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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2013-05-17 00:54:59 UTC

Update Date

2022-03-07 03:17:43 UTC

HMDB ID

HMDB0060341

Secondary Accession Numbers

HMDB60341

Metabolite Identification

Common Name

1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene

Description

1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene. 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene is an extremely weak basic (essentially neutral) compound (based on its pKa). 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene exists in all living organisms, ranging from bacteria to humans. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0060341
     RDKit          3D
1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene
 37 41  0  0  0  0  0  0  0  0999 V2000
   -2.1390    2.2519   -1.5075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5485    1.0826   -0.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3013    0.0935   -0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6728    0.1307   -0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4672   -0.8503    0.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8489   -1.8903    0.9088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4504   -1.9573    0.9842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6943   -0.9663    0.4082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2833   -1.0632    0.5147 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3159   -2.3065    1.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -0.0364   -0.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8055   -0.0460    0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860    0.9659   -0.6136 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9553    1.9862   -1.2516 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5886    2.0394   -1.3101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1553    1.0392   -0.7175 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9897    0.6421   -0.7088 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1563    0.9777   -0.2831 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4233    0.6504    0.7384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7082   -0.4115    1.3475 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4390   -0.8095    1.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7486    2.2689   -2.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2219    2.3475   -1.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7489    3.2024   -1.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2146    0.9197   -0.7870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5439   -0.7887    0.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4699   -2.6637    1.3569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0142   -2.7716    1.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1648   -2.7298    0.4116 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1915   -2.5910    2.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4359   -3.0920    0.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5779    2.7508   -1.7089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0630    2.8480   -1.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0974   -0.3500   -1.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2210    1.6630    1.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2166   -0.9965    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0445   -1.5396    1.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 13 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 16  2  1  0
 19 17  1  0
  8  3  1  0
 16 11  1  0
 21 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  5 26  1  0
  6 27  1  0
  7 28  1  0
 10 29  1  0
 10 30  1  0
 10 31  1  0
 14 32  1  0
 15 33  1  0
 17 34  1  0
 19 35  1  0
 20 36  1  0
 21 37  1  0
M  END


  Mrv0541 05161317542D          

 21 25  0  0  0  0            999 V2000
    3.9862    1.7440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1157    4.9271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7273    3.5031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5097    4.2989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1469    2.9167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7117    4.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3903    2.1628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5923    2.3722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7374    4.5502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9394    4.7596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7686    2.5398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3333    4.1313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3490    3.1261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1313    3.9219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9706    2.7492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9550    3.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3747    3.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3591    4.1732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7530    3.5450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5767    3.3774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2213    3.5869    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
  8  7  2  0  0  0  0
 10  9  2  0  0  0  0
 11  1  1  0  0  0  0
 12  2  1  0  0  0  0
 13  5  2  0  0  0  0
 13 11  1  0  0  0  0
 14  6  2  0  0  0  0
 14 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15  7  1  0  0  0  0
 15 11  2  0  0  0  0
 16  9  1  0  0  0  0
 17  8  1  0  0  0  0
 17 16  2  0  0  0  0
 18 10  1  0  0  0  0
 19 12  2  0  0  0  0
 19 15  1  0  0  0  0
 19 16  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 18  1  0  0  0  0
 21 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0060341

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=C2C=CC3=C(C=CC4OC34)C2=C(C)C2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O/c1-11-13-5-3-4-6-14(13)12(2)19-15(11)7-8-17-16(19)9-10-18-20(17)21-18/h3-10,18,20H,1-2H3

> <INCHI_KEY>
UZKWBBZEYBCHIN-UHFFFAOYSA-N

> <FORMULA>
C20H16O

> <MOLECULAR_WEIGHT>
272.3404

> <EXACT_MASS>
272.120115134

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
31.194407356173247

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12,19-dimethyl-6-oxapentacyclo[9.8.0.0²,⁸.0⁵,⁷.0¹³,¹⁸]nonadeca-1(19),2(8),3,9,11,13,15,17-octaene

> <ALOGPS_LOGP>
5.24

> <JCHEM_LOGP>
5.163971015666666

> <ALOGPS_LOGS>
-7.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.267011944497295

> <JCHEM_POLAR_SURFACE_AREA>
12.53

> <JCHEM_REFRACTIVITY>
86.85249999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.23e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12,19-dimethyl-6-oxapentacyclo[9.8.0.0²,⁸.0⁵,⁷.0¹³,¹⁸]nonadeca-1(19),2(8),3,9,11,13,15,17-octaene

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0060341
     RDKit          3D
1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene
 37 41  0  0  0  0  0  0  0  0999 V2000
   -2.1390    2.2519   -1.5075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5485    1.0826   -0.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3013    0.0935   -0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6728    0.1307   -0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4672   -0.8503    0.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8489   -1.8903    0.9088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4504   -1.9573    0.9842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6943   -0.9663    0.4082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2833   -1.0632    0.5147 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3159   -2.3065    1.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -0.0364   -0.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8055   -0.0460    0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860    0.9659   -0.6136 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9553    1.9862   -1.2516 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5886    2.0394   -1.3101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1553    1.0392   -0.7175 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9897    0.6421   -0.7088 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1563    0.9777   -0.2831 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4233    0.6504    0.7384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7082   -0.4115    1.3475 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4390   -0.8095    1.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7486    2.2689   -2.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2219    2.3475   -1.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7489    3.2024   -1.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2146    0.9197   -0.7870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5439   -0.7887    0.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4699   -2.6637    1.3569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0142   -2.7716    1.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1648   -2.7298    0.4116 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1915   -2.5910    2.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4359   -3.0920    0.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5779    2.7508   -1.7089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0630    2.8480   -1.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0974   -0.3500   -1.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2210    1.6630    1.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2166   -0.9965    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0445   -1.5396    1.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 13 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 16  2  1  0
 19 17  1  0
  8  3  1  0
 16 11  1  0
 21 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  5 26  1  0
  6 27  1  0
  7 28  1  0
 10 29  1  0
 10 30  1  0
 10 31  1  0
 14 32  1  0
 15 33  1  0
 17 34  1  0
 19 35  1  0
 20 36  1  0
 21 37  1  0
M  END

HEADER    PROTEIN                                 16-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-MAY-13         0                                  
HETATM    1  C   UNK     0       7.441   3.255   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.816   9.197   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.691   6.539   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.285   8.025   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.608   5.445   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.795   8.415   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.462   4.037   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.972   4.428   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.243   8.494   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.754   8.885   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.035   4.741   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.222   7.712   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.118   5.835   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.712   7.321   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.545   5.132   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.649   7.008   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.566   5.914   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.670   7.790   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.139   6.617   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.077   6.304   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.413   6.696   0.000  0.00  0.00           O+0
CONECT    1   11                                                            
CONECT    2   12                                                            
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3   13                                                       
CONECT    6    4   14                                                       
CONECT    7    8   15                                                       
CONECT    8    7   17                                                       
CONECT    9   10   16                                                       
CONECT   10    9   18                                                       
CONECT   11    1   13   15                                                  
CONECT   12    2   14   19                                                  
CONECT   13    5   11   14                                                  
CONECT   14    6   12   13                                                  
CONECT   15    7   11   19                                                  
CONECT   16    9   17   19                                                  
CONECT   17    8   16   20                                                  
CONECT   18   10   20   21                                                  
CONECT   19   12   15   16                                                  
CONECT   20   17   18   21                                                  
CONECT   21   18   20                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   50    0
END

COMPND    HMDB0060341
HETATM    1  C1  UNL     1      -2.139   2.252  -1.507  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.549   1.083  -0.798  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.301   0.093  -0.240  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.673   0.131  -0.298  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.467  -0.850   0.270  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.849  -1.890   0.909  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.450  -1.957   0.984  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.694  -0.966   0.408  1.00  0.00           C  
HETATM    9  C9  UNL     1      -0.283  -1.063   0.515  1.00  0.00           C  
HETATM   10  C10 UNL     1       0.316  -2.307   1.013  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.415  -0.036  -0.056  1.00  0.00           C  
HETATM   12  C12 UNL     1       1.805  -0.046   0.001  1.00  0.00           C  
HETATM   13  C13 UNL     1       2.586   0.966  -0.614  1.00  0.00           C  
HETATM   14  C14 UNL     1       1.955   1.986  -1.252  1.00  0.00           C  
HETATM   15  C15 UNL     1       0.589   2.039  -1.310  1.00  0.00           C  
HETATM   16  C16 UNL     1      -0.155   1.039  -0.717  1.00  0.00           C  
HETATM   17  C17 UNL     1       3.990   0.642  -0.709  1.00  0.00           C  
HETATM   18  O1  UNL     1       5.156   0.978  -0.283  1.00  0.00           O  
HETATM   19  C18 UNL     1       4.423   0.650   0.738  1.00  0.00           C  
HETATM   20  C19 UNL     1       3.708  -0.411   1.348  1.00  0.00           C  
HETATM   21  C20 UNL     1       2.439  -0.809   1.065  1.00  0.00           C  
HETATM   22  H1  UNL     1      -1.749   2.269  -2.547  1.00  0.00           H  
HETATM   23  H2  UNL     1      -3.222   2.347  -1.452  1.00  0.00           H  
HETATM   24  H3  UNL     1      -1.749   3.202  -1.025  1.00  0.00           H  
HETATM   25  H4  UNL     1      -4.215   0.920  -0.787  1.00  0.00           H  
HETATM   26  H5  UNL     1      -5.544  -0.789   0.205  1.00  0.00           H  
HETATM   27  H6  UNL     1      -4.470  -2.664   1.357  1.00  0.00           H  
HETATM   28  H7  UNL     1      -2.014  -2.772   1.504  1.00  0.00           H  
HETATM   29  H8  UNL     1       1.165  -2.730   0.412  1.00  0.00           H  
HETATM   30  H9  UNL     1       0.191  -2.591   2.035  1.00  0.00           H  
HETATM   31  H10 UNL     1      -0.436  -3.092   0.544  1.00  0.00           H  
HETATM   32  H11 UNL     1       2.578   2.751  -1.709  1.00  0.00           H  
HETATM   33  H12 UNL     1       0.063   2.848  -1.814  1.00  0.00           H  
HETATM   34  H13 UNL     1       4.097  -0.350  -1.294  1.00  0.00           H  
HETATM   35  H14 UNL     1       4.221   1.663   1.303  1.00  0.00           H  
HETATM   36  H15 UNL     1       4.217  -0.996   2.142  1.00  0.00           H  
HETATM   37  H16 UNL     1       2.044  -1.540   1.660  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3    3   16
CONECT    3    4    8
CONECT    4    5    5   25
CONECT    5    6   26
CONECT    6    7    7   27
CONECT    7    8   28
CONECT    8    9    9
CONECT    9   10   11
CONECT   10   29   30   31
CONECT   11   12   12   16
CONECT   12   13   21
CONECT   13   14   14   17
CONECT   14   15   32
CONECT   15   16   16   33
CONECT   17   18   19   34
CONECT   18   19
CONECT   19   20   35
CONECT   20   21   21   36
CONECT   21   37
END

HMDB0060341
     RDKit          3D
1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene
 37 41  0  0  0  0  0  0  0  0999 V2000
   -2.1390    2.2519   -1.5075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5485    1.0826   -0.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3013    0.0935   -0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6728    0.1307   -0.2975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4672   -0.8503    0.2696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8489   -1.8903    0.9088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4504   -1.9573    0.9842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6943   -0.9663    0.4082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2833   -1.0632    0.5147 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3159   -2.3065    1.0126 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4146   -0.0364   -0.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8055   -0.0460    0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5860    0.9659   -0.6136 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9553    1.9862   -1.2516 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5886    2.0394   -1.3101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1553    1.0392   -0.7175 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9897    0.6421   -0.7088 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1563    0.9777   -0.2831 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4233    0.6504    0.7384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7082   -0.4115    1.3475 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4390   -0.8095    1.0655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7486    2.2689   -2.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2219    2.3475   -1.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7489    3.2024   -1.0248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2146    0.9197   -0.7870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5439   -0.7887    0.2047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4699   -2.6637    1.3569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0142   -2.7716    1.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1648   -2.7298    0.4116 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1915   -2.5910    2.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4359   -3.0920    0.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5779    2.7508   -1.7089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0630    2.8480   -1.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0974   -0.3500   -1.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2210    1.6630    1.3030 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2166   -0.9965    2.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0445   -1.5396    1.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 13 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 16  2  1  0
 19 17  1  0
  8  3  1  0
 16 11  1  0
 21 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  5 26  1  0
  6 27  1  0
  7 28  1  0
 10 29  1  0
 10 30  1  0
 10 31  1  0
 14 32  1  0
 15 33  1  0
 17 34  1  0
 19 35  1  0
 20 36  1  0
 21 37  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₀H₁₆O

Average Molecular Weight

272.3404

Monoisotopic Molecular Weight

272.120115134

IUPAC Name

12,19-dimethyl-6-oxapentacyclo[9.8.0.0²,⁸.0⁵,⁷.0¹³,¹⁸]nonadeca-1(19),2(8),3,9,11,13,15,17-octaene

Traditional Name

12,19-dimethyl-6-oxapentacyclo[9.8.0.0²,⁸.0⁵,⁷.0¹³,¹⁸]nonadeca-1(19),2(8),3,9,11,13,15,17-octaene

CAS Registry Number

Not Available

SMILES

CC1=C2C=CC3=C(C=CC4OC34)C2=C(C)C2=CC=CC=C12

InChI Identifier

InChI=1S/C20H16O/c1-11-13-5-3-4-6-14(13)12(2)19-15(11)7-8-17-16(19)9-10-18-20(17)21-18/h3-10,18,20H,1-2H3

InChI Key

UZKWBBZEYBCHIN-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Not Available

Direct Parent

Phenanthrenes and derivatives

Alternative Parents

Substituents

Phenanthrene
Anthracene
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

phenanthrenes (CHEBI:82517 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Membrane (HMDB: HMDB0060341)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	2.2e-05 g/L	ALOGPS
logP	5.24	ALOGPS
logP	5.16	ChemAxon
logS	-7.1	ALOGPS
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	12.53 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	86.85 m³·mol⁻¹	ChemAxon
Polarizability	31.19 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	163.228	31661259
DarkChem	[M-H]-	162.645	31661259
DeepCCS	[M-2H]-	197.211	30932474
DeepCCS	[M+Na]+	172.776	30932474
AllCCS	[M+H]+	165.6	32859911
AllCCS	[M+H-H2O]+	161.8	32859911
AllCCS	[M+NH4]+	169.1	32859911
AllCCS	[M+Na]+	170.1	32859911
AllCCS	[M-H]-	173.1	32859911
AllCCS	[M+Na-2H]-	171.8	32859911
AllCCS	[M+HCOO]-	170.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene	CC1=C2C=CC3=C(C=CC4OC34)C2=C(C)C2=CC=CC=C12	3843.9	Standard polar	33892256
1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene	CC1=C2C=CC3=C(C=CC4OC34)C2=C(C)C2=CC=CC=C12	2593.1	Standard non polar	33892256
1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene	CC1=C2C=CC3=C(C=CC4OC34)C2=C(C)C2=CC=CC=C12	2828.8	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene GC-MS (Non-derivatized) - 70eV, Positive	splash10-0abc-0190000000-2d545c03ff847ffe89ec	2017-09-20	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene 10V, Positive-QTOF	splash10-00di-0090000000-2a16a794047535245ee6	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene 20V, Positive-QTOF	splash10-05fr-0090000000-e6a1bce61fdabaf55551	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene 40V, Positive-QTOF	splash10-0zi0-0490000000-8f802df6e498892784bf	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene 10V, Negative-QTOF	splash10-00di-0090000000-1b00db8ec13edbabb3b8	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene 20V, Negative-QTOF	splash10-00di-0090000000-ac6f4dfbf1dd0abc5391	2017-10-06	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene 40V, Negative-QTOF	splash10-0ki7-0090000000-a687b57eb267bb9dbe02	2017-10-06	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane (predicted from logP)

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C19489

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53297434

PDB ID

Not Available

ChEBI ID

82517

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Magrane M: UniProt Knowledgebase: a hub of integrated protein data. Database (Oxford). 2011 Mar 29;2011:bar009. doi: 10.1093/database/bar009. Print 2011. [PubMed:21447597 ]

Enzymes

Enzyme Details

1. Epoxide hydrolase 1

General function:: Involved in catalytic activity
Specific function:: Biotransformation enzyme that catalyzes the hydrolysis of arene and aliphatic epoxides to less reactive and more water soluble dihydrodiols by the trans addition of water.
Gene Name:: EPHX1
Uniprot ID:: P07099
Molecular weight:: 52948.48

Reactions

1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene + Water → trans-3,4-Dihydro-3,4-dihydroxy-7,12-dimethylbenz[a]anthracene	details

Showing metabocard for 1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene (HMDB0060341)

MOL for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

3D MOL for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

3D SDF for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

3D-SDF for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

PDB for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

3D PDB for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

SMILES for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

INCHI for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

Structure for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

3D Structure for HMDB0060341 (1a,11b-Dihydro-4,9-dimethylbenz[a]anthra[3,4-b]oxirene)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra

Enzymes

Reactions