MiMeDB: Showing metabocard for Avermectin B2a (MMDBc0006070)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 23:25:44 UTC

Update Date

2025-10-07 16:05:06 UTC

Metabolite ID

MMDBc0006070

Metabolite Identification

Common Name

Avermectin B2a

Description

Avermectin B2a is a member of the avermectin class of compounds, which are macrocyclic lactones produced by the fermentation of the bacterium Streptomyces avermitilis. This compound serves as a crucial starting material in the synthesis of various derivatives aimed at enhancing insecticidal properties. Recent studies have reported the synthesis of 23,24-alkene-avermectin B2a derivatives through a one-pot multistep reaction, highlighting its versatility in developing novel insecticidal agents (PMID:35584200 ). Additionally, three series of avermectin B2a oxime ester derivatives have been synthesized, demonstrating improved potency compared to the parent compound (PMID:35542930 ). Avermectin B2a has also been explored for its site-selective acylation, where organocatalytic methods have been employed to enhance the yield and selectivity of monoacylation at specific hydroxyl groups (PMID:27075247 ). These advancements indicate that avermectin B2a not only serves as an effective insecticidal and anti-parasitic drug but also as a valuable scaffold for the development of new derivatives with enhanced biological activity. The ongoing research into its derivatives underscores the potential for improving pest control strategies through chemical modifications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152101252D          

 86 92  0  0  1  0            999 V2000
   10.9458    4.2311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4172    3.6098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.3707    2.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6919   -2.8131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652305152101252D          

 86 92  0  0  1  0            999 V2000
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   11.3707    2.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.1815    3.9205    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1432   -1.2121    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.2576    1.2729    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3430   -3.3197    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0501   -4.2516    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8515   -0.4762    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7755    2.1714    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3516    2.3875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3801    0.1451    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8810   -4.6435    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1727   -5.3794    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4656   -4.4476    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0967   -2.7318    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2700    3.8147    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0471   -4.2501    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6812   -2.5359    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7195    2.5967    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6347   -4.0556    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4735    2.5257    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 11  1  1  0  0  0  0
 13 12  2  0  0  0  0
 14 12  1  0  0  0  0
 16 15  1  0  0  0  0
 24  2  1  1  0  0  0
 24 11  1  0  0  0  0
 25  3  1  1  0  0  0
 25 13  1  0  0  0  0
 26  4  1  0  0  0  0
 26 15  2  0  0  0  0
 27  5  1  0  0  0  0
 27 17  2  0  0  0  0
 28  6  1  1  0  0  0
 29  7  1  1  0  0  0
 30  8  1  1  0  0  0
 31 14  2  0  0  0  0
 31 23  1  0  0  0  0
 32 16  1  0  0  0  0
 32 18  1  0  0  0  0
 33 18  1  0  0  0  0
 33 21  1  0  0  0  0
 34 17  1  0  0  0  0
 35 22  1  0  0  0  0
 35 28  1  0  0  0  0
 36 19  1  0  0  0  0
 37 20  1  0  0  0  0
 38 19  1  0  0  0  0
 39 20  1  0  0  0  0
 40 27  1  0  0  0  0
 41 29  1  0  0  0  0
 41 36  1  0  0  0  0
 42 25  1  0  0  0  0
 42 26  1  0  0  0  0
 43 24  1  6  0  0  0
 43 28  1  0  0  0  0
 44 30  1  0  0  0  0
 44 37  1  0  0  0  0
 45 40  1  0  0  0  0
 46 34  1  0  0  0  0
 47 21  1  0  0  0  0
 47 22  1  0  0  0  0
 48 31  1  0  0  0  0
 48 34  1  0  0  0  0
 48 45  1  0  0  0  0
 35 49  1  1  0  0  0
 40 50  1  6  0  0  0
 41 51  1  6  0  0  0
 52 46  2  0  0  0  0
 48 53  1  1  0  0  0
 54  9  1  0  0  0  0
 36 54  1  1  0  0  0
 55 10  1  0  0  0  0
 37 55  1  1  0  0  0
 56 23  1  0  0  0  0
 56 45  1  0  0  0  0
 57 29  1  0  0  0  0
 57 38  1  0  0  0  0
 58 30  1  0  0  0  0
 58 39  1  0  0  0  0
 59 33  1  0  0  0  0
 59 46  1  0  0  0  0
 39 60  1  6  0  0  0
 42 60  1  1  0  0  0
 38 61  1  1  0  0  0
 44 61  1  1  0  0  0
 62 32  1  0  0  0  0
 47 62  1  1  0  0  0
 63 43  1  0  0  0  0
 63 47  1  0  0  0  0
 64 12  1  0  0  0  0
 65 13  1  0  0  0  0
 66 14  1  0  0  0  0
 67 15  1  0  0  0  0
 24 68  1  6  0  0  0
 25 69  1  6  0  0  0
 28 70  1  6  0  0  0
 29 71  1  6  0  0  0
 30 72  1  6  0  0  0
 32 73  1  1  0  0  0
 33 74  1  1  0  0  0
 34 75  1  6  0  0  0
 35 76  1  6  0  0  0
 36 77  1  6  0  0  0
 37 78  1  6  0  0  0
 38 79  1  1  0  0  0
 39 80  1  1  0  0  0
 40 81  1  1  0  0  0
 41 82  1  1  0  0  0
 42 83  1  6  0  0  0
 43 84  1  1  0  0  0
 44 85  1  1  0  0  0
 45 86  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0006070

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C1=C(C)/[C@@]([H])(O[C@@]2([H])C[C@]([H])(OC)[C@@]([H])(O[C@@]3([H])C[C@]([H])(OC)[C@@]([H])(O)[C@]([H])(C)O3)[C@]([H])(C)O2)[C@@]([H])(C)\C([H])=C(/[H])\C(\[H])=C2/CO[C@]3([H])[C@]([H])(O)C(C)=C[C@@]([H])(C(=O)O[C@@]4([H])C[C@@]([H])(C1)O[C@]1(C4)C[C@]([H])(O)[C@]([H])(C)[C@]([H])(O1)[C@@]([H])(C)CC)[C@]23O

> <INCHI_IDENTIFIER>
InChI=1S/C48H74O15/c1-11-24(2)43-28(6)35(49)22-47(63-43)21-33-18-32(62-47)16-15-26(4)42(25(3)13-12-14-31-23-56-45-40(50)27(5)17-34(46(52)59-33)48(31,45)53)60-39-20-37(55-10)44(30(8)58-39)61-38-19-36(54-9)41(51)29(7)57-38/h12-15,17,24-25,28-30,32-45,49-51,53H,11,16,18-23H2,1-10H3/b13-12+,26-15+,31-14+/t24-,25-,28-,29-,30-,32+,33-,34-,35-,36-,37-,38-,39-,40+,41-,42-,43+,44-,45+,47-,48+/m0/s1

> <INCHI_KEY>
CWGATOJEFAKFBK-PDVFGPFMSA-N

> <FORMULA>
C48H74O15

> <MOLECULAR_WEIGHT>
891.105

> <EXACT_MASS>
890.502771683

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
137

> <JCHEM_AVERAGE_POLARIZABILITY>
98.76395003614223

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'R,2R,4S,4'S,5S,6R,8'R,10'E,12'S,13'S,14'E,20'R,21'R,24'S)-6-[(2S)-butan-2-yl]-4,21',24'-trihydroxy-12'-{[(2R,4S,5S,6S)-5-{[(2S,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4-methoxy-6-methyloxan-2-yl]oxy}-5,11',13',22'-tetramethyl-3',7',19'-trioxaspiro[oxane-2,6'-tetracyclo[15.6.1.1^{4,8}.0^{20,24}]pentacosane]-10',14',16',22'-tetraen-2'-one

> <ALOGPS_LOGP>
3.54

> <JCHEM_LOGP>
4.846834697666666

> <ALOGPS_LOGS>
-4.75

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.159085315191298

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.465381576730142

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9289493922791

> <JCHEM_POLAR_SURFACE_AREA>
190.28999999999994

> <JCHEM_REFRACTIVITY>
231.33070000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.58e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,2R,4S,4'S,5S,6R,8'R,10'E,12'S,13'S,14'E,20'R,21'R,24'S)-6-[(2S)-butan-2-yl]-4,21',24'-trihydroxy-12'-{[(2R,4S,5S,6S)-5-{[(2S,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4-methoxy-6-methyloxan-2-yl]oxy}-5,11',13',22'-tetramethyl-3',7',19'-trioxaspiro[oxane-2,6'-tetracyclo[15.6.1.1^{4,8}.0^{20,24}]pentacosane]-10',14',16',22'-tetraen-2'-one

> <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      20.432   7.898   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.579   6.738   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.390  -3.788   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.674  -4.520   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.329   7.846   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.225   3.902   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.958  -5.251   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.105  -6.411   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      21.756 -11.719   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.045 -11.567   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.221   6.373   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.812  -0.737   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.027  -1.683   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.023   0.788   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.670  -2.049   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.096  -1.469   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.586   5.494   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.092   1.002   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      19.325  -9.828   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.825  -8.150   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      15.730   3.108   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      18.161   1.216   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.272   1.623   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      18.794   5.793   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.816  -3.208   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.458  -3.574   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.278   6.307   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      19.799   3.322   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      19.747  -6.777   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      15.678  -6.991   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.808   1.734   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      15.307   0.057   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.303   2.528   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.445   3.839   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      19.587   1.796   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      20.751  -9.248   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.040  -9.096   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      18.109  -8.882   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.036  -6.625   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.920   5.582   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      20.962  -7.722   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      12.032  -4.154   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      18.583   4.267   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      15.467  -8.516   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       7.869   4.042   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      11.661   2.894   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      16.945   2.162   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       9.019   3.259   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      20.803   0.851   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       6.612   6.395   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      22.389  -7.142   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0      11.450   1.368   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0       9.182   4.791   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      21.967 -10.193   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0      13.829 -10.621   0.000  0.00  0.00           O+0
HETATM   56  O   UNK     0       6.692   3.050   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      18.320  -7.356   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0      14.463  -6.045   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0      13.088   3.473   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      11.820  -5.679   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      16.682  -9.462   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0      16.734   0.637   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      17.156   3.687   0.000  0.00  0.00           O+0
HETATM   64  H   UNK     0       8.385  -1.317   0.000  0.00  0.00           H+0
HETATM   65  H   UNK     0      12.454  -1.103   0.000  0.00  0.00           H+0
HETATM   66  H   UNK     0      10.234   2.314   0.000  0.00  0.00           H+0
HETATM   67  H   UNK     0      12.243  -2.628   0.000  0.00  0.00           H+0
HETATM   68  H   UNK     0      19.006   7.318   0.000  0.00  0.00           H+0
HETATM   69  H   UNK     0       9.601  -2.263   0.000  0.00  0.00           H+0
HETATM   70  H   UNK     0      21.014   2.376   0.000  0.00  0.00           H+0
HETATM   71  H   UNK     0      21.174  -6.197   0.000  0.00  0.00           H+0
HETATM   72  H   UNK     0      16.894  -7.936   0.000  0.00  0.00           H+0
HETATM   73  H   UNK     0      16.523  -0.889   0.000  0.00  0.00           H+0
HETATM   74  H   UNK     0      14.514   4.053   0.000  0.00  0.00           H+0
HETATM   75  H   UNK     0      11.856   4.457   0.000  0.00  0.00           H+0
HETATM   76  H   UNK     0      19.376   0.271   0.000  0.00  0.00           H+0
HETATM   77  H   UNK     0      22.178  -8.668   0.000  0.00  0.00           H+0
HETATM   78  H   UNK     0      15.256 -10.042   0.000  0.00  0.00           H+0
HETATM   79  H   UNK     0      19.536  -8.302   0.000  0.00  0.00           H+0
HETATM   80  H   UNK     0      13.247  -5.099   0.000  0.00  0.00           H+0
HETATM   81  H   UNK     0       7.971   7.121   0.000  0.00  0.00           H+0
HETATM   82  H   UNK     0      22.488  -7.933   0.000  0.00  0.00           H+0
HETATM   83  H   UNK     0      10.605  -4.734   0.000  0.00  0.00           H+0
HETATM   84  H   UNK     0      20.010   4.847   0.000  0.00  0.00           H+0
HETATM   85  H   UNK     0      14.251  -7.570   0.000  0.00  0.00           H+0
HETATM   86  H   UNK     0       6.484   4.715   0.000  0.00  0.00           H+0
CONECT    1   11                                                            
CONECT    2   24                                                            
CONECT    3   25                                                            
CONECT    4   26                                                            
CONECT    5   27                                                            
CONECT    6   28                                                            
CONECT    7   29                                                            
CONECT    8   30                                                            
CONECT    9   54                                                            
CONECT   10   55                                                            
CONECT   11    1   24                                                       
CONECT   12   13   14   64                                                  
CONECT   13   12   25   65                                                  
CONECT   14   12   31   66                                                  
CONECT   15   16   26   67                                                  
CONECT   16   15   32                                                       
CONECT   17   27   34                                                       
CONECT   18   32   33                                                       
CONECT   19   36   38                                                       
CONECT   20   37   39                                                       
CONECT   21   33   47                                                       
CONECT   22   35   47                                                       
CONECT   23   31   56                                                       
CONECT   24    2   11   43   68                                             
CONECT   25    3   13   42   69                                             
CONECT   26    4   15   42                                                  
CONECT   27    5   17   40                                                  
CONECT   28    6   35   43   70                                             
CONECT   29    7   41   57   71                                             
CONECT   30    8   44   58   72                                             
CONECT   31   14   23   48                                                  
CONECT   32   16   18   62   73                                             
CONECT   33   18   21   59   74                                             
CONECT   34   17   46   48   75                                             
CONECT   35   22   28   49   76                                             
CONECT   36   19   41   54   77                                             
CONECT   37   20   44   55   78                                             
CONECT   38   19   57   61   79                                             
CONECT   39   20   58   60   80                                             
CONECT   40   27   45   50   81                                             
CONECT   41   29   36   51   82                                             
CONECT   42   25   26   60   83                                             
CONECT   43   24   28   63   84                                             
CONECT   44   30   37   61   85                                             
CONECT   45   40   48   56   86                                             
CONECT   46   34   52   59                                                  
CONECT   47   21   22   62   63                                             
CONECT   48   31   34   45   53                                             
CONECT   49   35                                                            
CONECT   50   40                                                            
CONECT   51   41                                                            
CONECT   52   46                                                            
CONECT   53   48                                                            
CONECT   54    9   36                                                       
CONECT   55   10   37                                                       
CONECT   56   23   45                                                       
CONECT   57   29   38                                                       
CONECT   58   30   39                                                       
CONECT   59   33   46                                                       
CONECT   60   39   42                                                       
CONECT   61   38   44                                                       
CONECT   62   32   47                                                       
CONECT   63   43   47                                                       
CONECT   64   12                                                            
CONECT   65   13                                                            
CONECT   66   14                                                            
CONECT   67   15                                                            
CONECT   68   24                                                            
CONECT   69   25                                                            
CONECT   70   28                                                            
CONECT   71   29                                                            
CONECT   72   30                                                            
CONECT   73   32                                                            
CONECT   74   33                                                            
CONECT   75   34                                                            
CONECT   76   35                                                            
CONECT   77   36                                                            
CONECT   78   37                                                            
CONECT   79   38                                                            
CONECT   80   39                                                            
CONECT   81   40                                                            
CONECT   82   41                                                            
CONECT   83   42                                                            
CONECT   84   43                                                            
CONECT   85   44                                                            
CONECT   86   45                                                            
MASTER        0    0    0    0    0    0    0    0   86    0  184    0
END

Synonyms

Value	Source
Avermectin b2a	MeSH

Molecular Formula

C₄₈H₇₄O₁₅

Average Mass

891.105

Monoisotopic Mass

890.502771683

IUPAC Name

(1'R,2R,4S,4'S,5S,6R,8'R,10'E,12'S,13'S,14'E,20'R,21'R,24'S)-6-[(2S)-butan-2-yl]-4,21',24'-trihydroxy-12'-{[(2R,4S,5S,6S)-5-{[(2S,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4-methoxy-6-methyloxan-2-yl]oxy}-5,11',13',22'-tetramethyl-3',7',19'-trioxaspiro[oxane-2,6'-tetracyclo[15.6.1.1^{4,8}.0^{20,24}]pentacosane]-10',14',16',22'-tetraen-2'-one

Traditional Name

CAS Registry Number

Not Available

SMILES

[H]\C1=C(C)/[C@@]([H])(O[C@@]2([H])C[C@]([H])(OC)[C@@]([H])(O[C@@]3([H])C[C@]([H])(OC)[C@@]([H])(O)[C@]([H])(C)O3)[C@]([H])(C)O2)[C@@]([H])(C)\C([H])=C(/[H])\C(\[H])=C2/CO[C@]3([H])[C@]([H])(O)C(C)=C[C@@]([H])(C(=O)O[C@@]4([H])C[C@@]([H])(C1)O[C@]1(C4)C[C@]([H])(O)[C@]([H])(C)[C@]([H])(O1)[C@@]([H])(C)CC)[C@]23O

InChI Identifier

InChI=1S/C48H74O15/c1-11-24(2)43-28(6)35(49)22-47(63-43)21-33-18-32(62-47)16-15-26(4)42(25(3)13-12-14-31-23-56-45-40(50)27(5)17-34(46(52)59-33)48(31,45)53)60-39-20-37(55-10)44(30(8)58-39)61-38-19-36(54-9)41(51)29(7)57-38/h12-15,17,24-25,28-30,32-45,49-51,53H,11,16,18-23H2,1-10H3/b13-12+,26-15+,31-14+/t24-,25-,28-,29-,30-,32+,33-,34-,35-,36-,37-,38-,39-,40+,41-,42-,43+,44-,45+,47-,48+/m0/s1

InChI Key

CWGATOJEFAKFBK-PDVFGPFMSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as milbemycins. These are a group of macrolides with a structure containing a 16-membered lactone ring fused to a 1,7-dioxaspiroundecane ring system and to either a benzofuran (or hydrogenated derivative thereof). In some cases (e.G. Milbemycin E), the tetrahydrofuranyl ring is missing. Milbemycins can be o-glycosylated at C13 to form Avermectins. Milbemycins are produced by Streptomyces species.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Milbemycins

Direct Parent

Milbemycins

Alternative Parents

Substituents

Milbemycin
Disaccharide
Glycosyl compound
O-glycosyl compound
Ketal
Oxane
Oxolane
Tertiary alcohol
Secondary alcohol
Carboxylic acid ester
Lactone
Polyol
Carboxylic acid derivative
Acetal
Dialkyl ether
Ether
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Oxacycle
Alcohol
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Macrolides and lactone polyketides (C11975 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.016 g/L	ALOGPS
logP	3.54	ALOGPS
logP	4.85	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	12.47	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	190.29 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	231.33 m³·mol⁻¹	ChemAxon
Polarizability	98.76 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

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

Microbial Pathways

Pathways

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank	Species

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

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/Eubacteria	Actinobacteria	1		Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	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

C00016540

Chemspider ID

4945321

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6441103

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Avermectin B2a (MMDBc0006070)

MOL for #<Metabolite:0x00007fb4d4ae5fe8>

3D MOL for #<Metabolite:0x00007fb4d4ae5fe8>

3D SDF for #<Metabolite:0x00007fb4d4ae5fe8>

3D-SDF for #<Metabolite:0x00007fb4d4ae5fe8>

PDB for #<Metabolite:0x00007fb4d4ae5fe8>

3D PDB for #<Metabolite:0x00007fb4d4ae5fe8>

SMILES for #<Metabolite:0x00007fb4d4ae5fe8>

INCHI for #<Metabolite:0x00007fb4d4ae5fe8>

Structure for #<Metabolite:0x00007fb4d4ae5fe8>

3D Structure for #<Metabolite:0x00007fb4d4ae5fe8>