018    4.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2028    1.7844    5.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7199    3.3657    4.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4554    3.7736    2.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6901    2.6133    0.9588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5990   -0.9428    1.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1025   -1.1660   -3.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240   -0.0242   -5.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9725    1.6746   -4.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    2.2368   -2.3003 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  8  2  0  0  0  0
 11 12  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10  5  1  0  0  0  0
  3  4  1  0  0  0  0
 14 12  1  0  0  0  0
 19 14  2  0  0  0  0
  4  5  1  0  0  0  0
 14 15  1  0  0  0  0
 19  2  1  0  0  0  0
 15 16  2  0  0  0  0
  5  6  2  0  0  0  0
 16 17  1  0  0  0  0
  2  3  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  6  7  1  0  0  0  0
  2  1  1  0  0  0  0
  3 11  2  0  0  0  0
 12 13  2  0  0  0  0
 11 28  1  0  0  0  0
  6 23  1  0  0  0  0
  7 24  1  0  0  0  0
  8 25  1  0  0  0  0
  9 26  1  0  0  0  0
 10 27  1  0  0  0  0
 15 29  1  0  0  0  0
 16 30  1  0  0  0  0
 17 31  1  0  0  0  0
 18 32  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0040470

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C([H])C([H])=C(OC2=C([H])C(=O)C3=C(C([H])=C([H])C([H])=C3[H])N2C([H])([H])[H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H13NO2/c1-17-14-10-6-5-9-13(14)15(18)11-16(17)19-12-7-3-2-4-8-12/h2-11H,1H3

> <INCHI_KEY>
HBIGNUYKQYQFSC-UHFFFAOYSA-N

> <FORMULA>
C16H13NO2

> <MOLECULAR_WEIGHT>
251.285

> <EXACT_MASS>
251.094628663

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
27.095407888278658

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-methyl-2-phenoxy-1,4-dihydroquinolin-4-one

> <ALOGPS_LOGP>
3.34

> <JCHEM_LOGP>
3.725696422333333

> <ALOGPS_LOGS>
-3.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.994166038965783

> <JCHEM_PKA_STRONGEST_BASIC>
-0.6236928070884232

> <JCHEM_POLAR_SURFACE_AREA>
29.54

> <JCHEM_REFRACTIVITY>
84.79190000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.22e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-methyl-2-phenoxyquinolin-4-one

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
    1.7786    2.1196    0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7747    1.1431   -0.2034 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0731    0.5036    0.7028 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0662    0.8220    2.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9579    1.5056    2.6733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0959    1.2919    4.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0918    1.9580    4.7614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9434    2.8468    4.1062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7960    3.0747    2.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7999    2.4095    2.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656   -0.4330    0.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1110   -0.7973   -1.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9278   -1.6466   -1.4049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2479   -0.1024   -2.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3782   -0.4205   -3.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4213    0.2191   -4.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3446    1.1708   -3.9259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4716    1.4847   -2.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6798    0.8563   -1.5884 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8103    2.2489    1.3109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7839    1.8020   -0.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5650    3.1065   -0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    0.6018    4.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2028    1.7844    5.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7199    3.3657    4.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4554    3.7736    2.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6901    2.6133    0.9588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5990   -0.9428    1.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1025   -1.1660   -3.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240   -0.0242   -5.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9725    1.6746   -4.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    2.2368   -2.3003 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  8  2  0
 11 12  1  0
  8  9  1  0
  9 10  2  0
 10  5  1  0
  3  4  1  0
 14 12  1  0
 19 14  2  0
  4  5  1  0
 14 15  1  0
 19  2  1  0
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  5  6  2  0
 16 17  1  0
  2  3  1  0
 17 18  2  0
 18 19  1  0
  6  7  1  0
  2  1  1  0
  3 11  2  0
 12 13  2  0
 11 28  1  0
  6 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 15 29  1  0
 16 30  1  0
 17 31  1  0
 18 32  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0       1.779   2.120   0.224  0.00  0.00           C+0
HETATM    2  N   UNK     0       0.775   1.143  -0.203  0.00  0.00           N+0
HETATM    3  C   UNK     0      -0.073   0.504   0.703  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.066   0.822   2.054  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.958   1.506   2.673  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.096   1.292   4.046  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.092   1.958   4.761  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.943   2.847   4.106  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.796   3.075   2.738  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.800   2.410   2.020  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.966  -0.433   0.351  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.111  -0.797  -1.065  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.928  -1.647  -1.405  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.248  -0.102  -2.045  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.378  -0.421  -3.405  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.421   0.219  -4.346  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.345   1.171  -3.926  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.472   1.485  -2.566  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.680   0.856  -1.588  0.00  0.00           C+0
HETATM   20  H   UNK     0       1.810   2.249   1.311  0.00  0.00           H+0
HETATM   21  H   UNK     0       2.784   1.802  -0.076  0.00  0.00           H+0
HETATM   22  H   UNK     0       1.565   3.107  -0.202  0.00  0.00           H+0
HETATM   23  H   UNK     0      -0.431   0.602   4.559  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.203   1.784   5.829  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.720   3.366   4.663  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.455   3.774   2.229  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.690   2.613   0.959  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.599  -0.943   1.064  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.103  -1.166  -3.726  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.324  -0.024  -5.401  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.972   1.675  -4.657  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.208   2.237  -2.300  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2   19    3    1                                                  
CONECT    3    4    2   11                                                  
CONECT    4    3    5                                                       
CONECT    5   10    4    6                                                  
CONECT    6    5    7   23                                                  
CONECT    7    8    6   24                                                  
CONECT    8    7    9   25                                                  
CONECT    9    8   10   26                                                  
CONECT   10    9    5   27                                                  
CONECT   11   12    3   28                                                  
CONECT   12   11   14   13                                                  
CONECT   13   12                                                            
CONECT   14   12   19   15                                                  
CONECT   15   14   16   29                                                  
CONECT   16   15   17   30                                                  
CONECT   17   16   18   31                                                  
CONECT   18   17   19   32                                                  
CONECT   19   14    2   18                                                  
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    6                                                            
CONECT   24    7                                                            
CONECT   25    8                                                            
CONECT   26    9                                                            
CONECT   27   10                                                            
CONECT   28   11                                                            
CONECT   29   15                                                            
CONECT   30   16                                                            
CONECT   31   17                                                            
CONECT   32   18                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

RDKit          3D

32 34  0  0  0  0  0  0  0  0999 V2000
    1.7786    2.1196    0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7747    1.1431   -0.2034 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0731    0.5036    0.7028 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0662    0.8220    2.0538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9579    1.5056    2.6733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0959    1.2919    4.0462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0918    1.9580    4.7614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9434    2.8468    4.1062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7960    3.0747    2.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7999    2.4095    2.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9656   -0.4330    0.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1110   -0.7973   -1.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9278   -1.6466   -1.4049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2479   -0.1024   -2.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3782   -0.4205   -3.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4213    0.2191   -4.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3446    1.1708   -3.9259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4716    1.4847   -2.5660 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6798    0.8563   -1.5884 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8103    2.2489    1.3109 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7839    1.8020   -0.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5650    3.1065   -0.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4310    0.6018    4.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2028    1.7844    5.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7199    3.3657    4.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4554    3.7736    2.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6901    2.6133    0.9588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5990   -0.9428    1.0639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1025   -1.1660   -3.7263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3240   -0.0242   -5.4005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9725    1.6746   -4.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2085    2.2368   -2.3003 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  8  2  0
 11 12  1  0
  8  9  1  0
  9 10  2  0
 10  5  1  0
  3  4  1  0
 14 12  1  0
 19 14  2  0
  4  5  1  0
 14 15  1  0
 19  2  1  0
 15 16  2  0
  5  6  2  0
 16 17  1  0
  2  3  1  0
 17 18  2  0
 18 19  1  0
  6  7  1  0
  2  1  1  0
  3 11  2  0
 12 13  2  0
 11 28  1  0
  6 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 15 29  1  0
 16 30  1  0
 17 31  1  0
 18 32  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₆H₁₃NO₂

Average Mass

251.2850 Da

Monoisotopic Mass

251.09463 Da

IUPAC Name

1-methyl-2-phenoxy-1,4-dihydroquinolin-4-one

Traditional Name

1-methyl-2-phenoxyquinolin-4-one

CAS Registry Number

Not Available

SMILES

[H]C1=C([H])C([H])=C(OC2=C([H])C(=O)C3=C(C([H])=C([H])C([H])=C3[H])N2C([H])([H])[H])C([H])=C1[H]

InChI Identifier

InChI=1S/C16H13NO2/c1-17-14-10-6-5-9-13(14)15(18)11-16(17)19-12-7-3-2-4-8-12/h2-11H,1H3

InChI Key

HBIGNUYKQYQFSC-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Raputia heptaphylla	JEOL database	Barrera, C. A. C., et al., Chem. Pharm. Bull., 59, 855 (2011)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroquinolones. Hydroquinolones are compounds containing a hydrogenated quinoline bearing a ketone group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Quinolones and derivatives

Direct Parent

Hydroquinolones

Alternative Parents

Substituents

Diaryl ether
Dihydroquinolone
Dihydroquinoline
Phenoxy compound
Phenol ether
Monocyclic benzene moiety
Pyridine
Benzenoid
Vinylogous ester
Vinylogous amide
Heteroaromatic compound
Ether
Azacycle
Organic nitrogen compound
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen 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	3.34	ALOGPS
logP	3.73	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	15.99	ChemAxon
pKa (Strongest Basic)	-0.62	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	29.54 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	84.79 m³·mol⁻¹	ChemAxon
Polarizability	27.1 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

53348958

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Barrera, C. A. C., et al. (2011). Barrera, C. A. C., et al., Chem. Pharm. Bull., 59, 855 (2011). Chem. Pharm. Bull..

Showing NP-Card for heptaphyllone A (NP0040470)

MOL for NP0040470 (heptaphyllone A)

3D MOL for NP0040470 (heptaphyllone A)

3D SDF for NP0040470 (heptaphyllone A)

3D-SDF for NP0040470 (heptaphyllone A)

PDB for NP0040470 (heptaphyllone A)

3D PDB for NP0040470 (heptaphyllone A)

SMILES for NP0040470 (heptaphyllone A)

INCHI for NP0040470 (heptaphyllone A)

Structure for NP0040470 (heptaphyllone A)

3D Structure for NP0040470 (heptaphyllone A)