MiMeDB: Showing metabocard for 6-O-adenylylstreptomycin (MMDBc0055607)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-17 20:00:09 UTC

Update Date

2022-08-12 20:09:25 UTC

Metabolite ID

MMDBc0055607

Metabolite Identification

Common Name

6-O-adenylylstreptomycin

Description

6-O-adenylylstreptomycin belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached. Based on a literature review very few articles have been published on 6-O-adenylylstreptomycin.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172222002D          

 80 85  0  0  1  0            999 V2000
   -7.2249    0.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4127    3.3371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5860    0.0271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5683   -1.4940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9108    2.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4179    0.6589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8409    0.8118    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0992   -1.0091    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9179   -1.1216    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0779   -2.2776    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3508    2.3810    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2889    1.4249    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8838   -1.2640    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8316   -1.9421    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5438    2.2095    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3687   -0.5966    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4967   -0.9722    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2504   -0.6367    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4105   -1.7927    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2619    1.3263    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.9029    1.7679    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0903    0.5194    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3390   -1.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0823    1.4126    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -7.0926   -0.9354    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -6.2527   -2.0914    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4128   -3.2475    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5729   -4.4035    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6058    3.1656    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6715   -0.7860    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9917   -3.0981    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7790   -0.1444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1262    2.4745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4819    1.2533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -2.0486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4991   -2.4270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9918    2.8226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1937   -0.5966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8293   -0.4873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8670    1.6675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4743   -0.9759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5045   -2.3108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3220   -1.1584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8048    0.1069    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0992   -0.1841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6479    0.9833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3367    0.1838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7098    1.9394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6568   -2.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9894   -1.6433    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9371    1.3000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0340    0.6402    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2282   -1.8239    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5853   -1.6065    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7454   -2.7626    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7988    2.9941    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7369    2.0379    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6986   -1.3931    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1642   -1.4572    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0959    1.5964    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7432    0.1385    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7431   -1.3078    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1578    2.5525    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4492    1.0386    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  1  0  0  0
  9  3  1  6  0  0  0
 10  4  1  1  0  0  0
 15  9  1  0  0  0  0
 16 10  1  0  0  0  0
 17 11  1  0  0  0  0
 17 12  1  0  0  0  0
 18 13  1  0  0  0  0
 18 15  1  0  0  0  0
 19 16  1  0  0  0  0
 21 11  1  0  0  0  0
 21 20  1  0  0  0  0
 22 12  1  0  0  0  0
 22 20  1  0  0  0  0
 24 14  2  0  0  0  0
 25 14  1  0  0  0  0
 26 19  1  0  0  0  0
 27 13  1  0  0  0  0
 28 23  1  0  0  0  0
 31  5  1  6  0  0  0
 31  8  1  0  0  0  0
 31 23  1  0  0  0  0
 32 24  1  0  0  0  0
 33 29  2  0  0  0  0
 34 29  1  0  0  0  0
 35 30  2  0  0  0  0
 36 30  1  0  0  0  0
 37  2  1  0  0  0  0
 13 37  1  1  0  0  0
 38  6  2  0  0  0  0
 38 24  1  0  0  0  0
 39  6  1  0  0  0  0
 39 25  2  0  0  0  0
 40  7  2  0  0  0  0
 40 14  1  0  0  0  0
 11 41  1  6  0  0  0
 41 29  1  0  0  0  0
 12 42  1  6  0  0  0
 42 30  1  0  0  0  0
 43  7  1  0  0  0  0
 43 25  1  0  0  0  0
 26 43  1  1  0  0  0
 44  3  1  0  0  0  0
 45  5  2  0  0  0  0
 15 46  1  1  0  0  0
 16 47  1  6  0  0  0
 17 48  1  6  0  0  0
 18 49  1  1  0  0  0
 19 50  1  6  0  0  0
 20 51  1  6  0  0  0
 31 52  1  1  0  0  0
 55  4  1  0  0  0  0
 56  8  1  0  0  0  0
 56 28  1  0  0  0  0
 57 10  1  0  0  0  0
 57 26  1  0  0  0  0
 58  9  1  0  0  0  0
 58 27  1  0  0  0  0
 21 59  1  1  0  0  0
 28 59  1  6  0  0  0
 23 60  1  1  0  0  0
 27 60  1  1  0  0  0
 22 61  1  1  0  0  0
 62 53  1  0  0  0  0
 62 54  2  0  0  0  0
 62 55  1  0  0  0  0
 62 61  1  0  0  0  0
  8 63  1  6  0  0  0
  9 64  1  1  0  0  0
 10 65  1  6  0  0  0
 11 66  1  1  0  0  0
 12 67  1  1  0  0  0
 13 68  1  6  0  0  0
 15 69  1  6  0  0  0
 16 70  1  1  0  0  0
 17 71  1  6  0  0  0
 18 72  1  1  0  0  0
 19 73  1  1  0  0  0
 20 74  1  1  0  0  0
 21 75  1  6  0  0  0
 22 76  1  6  0  0  0
 23 77  1  6  0  0  0
 26 78  1  6  0  0  0
 27 79  1  6  0  0  0
 28 80  1  1  0  0  0
M  CHG  2  32   1  33   1
M  END


  Mrv1652306172222002D          

 80 85  0  0  1  0            999 V2000
   -7.2249    0.4874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4127    3.3371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.9108    2.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4179    0.6589    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8409    0.8118    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -5.5575    2.0965    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3004    0.6542    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1578    2.5525    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4492    1.0386    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  1  0  0  0
  9  3  1  6  0  0  0
 10  4  1  1  0  0  0
 15  9  1  0  0  0  0
 16 10  1  0  0  0  0
 17 11  1  0  0  0  0
 17 12  1  0  0  0  0
 18 13  1  0  0  0  0
 18 15  1  0  0  0  0
 19 16  1  0  0  0  0
 21 11  1  0  0  0  0
 21 20  1  0  0  0  0
 22 12  1  0  0  0  0
 22 20  1  0  0  0  0
 24 14  2  0  0  0  0
 25 14  1  0  0  0  0
 26 19  1  0  0  0  0
 27 13  1  0  0  0  0
 28 23  1  0  0  0  0
 31  5  1  6  0  0  0
 31  8  1  0  0  0  0
 31 23  1  0  0  0  0
 32 24  1  0  0  0  0
 33 29  2  0  0  0  0
 34 29  1  0  0  0  0
 35 30  2  0  0  0  0
 36 30  1  0  0  0  0
 37  2  1  0  0  0  0
 13 37  1  1  0  0  0
 38  6  2  0  0  0  0
 38 24  1  0  0  0  0
 39  6  1  0  0  0  0
 39 25  2  0  0  0  0
 40  7  2  0  0  0  0
 40 14  1  0  0  0  0
 11 41  1  6  0  0  0
 41 29  1  0  0  0  0
 12 42  1  6  0  0  0
 42 30  1  0  0  0  0
 43  7  1  0  0  0  0
 43 25  1  0  0  0  0
 26 43  1  1  0  0  0
 44  3  1  0  0  0  0
 45  5  2  0  0  0  0
 15 46  1  1  0  0  0
 16 47  1  6  0  0  0
 17 48  1  6  0  0  0
 18 49  1  1  0  0  0
 19 50  1  6  0  0  0
 20 51  1  6  0  0  0
 31 52  1  1  0  0  0
 55  4  1  0  0  0  0
 56  8  1  0  0  0  0
 56 28  1  0  0  0  0
 57 10  1  0  0  0  0
 57 26  1  0  0  0  0
 58  9  1  0  0  0  0
 58 27  1  0  0  0  0
 21 59  1  1  0  0  0
 28 59  1  6  0  0  0
 23 60  1  1  0  0  0
 27 60  1  1  0  0  0
 22 61  1  1  0  0  0
 62 53  1  0  0  0  0
 62 54  2  0  0  0  0
 62 55  1  0  0  0  0
 62 61  1  0  0  0  0
  8 63  1  6  0  0  0
  9 64  1  1  0  0  0
 10 65  1  6  0  0  0
 11 66  1  1  0  0  0
 12 67  1  1  0  0  0
 13 68  1  6  0  0  0
 15 69  1  6  0  0  0
 16 70  1  1  0  0  0
 17 71  1  6  0  0  0
 18 72  1  1  0  0  0
 19 73  1  1  0  0  0
 20 74  1  1  0  0  0
 21 75  1  6  0  0  0
 22 76  1  6  0  0  0
 23 77  1  6  0  0  0
 26 78  1  6  0  0  0
 27 79  1  6  0  0  0
 28 80  1  1  0  0  0
M  CHG  2  32   1  33   1
M  END
> <DATABASE_ID>
MMDBc0055607

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(C)O[C@@]([H])(O[C@@]2([H])[C@]([H])(O)[C@@]([H])(OP(O)(=O)OC[C@@]3([H])O[C@@]([H])(N4C=NC5=C([NH3+])N=CN=C45)[C@]([H])(O)[C@]3([H])O)[C@]([H])(NC(N)=N)[C@@]([H])(O)[C@]2([H])NC(N)=[NH2+])[C@]([H])(O[C@]2([H])O[C@@]([H])(CO)[C@]([H])(O)[C@@]([H])(O)[C@]2([H])NC)[C@@]1(O)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H51N12O18P/c1-8-31(52,5-45)23(60-27-13(37-2)18(49)15(46)9(3-44)58-27)28(56-8)59-21-11(41-29(33)34)17(48)12(42-30(35)36)22(20(21)51)61-62(53,54)55-4-10-16(47)19(50)26(57-10)43-7-40-14-24(32)38-6-39-25(14)43/h5-13,15-23,26-28,37,44,46-52H,3-4H2,1-2H3,(H,53,54)(H2,32,38,39)(H4,33,34,41)(H4,35,36,42)/p+2/t8-,9-,10+,11-,12+,13-,15-,16+,17-,18-,19+,20-,21+,22-,23-,26+,27-,28-,31+/m0/s1

> <INCHI_KEY>
WTARMSKPYZJSQR-ZJVZNLSDSA-P

> <FORMULA>
C31H53N12O18P

> <MOLECULAR_WEIGHT>
912.804

> <EXACT_MASS>
912.332742753

> <JCHEM_ACCEPTOR_COUNT>
25

> <JCHEM_ATOM_COUNT>
115

> <JCHEM_AVERAGE_POLARIZABILITY>
85.6242446291479

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
17

> <JCHEM_FORMAL_CHARGE>
2

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
9-[(2R,3R,4S,5R)-5-{[({[(1S,2R,3S,4S,5R,6S)-4-{[amino(iminiumyl)methyl]amino}-2-carbamimidamido-5-{[(2R,3R,4R,5S)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-4-formyl-4-hydroxy-5-methyloxolan-2-yl]oxy}-3,6-dihydroxycyclohexyl]oxy}(hydroxy)phosphoryl)oxy]methyl}-3,4-dihydroxyoxolan-2-yl]-9H-purin-6-aminium

> <JCHEM_LOGP>
-8.90621541941536

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
10.693254876002278

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.797551069656686

> <JCHEM_PKA_STRONGEST_BASIC>
11.654554908313962

> <JCHEM_POLAR_SURFACE_AREA>
489.6300000000002

> <JCHEM_REFRACTIVITY>
230.79100000000014

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
9-[(2R,3R,4S,5R)-5-[({[(1S,2R,3S,4S,5R,6S)-4-{[amino(iminio)methyl]amino}-2-carbamimidamido-5-{[(2R,3R,4R,5S)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-4-formyl-4-hydroxy-5-methyloxolan-2-yl]oxy}-3,6-dihydroxycyclohexyl]oxy(hydroxy)phosphoryl}oxy)methyl]-3,4-dihydroxyoxolan-2-yl]purin-6-aminium

> <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     -13.486   0.910   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.237   6.229   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.827   0.051   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.061  -2.789   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -11.034   4.143   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -11.980   1.230   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.303   1.515   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.185  -1.884   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.180  -2.094   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -7.612  -4.252   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.255   4.445   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.273   2.660   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.650  -2.359   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -9.019  -3.625   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.749   4.124   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.555  -1.114   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.527  -1.815   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -7.934  -1.188   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.366  -3.346   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -9.822   2.476   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.650   0.132   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -7.285   3.300   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -9.502   0.969   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -11.833  -2.372   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -8.697  -6.688   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -11.354   2.637   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       4.924   5.923   0.000  0.00  0.00           N+1
HETATM   33  N   UNK     0     -13.240  -1.746   0.000  0.00  0.00           N+1
HETATM   34  N   UNK     0     -11.672  -3.904   0.000  0.00  0.00           N+0
HETATM   35  N   UNK     0     -10.104  -6.062   0.000  0.00  0.00           N+0
HETATM   36  N   UNK     0      -8.536  -8.220   0.000  0.00  0.00           N+0
HETATM   37  N   UNK     0      -6.731   5.909   0.000  0.00  0.00           N+0
HETATM   38  N   UNK     0       6.258   3.613   0.000  0.00  0.00           N+0
HETATM   39  N   UNK     0       4.924   1.303   0.000  0.00  0.00           N+0
HETATM   40  N   UNK     0       2.126   4.089   0.000  0.00  0.00           N+0
HETATM   41  N   UNK     0     -10.587  -1.467   0.000  0.00  0.00           N+0
HETATM   42  N   UNK     0      -7.451  -5.783   0.000  0.00  0.00           N+0
HETATM   43  N   UNK     0       2.126   1.597   0.000  0.00  0.00           N+0
HETATM   44  O   UNK     0      -3.321  -0.270   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      -9.569   4.619   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      -2.766   2.340   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0       2.126  -3.824   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0     -10.265  -4.530   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      -3.718   5.269   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       4.095  -1.114   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      -5.281  -0.910   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0     -12.818   3.113   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0      -4.619  -1.822   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      -2.808  -4.313   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0      -2.468  -2.162   0.000  0.00  0.00           O+0
HETATM   56  O   UNK     0     -10.836   0.199   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0       0.185  -0.344   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0      -6.809   1.835   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0      -8.095   0.343   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      -8.792   3.620   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      -4.959  -3.973   0.000  0.00  0.00           O+0
HETATM   62  P   UNK     0      -3.714  -3.068   0.000  0.00  0.00           P+0
HETATM   63  H   UNK     0     -12.949   2.427   0.000  0.00  0.00           H+0
HETATM   64  H   UNK     0      -3.797   1.195   0.000  0.00  0.00           H+0
HETATM   65  H   UNK     0       0.426  -3.405   0.000  0.00  0.00           H+0
HETATM   66  H   UNK     0     -10.426  -2.999   0.000  0.00  0.00           H+0
HETATM   67  H   UNK     0      -8.858  -5.157   0.000  0.00  0.00           H+0
HETATM   68  H   UNK     0      -5.224   5.589   0.000  0.00  0.00           H+0
HETATM   69  H   UNK     0      -3.242   3.804   0.000  0.00  0.00           H+0
HETATM   70  H   UNK     0       3.171  -2.600   0.000  0.00  0.00           H+0
HETATM   71  H   UNK     0      -7.773  -2.720   0.000  0.00  0.00           H+0
HETATM   72  H   UNK     0      -5.779   2.980   0.000  0.00  0.00           H+0
HETATM   73  H   UNK     0       3.254   0.259   0.000  0.00  0.00           H+0
HETATM   74  H   UNK     0      -5.120  -2.441   0.000  0.00  0.00           H+0
HETATM   75  H   UNK     0      -6.688  -0.283   0.000  0.00  0.00           H+0
HETATM   76  H   UNK     0      -6.205  -4.878   0.000  0.00  0.00           H+0
HETATM   77  H   UNK     0     -10.374   3.914   0.000  0.00  0.00           H+0
HETATM   78  H   UNK     0       0.561   1.221   0.000  0.00  0.00           H+0
HETATM   79  H   UNK     0      -7.761   4.765   0.000  0.00  0.00           H+0
HETATM   80  H   UNK     0      -8.305   1.939   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2   37                                                            
CONECT    3    9   44                                                       
CONECT    4   10   55                                                       
CONECT    5   31   45                                                       
CONECT    6   38   39                                                       
CONECT    7   40   43                                                       
CONECT    8    1   31   56   63                                             
CONECT    9    3   15   58   64                                             
CONECT   10    4   16   57   65                                             
CONECT   11   17   21   41   66                                             
CONECT   12   17   22   42   67                                             
CONECT   13   18   27   37   68                                             
CONECT   14   24   25   40                                                  
CONECT   15    9   18   46   69                                             
CONECT   16   10   19   47   70                                             
CONECT   17   11   12   48   71                                             
CONECT   18   13   15   49   72                                             
CONECT   19   16   26   50   73                                             
CONECT   20   21   22   51   74                                             
CONECT   21   11   20   59   75                                             
CONECT   22   12   20   61   76                                             
CONECT   23   28   31   60   77                                             
CONECT   24   14   32   38                                                  
CONECT   25   14   39   43                                                  
CONECT   26   19   43   57   78                                             
CONECT   27   13   58   60   79                                             
CONECT   28   23   56   59   80                                             
CONECT   29   33   34   41                                                  
CONECT   30   35   36   42                                                  
CONECT   31    5    8   23   52                                             
CONECT   32   24                                                            
CONECT   33   29                                                            
CONECT   34   29                                                            
CONECT   35   30                                                            
CONECT   36   30                                                            
CONECT   37    2   13                                                       
CONECT   38    6   24                                                       
CONECT   39    6   25                                                       
CONECT   40    7   14                                                       
CONECT   41   11   29                                                       
CONECT   42   12   30                                                       
CONECT   43    7   25   26                                                  
CONECT   44    3                                                            
CONECT   45    5                                                            
CONECT   46   15                                                            
CONECT   47   16                                                            
CONECT   48   17                                                            
CONECT   49   18                                                            
CONECT   50   19                                                            
CONECT   51   20                                                            
CONECT   52   31                                                            
CONECT   53   62                                                            
CONECT   54   62                                                            
CONECT   55    4   62                                                       
CONECT   56    8   28                                                       
CONECT   57   10   26                                                       
CONECT   58    9   27                                                       
CONECT   59   21   28                                                       
CONECT   60   23   27                                                       
CONECT   61   22   62                                                       
CONECT   62   53   54   55   61                                             
CONECT   63    8                                                            
CONECT   64    9                                                            
CONECT   65   10                                                            
CONECT   66   11                                                            
CONECT   67   12                                                            
CONECT   68   13                                                            
CONECT   69   15                                                            
CONECT   70   16                                                            
CONECT   71   17                                                            
CONECT   72   18                                                            
CONECT   73   19                                                            
CONECT   74   20                                                            
CONECT   75   21                                                            
CONECT   76   22                                                            
CONECT   77   23                                                            
CONECT   78   26                                                            
CONECT   79   27                                                            
CONECT   80   28                                                            
MASTER        0    0    0    0    0    0    0    0   80    0  170    0
END

Synonyms

Not Available

Molecular Formula

C₃₁H₅₃N₁₂O₁₈P

Average Mass

912.804

Monoisotopic Mass

912.332742753

IUPAC Name

9-[(2R,3R,4S,5R)-5-{[({[(1S,2R,3S,4S,5R,6S)-4-{[amino(iminiumyl)methyl]amino}-2-carbamimidamido-5-{[(2R,3R,4R,5S)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-4-formyl-4-hydroxy-5-methyloxolan-2-yl]oxy}-3,6-dihydroxycyclohexyl]oxy}(hydroxy)phosphoryl)oxy]methyl}-3,4-dihydroxyoxolan-2-yl]-9H-purin-6-aminium

Traditional Name

9-[(2R,3R,4S,5R)-5-[({[(1S,2R,3S,4S,5R,6S)-4-{[amino(iminio)methyl]amino}-2-carbamimidamido-5-{[(2R,3R,4R,5S)-3-{[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy}-4-formyl-4-hydroxy-5-methyloxolan-2-yl]oxy}-3,6-dihydroxycyclohexyl]oxy(hydroxy)phosphoryl}oxy)methyl]-3,4-dihydroxyoxolan-2-yl]purin-6-aminium

CAS Registry Number

Not Available

SMILES

[H][C@@]1(C)O[C@@]([H])(O[C@@]2([H])[C@]([H])(O)[C@@]([H])(OP(O)(=O)OC[C@@]3([H])O[C@@]([H])(N4C=NC5=C([NH3+])N=CN=C45)[C@]([H])(O)[C@]3([H])O)[C@]([H])(NC(N)=N)[C@@]([H])(O)[C@]2([H])NC(N)=[NH2+])[C@]([H])(O[C@]2([H])O[C@@]([H])(CO)[C@]([H])(O)[C@@]([H])(O)[C@]2([H])NC)[C@@]1(O)C=O

InChI Identifier

InChI=1S/C31H51N12O18P/c1-8-31(52,5-45)23(60-27-13(37-2)18(49)15(46)9(3-44)58-27)28(56-8)59-21-11(41-29(33)34)17(48)12(42-30(35)36)22(20(21)51)61-62(53,54)55-4-10-16(47)19(50)26(57-10)43-7-40-14-24(32)38-6-39-25(14)43/h5-13,15-23,26-28,37,44,46-52H,3-4H2,1-2H3,(H,53,54)(H2,32,38,39)(H4,33,34,41)(H4,35,36,42)/p+2/t8-,9-,10+,11-,12+,13-,15-,16+,17-,18-,19+,20-,21+,22-,23-,26+,27-,28-,31+/m0/s1

InChI Key

WTARMSKPYZJSQR-ZJVZNLSDSA-P

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Sub Class

Purine ribonucleotides

Direct Parent

Purine ribonucleoside monophosphates

Alternative Parents

Substituents

Purine ribonucleoside monophosphate
Aminoglycoside core
Streptamine aminoglycoside
Amino cyclitol glycoside
Pentose-5-phosphate
Pentose phosphate
O-glycosyl compound
N-glycosyl compound
Glycosyl compound
Monosaccharide phosphate
6-aminopurine
Purine
Imidazopyrimidine
Dialkyl phosphate
Amino saccharide
Cyclohexanol
Aminopyrimidine
Alkyl phosphate
Pyrimidine
Phosphoric acid ester
Oxane
Organic phosphoric acid derivative
N-substituted imidazole
Monosaccharide
Cyclitol or derivatives
Heteroaromatic compound
Tetrahydrofuran
Tertiary alcohol
Imidazole
Cyclic alcohol
Azole
Secondary alcohol
Guanidine
1,2-aminoalcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Carboximidamide
Secondary amine
Secondary aliphatic amine
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Primary alcohol
Organooxygen compound
Organonitrogen compound
Imine
Carbonyl group
Amine
Aldehyde
Alcohol
Organic cation
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
logP	-8.9	ChemAxon
pKa (Strongest Acidic)	1.8	ChemAxon
pKa (Strongest Basic)	11.65	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	25	ChemAxon
Hydrogen Donor Count	17	ChemAxon
Polar Surface Area	489.63 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	230.79 m³·mol⁻¹	ChemAxon
Polarizability	85.62 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

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

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	Firmicutes	2	Human feces; Human ; Human subgingival plaque; Human saliva
Bacteria/Eubacteria	Proteobacteria	1	Human ; Human feces

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

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

146014766

PDB ID

Not Available

ChEBI ID

Not Available

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 6-O-adenylylstreptomycin (MMDBc0055607)

MOL for #<Metabolite:0x00007f922c352648>

3D MOL for #<Metabolite:0x00007f922c352648>

3D SDF for #<Metabolite:0x00007f922c352648>

3D-SDF for #<Metabolite:0x00007f922c352648>

PDB for #<Metabolite:0x00007f922c352648>

3D PDB for #<Metabolite:0x00007f922c352648>

SMILES for #<Metabolite:0x00007f922c352648>

INCHI for #<Metabolite:0x00007f922c352648>

Structure for #<Metabolite:0x00007f922c352648>

3D Structure for #<Metabolite:0x00007f922c352648>