MiMeDB: Showing metabocard for adenosylcob(III)yrinate a,c-diamide (MMDBc0055687)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-17 20:02:14 UTC

Update Date

2022-08-12 20:09:27 UTC

Metabolite ID

MMDBc0055687

Metabolite Identification

Common Name

adenosylcob(III)yrinate a,c-diamide

Description

adenosylcob(III)yrinate a,c-diamide(4-) belongs to the class of organic compounds known as metallotetrapyrroles. These are polycyclic compounds containing a tetrapyrrole skeleton combined with a metal atom. Based on a literature review very few articles have been published on adenosylcob(III)yrinate a,c-diamide(4-).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172222022D          

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M  CHG  7  46  -1  53  -1  55  -1  57  -1  59  -1  61  -1  82   2
M  RAD  1  64   2
M  END


  Mrv1652306172222022D          

 91 96  0  0  1  0            999 V2000
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    4.3873   -1.0925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1889   -1.8273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1094    0.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4110    1.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8563   -1.3424    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.6805    1.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6409   -1.5973    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.1259   -0.9299    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.3950    2.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6805    0.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6409   -0.2624    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.3950    2.8396    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.1094    1.6021    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.3950    0.3646    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8959    1.8570    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8959    0.5222    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.8959   -2.3819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9509   -0.9299    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8563   -0.5174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5769   -0.5507    0.0000 Co  0  2  0  0  0  0  0  0  0  0  0  0
   -2.5773    1.6075    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0929    1.6890    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8024   -1.9869    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1717   -0.8879    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8014   -0.1442    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9854   -2.1572    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4558   -1.7264    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5004   -0.1948    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0576    0.3209    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 12  9  1  0  0  0  0
 13 10  1  0  0  0  0
 14 11  1  0  0  0  0
 16 15  1  0  0  0  0
 21  1  1  4  0  0  0
 22  2  1  4  0  0  0
 23  9  1  6  0  0  0
 24 10  1  1  0  0  0
 25 11  1  6  0  0  0
 26 17  1  1  0  0  0
 27 18  2  0  0  0  0
 27 23  1  0  0  0  0
 18 28  1  4  0  0  0
 29 19  1  0  0  0  0
 30 20  1  0  0  0  0
 31 12  1  0  0  0  0
 32 13  1  0  0  0  0
 33 14  1  0  0  0  0
 34 15  1  0  0  0  0
 35 17  1  0  0  0  0
 36 21  2  0  0  0  0
 36 24  1  0  0  0  0
 37 22  2  0  0  0  0
 37 25  1  0  0  0  0
 38 21  1  0  0  0  0
 39 22  1  0  0  0  0
 40 26  1  0  0  0  0
 41  3  1  0  0  0  0
 41  4  1  0  0  0  0
 41 24  1  0  0  0  0
 41 28  1  0  0  0  0
 42  5  1  1  0  0  0
 42 16  1  6  0  0  0
 42 26  1  0  0  0  0
 42 38  1  0  0  0  0
 43  6  1  6  0  0  0
 43 19  1  1  0  0  0
 43 23  1  0  0  0  0
 43 39  1  0  0  0  0
 44  7  1  6  0  0  0
 44 20  1  1  0  0  0
 44 25  1  0  0  0  0
 45  8  1  6  0  0  0
 45 40  1  0  0  0  0
 45 44  1  0  0  0  0
 46 29  1  0  0  0  0
 47 30  2  0  0  0  0
 48 27  1  0  0  0  0
 48 39  2  0  0  0  0
 49 28  2  0  0  0  0
 49 36  1  0  0  0  0
 50 38  2  0  0  0  0
 50 40  1  0  0  0  0
 51 37  1  0  0  0  0
 51 45  1  0  0  0  0
 52 29  2  0  0  0  0
 53 30  1  0  0  0  0
 54 31  2  0  0  0  0
 55 31  1  0  0  0  0
 56 32  2  0  0  0  0
 57 32  1  0  0  0  0
 58 33  2  0  0  0  0
 59 33  1  0  0  0  0
 60 34  2  0  0  0  0
 61 34  1  0  0  0  0
 62 35  2  0  0  0  0
 63 35  1  0  0  0  0
 67 64  1  1  0  0  0
 69 67  1  0  0  0  0
 70 69  1  0  0  0  0
 71 68  2  0  0  0  0
 72 68  1  0  0  0  0
 73 70  1  0  0  0  0
 74 71  1  0  0  0  0
 75 65  2  0  0  0  0
 75 71  1  0  0  0  0
 76 65  1  0  0  0  0
 76 72  2  0  0  0  0
 77 66  2  0  0  0  0
 77 68  1  0  0  0  0
 78 66  1  0  0  0  0
 78 72  1  0  0  0  0
 73 78  1  1  0  0  0
 69 79  1  6  0  0  0
 70 80  1  6  0  0  0
 81 67  1  0  0  0  0
 81 73  1  0  0  0  0
 23 83  1  1  0  0  0
 24 84  1  6  0  0  0
 25 85  1  1  0  0  0
 26 86  1  6  0  0  0
 40 87  1  1  0  0  0
 67 88  1  6  0  0  0
 69 89  1  1  0  0  0
 70 90  1  1  0  0  0
 73 91  1  6  0  0  0
M  CHG  7  46  -1  53  -1  55  -1  57  -1  59  -1  61  -1  82   2
M  RAD  1  64   2
M  END
> <DATABASE_ID>
MMDBc0055687

> <DATABASE_NAME>
MIME

> <SMILES>
[Co++].[H][C@]1([CH2])O[C@@]([H])(N2C=NC3=C(N)N=CN=C23)[C@]([H])(O)[C@]1([H])O.[H][C@@]1(CCC([O-])=O)C2=C(C)C3=N[C@]([H])([C@]([H])(CC(O)=O)[C@@]3(C)CCC([O-])=O)[C@]3(C)NC(=C(C)C4=NC(=CC(=N2)C1(C)C)[C@@]([H])(CCC([O-])=O)[C@]4(C)CC([NH-])=O)[C@@]([H])(CCC([O-])=O)[C@]3(C)CC([O-])=N

> <INCHI_IDENTIFIER>
InChI=1S/C45H62N6O12.C10H12N5O3.Co/c1-21-36-24(10-13-32(56)57)41(3,4)28(49-36)18-27-23(9-12-31(54)55)43(6,19-29(46)52)39(48-27)22(2)37-25(11-14-33(58)59)44(7,20-30(47)53)45(8,51-37)40-26(17-35(62)63)42(5,38(21)50-40)16-15-34(60)61;1-4-6(16)7(17)10(18-4)15-3-14-5-8(11)12-2-13-9(5)15;/h18,23-26,40H,9-17,19-20H2,1-8H3,(H10,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63);2-4,6-7,10,16-17H,1H2,(H2,11,12,13);/q;;+2/p-6/t23-,24-,25-,26+,40-,42-,43+,44+,45+;4-,6-,7-,10-;/m11./s1

> <INCHI_KEY>
OCNLJCZKGHKJGF-NQYRMHKHSA-H

> <FORMULA>
C55H68CoN11O15

> <MOLECULAR_WEIGHT>
1182.146

> <EXACT_MASS>
1181.425024

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
150

> <JCHEM_AVERAGE_POLARIZABILITY>
89.51019968634165

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
-4

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
lambda2-cobalt(2+) ion [(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl 3-[(1R,2R,3S,4S,8S,9S,14S,18R,19R)-8-(2-azanidyl-2-oxoethyl)-4,14,18-tris(2-carboxyethyl)-19-(carboxymethyl)-3-[(C-hydroxycarbonimidoyl)methyl]-2,3,6,8,13,13,16,18-octamethyl-20,21,22,23-tetraazapentacyclo[15.2.1.1^{2,5}.1^{7,10}.1^{12,15}]tricosa-5,7(22),10,12(21),15,17(20)-hexaen-9-yl]propanoate

> <JCHEM_LOGP>
-2.7627993607160444

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.9187169015639407

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5174993822301643

> <JCHEM_PKA_STRONGEST_BASIC>
8.943674899598886

> <JCHEM_POLAR_SURFACE_AREA>
331.14

> <JCHEM_REFRACTIVITY>
293.32480000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
lambda2-cobalt(2+) ion [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl 3-[(1R,2R,3S,4S,8S,9S,14S,18R,19R)-8-(2-azanidyl-2-oxoethyl)-4,14,18-tris(2-carboxyethyl)-19-(carboxymethyl)-3-(C-hydroxycarbonimidoylmethyl)-2,3,6,8,13,13,16,18-octamethyl-20,21,22,23-tetraazapentacyclo[15.2.1.1^{2,5}.1^{7,10}.1^{12,15}]tricosa-5,7(22),10,12(21),15,17(20)-hexaen-9-yl]propanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-JUN-22         0                                  
HETATM    1  C   UNK     0       3.917   4.461   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.405  -2.956   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.555   2.906   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.975   1.583   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.300   0.894   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.207  -1.584   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.103  -3.623   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.245  -2.615   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.275   2.332   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.324   1.712   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.679  -5.095   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.169   3.868   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.602   0.351   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.218  -5.150   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.919   2.961   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.394   2.745   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.625  -1.307   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.710   3.799   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.478   0.039   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.622  -5.057   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.782   3.421   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.511  -1.702   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.997   1.472   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.506   3.017   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.042  -3.734   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.554  -0.201   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.550   2.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.404   4.616   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -7.337  -1.239   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.983  -5.778   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.786   4.545   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.937   0.296   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.940  -6.511   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.494   4.389   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.118  -0.933   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.081   4.445   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -0.635  -2.351   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.459   2.038   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.461  -0.490   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.029  -0.417   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -1.030   3.122   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.819   1.316   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -4.941  -0.067   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.567  -3.518   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.832  -2.001   0.000  0.00  0.00           C+0
HETATM   46  N   UNK     0      -8.874  -1.134   0.000  0.00  0.00           N-1
HETATM   47  N   UNK     0       4.288  -4.961   0.000  0.00  0.00           N+0
HETATM   48  N   UNK     0      -2.601   0.788   0.000  0.00  0.00           N+0
HETATM   49  N   UNK     0      -0.099   5.434   0.000  0.00  0.00           N+0
HETATM   50  N   UNK     0       2.352   0.967   0.000  0.00  0.00           N+0
HETATM   51  N   UNK     0       0.472  -1.280   0.000  0.00  0.00           N+0
HETATM   52  O   UNK     0      -6.661  -2.623   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0       3.038  -7.317   0.000  0.00  0.00           O-1
HETATM   54  O   UNK     0      -4.680   6.081   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0      -3.508   3.685   0.000  0.00  0.00           O-1
HETATM   56  O   UNK     0      -1.754   1.601   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      -1.658  -1.065   0.000  0.00  0.00           O-1
HETATM   58  O   UNK     0      -2.122  -7.816   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0      -4.479  -6.566   0.000  0.00  0.00           O-1
HETATM   60  O   UNK     0       6.545   5.602   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0       9.019   4.606   0.000  0.00  0.00           O-1
HETATM   62  O   UNK     0       7.541   0.548   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0       8.190  -2.039   0.000  0.00  0.00           O+0
HETATM   64  C   UNK     0      13.419  -3.411   0.000  0.00  0.00           C+0
HETATM   65  C   UNK     0      20.738   1.451   0.000  0.00  0.00           C+0
HETATM   66  C   UNK     0      15.700   2.221   0.000  0.00  0.00           C+0
HETATM   67  C   UNK     0      14.665  -2.506   0.000  0.00  0.00           C+0
HETATM   68  C   UNK     0      18.070   2.991   0.000  0.00  0.00           C+0
HETATM   69  C   UNK     0      16.130  -2.982   0.000  0.00  0.00           C+0
HETATM   70  C   UNK     0      17.035  -1.736   0.000  0.00  0.00           C+0
HETATM   71  C   UNK     0      19.404   3.761   0.000  0.00  0.00           C+0
HETATM   72  C   UNK     0      18.070   1.451   0.000  0.00  0.00           C+0
HETATM   73  C   UNK     0      16.130  -0.490   0.000  0.00  0.00           C+0
HETATM   74  N   UNK     0      19.404   5.301   0.000  0.00  0.00           N+0
HETATM   75  N   UNK     0      20.738   2.991   0.000  0.00  0.00           N+0
HETATM   76  N   UNK     0      19.404   0.681   0.000  0.00  0.00           N+0
HETATM   77  N   UNK     0      16.606   3.466   0.000  0.00  0.00           N+0
HETATM   78  N   UNK     0      16.606   0.975   0.000  0.00  0.00           N+0
HETATM   79  O   UNK     0      16.606  -4.446   0.000  0.00  0.00           O+0
HETATM   80  O   UNK     0      18.575  -1.736   0.000  0.00  0.00           O+0
HETATM   81  O   UNK     0      14.665  -0.966   0.000  0.00  0.00           O+0
HETATM   82 Co   UNK     0     -10.410  -1.028   0.000  0.00  0.00          Co+2
HETATM   83  H   UNK     0      -4.811   3.001   0.000  0.00  0.00           H+0
HETATM   84  H   UNK     0       2.040   3.153   0.000  0.00  0.00           H+0
HETATM   85  H   UNK     0      -1.498  -3.709   0.000  0.00  0.00           H+0
HETATM   86  H   UNK     0       4.054  -1.657   0.000  0.00  0.00           H+0
HETATM   87  H   UNK     0       1.496  -0.269   0.000  0.00  0.00           H+0
HETATM   88  H   UNK     0      14.906  -4.027   0.000  0.00  0.00           H+0
HETATM   89  H   UNK     0      17.651  -3.223   0.000  0.00  0.00           H+0
HETATM   90  H   UNK     0      17.734  -0.364   0.000  0.00  0.00           H+0
HETATM   91  H   UNK     0      15.041   0.599   0.000  0.00  0.00           H+0
CONECT    1   21                                                            
CONECT    2   22                                                            
CONECT    3   41                                                            
CONECT    4   41                                                            
CONECT    5   42                                                            
CONECT    6   43                                                            
CONECT    7   44                                                            
CONECT    8   45                                                            
CONECT    9   12   23                                                       
CONECT   10   13   24                                                       
CONECT   11   14   25                                                       
CONECT   12    9   31                                                       
CONECT   13   10   32                                                       
CONECT   14   11   33                                                       
CONECT   15   16   34                                                       
CONECT   16   15   42                                                       
CONECT   17   26   35                                                       
CONECT   18   27   28                                                       
CONECT   19   29   43                                                       
CONECT   20   30   44                                                       
CONECT   21    1   36   38                                                  
CONECT   22    2   37   39                                                  
CONECT   23    9   27   43   83                                             
CONECT   24   10   36   41   84                                             
CONECT   25   11   37   44   85                                             
CONECT   26   17   40   42   86                                             
CONECT   27   18   23   48                                                  
CONECT   28   18   41   49                                                  
CONECT   29   19   46   52                                                  
CONECT   30   20   47   53                                                  
CONECT   31   12   54   55                                                  
CONECT   32   13   56   57                                                  
CONECT   33   14   58   59                                                  
CONECT   34   15   60   61                                                  
CONECT   35   17   62   63                                                  
CONECT   36   21   24   49                                                  
CONECT   37   22   25   51                                                  
CONECT   38   21   42   50                                                  
CONECT   39   22   43   48                                                  
CONECT   40   26   45   50   87                                             
CONECT   41    3    4   24   28                                             
CONECT   42    5   16   26   38                                             
CONECT   43    6   19   23   39                                             
CONECT   44    7   20   25   45                                             
CONECT   45    8   40   44   51                                             
CONECT   46   29                                                            
CONECT   47   30                                                            
CONECT   48   27   39                                                       
CONECT   49   28   36                                                       
CONECT   50   38   40                                                       
CONECT   51   37   45                                                       
CONECT   52   29                                                            
CONECT   53   30                                                            
CONECT   54   31                                                            
CONECT   55   31                                                            
CONECT   56   32                                                            
CONECT   57   32                                                            
CONECT   58   33                                                            
CONECT   59   33                                                            
CONECT   60   34                                                            
CONECT   61   34                                                            
CONECT   62   35                                                            
CONECT   63   35                                                            
CONECT   64   67                                                            
CONECT   65   75   76                                                       
CONECT   66   77   78                                                       
CONECT   67   64   69   81   88                                             
CONECT   68   71   72   77                                                  
CONECT   69   67   70   79   89                                             
CONECT   70   69   73   80   90                                             
CONECT   71   68   74   75                                                  
CONECT   72   68   76   78                                                  
CONECT   73   70   78   81   91                                             
CONECT   74   71                                                            
CONECT   75   65   71                                                       
CONECT   76   65   72                                                       
CONECT   77   66   68                                                       
CONECT   78   66   72   73                                                  
CONECT   79   69                                                            
CONECT   80   70                                                            
CONECT   81   67   73                                                       
CONECT   83   23                                                            
CONECT   84   24                                                            
CONECT   85   25                                                            
CONECT   86   26                                                            
CONECT   87   40                                                            
CONECT   88   67                                                            
CONECT   89   69                                                            
CONECT   90   70                                                            
CONECT   91   73                                                            
MASTER        0    0    0    0    0    0    0    0   91    0  192    0
END

Synonyms

Value	Source
Adenosylcob(III)yrinate a,c-diamide	ChEBI
Adenosylcob(III)yrinic acid a,c-diamide	Generator
Adenosylcob(III)yrinic acid a,c-diamide(4-)	Generator

Molecular Formula

C₅₅H₆₈CoN₁₁O₁₅

Average Mass

1182.146

Monoisotopic Mass

1181.425024

IUPAC Name

lambda2-cobalt(2+) ion [(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl 3-[(1R,2R,3S,4S,8S,9S,14S,18R,19R)-8-(2-azanidyl-2-oxoethyl)-4,14,18-tris(2-carboxyethyl)-19-(carboxymethyl)-3-[(C-hydroxycarbonimidoyl)methyl]-2,3,6,8,13,13,16,18-octamethyl-20,21,22,23-tetraazapentacyclo[15.2.1.1^{2,5}.1^{7,10}.1^{12,15}]tricosa-5,7(22),10,12(21),15,17(20)-hexaen-9-yl]propanoate

Traditional Name

lambda2-cobalt(2+) ion [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl 3-[(1R,2R,3S,4S,8S,9S,14S,18R,19R)-8-(2-azanidyl-2-oxoethyl)-4,14,18-tris(2-carboxyethyl)-19-(carboxymethyl)-3-(C-hydroxycarbonimidoylmethyl)-2,3,6,8,13,13,16,18-octamethyl-20,21,22,23-tetraazapentacyclo[15.2.1.1^{2,5}.1^{7,10}.1^{12,15}]tricosa-5,7(22),10,12(21),15,17(20)-hexaen-9-yl]propanoate

CAS Registry Number

Not Available

SMILES

[Co++].[H][C@]1([CH2])O[C@@]([H])(N2C=NC3=C(N)N=CN=C23)[C@]([H])(O)[C@]1([H])O.[H][C@@]1(CCC([O-])=O)C2=C(C)C3=N[C@]([H])([C@]([H])(CC(O)=O)[C@@]3(C)CCC([O-])=O)[C@]3(C)NC(=C(C)C4=NC(=CC(=N2)C1(C)C)[C@@]([H])(CCC([O-])=O)[C@]4(C)CC([NH-])=O)[C@@]([H])(CCC([O-])=O)[C@]3(C)CC([O-])=N

InChI Identifier

InChI=1S/C45H62N6O12.C10H12N5O3.Co/c1-21-36-24(10-13-32(56)57)41(3,4)28(49-36)18-27-23(9-12-31(54)55)43(6,19-29(46)52)39(48-27)22(2)37-25(11-14-33(58)59)44(7,20-30(47)53)45(8,51-37)40-26(17-35(62)63)42(5,38(21)50-40)16-15-34(60)61;1-4-6(16)7(17)10(18-4)15-3-14-5-8(11)12-2-13-9(5)15;/h18,23-26,40H,9-17,19-20H2,1-8H3,(H10,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63);2-4,6-7,10,16-17H,1H2,(H2,11,12,13);/q;;+2/p-6/t23-,24-,25-,26+,40-,42-,43+,44+,45+;4-,6-,7-,10-;/m11./s1

InChI Key

OCNLJCZKGHKJGF-NQYRMHKHSA-H

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as metallotetrapyrroles. These are polycyclic compounds containing a tetrapyrrole skeleton combined with a metal atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrapyrroles and derivatives

Sub Class

Metallotetrapyrroles

Direct Parent

Metallotetrapyrroles

Alternative Parents

Substituents

Metallotetrapyrrole skeleton
Pentacarboxylic acid or derivatives
5'-deoxyribonucleoside
Delta amino acid or derivatives
N-glycosyl compound
Glycosyl compound
6-aminopurine
Purine
Imidazopyrimidine
Aminopyrimidine
N-substituted imidazole
Pyrimidine
Fatty amide
Fatty acyl
Imidolactam
Azole
Heteroaromatic compound
Pyrrolidine
Pyrroline
Tetrahydrofuran
Imidazole
Amino acid
Amino acid or derivatives
Ketimine
Secondary alcohol
Carboxamide group
Primary carboxylic acid amide
1,2-diol
Carboxylic acid salt
Carboximidic acid
Carboximidic acid derivative
Oxacycle
Carboxylic acid derivative
Azacycle
Carboxylic acid
Organic transition metal salt
Secondary aliphatic amine
Enamine
Carbene-type 1,3-dipolar compound
Secondary amine
Organic oxide
Organopnictogen compound
Amine
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic cobalt salt
Organic salt
Organic nitrogen compound
Organic oxygen compound
Imine
Primary amine
Organooxygen compound
Organonitrogen compound
Organic anion
Aromatic heteropolycyclic compound

Molecular Framework

Not Available

External Descriptors

pentacarboxylic acid anion (CHEBI:58503 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
logP	-2.8	ChemAxon
pKa (Strongest Acidic)	3.52	ChemAxon
pKa (Strongest Basic)	8.94	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	331.14 Å²	ChemAxon
Rotatable Bond Count	19	ChemAxon
Refractivity	293.32 m³·mol⁻¹	ChemAxon
Polarizability	89.51 Å³	ChemAxon
Number of Rings	8	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 GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2022-08-08	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

Metabolic Reactions

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
Bacteria	Proteobacteria	6	Human ; Human feces
Bacteria	Firmicutes	1	Human feces
Bacteria	Actinobacteria	4	Cattle ; Human

Exposure Sources

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

26331207

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

58503

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for adenosylcob(III)yrinate a,c-diamide (MMDBc0055687)

MOL for #<Metabolite:0x00007fdb4ccd61b0>

3D MOL for #<Metabolite:0x00007fdb4ccd61b0>

3D SDF for #<Metabolite:0x00007fdb4ccd61b0>

3D-SDF for #<Metabolite:0x00007fdb4ccd61b0>

PDB for #<Metabolite:0x00007fdb4ccd61b0>

3D PDB for #<Metabolite:0x00007fdb4ccd61b0>

SMILES for #<Metabolite:0x00007fdb4ccd61b0>

INCHI for #<Metabolite:0x00007fdb4ccd61b0>

Structure for #<Metabolite:0x00007fdb4ccd61b0>

3D Structure for #<Metabolite:0x00007fdb4ccd61b0>