MiMeDB: Showing metabocard for 6-Deoxy-8,17-dihydroxyerythronolide B (MMDBc0019411)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 09:29:19 UTC

Update Date

2022-08-31 06:45:24 UTC

Metabolite ID

MMDBc0019411

Metabolite Identification

Common Name

6-Deoxy-8,17-dihydroxyerythronolide B

Description

6-Deoxy-8,17-dihydroxyerythronolide B 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. 6-Deoxy-8,17-dihydroxyerythronolide B is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152111292D          

 38 38  0  0  1  0            999 V2000
    1.5161   -2.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5161    1.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8664   -2.2331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3742    0.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0562    0.1056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6442   -0.8299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0562   -2.0772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263    1.5088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1493    2.1778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7862    0.8851    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5963   -1.4535    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4360    0.4174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8664   -0.0503    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1659   -0.9858    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7862   -1.2976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9760    1.0410    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1364   -0.8299    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7060   -0.3622    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4064    0.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4360   -1.7654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1364    1.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8701    2.5791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7060    1.8206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9465   -0.9858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5161   -0.5181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2166    0.4174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1041   -2.3890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9510    1.4834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2461   -1.9213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2461    0.2615    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263   -0.6740    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659    1.1969    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5963    0.7292    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1041   -0.2062    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9760   -1.1417    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1320    1.8512    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4064   -1.6094    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8619    0.4480    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  0  0  0  0
 10  2  1  6  0  0  0
 10  8  1  0  0  0  0
 11  3  1  6  0  0  0
 12  4  1  6  0  0  0
 13  5  1  1  0  0  0
 14  6  1  6  0  0  0
 15  7  1  6  0  0  0
 15 11  1  0  0  0  0
 16 10  1  0  0  0  0
 16 12  1  0  0  0  0
 17 11  1  0  0  0  0
 17 13  1  0  0  0  0
 18 12  1  0  0  0  0
 18 14  1  0  0  0  0
 19 13  1  0  0  0  0
 20 14  1  0  0  0  0
 21  8  1  0  0  0  0
 21  9  1  0  0  0  0
 21 19  1  0  0  0  0
 22  9  1  0  0  0  0
 16 23  1  1  0  0  0
 17 24  1  1  0  0  0
 18 25  1  6  0  0  0
 26 19  2  0  0  0  0
 27 20  2  0  0  0  0
 28 21  1  0  0  0  0
 29 15  1  0  0  0  0
 29 20  1  0  0  0  0
 10 30  1  6  0  0  0
 11 31  1  6  0  0  0
 12 32  1  1  0  0  0
 13 33  1  6  0  0  0
 14 34  1  1  0  0  0
 15 35  1  6  0  0  0
 16 36  1  6  0  0  0
 17 37  1  6  0  0  0
 18 38  1  1  0  0  0
M  END


  Mrv1652305152111292D          

 38 38  0  0  1  0            999 V2000
    1.5161   -2.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5161    1.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8664   -2.2331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3742    0.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0562    0.1056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6442   -0.8299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0562   -2.0772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263    1.5088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1493    2.1778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7862    0.8851    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5963   -1.4535    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4360    0.4174    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8664   -0.0503    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1659   -0.9858    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7862   -1.2976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9760    1.0410    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1364   -0.8299    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7060   -0.3622    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4064    0.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4360   -1.7654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1364    1.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8701    2.5791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7060    1.8206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9465   -0.9858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5161   -0.5181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2166    0.4174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1041   -2.3890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9510    1.4834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2461   -1.9213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2461    0.2615    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263   -0.6740    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659    1.1969    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5963    0.7292    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1041   -0.2062    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9760   -1.1417    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1320    1.8512    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4064   -1.6094    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8619    0.4480    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  0  0  0  0
 10  2  1  6  0  0  0
 10  8  1  0  0  0  0
 11  3  1  6  0  0  0
 12  4  1  6  0  0  0
 13  5  1  1  0  0  0
 14  6  1  6  0  0  0
 15  7  1  6  0  0  0
 15 11  1  0  0  0  0
 16 10  1  0  0  0  0
 16 12  1  0  0  0  0
 17 11  1  0  0  0  0
 17 13  1  0  0  0  0
 18 12  1  0  0  0  0
 18 14  1  0  0  0  0
 19 13  1  0  0  0  0
 20 14  1  0  0  0  0
 21  8  1  0  0  0  0
 21  9  1  0  0  0  0
 21 19  1  0  0  0  0
 22  9  1  0  0  0  0
 16 23  1  1  0  0  0
 17 24  1  1  0  0  0
 18 25  1  6  0  0  0
 26 19  2  0  0  0  0
 27 20  2  0  0  0  0
 28 21  1  0  0  0  0
 29 15  1  0  0  0  0
 29 20  1  0  0  0  0
 10 30  1  6  0  0  0
 11 31  1  6  0  0  0
 12 32  1  1  0  0  0
 13 33  1  6  0  0  0
 14 34  1  1  0  0  0
 15 35  1  6  0  0  0
 16 36  1  6  0  0  0
 17 37  1  6  0  0  0
 18 38  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0019411

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]1(C)CC(O)(CO)C(=O)[C@]([H])(C)[C@@]([H])(O)[C@@]([H])(C)[C@@]([H])(CC)OC(=O)[C@]([H])(C)[C@@]([H])(O)[C@]([H])(C)[C@@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C21H38O8/c1-7-15-11(3)17(24)13(5)19(26)21(28,9-22)8-10(2)16(23)12(4)18(25)14(6)20(27)29-15/h10-18,22-25,28H,7-9H2,1-6H3/t10-,11-,12+,13+,14+,15+,16-,17-,18-,21?/m0/s1

> <INCHI_KEY>
PREIDDIPLSAKJR-CFWJUOAESA-N

> <FORMULA>
C21H38O8

> <MOLECULAR_WEIGHT>
418.527

> <EXACT_MASS>
418.256668184

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
44.618438813986394

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4S,5R,6S,7S,11R,12S,13R,14R)-14-ethyl-4,6,9,12-tetrahydroxy-9-(hydroxymethyl)-3,5,7,11,13-pentamethyl-1-oxacyclotetradecane-2,10-dione

> <ALOGPS_LOGP>
0.21

> <JCHEM_LOGP>
0.8410028123333337

> <ALOGPS_LOGS>
-2.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.810867964022325

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.249327805192154

> <JCHEM_PKA_STRONGEST_BASIC>
-2.962847164146188

> <JCHEM_POLAR_SURFACE_AREA>
144.52

> <JCHEM_REFRACTIVITY>
106.1172

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.56e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4S,5R,6S,7S,11R,12S,13R,14R)-14-ethyl-4,6,9,12-tetrahydroxy-9-(hydroxymethyl)-3,5,7,11,13-pentamethyl-1-oxacyclotetradecane-2,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       2.830  -5.042   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.830   3.107   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.351  -4.168   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.698   1.070   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.838   0.197   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.203  -1.549   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.838  -3.877   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.342   2.816   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.879   4.065   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.334   1.652   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.846  -2.713   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.814   0.779   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.351  -0.094   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.310  -1.840   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.334  -2.422   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.822   1.943   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.855  -1.549   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.318  -0.676   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.359   1.070   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.814  -3.295   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.855   2.525   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.224   4.814   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       1.318   3.398   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       7.367  -1.840   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       2.830  -0.967   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       7.871   0.779   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -0.194  -4.459   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       7.375   2.769   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.326  -3.586   0.000  0.00  0.00           O+0
HETATM   30  H   UNK     0       2.326   0.488   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.342  -1.258   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.310   2.234   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       4.846   1.361   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.194  -0.385   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.822  -2.131   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.113   3.456   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       6.359  -3.004   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.609   0.836   0.000  0.00  0.00           H+0
CONECT    1    7                                                            
CONECT    2   10                                                            
CONECT    3   11                                                            
CONECT    4   12                                                            
CONECT    5   13                                                            
CONECT    6   14                                                            
CONECT    7    1   15                                                       
CONECT    8   10   21                                                       
CONECT    9   21   22                                                       
CONECT   10    2    8   16   30                                             
CONECT   11    3   15   17   31                                             
CONECT   12    4   16   18   32                                             
CONECT   13    5   17   19   33                                             
CONECT   14    6   18   20   34                                             
CONECT   15    7   11   29   35                                             
CONECT   16   10   12   23   36                                             
CONECT   17   11   13   24   37                                             
CONECT   18   12   14   25   38                                             
CONECT   19   13   21   26                                                  
CONECT   20   14   27   29                                                  
CONECT   21    8    9   19   28                                             
CONECT   22    9                                                            
CONECT   23   16                                                            
CONECT   24   17                                                            
CONECT   25   18                                                            
CONECT   26   19                                                            
CONECT   27   20                                                            
CONECT   28   21                                                            
CONECT   29   15   20                                                       
CONECT   30   10                                                            
CONECT   31   11                                                            
CONECT   32   12                                                            
CONECT   33   13                                                            
CONECT   34   14                                                            
CONECT   35   15                                                            
CONECT   36   16                                                            
CONECT   37   17                                                            
CONECT   38   18                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   76    0
END

Synonyms

Not Available

Molecular Formula

C₂₁H₃₈O₈

Average Mass

418.527

Monoisotopic Mass

418.256668184

IUPAC Name

(3R,4S,5R,6S,7S,11R,12S,13R,14R)-14-ethyl-4,6,9,12-tetrahydroxy-9-(hydroxymethyl)-3,5,7,11,13-pentamethyl-1-oxacyclotetradecane-2,10-dione

Traditional Name

(3R,4S,5R,6S,7S,11R,12S,13R,14R)-14-ethyl-4,6,9,12-tetrahydroxy-9-(hydroxymethyl)-3,5,7,11,13-pentamethyl-1-oxacyclotetradecane-2,10-dione

CAS Registry Number

Not Available

SMILES

[H][C@]1(C)CC(O)(CO)C(=O)[C@]([H])(C)[C@@]([H])(O)[C@@]([H])(C)[C@@]([H])(CC)OC(=O)[C@]([H])(C)[C@@]([H])(O)[C@]([H])(C)[C@@]1([H])O

InChI Identifier

InChI=1S/C21H38O8/c1-7-15-11(3)17(24)13(5)19(26)21(28,9-22)8-10(2)16(23)12(4)18(25)14(6)20(27)29-15/h10-18,22-25,28H,7-9H2,1-6H3/t10-,11-,12+,13+,14+,15+,16-,17-,18-,21?/m0/s1

InChI Key

PREIDDIPLSAKJR-CFWJUOAESA-N

Chemical Taxonomy

Description

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
Acyloin
Tertiary alcohol
Carboxylic acid ester
Ketone
Lactone
Secondary alcohol
Cyclic ketone
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Primary alcohol
Organooxygen compound
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	3.56 g/L	ALOGPS
logP	0.21	ALOGPS
logP	0.84	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	12.25	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	144.52 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	106.12 m³·mol⁻¹	ChemAxon
Polarizability	44.62 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Actinobacteria	1		Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78438587

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588485

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for 6-Deoxy-8,17-dihydroxyerythronolide B (MMDBc0019411)

MOL for #<Metabolite:0x00005634c2ae0b08>

3D MOL for #<Metabolite:0x00005634c2ae0b08>

3D SDF for #<Metabolite:0x00005634c2ae0b08>

3D-SDF for #<Metabolite:0x00005634c2ae0b08>

PDB for #<Metabolite:0x00005634c2ae0b08>

3D PDB for #<Metabolite:0x00005634c2ae0b08>

SMILES for #<Metabolite:0x00005634c2ae0b08>

INCHI for #<Metabolite:0x00005634c2ae0b08>

Structure for #<Metabolite:0x00005634c2ae0b08>

3D Structure for #<Metabolite:0x00005634c2ae0b08>