NP-MRD: Showing NP-Card for Antibiotic A 130C (NP0062085)

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Record Information

Version

2.0

Created at

2022-04-28 06:45:30 UTC

Updated at

2022-04-28 06:45:31 UTC

NP-MRD ID

NP0062085

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Antibiotic A 130C

Description

(2S,4R,6E,8S)-8-[(2S,5R,7S,9R,10R)-2-[(2R,4S,5R,7R,10R)-2-[(2S,3S,5S,6R)-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-4,10-dimethyl-1,6-dioxaspiro[4.5]Decan-7-yl]-9-{[(2R,5S,6R)-5-methoxy-6-methyloxan-2-yl]oxy}-2,10-dimethyl-1,6-dioxaspiro[4.5]Decan-7-yl]-2,4,6-trimethyl-5-oxonon-6-enoic acid belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. Antibiotic A 130C is found in Streptomyces hygroscopicus A-130. Based on a literature review very few articles have been published on (2S,4R,6E,8S)-8-[(2S,5R,7S,9R,10R)-2-[(2R,4S,5R,7R,10R)-2-[(2S,3S,5S,6R)-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-4,10-dimethyl-1,6-dioxaspiro[4.5]Decan-7-yl]-9-{[(2R,5S,6R)-5-methoxy-6-methyloxan-2-yl]oxy}-2,10-dimethyl-1,6-dioxaspiro[4.5]Decan-7-yl]-2,4,6-trimethyl-5-oxonon-6-enoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282208452D          

 60 65  0  0  1  0            999 V2000
    8.4634   -2.3420    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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  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  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  4  8  1  1  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
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 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 13 15  1  6  0  0  0
 15 16  1  1  0  0  0
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 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  1  0  0  0
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 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
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 32 33  1  0  0  0  0
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  1 59  1  6  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652304282208452D          

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M  END
> <DATABASE_ID>
NP0062085

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1CC[C@H](O[C@@H]2C[C@H](O[C@@]3(CC[C@](C)(O3)[C@H]3CC[C@@H](C)[C@@]4(O[C@H](C[C@@H]4C)[C@H]4O[C@@](O)(CO)[C@@H](C)C[C@@H]4C)O3)[C@@H]2C)[C@@H](C)\C=C(/C)C(=O)[C@H](C)C[C@H](C)C(O)=O)O[C@@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C47H78O13/c1-25(19-26(2)41(49)27(3)20-29(5)43(50)51)36-23-37(55-40-16-14-35(53-12)34(10)54-40)33(9)46(56-36)18-17-44(11,60-46)39-15-13-30(6)47(58-39)32(8)22-38(57-47)42-28(4)21-31(7)45(52,24-48)59-42/h19,25,27-40,42,48,52H,13-18,20-24H2,1-12H3,(H,50,51)/b26-19+/t25-,27+,28-,29-,30+,31-,32-,33+,34+,35-,36-,37+,38+,39+,40-,42-,44-,45-,46+,47+/m0/s1

> <INCHI_KEY>
LQFPDTISEHAMNQ-XAOGPWCZSA-N

> <FORMULA>
C47H78O13

> <MOLECULAR_WEIGHT>
851.128

> <EXACT_MASS>
850.544242572

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
138

> <JCHEM_AVERAGE_POLARIZABILITY>
96.22764786101398

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,4R,6E,8S)-8-[(2S,5R,7S,9R,10R)-2-[(2R,4S,5R,7R,10R)-2-[(2S,3S,5S,6R)-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-4,10-dimethyl-1,6-dioxaspiro[4.5]decan-7-yl]-9-{[(2R,5S,6R)-5-methoxy-6-methyloxan-2-yl]oxy}-2,10-dimethyl-1,6-dioxaspiro[4.5]decan-7-yl]-2,4,6-trimethyl-5-oxonon-6-enoic acid

> <ALOGPS_LOGP>
4.53

> <JCHEM_LOGP>
8.539524061000002

> <ALOGPS_LOGS>
-5.68

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.107358260252239

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.48199082305617

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4152912705100116

> <JCHEM_POLAR_SURFACE_AREA>
168.67

> <JCHEM_REFRACTIVITY>
224.3308

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.77e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4R,6E,8S)-8-[(2S,5R,7S,9R,10R)-2-[(2R,4S,5R,7R,10R)-2-[(2S,3S,5S,6R)-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-4,10-dimethyl-1,6-dioxaspiro[4.5]decan-7-yl]-9-{[(2R,5S,6R)-5-methoxy-6-methyloxan-2-yl]oxy}-2,10-dimethyl-1,6-dioxaspiro[4.5]decan-7-yl]-2,4,6-trimethyl-5-oxonon-6-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      15.798  -4.372   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.906  -3.117   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.373  -3.261   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.732  -4.662   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      13.624  -5.917   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      15.157  -5.772   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.049  -7.027   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.199  -4.807   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.307  -3.551   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.774  -3.696   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.882  -2.441   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.523  -1.041   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.056  -0.896   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.948  -2.151   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.697   0.504   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.805   1.760   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.230   0.649   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.122  -0.606   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.481  -2.006   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.655  -0.461   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      15.547  -1.716   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      15.296   0.939   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.830   1.084   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.404   2.195   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      15.045   3.595   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.579   3.740   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.153   4.850   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      14.794   6.250   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      12.620   4.705   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.098  -3.766   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.595  -3.431   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.450  -1.897   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.863  -1.286   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.910  -1.865   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.680  -0.564   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.140  -0.564   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.140   2.104   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.680   2.104   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.450   0.770   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       2.370   3.437   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       1.465   2.016   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -1.246   2.445   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -2.653   1.819   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -3.899   2.724   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -3.738   4.256   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -2.331   4.882   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -1.085   3.977   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      -2.908   6.310   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      -4.433   6.524   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      -1.470   6.159   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      -4.984   5.161   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      -2.814   0.287   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0       1.941  -1.941   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0       8.133  -5.096   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      17.332  -4.227   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0      18.224  -5.482   0.000  0.00  0.00           C+0
CONECT    1    2    6   59                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    4    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11   58                                                  
CONECT   11   10   12   30   33                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13    9                                                       
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   11   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   35                                             
CONECT   33   32   11                                                       
CONECT   34   32                                                            
CONECT   35   32   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   42   45                                             
CONECT   38   37   39   41                                                  
CONECT   39   38   40                                                       
CONECT   40   39   35                                                       
CONECT   41   38                                                            
CONECT   42   37   43   57                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45   46                                                  
CONECT   45   44   37                                                       
CONECT   46   44   47   51                                                  
CONECT   47   46   48   56                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50   55                                                  
CONECT   50   49   51   52   54                                             
CONECT   51   50   46                                                       
CONECT   52   50   53                                                       
CONECT   53   52                                                            
CONECT   54   50                                                            
CONECT   55   49                                                            
CONECT   56   47                                                            
CONECT   57   42                                                            
CONECT   58   10                                                            
CONECT   59    1   60                                                       
CONECT   60   59                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  130    0
END

View in JSmol

Synonyms

Value	Source
(2S,4R,6E,8S)-8-[(2S,5R,7S,9R,10R)-2-[(2R,4S,5R,7R,10R)-2-[(2S,3S,5S,6R)-6-Hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-4,10-dimethyl-1,6-dioxaspiro[4.5]decan-7-yl]-9-{[(2R,5S,6R)-5-methoxy-6-methyloxan-2-yl]oxy}-2,10-dimethyl-1,6-dioxaspiro[4.5]decan-7-yl]-2,4,6-trimethyl-5-oxonon-6-enoate	Generator

Chemical Formula

C₄₇H₇₈O₁₃

Average Mass

851.1280 Da

Monoisotopic Mass

850.54424 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CO[C@H]1CC[C@H](O[C@@H]2C[C@H](O[C@@]3(CC[C@](C)(O3)[C@H]3CC[C@@H](C)[C@@]4(O[C@H](C[C@@H]4C)[C@H]4O[C@@](O)(CO)[C@@H](C)C[C@@H]4C)O3)[C@@H]2C)[C@@H](C)\C=C(/C)C(=O)[C@H](C)C[C@H](C)C(O)=O)O[C@@H]1C

InChI Identifier

InChI=1S/C47H78O13/c1-25(19-26(2)41(49)27(3)20-29(5)43(50)51)36-23-37(55-40-16-14-35(53-12)34(10)54-40)33(9)46(56-36)18-17-44(11,60-46)39-15-13-30(6)47(58-39)32(8)22-38(57-47)42-28(4)21-31(7)45(52,24-48)59-42/h19,25,27-40,42,48,52H,13-18,20-24H2,1-12H3,(H,50,51)/b26-19+/t25-,27+,28-,29-,30+,31-,32-,33+,34+,35-,36-,37+,38+,39+,40-,42-,44-,45-,46+,47+/m0/s1

InChI Key

LQFPDTISEHAMNQ-XAOGPWCZSA-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 hygroscopicus A-130	Bacteria	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Terpene glycoside
Medium-chain fatty acid
Ketal
Methyl-branched fatty acid
Hydroxy fatty acid
Heterocyclic fatty acid
Branched fatty acid
Fatty acyl
Fatty acid
Alpha-branched alpha,beta-unsaturated-ketone
Unsaturated fatty acid
Oxane
Alpha,beta-unsaturated ketone
Tetrahydrofuran
Enone
Acryloyl-group
Ketone
Hemiacetal
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	4.53	ALOGPS
logP	8.54	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	4.48	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	168.67 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	224.33 m³·mol⁻¹	ChemAxon
Polarizability	96.23 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

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

162996251

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Antibiotic A 130C (NP0062085)

MOL for NP0062085 (Antibiotic A 130C)

3D MOL for NP0062085 (Antibiotic A 130C)

3D SDF for NP0062085 (Antibiotic A 130C)

3D-SDF for NP0062085 (Antibiotic A 130C)

PDB for NP0062085 (Antibiotic A 130C)

3D PDB for NP0062085 (Antibiotic A 130C)

SMILES for NP0062085 (Antibiotic A 130C)

INCHI for NP0062085 (Antibiotic A 130C)

Structure for NP0062085 (Antibiotic A 130C)

3D Structure for NP0062085 (Antibiotic A 130C)