NP-MRD: Showing NP-Card for Luminacin A1/A2 (NP0003395)

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Record Information

Version

2.0

Created at

2020-12-09 00:39:57 UTC

Updated at

2021-07-15 16:46:19 UTC

NP-MRD ID

NP0003395

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Luminacin A1/A2

Provided By

NPAtlas

Description

Luminacin A1/A2 is found in Streptomyces and Streptomyces sp. Mer-VD1207. Based on a literature review very few articles have been published on Luminacin A1/A2.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117473D          

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     RDKit          3D

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M  END


  Mrv1652306242117473D          

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    2.4808   -0.0365   -1.1807 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7244    0.7903   -0.8354 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6173    2.0750   -1.3552 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1056   -0.2257    1.4279 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0010    0.8545    1.4416 C   0  0  1  0  0  0  0  0  0  0  0  0
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    6.5119   -0.6548    0.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6689    1.7884    1.1071 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -2.5525   -0.3168   -0.0845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6541    0.7739   -0.6063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8578    1.3478    2.2767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7099   -0.0539    1.9660 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.7964    0.5473    1.5643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5017    1.9837    0.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3558   -4.8680    0.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0447   -5.1415   -0.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6576   -0.3639    0.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2121    0.2304   -2.2155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7975   -1.0773   -1.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5807    0.3126   -1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4639    2.0969   -2.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9815    1.3807    2.4402 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6562    1.4614    0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1235    0.7294    1.6892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5738   -1.2467    0.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3160   -1.2378    0.6358 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7956   -0.5071   -0.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0295    2.8279    0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0438    2.2665    2.9496 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  9 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
  4 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  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 18  7  1  0  0  0  0
 31 20  1  0  0  0  0
 26 24  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
  2 35  1  0  0  0  0
  2 36  1  0  0  0  0
  3 37  1  0  0  0  0
  3 38  1  0  0  0  0
  4 39  1  1  0  0  0
  8 40  1  0  0  0  0
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 28 60  1  0  0  0  0
 28 61  1  0  0  0  0
 29 62  1  1  0  0  0
 30 63  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0003395

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C(O[H])=C(C([H])=C1C(=O)[C@]([H])(C([H])([H])C([H])([H])C([H])([H])[H])[C@]1([H])O[C@@]([H])(O[H])[C@@]2(O[C@@]2([H])C([H])([H])C([H])([H])[H])[C@]([H])(O[H])C1([H])[H])C(=O)C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H32O8/c1-5-7-12(17-10-18(26)23(22(29)30-17)19(6-2)31-23)21(28)14-8-13(20(27)11(3)4)15(24)9-16(14)25/h8-9,11-12,17-19,22,24-26,29H,5-7,10H2,1-4H3/t12-,17-,18-,19+,22-,23-/m1/s1

> <INCHI_KEY>
ZVHCTEUOWHUIMG-BTOYHFQMSA-N

> <FORMULA>
C23H32O8

> <MOLECULAR_WEIGHT>
436.501

> <EXACT_MASS>
436.20971799

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
46.31542343719293

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R)-1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-[(2S,3R,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl]pentan-1-one

> <ALOGPS_LOGP>
2.48

> <JCHEM_LOGP>
4.177722871333333

> <ALOGPS_LOGS>
-2.73

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.405530921843912

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.157092582590205

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3808523254602534

> <JCHEM_POLAR_SURFACE_AREA>
136.82000000000002

> <JCHEM_REFRACTIVITY>
112.09219999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.11e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-[(2S,3R,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl]pentan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 63 65  0  0  0  0  0  0  0  0999 V2000
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    4.1056   -0.2257    1.4279 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5119   -0.6548    0.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0295    2.8279    0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0438    2.2665    2.9496 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
  9 15  2  0
 15 16  1  0
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 17 18  2  0
 18 19  1  0
  4 20  1  0
 20 21  1  0
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 22 24  1  0
 24 25  1  1
 25 26  1  0
 26 27  1  0
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 24 29  1  0
 29 30  1  0
 29 31  1  0
 18  7  1  0
 31 20  1  0
 26 24  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  1
  8 40  1  0
 12 41  1  6
 13 42  1  0
 13 43  1  0
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 17 49  1  0
 19 50  1  0
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 26 56  1  1
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 28 59  1  0
 28 60  1  0
 28 61  1  0
 29 62  1  1
 30 63  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.865   2.815  -0.706  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.194   2.079  -1.822  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.468   0.617  -1.809  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.033  -0.027  -0.561  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.214  -1.507  -0.503  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.843  -2.192  -0.621  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.479  -2.139  -0.344  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.631  -1.375  -0.117  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.874  -1.930   0.090  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.070  -1.107   0.314  0.00  0.00           C+0
HETATM   11  O   UNK     0      -6.188  -1.693   0.478  0.00  0.00           O+0
HETATM   12  C   UNK     0      -5.059   0.363   0.364  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.213   0.822   1.521  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.465   0.876   0.559  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.010  -3.298   0.078  0.00  0.00           C+0
HETATM   16  O   UNK     0      -5.288  -3.862   0.291  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.915  -4.068  -0.138  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.637  -3.497  -0.351  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.632  -4.402  -0.556  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.432   0.314  -0.166  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.481  -0.037  -1.181  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.724   0.790  -0.835  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.617   2.075  -1.355  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.824   0.885   0.651  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.106  -0.226   1.428  0.00  0.00           O+0
HETATM   26  C   UNK     0       5.001   0.855   1.442  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.371   0.654   0.865  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.512  -0.655   0.137  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.669   1.788   1.107  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.440   1.650   2.465  0.00  0.00           O+0
HETATM   31  O   UNK     0       1.550   1.590   0.335  0.00  0.00           O+0
HETATM   32  H   UNK     0      -0.179   3.615  -0.325  0.00  0.00           H+0
HETATM   33  H   UNK     0      -1.821   3.284  -1.061  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.124   2.196   0.165  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.463   2.539  -2.823  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.913   2.309  -1.752  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.545   0.468  -1.918  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.031   0.115  -2.728  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.630   0.349   0.285  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.553  -0.317  -0.085  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.654   0.774  -0.606  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.858   1.348   2.277  0.00  0.00           H+0
HETATM   43  H   UNK     0      -3.710  -0.054   1.966  0.00  0.00           H+0
HETATM   44  H   UNK     0      -3.442   1.527   1.117  0.00  0.00           H+0
HETATM   45  H   UNK     0      -7.137   0.507  -0.248  0.00  0.00           H+0
HETATM   46  H   UNK     0      -6.796   0.547   1.564  0.00  0.00           H+0
HETATM   47  H   UNK     0      -6.502   1.984   0.504  0.00  0.00           H+0
HETATM   48  H   UNK     0      -5.356  -4.868   0.276  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.045  -5.141  -0.143  0.00  0.00           H+0
HETATM   50  H   UNK     0       0.300  -4.212  -0.723  0.00  0.00           H+0
HETATM   51  H   UNK     0       1.658  -0.364   0.725  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.212   0.230  -2.216  0.00  0.00           H+0
HETATM   53  H   UNK     0       2.797  -1.077  -1.160  0.00  0.00           H+0
HETATM   54  H   UNK     0       4.581   0.313  -1.332  0.00  0.00           H+0
HETATM   55  H   UNK     0       3.464   2.097  -2.329  0.00  0.00           H+0
HETATM   56  H   UNK     0       4.981   1.381   2.440  0.00  0.00           H+0
HETATM   57  H   UNK     0       6.656   1.461   0.152  0.00  0.00           H+0
HETATM   58  H   UNK     0       7.123   0.729   1.689  0.00  0.00           H+0
HETATM   59  H   UNK     0       5.574  -1.247   0.194  0.00  0.00           H+0
HETATM   60  H   UNK     0       7.316  -1.238   0.636  0.00  0.00           H+0
HETATM   61  H   UNK     0       6.796  -0.507  -0.922  0.00  0.00           H+0
HETATM   62  H   UNK     0       3.030   2.828   0.929  0.00  0.00           H+0
HETATM   63  H   UNK     0       3.044   2.267   2.950  0.00  0.00           H+0
CONECT    1    2   32   33   34                                             
CONECT    2    1    3   35   36                                             
CONECT    3    2    4   37   38                                             
CONECT    4    3    5   20   39                                             
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   18                                                  
CONECT    8    7    9   40                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14   41                                             
CONECT   13   12   42   43   44                                             
CONECT   14   12   45   46   47                                             
CONECT   15    9   16   17                                                  
CONECT   16   15   48                                                       
CONECT   17   15   18   49                                                  
CONECT   18   17   19    7                                                  
CONECT   19   18   50                                                       
CONECT   20    4   21   31   51                                             
CONECT   21   20   22   52   53                                             
CONECT   22   21   23   24   54                                             
CONECT   23   22   55                                                       
CONECT   24   22   25   29   26                                             
CONECT   25   24   26                                                       
CONECT   26   25   27   24   56                                             
CONECT   27   26   28   57   58                                             
CONECT   28   27   59   60   61                                             
CONECT   29   24   30   31   62                                             
CONECT   30   29   63                                                       
CONECT   31   29   20                                                       
CONECT   32    1                                                            
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    2                                                            
CONECT   36    2                                                            
CONECT   37    3                                                            
CONECT   38    3                                                            
CONECT   39    4                                                            
CONECT   40    8                                                            
CONECT   41   12                                                            
CONECT   42   13                                                            
CONECT   43   13                                                            
CONECT   44   13                                                            
CONECT   45   14                                                            
CONECT   46   14                                                            
CONECT   47   14                                                            
CONECT   48   16                                                            
CONECT   49   17                                                            
CONECT   50   19                                                            
CONECT   51   20                                                            
CONECT   52   21                                                            
CONECT   53   21                                                            
CONECT   54   22                                                            
CONECT   55   23                                                            
CONECT   56   26                                                            
CONECT   57   27                                                            
CONECT   58   27                                                            
CONECT   59   28                                                            
CONECT   60   28                                                            
CONECT   61   28                                                            
CONECT   62   29                                                            
CONECT   63   30                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  130    0
END

RDKit          3D

63 65  0  0  0  0  0  0  0  0999 V2000
   -0.8649    2.8153   -0.7057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1936    2.0791   -1.8219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4676    0.6170   -1.8090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0326   -0.0271   -0.5607 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2142   -1.5069   -0.5030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8429   -2.1925   -0.6214 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4792   -2.1387   -0.3439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6310   -1.3751   -0.1173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8743   -1.9303    0.0899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0696   -1.1067    0.3137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1883   -1.6926    0.4779 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0590    0.3628    0.3635 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2130    0.8217    1.5213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4645    0.8760    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0100   -3.2977    0.0778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2880   -3.8618    0.2908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9151   -4.0684   -0.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6367   -3.4971   -0.3514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6321   -4.4021   -0.5557 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4315    0.3136   -0.1664 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4808   -0.0365   -1.1807 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7244    0.7903   -0.8354 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6173    2.0750   -1.3552 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8239    0.8853    0.6506 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1056   -0.2257    1.4279 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0010    0.8545    1.4416 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3708    0.6537    0.8649 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5119   -0.6548    0.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6689    1.7884    1.1071 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4401    1.6495    2.4654 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5495    1.5899    0.3354 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1789    3.6150   -0.3247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8210    3.2836   -1.0610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1237    2.1964    0.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4628    2.5385   -2.8231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9128    2.3088   -1.7520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5447    0.4677   -1.9175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0307    0.1149   -2.7284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6304    0.3490    0.2849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5525   -0.3168   -0.0845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6541    0.7739   -0.6063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8578    1.3478    2.2767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7099   -0.0539    1.9660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4422    1.5272    1.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1371    0.5069   -0.2482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7964    0.5473    1.5643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5017    1.9837    0.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3558   -4.8680    0.2762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0447   -5.1415   -0.1429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2995   -4.2118   -0.7233 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6576   -0.3639    0.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2121    0.2304   -2.2155 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7975   -1.0773   -1.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5807    0.3126   -1.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4639    2.0969   -2.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9815    1.3807    2.4402 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6562    1.4614    0.1516 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1235    0.7294    1.6892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5738   -1.2467    0.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3160   -1.2378    0.6358 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7956   -0.5071   -0.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0295    2.8279    0.9288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0438    2.2665    2.9496 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
  9 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
  4 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  1
 25 26  1  0
 26 27  1  0
 27 28  1  0
 24 29  1  0
 29 30  1  0
 29 31  1  0
 18  7  1  0
 31 20  1  0
 26 24  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  1
  8 40  1  0
 12 41  1  6
 13 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 14 47  1  0
 16 48  1  0
 17 49  1  0
 19 50  1  0
 20 51  1  1
 21 52  1  0
 21 53  1  0
 22 54  1  6
 23 55  1  0
 26 56  1  1
 27 57  1  0
 27 58  1  0
 28 59  1  0
 28 60  1  0
 28 61  1  0
 29 62  1  1
 30 63  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₃H₃₂O₈

Average Mass

436.5010 Da

Monoisotopic Mass

436.20972 Da

IUPAC Name

(2R)-1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-[(2S,3R,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl]pentan-1-one

Traditional Name

(2R)-1-[2,4-dihydroxy-5-(2-methylpropanoyl)phenyl]-2-[(2S,3R,4R,6R,8R)-2-ethyl-4,8-dihydroxy-1,5-dioxaspiro[2.5]octan-6-yl]pentan-1-one

CAS Registry Number

Not Available

SMILES

CCCC(C1C[C@@H](O)C2(O[C@H]2CC)[C@H](O)O1)C(=O)C1=CC(C(=O)C(C)C)=C(O)C=C1O

InChI Identifier

InChI=1S/C23H32O8/c1-5-7-12(17-10-18(26)23(22(29)30-17)19(6-2)31-23)21(28)14-8-13(20(27)11(3)4)15(24)9-16(14)25/h8-9,11-12,17-19,22,24-26,29H,5-7,10H2,1-4H3/t12?,17?,18-,19+,22-,23?/m1/s1

InChI Key

ZVHCTEUOWHUIMG-BTOYHFQMSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Streptomyces	NPAtlas	10966073
Streptomyces sp. Mer-VD1207	Bacteria	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	2.48	ALOGPS
logP	4.18	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	7.16	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	136.82 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	112.09 m³·mol⁻¹	ChemAxon
Polarizability	46.32 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

NPAtlas ID

NPA008890

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78443739

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585568

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Luminacin A1/A2 (NP0003395)

MOL for NP0003395 (Luminacin A1/A2)

3D MOL for NP0003395 (Luminacin A1/A2)

3D SDF for NP0003395 (Luminacin A1/A2)

3D-SDF for NP0003395 (Luminacin A1/A2)

PDB for NP0003395 (Luminacin A1/A2)

3D PDB for NP0003395 (Luminacin A1/A2)

SMILES for NP0003395 (Luminacin A1/A2)

INCHI for NP0003395 (Luminacin A1/A2)

Structure for NP0003395 (Luminacin A1/A2)

3D Structure for NP0003395 (Luminacin A1/A2)