NP-MRD: Showing NP-Card for Antarlide E (NP0015138)

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Record Information

Version

2.0

Created at

2021-01-06 00:16:02 UTC

Updated at

2024-09-12 20:24:51 UTC

NP-MRD ID

NP0015138

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Antarlide E

Provided By

NPAtlas

Description

Antarlide E belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. Antarlide E is found in Streptomyces. Based on a literature review very few articles have been published on Antarlide E.

Structure

MOL SDF PDB SMILES InChI

NP0015138
  Mrv2104 05272322573D          

 83 84  0  0  0  0            999 V2000
    2.0743    4.1849    0.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9329    3.2179    0.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3857    3.4897    0.5599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9649    4.8177    0.5872 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2659    5.1441    0.5017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4203    4.2944    0.3211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7943    3.2957    1.1343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0280    2.5688    0.9337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4540    1.5736    1.7256 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

NP0015138
  Mrv2104 05272322573D          

 83 84  0  0  0  0            999 V2000
    2.0743    4.1849    0.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9329    3.2179    0.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0280    2.5688    0.9337 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5885   -2.3918    0.6189 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3462   -0.2809   -2.2619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6539   -0.4901   -0.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8979   -0.1480    0.4014 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7213   -0.0200   -2.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5299    1.6391   -2.1368 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7960    2.0939   -0.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9175    2.3266   -2.1038 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6008   -1.8134   -1.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7390   -1.2731   -2.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825   -2.0602    1.3487 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3390   -1.7230    3.5882 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1810   -0.0829    3.9253 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5869    1.6869    1.2186 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1131    0.8562   -0.2710 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 25 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38  2  1  0  0  0  0
 36 30  1  0  0  0  0
  1 40  1  0  0  0  0
  1 41  1  0  0  0  0
  1 42  1  0  0  0  0
  3 43  1  0  0  0  0
  4 44  1  0  0  0  0
  5 45  1  0  0  0  0
  6 46  1  0  0  0  0
  7 47  1  0  0  0  0
  8 48  1  0  0  0  0
  9 49  1  0  0  0  0
 10 50  1  0  0  0  0
 10 51  1  0  0  0  0
 11 52  1  1  0  0  0
 12 53  1  0  0  0  0
 14 54  1  0  0  0  0
 14 55  1  0  0  0  0
 14 56  1  0  0  0  0
 15 57  1  0  0  0  0
 16 58  1  0  0  0  0
 17 59  1  0  0  0  0
 18 60  1  6  0  0  0
 19 61  1  0  0  0  0
 19 62  1  0  0  0  0
 19 63  1  0  0  0  0
 20 64  1  0  0  0  0
 20 65  1  0  0  0  0
 21 66  1  0  0  0  0
 21 67  1  0  0  0  0
 22 68  1  6  0  0  0
 23 69  1  0  0  0  0
 24 70  1  0  0  0  0
 24 71  1  0  0  0  0
 25 72  1  1  0  0  0
 26 73  1  6  0  0  0
 27 74  1  0  0  0  0
 27 75  1  0  0  0  0
 27 76  1  0  0  0  0
 28 77  1  1  0  0  0
 29 78  1  0  0  0  0
 31 79  1  0  0  0  0
 32 80  1  0  0  0  0
 33 81  1  0  0  0  0
 35 82  1  0  0  0  0
 36 83  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0015138

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(=C([H])C([H])=C1[H])[C@]([H])(O[H])[C@]([H])(C([H])([H])[H])[C@@]1([H])OC(=O)\C(=C(/[H])\C(\[H])=C(\[H])/C(/[H])=C(\[H])/C(/[H])=C([H])/C([H])([H])[C@@]([H])(O[H])\C(=C(/[H])\C(\[H])=C([H])\[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[C@]([H])(O[H])C1([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1/C33H44O6/c1-23-13-11-15-24(2)30(36)18-10-8-6-5-7-9-14-25(3)33(38)39-31(22-29(35)20-19-23)26(4)32(37)27-16-12-17-28(34)21-27/h5-17,21,23,26,29-32,34-37H,18-20,22H2,1-4H3/b6-5+,9-7-,10-8+,13-11+,24-15+,25-14+/t23-,26+,29-,30+,31-,32+/s2

> <INCHI_KEY>
YNAQNPGWTKBAKU-IZAGOXLGNA-N

> <FORMULA>
C33H44O6

> <MOLECULAR_WEIGHT>
536.709

> <EXACT_MASS>
536.313789137

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
61.98239828628155

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3E,5Z,7E,9E,12R,13E,15E,17R,20S,22S)-12,20-dihydroxy-22-[(1R,2S)-1-hydroxy-1-(3-hydroxyphenyl)propan-2-yl]-3,13,17-trimethyl-1-oxacyclodocosa-3,5,7,9,13,15-hexaen-2-one

> <JCHEM_LOGP>
5.7539976296666655

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.21385280662631

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.364429630823718

> <JCHEM_PKA_STRONGEST_BASIC>
-1.323666134479385

> <JCHEM_POLAR_SURFACE_AREA>
107.22

> <JCHEM_REFRACTIVITY>
163.0385

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3E,5Z,7E,9E,12R,13E,15E,17R,20S,22S)-12,20-dihydroxy-22-[(1R,2S)-1-hydroxy-1-(3-hydroxyphenyl)propan-2-yl]-3,13,17-trimethyl-1-oxacyclodocosa-3,5,7,9,13,15-hexaen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-MAY-23   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: NP0015138                                         
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-MAY-23         0                                  
HETATM    1  C   UNK     0       2.074   4.185   0.609  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.933   3.218   0.555  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.386   3.490   0.560  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.965   4.818   0.587  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.266   5.144   0.502  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.420   4.294   0.321  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.794   3.296   1.134  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.028   2.569   0.934  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.454   1.574   1.726  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.780   0.882   1.526  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.696  -0.643   1.300  0.00  0.00           C+0
HETATM   12  O   UNK     0      -8.027  -1.143   1.159  0.00  0.00           O+0
HETATM   13  C   UNK     0      -5.871  -1.075   0.096  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.248  -0.458  -1.227  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.866  -1.959   0.274  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.904  -2.392  -0.715  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.950  -3.294  -0.439  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.822  -3.626  -1.389  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.720  -5.135  -1.595  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.532  -3.022  -0.802  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.637  -2.987  -1.796  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.845  -2.164  -1.313  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.271  -2.636  -0.037  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.571  -0.658  -1.256  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.678   0.207  -0.610  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.987   0.242  -1.452  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.596   1.652  -1.569  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.040  -0.813  -1.002  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.098  -0.850  -1.967  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.658  -0.601   0.369  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.179  -1.330   1.473  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.721  -1.143   2.748  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.756  -0.228   2.938  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.248   0.482   1.850  0.00  0.00           C+0
HETATM   35  O   UNK     0       8.272   1.352   2.074  0.00  0.00           O+0
HETATM   36  C   UNK     0       6.714   0.303   0.575  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.148   1.556  -0.494  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.303   1.783   0.543  0.00  0.00           C+0
HETATM   39  O   UNK     0       0.884   0.956   1.338  0.00  0.00           O+0
HETATM   40  H   UNK     0       1.814   5.117   1.121  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.916   3.763   1.171  0.00  0.00           H+0
HETATM   42  H   UNK     0       2.424   4.423  -0.401  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.087   2.653   0.534  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.268   5.651   0.661  0.00  0.00           H+0
HETATM   45  H   UNK     0      -2.510   6.208   0.489  0.00  0.00           H+0
HETATM   46  H   UNK     0      -4.059   4.581  -0.513  0.00  0.00           H+0
HETATM   47  H   UNK     0      -3.184   3.033   1.995  0.00  0.00           H+0
HETATM   48  H   UNK     0      -5.655   2.883   0.097  0.00  0.00           H+0
HETATM   49  H   UNK     0      -4.857   1.252   2.575  0.00  0.00           H+0
HETATM   50  H   UNK     0      -7.391   1.060   2.420  0.00  0.00           H+0
HETATM   51  H   UNK     0      -7.348   1.347   0.710  0.00  0.00           H+0
HETATM   52  H   UNK     0      -6.297  -1.095   2.216  0.00  0.00           H+0
HETATM   53  H   UNK     0      -8.023  -1.820   0.457  0.00  0.00           H+0
HETATM   54  H   UNK     0      -5.894   0.576  -1.282  0.00  0.00           H+0
HETATM   55  H   UNK     0      -5.831  -0.999  -2.081  0.00  0.00           H+0
HETATM   56  H   UNK     0      -7.335  -0.465  -1.361  0.00  0.00           H+0
HETATM   57  H   UNK     0      -4.698  -2.361   1.274  0.00  0.00           H+0
HETATM   58  H   UNK     0      -3.909  -1.906  -1.685  0.00  0.00           H+0
HETATM   59  H   UNK     0      -2.918  -3.772   0.540  0.00  0.00           H+0
HETATM   60  H   UNK     0      -2.018  -3.162  -2.365  0.00  0.00           H+0
HETATM   61  H   UNK     0      -0.936  -5.383  -2.317  0.00  0.00           H+0
HETATM   62  H   UNK     0      -1.496  -5.658  -0.658  0.00  0.00           H+0
HETATM   63  H   UNK     0      -2.661  -5.541  -1.984  0.00  0.00           H+0
HETATM   64  H   UNK     0      -0.236  -3.586   0.093  0.00  0.00           H+0
HETATM   65  H   UNK     0      -0.755  -2.004  -0.465  0.00  0.00           H+0
HETATM   66  H   UNK     0       0.972  -4.019  -1.965  0.00  0.00           H+0
HETATM   67  H   UNK     0       0.299  -2.594  -2.763  0.00  0.00           H+0
HETATM   68  H   UNK     0       2.665  -2.346  -2.015  0.00  0.00           H+0
HETATM   69  H   UNK     0       1.589  -2.392   0.619  0.00  0.00           H+0
HETATM   70  H   UNK     0       1.346  -0.281  -2.262  0.00  0.00           H+0
HETATM   71  H   UNK     0       0.654  -0.490  -0.684  0.00  0.00           H+0
HETATM   72  H   UNK     0       2.898  -0.148   0.401  0.00  0.00           H+0
HETATM   73  H   UNK     0       3.721  -0.020  -2.488  0.00  0.00           H+0
HETATM   74  H   UNK     0       5.530   1.639  -2.137  0.00  0.00           H+0
HETATM   75  H   UNK     0       4.796   2.094  -0.589  0.00  0.00           H+0
HETATM   76  H   UNK     0       3.918   2.327  -2.104  0.00  0.00           H+0
HETATM   77  H   UNK     0       4.601  -1.813  -1.016  0.00  0.00           H+0
HETATM   78  H   UNK     0       5.739  -1.273  -2.766  0.00  0.00           H+0
HETATM   79  H   UNK     0       4.383  -2.060   1.349  0.00  0.00           H+0
HETATM   80  H   UNK     0       5.339  -1.723   3.588  0.00  0.00           H+0
HETATM   81  H   UNK     0       7.181  -0.083   3.925  0.00  0.00           H+0
HETATM   82  H   UNK     0       8.587   1.687   1.219  0.00  0.00           H+0
HETATM   83  H   UNK     0       7.113   0.856  -0.271  0.00  0.00           H+0
CONECT    1    2   40   41   42                                             
CONECT    2    1    3   38                                                  
CONECT    3    2    4   43                                                  
CONECT    4    3    5   44                                                  
CONECT    5    4    6   45                                                  
CONECT    6    5    7   46                                                  
CONECT    7    6    8   47                                                  
CONECT    8    7    9   48                                                  
CONECT    9    8   10   49                                                  
CONECT   10    9   11   50   51                                             
CONECT   11   10   12   13   52                                             
CONECT   12   11   53                                                       
CONECT   13   11   14   15                                                  
CONECT   14   13   54   55   56                                             
CONECT   15   13   16   57                                                  
CONECT   16   15   17   58                                                  
CONECT   17   16   18   59                                                  
CONECT   18   17   19   20   60                                             
CONECT   19   18   61   62   63                                             
CONECT   20   18   21   64   65                                             
CONECT   21   20   22   66   67                                             
CONECT   22   21   23   24   68                                             
CONECT   23   22   69                                                       
CONECT   24   22   25   70   71                                             
CONECT   25   24   26   37   72                                             
CONECT   26   25   27   28   73                                             
CONECT   27   26   74   75   76                                             
CONECT   28   26   29   30   77                                             
CONECT   29   28   78                                                       
CONECT   30   28   31   36                                                  
CONECT   31   30   32   79                                                  
CONECT   32   31   33   80                                                  
CONECT   33   32   34   81                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34   82                                                       
CONECT   36   34   30   83                                                  
CONECT   37   25   38                                                       
CONECT   38   37   39    2                                                  
CONECT   39   38                                                            
CONECT   40    1                                                            
CONECT   41    1                                                            
CONECT   42    1                                                            
CONECT   43    3                                                            
CONECT   44    4                                                            
CONECT   45    5                                                            
CONECT   46    6                                                            
CONECT   47    7                                                            
CONECT   48    8                                                            
CONECT   49    9                                                            
CONECT   50   10                                                            
CONECT   51   10                                                            
CONECT   52   11                                                            
CONECT   53   12                                                            
CONECT   54   14                                                            
CONECT   55   14                                                            
CONECT   56   14                                                            
CONECT   57   15                                                            
CONECT   58   16                                                            
CONECT   59   17                                                            
CONECT   60   18                                                            
CONECT   61   19                                                            
CONECT   62   19                                                            
CONECT   63   19                                                            
CONECT   64   20                                                            
CONECT   65   20                                                            
CONECT   66   21                                                            
CONECT   67   21                                                            
CONECT   68   22                                                            
CONECT   69   23                                                            
CONECT   70   24                                                            
CONECT   71   24                                                            
CONECT   72   25                                                            
CONECT   73   26                                                            
CONECT   74   27                                                            
CONECT   75   27                                                            
CONECT   76   27                                                            
CONECT   77   28                                                            
CONECT   78   29                                                            
CONECT   79   31                                                            
CONECT   80   32                                                            
CONECT   81   33                                                            
CONECT   82   35                                                            
CONECT   83   36                                                            
MASTER        0    0    0    0    0    0    0    0   83    0  168    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₄O₆

Average Mass

536.7090 Da

Monoisotopic Mass

536.31379 Da

IUPAC Name

(3E,5Z,7E,9E,12R,13E,15E,17R,20S,22S)-12,20-dihydroxy-22-[(1R,2S)-1-hydroxy-1-(3-hydroxyphenyl)propan-2-yl]-3,13,17-trimethyl-1-oxacyclodocosa-3,5,7,9,13,15-hexaen-2-one

Traditional Name

(3E,5Z,7E,9E,12R,13E,15E,17R,20S,22S)-12,20-dihydroxy-22-[(1R,2S)-1-hydroxy-1-(3-hydroxyphenyl)propan-2-yl]-3,13,17-trimethyl-1-oxacyclodocosa-3,5,7,9,13,15-hexaen-2-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C(=C([H])C([H])=C1[H])[C@]([H])(O[H])[C@]([H])(C([H])([H])[H])[C@@]1([H])OC(=O)\C(=C(/[H])\C(\[H])=C(\[H])/C(/[H])=C(\[H])/C(/[H])=C([H])/C([H])([H])[C@@]([H])(O[H])\C(=C(/[H])\C(\[H])=C([H])\[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[C@]([H])(O[H])C1([H])[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1/C33H44O6/c1-23-13-11-15-24(2)30(36)18-10-8-6-5-7-9-14-25(3)33(38)39-31(22-29(35)20-19-23)26(4)32(37)27-16-12-17-28(34)21-27/h5-17,21,23,26,29-32,34-37H,18-20,22H2,1-4H3/b6-5+,9-7-,10-8+,13-11+,24-15+,25-14+/t23-,26+,29-,30+,31-,32+/s2

InChI Key

YNAQNPGWTKBAKU-IZAGOXLGNA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Streptomyces	NPAtlas	26805525

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Phenylpropane
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	5.75	ChemAxon
pKa (Strongest Acidic)	9.36	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	163.04 m³·mol⁻¹	ChemAxon
Polarizability	61.98 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA024330

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

Showing NP-Card for Antarlide E (NP0015138)

MOL for NP0015138 (Antarlide E)

3D MOL for NP0015138 (Antarlide E)

3D SDF for NP0015138 (Antarlide E)

3D-SDF for NP0015138 (Antarlide E)

PDB for NP0015138 (Antarlide E)

3D PDB for NP0015138 (Antarlide E)

SMILES for NP0015138 (Antarlide E)

INCHI for NP0015138 (Antarlide E)

Structure for NP0015138 (Antarlide E)

3D Structure for NP0015138 (Antarlide E)