NP-MRD: Showing NP-Card for 6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one (NP0199218)

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Record Information

Version

2.0

Created at

2022-09-04 17:49:13 UTC

Updated at

2022-09-04 17:49:13 UTC

NP-MRD ID

NP0199218

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one

Description

Rutagravine belongs to the class of organic compounds known as acridones. These are acridines containing a ketone group attached to the C9 carbon atom of the acridine moiety. Rutagravine is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, rutagravine has been detected, but not quantified in, herbs and spices. 6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one is found in Ruta graveolens. This could make rutagravine a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061307082D          

 25 29  0  0  0  0            999 V2000
    2.4245    0.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5822    1.5688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5082    1.0333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0526    1.7211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1405    0.2948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2291    1.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9347   -1.3345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3055    1.6049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3170    0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8614    0.9318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7581   -1.2837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4790   -0.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1259   -0.5452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8467    0.0918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6702    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9493   -0.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2580    0.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5264    0.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9377    0.8664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0379    0.8810    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2138   -1.9714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4050   -1.1822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2417    1.3093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1215    1.4833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6630   -0.5252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  9  5  2  0  0  0  0
 10  6  2  0  0  0  0
 10  9  1  0  0  0  0
 11  7  2  0  0  0  0
 12  7  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  2  0  0  0  0
 15 13  2  0  0  0  0
 15 14  1  0  0  0  0
 16  9  1  0  0  0  0
 16 13  1  0  0  0  0
 17 14  1  0  0  0  0
 18 17  1  0  0  0  0
 19  1  1  0  0  0  0
 19  8  1  0  0  0  0
 19 18  1  0  0  0  0
 20  2  1  0  0  0  0
 20 10  1  0  0  0  0
 20 15  1  0  0  0  0
 21 11  1  0  0  0  0
 22 16  2  0  0  0  0
 23 19  1  0  0  0  0
 24  8  1  0  0  0  0
 24 17  1  0  0  0  0
 25 12  1  0  0  0  0
 25 18  1  0  0  0  0
M  END

     RDKit          3D

 42 46  0  0  0  0  0  0  0  0999 V2000
    0.8937    0.6527    2.1389 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3336    0.2017    0.8320 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5811   -0.3743    0.7725 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2953   -0.6333    1.9270 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5378   -1.2307    1.8369 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0477   -1.5612    0.6032 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3551   -1.3161   -0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108   -0.7185   -0.4677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3627   -0.4706   -1.5906 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8676   -0.7901   -2.7060 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1194    0.1016   -1.4835 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3962    0.3066   -2.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9672   -0.0494   -3.8582 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363    0.8400   -2.5930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3659    1.1788   -1.3556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6846    0.9963   -0.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5752    0.4518   -0.2432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5350    1.3980    0.9357 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8663    0.3866    1.8509 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4633   -0.6221    1.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5790    0.1420    0.4469 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0326   -0.5090   -0.8403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6185    0.2403    1.3694 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9122    1.4626    0.2084 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5935    1.7260   -1.1127 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4204    1.6524    2.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8799    1.0077    2.6565 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5916   -0.0917    2.8414 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8625   -0.3941    2.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0518   -1.4085    2.7710 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0306   -2.0323    0.5354 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7200   -1.5608   -1.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4696    0.0869   -4.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3828    0.9918   -3.5210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4921    2.4016    1.3368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8063   -1.3903    1.8042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7710   -1.0835    0.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9872   -1.0605   -0.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2801    0.3372   -1.5430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2296   -1.0865   -1.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4890    0.4237    0.9579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5449    2.2697    0.5881 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
  9 11  1  0
 11 17  2  0
 17 16  1  0
 16 15  2  0
 15 25  1  0
 25 24  1  0
 24 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  1
 15 14  1  0
 14 12  2  0
 12 13  1  0
 17  2  1  0
 18 16  1  0
  8  3  1  0
 12 11  1  0
 21 24  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  5 30  1  0
  6 31  1  0
  7 32  1  0
 24 42  1  1
 18 35  1  1
 20 36  1  0
 20 37  1  0
 22 38  1  0
 22 39  1  0
 22 40  1  0
 23 41  1  0
 14 34  1  0
 13 33  1  0
M  END


  Mrv0541 05061307082D          

 25 29  0  0  0  0            999 V2000
    2.4245    0.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5822    1.5688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5082    1.0333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0526    1.7211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1405    0.2948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2291    1.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9347   -1.3345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3055    1.6049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3170    0.2441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8614    0.9318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7581   -1.2837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4790   -0.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1259   -0.5452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8467    0.0918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6702    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9493   -0.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2580    0.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5264    0.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9377    0.8664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0379    0.8810    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2138   -1.9714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4050   -1.1822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2417    1.3093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1215    1.4833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6630   -0.5252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  9  5  2  0  0  0  0
 10  6  2  0  0  0  0
 10  9  1  0  0  0  0
 11  7  2  0  0  0  0
 12  7  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  2  0  0  0  0
 15 13  2  0  0  0  0
 15 14  1  0  0  0  0
 16  9  1  0  0  0  0
 16 13  1  0  0  0  0
 17 14  1  0  0  0  0
 18 17  1  0  0  0  0
 19  1  1  0  0  0  0
 19  8  1  0  0  0  0
 19 18  1  0  0  0  0
 20  2  1  0  0  0  0
 20 10  1  0  0  0  0
 20 15  1  0  0  0  0
 21 11  1  0  0  0  0
 22 16  2  0  0  0  0
 23 19  1  0  0  0  0
 24  8  1  0  0  0  0
 24 17  1  0  0  0  0
 25 12  1  0  0  0  0
 25 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0199218

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C2=CC=CC=C2C(=O)C2=C1C1=C(OC3C1OCC3(C)O)C=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C19H17NO5/c1-19(23)8-24-17-14-12(25-18(17)19)7-11(21)13-15(14)20(2)10-6-4-3-5-9(10)16(13)22/h3-7,17-18,21,23H,8H2,1-2H3

> <INCHI_KEY>
SWALXCKAJQTSAC-UHFFFAOYSA-N

> <FORMULA>
C19H17NO5

> <MOLECULAR_WEIGHT>
339.342

> <EXACT_MASS>
339.110672659

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
34.9864272249543

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1(12),2(9),10,14,16,18-hexaen-13-one

> <ALOGPS_LOGP>
2.30

> <JCHEM_LOGP>
2.6142210069999994

> <ALOGPS_LOGS>
-2.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.181530603776356

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.961612033479478

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5943146777169606

> <JCHEM_POLAR_SURFACE_AREA>
79.23

> <JCHEM_REFRACTIVITY>
89.9727

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.06e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1(12),2(9),10,14,16,18-hexaen-13-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       4.526   0.412   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.420   2.928   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.882   1.929   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.032   3.213   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.196   0.550   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.494   3.118   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.211  -2.491   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.170   2.996   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.658   0.456   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.808   1.739   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.748  -2.396   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.361  -1.207   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.435  -1.018   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.047   0.171   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.584   0.266   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.972  -0.923   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.948   1.250   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.583   0.538   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.484   1.617   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0      11.271   1.645   0.000  0.00  0.00           N+0
HETATM   21  O   UNK     0      11.599  -3.680   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      13.823  -2.207   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       4.185   2.444   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       7.693   2.769   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       6.838  -0.980   0.000  0.00  0.00           O+0
CONECT    1   19                                                            
CONECT    2   20                                                            
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3    9                                                       
CONECT    6    4   10                                                       
CONECT    7   11   12                                                       
CONECT    8   19   24                                                       
CONECT    9    5   10   16                                                  
CONECT   10    6    9   20                                                  
CONECT   11    7   13   21                                                  
CONECT   12    7   14   25                                                  
CONECT   13   11   15   16                                                  
CONECT   14   12   15   17                                                  
CONECT   15   13   14   20                                                  
CONECT   16    9   13   22                                                  
CONECT   17   14   18   24                                                  
CONECT   18   17   19   25                                                  
CONECT   19    1    8   18   23                                             
CONECT   20    2   10   15                                                  
CONECT   21   11                                                            
CONECT   22   16                                                            
CONECT   23   19                                                            
CONECT   24    8   17                                                       
CONECT   25   12   18                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₇NO₅

Average Mass

339.3420 Da

Monoisotopic Mass

339.11067 Da

IUPAC Name

6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1(12),2(9),10,14,16,18-hexaen-13-one

Traditional Name

6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1(12),2(9),10,14,16,18-hexaen-13-one

CAS Registry Number

Not Available

SMILES

CN1C2=CC=CC=C2C(=O)C2=C1C1=C(OC3C1OCC3(C)O)C=C2O

InChI Identifier

InChI=1S/C19H17NO5/c1-19(23)8-24-17-14-12(25-18(17)19)7-11(21)13-15(14)20(2)10-6-4-3-5-9(10)16(13)22/h3-7,17-18,21,23H,8H2,1-2H3

InChI Key

SWALXCKAJQTSAC-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
Ruta graveolens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acridones. These are acridines containing a ketone group attached to the C9 carbon atom of the acridine moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Benzoquinolines

Direct Parent

Acridones

Alternative Parents

Substituents

Acridone
Dihydroquinolone
Dihydroquinoline
Coumaran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyridine
Benzenoid
Vinylogous amide
Vinylogous acid
Heteroaromatic compound
Tetrahydrofuran
Tertiary alcohol
Oxacycle
Azacycle
Dialkyl ether
Ether
Hydrocarbon derivative
Organonitrogen compound
Organic oxide
Organopnictogen compound
Organooxygen compound
Organic nitrogen compound
Organic oxygen compound
Alcohol
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	2.3	ALOGPS
logP	2.61	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	9.96	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.23 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	89.97 m³·mol⁻¹	ChemAxon
Polarizability	34.99 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

HMDB0033446

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB011484

KNApSAcK ID

Not Available

Chemspider ID

4577337

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5465778

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one (NP0199218)

MOL for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)

3D MOL for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)

3D SDF for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)

3D-SDF for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)

PDB for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)

3D PDB for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)

SMILES for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)

INCHI for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)

Structure for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)

3D Structure for NP0199218 (6,11-dihydroxy-6,20-dimethyl-4,8-dioxa-20-azapentacyclo[10.8.0.0²,⁹.0³,⁷.0¹⁴,¹⁹]icosa-1,9,11,14,16,18-hexaen-13-one)