NP-MRD: Showing NP-Card for 9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one (NP0223492)

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Record Information

Version

2.0

Created at

2022-09-06 01:36:21 UTC

Updated at

2022-09-06 01:36:22 UTC

NP-MRD ID

NP0223492

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one

Description

9-Hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]Heptadeca-1(10),2,4,6,8-pentaen-17-one belongs to the class of organic compounds known as quinolones and derivatives. Quinolones and derivatives are compounds containing a quinoline moiety which bears a ketone group. 9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one is found in Isatis tinctoria. 9-Hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]Heptadeca-1(10),2,4,6,8-pentaen-17-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171512392D          

 30 34  0  0  0  0            999 V2000
    3.2084   -4.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9281   -3.6123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4599   -2.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1796   -2.2057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7114   -1.5750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5235   -1.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8038   -2.4961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6160   -2.6413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8963   -3.4173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2720   -3.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5523   -3.9028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902    1.5287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0872   -1.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3675   -2.0605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -1.1393    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    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  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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 20 30  1  0  0  0  0
 25 30  1  0  0  0  0
M  END

     RDKit          3D

 52 56  0  0  0  0  0  0  0  0999 V2000
   -2.8370    0.0164   -3.7362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5794   -0.4446   -2.6503 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1207   -0.4514   -1.3401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8635    0.0079   -0.9966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3901    0.0088    0.3019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0363    0.5310    0.6028 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0388   -0.4191    0.2149 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3544    0.0384    0.0099 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3649   -0.8478   -0.3258 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6498   -0.4212   -0.5283 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6217   -1.3530   -0.8631 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3184   -2.6960   -0.9951 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0296   -3.1232   -0.7919 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0380   -2.2085   -0.4556 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7770   -2.6138   -0.2554 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7968   -1.7645    0.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3990   -2.1835    0.2537 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6368    1.4569    0.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7461    1.9471   -0.0327 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5067    2.3005    0.4411 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4041    3.5257    1.1542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0297    3.5070    1.6395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7365    2.9269    0.4043 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2288    1.8492   -0.0433 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2419   -0.4789    1.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5011   -0.9468    0.9773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3782   -1.4434    1.9338 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9789   -1.4830    3.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9436   -0.9315   -0.3458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2231   -1.4075   -0.6379 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4932    0.3480   -4.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2540    0.9222   -3.4405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1347   -0.7218   -4.1503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2280    0.3785   -1.7633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0345    0.7234    1.7236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9842    0.5786   -0.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6592   -1.0701   -1.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0568   -3.4353   -1.2540 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7779   -4.1794   -0.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5547   -3.6216   -0.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1243    3.6550    1.9806 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4701    4.3692    0.4141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4103    4.5135    1.8678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1807    2.7716    2.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7094    3.7230   -0.3693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7333    2.5555    0.6386 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2677    1.7803   -1.1437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9046   -0.4927    2.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1963   -2.2391    3.4699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5363   -0.4779    3.5148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8511   -1.5796    3.9750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5502   -1.3996   -1.5929 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 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  2  0
 29 30  1  0
  5  6  1  0
  6 24  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
 18  8  1  0
  8  7  2  0
  7 16  1  0
 16 17  2  0
 16 15  1  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
 10  9  2  0
 29  3  1  0
  7  6  1  0
  9 14  1  0
 20 24  1  0
  9  8  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
 25 48  1  0
 28 49  1  0
 28 50  1  0
 28 51  1  0
 30 52  1  0
  6 35  1  1
 24 47  1  6
 23 45  1  0
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 22 43  1  0
 22 44  1  0
 21 41  1  0
 21 42  1  0
 15 40  1  0
 13 39  1  0
 12 38  1  0
 11 37  1  0
 10 36  1  0
M  END


  Mrv1533004171512392D          

 30 34  0  0  0  0            999 V2000
    3.2084   -4.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9281   -3.6123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4599   -2.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1796   -2.2057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7114   -1.5750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5235   -1.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8038   -2.4961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6160   -2.6413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8963   -3.4173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2720   -3.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5523   -3.9028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902    1.5287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0872   -1.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3675   -2.0605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751   -1.1393    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    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  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  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
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 12 21  1  0  0  0  0
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 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 20 30  1  0  0  0  0
 25 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0223492

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(OC)=C1O)C1C2CCCN2C(=O)C2=C1C(=O)NC1=CC=CC=C21

> <INCHI_IDENTIFIER>
InChI=1S/C23H22N2O5/c1-29-16-10-12(11-17(30-2)21(16)26)18-15-8-5-9-25(15)23(28)19-13-6-3-4-7-14(13)24-22(27)20(18)19/h3-4,6-7,10-11,15,18,26H,5,8-9H2,1-2H3,(H,24,27)

> <INCHI_KEY>
IWGANRXBUPWVLV-UHFFFAOYSA-N

> <FORMULA>
C23H22N2O5

> <MOLECULAR_WEIGHT>
406.438

> <EXACT_MASS>
406.152871816

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
42.528154557727895

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6-tetraene-9,17-dione

> <ALOGPS_LOGP>
2.95

> <JCHEM_LOGP>
1.9960901523333345

> <ALOGPS_LOGS>
-3.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.076603762456589

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.32943261897623

> <JCHEM_PKA_STRONGEST_BASIC>
-0.31524731323915256

> <JCHEM_POLAR_SURFACE_AREA>
88.1

> <JCHEM_REFRACTIVITY>
112.2046

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.39e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6-tetraene-9,17-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       5.989  -8.191   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.466  -6.743   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.458  -5.566   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.935  -4.117   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.928  -2.940   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.444  -3.211   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.967  -4.659   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.483  -4.931   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      11.006  -6.379   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.974  -5.837   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.498  -7.285   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.405  -1.492   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.398  -0.314   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.937  -0.264   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.365   1.215   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.090   2.079   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       6.874   1.134   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       5.358   1.405   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.835   2.854   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.366   0.228   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.889  -1.221   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.896  -2.398   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.419  -3.846   0.000  0.00  0.00           O+0
HETATM   24  N   UNK     0       2.380  -2.127   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       1.857  -0.678   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.341  -0.407   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.182   1.041   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.810   2.218   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.326   1.947   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.850   0.499   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7    3   11                                                  
CONECT   11   10                                                            
CONECT   12    5   13   21                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13   18                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   30                                                  
CONECT   21   20   12   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   20   25                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₂N₂O₅

Average Mass

406.4380 Da

Monoisotopic Mass

406.15287 Da

IUPAC Name

11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6-tetraene-9,17-dione

Traditional Name

11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6-tetraene-9,17-dione

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(OC)=C1O)C1C2CCCN2C(=O)C2=C1C(=O)NC1=CC=CC=C21

InChI Identifier

InChI=1S/C23H22N2O5/c1-29-16-10-12(11-17(30-2)21(16)26)18-15-8-5-9-25(15)23(28)19-13-6-3-4-7-14(13)24-22(27)20(18)19/h3-4,6-7,10-11,15,18,26H,5,8-9H2,1-2H3,(H,24,27)

InChI Key

IWGANRXBUPWVLV-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
Isatis tinctoria	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolones and derivatives. Quinolones and derivatives are compounds containing a quinoline moiety which bears a ketone group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Quinolones and derivatives

Direct Parent

Quinolones and derivatives

Alternative Parents

Substituents

Quinolone
Methoxyphenol
Naphthyridine
M-dimethoxybenzene
Dimethoxybenzene
Pyridine carboxylic acid or derivatives
Phenoxy compound
Anisole
Phenol ether
Methoxybenzene
Alkyl aryl ether
Hydroxypyridine
Phenol
Monocyclic benzene moiety
Benzenoid
Pyridine
Heteroaromatic compound
Pyrrolidine
Tertiary carboxylic acid amide
Lactam
Carboxamide group
Azacycle
Ether
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic nitrogen 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	2.95	ALOGPS
logP	2	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	9.33	ChemAxon
pKa (Strongest Basic)	-0.32	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	88.1 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	112.2 m³·mol⁻¹	ChemAxon
Polarizability	42.53 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one (NP0223492)

MOL for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)

3D MOL for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)

3D SDF for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)

3D-SDF for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)

PDB for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)

3D PDB for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)

SMILES for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)

INCHI for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)

Structure for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)

3D Structure for NP0223492 (9-hydroxy-11-(4-hydroxy-3,5-dimethoxyphenyl)-8,16-diazatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-1(10),2,4,6,8-pentaen-17-one)