NP-MRD: Showing NP-Card for Citropone B (NP0083503)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-29 04:31:51 UTC

Updated at

2022-04-29 04:31:51 UTC

NP-MRD ID

NP0083503

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Citropone B

Description

7-Acetyl-1,8-dihydroxy-3-methoxy-5-methyl-4-(3-methylbut-2-en-1-yl)-5H,6H,11H-cyclohepta[b]quinoline-6,11-dione belongs to the class of organic compounds known as hydroquinolones. Hydroquinolones are compounds containing a hydrogenated quinoline bearing a ketone group. Citropone B is found in Citrus maxima and Citrus natsudaidai . 7-Acetyl-1,8-dihydroxy-3-methoxy-5-methyl-4-(3-methylbut-2-en-1-yl)-5H,6H,11H-cyclohepta[b]quinoline-6,11-dione is a moderately basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231522452D          

 30 32  0  0  0  0            999 V2000
   -2.4428   -0.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4428   -1.1080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7284   -1.5205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7284   -2.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139   -2.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139   -3.5830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2994   -2.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4151   -2.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4151   -3.5830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1295   -2.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1295   -1.5205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4151   -1.1080    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4151   -0.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2994   -1.5205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139   -1.1080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139   -0.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7284    0.1295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7284    0.9545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4428    1.3670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139    1.3670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7745   -1.0061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5910   -0.2018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5788   -1.1897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9368   -1.9330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7618   -1.9330    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5788   -2.6763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7745   -2.8599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0932   -0.5447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9090   -0.6676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7918    0.2233    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  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  2  0  0  0  0
  3 15  1  0  0  0  0
 15 16  1  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
 18 20  1  0  0  0  0
 11 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 10 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
   -4.6474   -2.4176   -1.4660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6740   -1.4385   -1.2769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3662   -1.7365   -0.8490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9898   -3.0255   -0.5962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7193   -3.2579   -0.1858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2998   -4.5508    0.0823 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1714   -2.2238   -0.0285 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4368   -2.4857    0.4337 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7814   -3.7042    0.6705 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3000   -1.4789    0.6345 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5226   -1.9267    1.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7184   -1.2248    1.0596 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8989    0.1021    0.6295 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1750    0.4285    0.2513 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862    1.1357    0.5275 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4102    2.4927    0.3194 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8168    2.8690    0.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5005    3.3893    0.2329 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6106    0.9454    0.6343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8937    1.9103    1.0357 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8758   -0.1925    0.3612 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6343    0.1187   -0.1066 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4104    1.4225   -0.5028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2199   -0.9086   -0.2922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5039   -0.6184   -0.7086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9650    0.7417   -0.8577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6487    1.2849    0.3717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8532    1.7762    0.4380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3902    2.2738    1.7272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6981    1.8514   -0.7762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0070   -2.7293   -0.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2142   -3.2867   -2.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4871   -1.9438   -2.0444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6929   -3.8231   -0.7235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9069   -5.3546   -0.0143 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6143   -2.9168    1.4773 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6166   -1.7275    1.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9739   -0.1823    0.2551 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3971    2.5314    1.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8798    3.9815    0.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2297    2.4699   -0.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0869    2.2276   -0.1454 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4539    1.8775   -0.8445 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2244    1.3521   -1.6515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7233    1.4359   -1.6177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0028    0.5188   -1.3918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0499    1.2540    1.3009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5412    2.7637    2.2871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7910    1.4468    2.3682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2148    2.9958    1.6015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1305    0.8497   -0.9670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5726    2.5438   -0.6016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1363    2.1638   -1.6850 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  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  2  3
 28 29  1  0
 28 30  1  0
 21 19  1  0
 19 20  2  0
 19 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 15 13  2  0
 13 14  1  0
 13 12  1  0
 12 11  2  0
 25  3  1  0
 24  7  1  0
 11 10  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  6 35  1  0
 23 42  1  0
 23 43  1  0
 23 44  1  0
 26 45  1  0
 26 46  1  0
 27 47  1  0
 29 48  1  0
 29 49  1  0
 29 50  1  0
 30 51  1  0
 30 52  1  0
 30 53  1  0
 17 39  1  0
 17 40  1  0
 17 41  1  0
 14 38  1  0
 12 37  1  0
 11 36  1  0
M  END


  Mrv1533004231522452D          

 30 32  0  0  0  0            999 V2000
   -2.4428   -0.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4428   -1.1080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7284   -1.5205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7284   -2.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139   -2.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139   -3.5830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2994   -2.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4151   -2.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4151   -3.5830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1295   -2.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1295   -1.5205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4151   -1.1080    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4151   -0.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2994   -1.5205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139   -1.1080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139   -0.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7284    0.1295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7284    0.9545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4428    1.3670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0139    1.3670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7745   -1.0061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5910   -0.2018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5788   -1.1897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9368   -1.9330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7618   -1.9330    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5788   -2.6763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7745   -2.8599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0932   -0.5447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9090   -0.6676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7918    0.2233    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  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  2  0  0  0  0
  3 15  1  0  0  0  0
 15 16  1  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
 18 20  1  0  0  0  0
 11 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 10 27  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0083503

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(=O)C3=C(N(C)C2=C1CC=C(C)C)C(=O)C(C(C)=O)=C(O)C=C3

> <INCHI_IDENTIFIER>
InChI=1S/C23H23NO6/c1-11(2)6-7-13-17(30-5)10-16(27)19-20(13)24(4)21-14(22(19)28)8-9-15(26)18(12(3)25)23(21)29/h6,8-10,26-27H,7H2,1-5H3

> <INCHI_KEY>
GBAAKPNKBNCFBH-UHFFFAOYSA-N

> <FORMULA>
C23H23NO6

> <MOLECULAR_WEIGHT>
409.438

> <EXACT_MASS>
409.152537465

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
42.6548983555427

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-acetyl-1,8-dihydroxy-3-methoxy-5-methyl-4-(3-methylbut-2-en-1-yl)-5H,6H,11H-cyclohepta[b]quinoline-6,11-dione

> <ALOGPS_LOGP>
2.65

> <JCHEM_LOGP>
3.6589640943333346

> <ALOGPS_LOGS>
-4.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.373193562524884

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.419203551731494

> <JCHEM_PKA_STRONGEST_BASIC>
2.2455101429124613

> <JCHEM_POLAR_SURFACE_AREA>
104.14000000000001

> <JCHEM_REFRACTIVITY>
118.30719999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.43e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-acetyl-1,8-dihydroxy-3-methoxy-5-methyl-4-(3-methylbut-2-en-1-yl)cyclohepta[b]quinoline-6,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      -4.560  -0.528   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -4.560  -2.068   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.226  -2.838   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.226  -4.378   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.893  -5.148   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.893  -6.688   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.559  -4.378   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.775  -5.148   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.775  -6.688   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.108  -4.378   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.108  -2.838   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       0.775  -2.068   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       0.775  -0.528   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.559  -2.838   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.893  -2.068   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.893  -0.528   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.226   0.242   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.226   1.782   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.560   2.552   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.893   2.552   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.312  -1.878   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.970  -0.377   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.814  -2.221   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.482  -3.608   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.022  -3.608   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.814  -4.996   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.312  -5.338   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.774  -1.017   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.297  -1.246   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.211   0.417   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    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   14                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   27                                                  
CONECT   11   10   12   21                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    7   15                                                  
CONECT   15   14    3   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   11   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   28                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   10                                                       
CONECT   28   23   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₃NO₆

Average Mass

409.4380 Da

Monoisotopic Mass

409.15254 Da

IUPAC Name

7-acetyl-1,8-dihydroxy-3-methoxy-5-methyl-4-(3-methylbut-2-en-1-yl)-5H,6H,11H-cyclohepta[b]quinoline-6,11-dione

Traditional Name

7-acetyl-1,8-dihydroxy-3-methoxy-5-methyl-4-(3-methylbut-2-en-1-yl)cyclohepta[b]quinoline-6,11-dione

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(=O)C3=C(N(C)C2=C1CC=C(C)C)C(=O)C(C(C)=O)=C(O)C=C3

InChI Identifier

InChI=1S/C23H23NO6/c1-11(2)6-7-13-17(30-5)10-16(27)19-20(13)24(4)21-14(22(19)28)8-9-15(26)18(12(3)25)23(21)29/h6,8-10,26-27H,7H2,1-5H3

InChI Key

GBAAKPNKBNCFBH-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
Citrus maxima	LOTUS Database	35616633
Citrus natsudaidai	Plant	KNApSAcK

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

Dihydroquinolone
Dihydroquinoline
Anisole
Tropone
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Pyridine
Benzenoid
Heteroaromatic compound
Vinylogous amide
Vinylogous acid
Ketone
Ether
Azacycle
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxide
Organopnictogen compound
Organic oxygen 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	2.65	ALOGPS
logP	3.66	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	7.42	ChemAxon
pKa (Strongest Basic)	2.25	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	104.14 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	118.31 m³·mol⁻¹	ChemAxon
Polarizability	42.65 Å³	ChemAxon
Number of Rings	3	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

Not Available

Showing NP-Card for Citropone B (NP0083503)

MOL for NP0083503 (Citropone B)

3D MOL for NP0083503 (Citropone B)

3D SDF for NP0083503 (Citropone B)

3D-SDF for NP0083503 (Citropone B)

PDB for NP0083503 (Citropone B)

3D PDB for NP0083503 (Citropone B)

SMILES for NP0083503 (Citropone B)

INCHI for NP0083503 (Citropone B)

Structure for NP0083503 (Citropone B)

3D Structure for NP0083503 (Citropone B)