NP-MRD: Showing NP-Card for 2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one (NP0144701)

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Record Information

Version

2.0

Created at

2022-09-01 23:44:32 UTC

Updated at

2022-09-01 23:44:32 UTC

NP-MRD ID

NP0144701

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one

Description

Isogravacridonechlorine 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. Isogravacridonechlorine is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Isogravacridonechlorine has been detected, but not quantified in, herbs and spices. 2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one is found in Ruta chalepensis, Ruta graveolens and Thamnosma montana. This could make isogravacridonechlorine a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061305032D          

 25 28  0  0  0  0            999 V2000
    1.0274    2.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5210    2.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1879    1.4729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9384    2.2593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6317    0.8636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1326    2.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0010    2.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1019    0.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9743    3.2356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8259    1.0407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4086    1.5719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5764    1.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9077   -0.0008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8524    0.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1929    2.1231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4639    0.6085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2144    1.3948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2697    0.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5836    2.6794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1879    2.9860    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.7706    2.0041    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1573   -0.7872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5193   -0.3549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1398    3.2887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1010    1.3033    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
 10  5  2  0  0  0  0
 11  7  1  0  0  0  0
 12  6  2  0  0  0  0
 12 10  1  0  0  0  0
 13  8  2  0  0  0  0
 14  8  1  0  0  0  0
 14 11  2  0  0  0  0
 15  7  1  0  0  0  0
 16 13  1  0  0  0  0
 17 11  1  0  0  0  0
 17 16  2  0  0  0  0
 18 10  1  0  0  0  0
 18 16  1  0  0  0  0
 19  1  1  0  0  0  0
 19  9  1  0  0  0  0
 19 15  1  0  0  0  0
 20  9  1  0  0  0  0
 21  2  1  0  0  0  0
 21 12  1  0  0  0  0
 21 17  1  0  0  0  0
 22 13  1  0  0  0  0
 23 18  2  0  0  0  0
 24 19  1  0  0  0  0
 25 14  1  0  0  0  0
 25 15  1  0  0  0  0
M  END

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
    0.7833   -0.4154    2.0040 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5739   -0.2360    0.8188 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9371   -0.3253    0.9143 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5457   -0.6951    2.0933 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9392   -0.8164    2.2312 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6937   -0.5489    1.1246 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1071   -0.1808   -0.0618 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7431   -0.0732   -0.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1397    0.2776   -1.3636 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9365    0.4973   -2.3061 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7665    0.3590   -1.4452 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2075    0.6809   -2.6428 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9162    0.9552   -3.7773 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2085    0.7373   -2.7251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9679    0.4743   -1.6309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4155    0.1413   -0.3843 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9611    0.0960   -0.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5218   -0.0968    0.5275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6834   -0.3682   -0.4719 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9938    0.0270    0.0991 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0441    1.4383    0.6205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3265   -0.8120    1.1813 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1042   -0.1180   -0.9175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6385    0.3769   -0.1484 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.3751    0.4860   -1.5524 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4725   -1.4083    2.2560 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0137    0.4106    2.1445 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4331   -0.0987    2.9063 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9321   -0.9311    2.9511 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3302   -1.1104    3.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7832   -0.6324    1.1958 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7160    0.0254   -0.9226 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8432    0.9791   -3.9543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6309    0.9979   -3.6920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5017   -1.0342    1.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9342    0.7815    1.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6930   -1.3942   -0.8218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4939    2.1613    0.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1103    1.7518    0.6181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7408    1.4753    1.7075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2228   -0.6112    1.5308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2139   -1.1884   -1.1861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9540    0.5218   -1.8046 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 19  1  0
 19 18  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  1
 20 23  1  0
 23 24  1  0
 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
  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
 19 37  1  6
 18 35  1  0
 18 36  1  0
 21 38  1  0
 21 39  1  0
 21 40  1  0
 22 41  1  0
 23 42  1  0
 23 43  1  0
 14 34  1  0
 13 33  1  0
M  END


  Mrv0541 05061305032D          

 25 28  0  0  0  0            999 V2000
    1.0274    2.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5210    2.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1879    1.4729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9384    2.2593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6317    0.8636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1326    2.4364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0010    2.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1019    0.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9743    3.2356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8259    1.0407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4086    1.5719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5764    1.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9077   -0.0008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8524    0.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1929    2.1231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4639    0.6085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2144    1.3948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2697    0.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5836    2.6794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1879    2.9860    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.7706    2.0041    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1573   -0.7872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5193   -0.3549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1398    3.2887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1010    1.3033    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
 10  5  2  0  0  0  0
 11  7  1  0  0  0  0
 12  6  2  0  0  0  0
 12 10  1  0  0  0  0
 13  8  2  0  0  0  0
 14  8  1  0  0  0  0
 14 11  2  0  0  0  0
 15  7  1  0  0  0  0
 16 13  1  0  0  0  0
 17 11  1  0  0  0  0
 17 16  2  0  0  0  0
 18 10  1  0  0  0  0
 18 16  1  0  0  0  0
 19  1  1  0  0  0  0
 19  9  1  0  0  0  0
 19 15  1  0  0  0  0
 20  9  1  0  0  0  0
 21  2  1  0  0  0  0
 21 12  1  0  0  0  0
 21 17  1  0  0  0  0
 22 13  1  0  0  0  0
 23 18  2  0  0  0  0
 24 19  1  0  0  0  0
 25 14  1  0  0  0  0
 25 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0144701

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C2=CC=CC=C2C(=O)C2=C1C1=C(OC(C1)C(C)(O)CCl)C=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C19H18ClNO4/c1-19(24,9-20)15-7-11-14(25-15)8-13(22)16-17(11)21(2)12-6-4-3-5-10(12)18(16)23/h3-6,8,15,22,24H,7,9H2,1-2H3

> <INCHI_KEY>
PGOOUZZLZBIMRI-UHFFFAOYSA-N

> <FORMULA>
C19H18ClNO4

> <MOLECULAR_WEIGHT>
359.804

> <EXACT_MASS>
359.092435776

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
36.94039797813048

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1H,2H,6H,11H-furo[2,3-c]acridin-6-one

> <ALOGPS_LOGP>
2.94

> <JCHEM_LOGP>
3.726105437666666

> <ALOGPS_LOGS>
-3.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.265837796383028

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.280038082886147

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5575206997625015

> <JCHEM_POLAR_SURFACE_AREA>
70

> <JCHEM_REFRACTIVITY>
95.32629999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.55e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1H,2H-furo[2,3-c]acridin-6-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       1.918   3.864   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.439   5.209   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.417   2.749   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.952   4.217   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.379   1.612   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.448   4.548   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.602   4.273   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.790   0.329   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.819   6.040   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.875   1.943   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.363   2.934   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.409   3.411   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.294  -0.001   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.324   1.797   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.093   3.963   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.333   1.136   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.867   2.604   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.837   0.805   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.956   5.002   0.000  0.00  0.00           C+0
HETATM   20 Cl   UNK     0       0.351   5.574   0.000  0.00  0.00          Cl+0
HETATM   21  N   UNK     0       8.905   3.741   0.000  0.00  0.00           N+0
HETATM   22  O   UNK     0       7.760  -1.469   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      10.303  -0.662   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       3.994   6.139   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       3.922   2.433   0.000  0.00  0.00           O+0
CONECT    1   19                                                            
CONECT    2   21                                                            
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3   10                                                       
CONECT    6    4   12                                                       
CONECT    7   11   15                                                       
CONECT    8   13   14                                                       
CONECT    9   19   20                                                       
CONECT   10    5   12   18                                                  
CONECT   11    7   14   17                                                  
CONECT   12    6   10   21                                                  
CONECT   13    8   16   22                                                  
CONECT   14    8   11   25                                                  
CONECT   15    7   19   25                                                  
CONECT   16   13   17   18                                                  
CONECT   17   11   16   21                                                  
CONECT   18   10   16   23                                                  
CONECT   19    1    9   15   24                                             
CONECT   20    9                                                            
CONECT   21    2   12   17                                                  
CONECT   22   13                                                            
CONECT   23   18                                                            
CONECT   24   19                                                            
CONECT   25   14   15                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Value	Source
2-(2-Chloro-1-hydroxy-1-methylethyl)-1,11-dihydro-5-hydroxy-11-methylfuro[2,3-c]acridin-6(2H)-one	HMDB
Isogravacridonchlorine	HMDB
Isogravacridone chlorine	HMDB

Chemical Formula

C₁₉H₁₈ClNO₄

Average Mass

359.8040 Da

Monoisotopic Mass

359.09244 Da

IUPAC Name

2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1H,2H,6H,11H-furo[2,3-c]acridin-6-one

Traditional Name

2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1H,2H-furo[2,3-c]acridin-6-one

CAS Registry Number

Not Available

SMILES

CN1C2=CC=CC=C2C(=O)C2=C1C1=C(OC(C1)C(C)(O)CCl)C=C2O

InChI Identifier

InChI=1S/C19H18ClNO4/c1-19(24,9-20)15-7-11-14(25-15)8-13(22)16-17(11)21(2)12-6-4-3-5-10(12)18(16)23/h3-6,8,15,22,24H,7,9H2,1-2H3

InChI Key

PGOOUZZLZBIMRI-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 chalepensis	LOTUS Database	35616633
Ruta graveolens	LOTUS Database	35616633
Thamnosma montana	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
Tertiary alcohol
Heteroaromatic compound
Vinylogous acid
Vinylogous amide
Chlorohydrin
Halohydrin
Oxacycle
Azacycle
Ether
Alcohol
Organochloride
Organohalogen compound
Organic oxide
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Alkyl halide
Organic oxygen compound
Alkyl chloride
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	2.94	ALOGPS
logP	3.73	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	10.28	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	70 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	95.33 m³·mol⁻¹	ChemAxon
Polarizability	36.94 Å³	ChemAxon
Number of Rings	4	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

HMDB0030189

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB002007

KNApSAcK ID

Not Available

Chemspider ID

4589118

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5486900

PDB ID

Not Available

ChEBI ID

542693

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one (NP0144701)

MOL for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)

3D MOL for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)

3D SDF for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)

3D-SDF for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)

PDB for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)

3D PDB for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)

SMILES for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)

INCHI for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)

Structure for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)

3D Structure for NP0144701 (2-(1-chloro-2-hydroxypropan-2-yl)-5-hydroxy-11-methyl-1h,2h-furo[2,3-c]acridin-6-one)