MiMeDB: Showing metabocard for (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene (MMDBc0029944)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-17 23:47:48 UTC

Update Date

2024-04-30 19:43:26 UTC

Metabolite ID

MMDBc0029944

Metabolite Identification

Common Name

(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene

Description

(1r)-glutathionyl-(2r)-hydroxy-1,2-dihydronaphthalene belongs to the class of Peptides. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another. (inferred from compound structure)

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 08131209212D          

 35 36  0  0  0  0            999 V2000
   -0.7145    7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    5.3625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.9500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    5.7750    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  7  5  2  0  0  0  0
  8  6  1  0  0  0  0
 11  3  2  0  0  0  0
 11  5  1  0  0  0  0
 12  4  2  0  0  0  0
 12 11  1  0  0  0  0
 13  6  1  0  0  0  0
 14 10  1  0  0  0  0
 15  7  1  0  0  0  0
 16  8  1  0  0  0  0
 17  9  1  0  0  0  0
 18 12  1  0  0  0  0
 18 15  1  0  0  0  0
 19 14  1  0  0  0  0
 20 13  1  0  0  0  0
 13 21  1  1  0  0  0
 22  9  1  4  0  0  0
 22 19  2  0  0  0  0
 14 23  1  1  0  0  0
 23 16  2  0  0  0  0
 15 24  1  6  0  0  0
 16 25  1  4  0  0  0
 26 17  2  0  0  0  0
 27 17  1  0  0  0  0
 28 19  1  0  0  0  0
 29 20  2  0  0  0  0
 30 20  1  0  0  0  0
 31 10  1  0  0  0  0
 18 31  1  1  0  0  0
 13 32  1  1  0  0  0
 14 33  1  1  0  0  0
 15 34  1  1  0  0  0
 18 35  1  6  0  0  0
M  END

HMDB0060299
     RDKit          3D
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene
 56 57  0  0  0  0  0  0  0  0999 V2000
    5.6731   -3.0934   -0.6763 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8681   -1.6540   -0.7080 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6915   -0.9440   -0.0752 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4124   -1.2698   -0.8189 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2438   -0.5739   -0.2025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9933   -0.8878    1.1321 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5646    0.2375   -0.9013 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4244    0.9990   -0.5145 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6789    0.0775   -0.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1356    1.0162    0.4679 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4342   -0.1258    0.9749 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0708   -0.8440   -0.1468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5460   -0.7755   -1.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0521   -1.6234   -2.4144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0609   -2.5007   -2.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5721   -2.5474   -0.8051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0823   -1.7113    0.1833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7793   -1.5922    1.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4312   -0.6195    2.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3801    0.3629    1.9703 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7751    0.8448    3.1410 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6746    1.9780    0.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1193    1.5425    1.7818 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4867    3.2351    0.3390 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0291    3.6955   -0.9322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0104    5.1679   -0.9536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3969    5.7707   -2.0131 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3712    5.8694    0.1727 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1236   -1.2609   -0.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9090   -2.1188    0.4812 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4431    0.0821    0.0204 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4132   -3.3875    0.2882 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6004   -3.5357   -0.9310 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9595   -1.3644   -1.7881 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9024    0.1582   -0.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6264   -1.2407    0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5123   -1.0016   -1.8840 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2684   -2.3718   -0.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6729   -0.7171    1.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0124    1.4880   -1.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2768   -0.3932    0.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8354   -0.7301   -0.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8710   -1.0004    1.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7718   -0.0796   -1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6259   -1.5531   -3.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4404   -3.1486   -2.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3723   -3.2354   -0.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5410   -2.3166    1.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9591   -0.5652    3.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9090    1.2660    1.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3610    1.5480    3.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0857    1.7147    2.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7090    3.3751   -1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9772    3.2743   -1.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3248    6.4686    0.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8813    0.6114   -0.7017 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
  8 22  1  0
 22 23  1  0
 22 24  2  3
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
  2 29  1  0
 29 30  2  0
 29 31  1  0
 20 11  1  0
 17 12  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  6
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  6 39  1  0
  8 40  1  6
  9 41  1  0
  9 42  1  0
 11 43  1  1
 13 44  1  0
 14 45  1  0
 15 46  1  0
 16 47  1  0
 18 48  1  0
 19 49  1  0
 20 50  1  6
 21 51  1  0
 23 52  1  0
 25 53  1  0
 25 54  1  0
 28 55  1  0
 31 56  1  0
M  END


  Mrv0541 08131209212D          

 35 36  0  0  0  0            999 V2000
   -0.7145    7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    5.3625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.3625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.3625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.9500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    5.7750    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  7  5  2  0  0  0  0
  8  6  1  0  0  0  0
 11  3  2  0  0  0  0
 11  5  1  0  0  0  0
 12  4  2  0  0  0  0
 12 11  1  0  0  0  0
 13  6  1  0  0  0  0
 14 10  1  0  0  0  0
 15  7  1  0  0  0  0
 16  8  1  0  0  0  0
 17  9  1  0  0  0  0
 18 12  1  0  0  0  0
 18 15  1  0  0  0  0
 19 14  1  0  0  0  0
 20 13  1  0  0  0  0
 13 21  1  1  0  0  0
 22  9  1  4  0  0  0
 22 19  2  0  0  0  0
 14 23  1  1  0  0  0
 23 16  2  0  0  0  0
 15 24  1  6  0  0  0
 16 25  1  4  0  0  0
 26 17  2  0  0  0  0
 27 17  1  0  0  0  0
 28 19  1  0  0  0  0
 29 20  2  0  0  0  0
 30 20  1  0  0  0  0
 31 10  1  0  0  0  0
 18 31  1  1  0  0  0
 13 32  1  1  0  0  0
 14 33  1  1  0  0  0
 15 34  1  1  0  0  0
 18 35  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0029944

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](N)(CCC(O)=N[C@@]([H])(CS[C@]1([H])C2=CC=CC=C2C=C[C@@]1([H])O)C(O)=NCC(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H25N3O7S/c21-13(20(29)30)6-8-16(25)23-14(19(28)22-9-17(26)27)10-31-18-12-4-2-1-3-11(12)5-7-15(18)24/h1-5,7,13-15,18,24H,6,8-10,21H2,(H,22,28)(H,23,25)(H,26,27)(H,29,30)/t13-,14-,15+,18+/m0/s1

> <INCHI_KEY>
UWBZAZWPTVBBEL-OIPACUDHSA-N

> <FORMULA>
C20H25N3O7S

> <MOLECULAR_WEIGHT>
451.493

> <EXACT_MASS>
451.141320859

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
44.998077996752514

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-{[(1R,2R)-2-hydroxy-1,2-dihydronaphthalen-1-yl]sulfanyl}ethyl]-C-hydroxycarbonimidoyl}butanoic acid

> <ALOGPS_LOGP>
-1.59

> <JCHEM_LOGP>
-1.6711648715767475

> <ALOGPS_LOGS>
-3.89

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.5552857881517927

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.9619963685797543

> <JCHEM_PKA_STRONGEST_BASIC>
9.538964729742805

> <JCHEM_POLAR_SURFACE_AREA>
186.02999999999997

> <JCHEM_REFRACTIVITY>
114.10319999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.81e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-amino-4-{[(1R)-1-(carboxymethyl-C-hydroxycarbonimidoyl)-2-{[(1R,2R)-2-hydroxy-1,2-dihydronaphthalen-1-yl]sulfanyl}ethyl]-C-hydroxycarbonimidoyl}butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0060299
     RDKit          3D
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene
 56 57  0  0  0  0  0  0  0  0999 V2000
    5.6731   -3.0934   -0.6763 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8681   -1.6540   -0.7080 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6915   -0.9440   -0.0752 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4124   -1.2698   -0.8189 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2438   -0.5739   -0.2025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9933   -0.8878    1.1321 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5646    0.2375   -0.9013 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4244    0.9990   -0.5145 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6789    0.0775   -0.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1356    1.0162    0.4679 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4342   -0.1258    0.9749 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0708   -0.8440   -0.1468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5460   -0.7755   -1.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0521   -1.6234   -2.4144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0609   -2.5007   -2.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5721   -2.5474   -0.8051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0823   -1.7113    0.1833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7793   -1.5922    1.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4312   -0.6195    2.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3801    0.3629    1.9703 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7751    0.8448    3.1410 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6746    1.9780    0.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1193    1.5425    1.7818 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4867    3.2351    0.3390 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0291    3.6955   -0.9322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0104    5.1679   -0.9536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3969    5.7707   -2.0131 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3712    5.8694    0.1727 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1236   -1.2609   -0.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9090   -2.1188    0.4812 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4431    0.0821    0.0204 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4132   -3.3875    0.2882 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6004   -3.5357   -0.9310 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9595   -1.3644   -1.7881 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9024    0.1582   -0.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6264   -1.2407    0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5123   -1.0016   -1.8840 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2684   -2.3718   -0.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6729   -0.7171    1.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0124    1.4880   -1.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2768   -0.3932    0.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8354   -0.7301   -0.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8710   -1.0004    1.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7718   -0.0796   -1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6259   -1.5531   -3.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4404   -3.1486   -2.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3723   -3.2354   -0.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5410   -2.3166    1.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9591   -0.5652    3.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9090    1.2660    1.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3610    1.5480    3.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0857    1.7147    2.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7090    3.3751   -1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9772    3.2743   -1.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3248    6.4686    0.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8813    0.6114   -0.7017 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
  8 22  1  0
 22 23  1  0
 22 24  2  3
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
  2 29  1  0
 29 30  2  0
 29 31  1  0
 20 11  1  0
 17 12  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  6
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  6 39  1  0
  8 40  1  6
  9 41  1  0
  9 42  1  0
 11 43  1  1
 13 44  1  0
 14 45  1  0
 15 46  1  0
 16 47  1  0
 18 48  1  0
 19 49  1  0
 20 50  1  6
 21 51  1  0
 23 52  1  0
 25 53  1  0
 25 54  1  0
 28 55  1  0
 31 56  1  0
M  END

HEADER    PROTEIN                                 13-AUG-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   13-AUG-12         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   22  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   23  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   24  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   31  S   UNK     0       0.000   0.000   0.000  0.00  0.00           S+0
HETATM   32  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
CONECT    1    2    3                                                       
CONECT    2    1    4                                                       
CONECT    3    1   11                                                       
CONECT    4    2   12                                                       
CONECT    5    7   11                                                       
CONECT    6    8   13                                                       
CONECT    7    5   15                                                       
CONECT    8    6   16                                                       
CONECT    9   17   22                                                       
CONECT   10   14   31                                                       
CONECT   11    3    5   12                                                  
CONECT   12    4   11   18                                                  
CONECT   13    6   20   21   32                                             
CONECT   14   10   19   23   33                                             
CONECT   15    7   18   24   34                                             
CONECT   16    8   23   25                                                  
CONECT   17    9   26   27                                                  
CONECT   18   12   15   31   35                                             
CONECT   19   14   22   28                                                  
CONECT   20   13   29   30                                                  
CONECT   21   13                                                            
CONECT   22    9   19                                                       
CONECT   23   14   16                                                       
CONECT   24   15                                                            
CONECT   25   16                                                            
CONECT   26   17                                                            
CONECT   27   17                                                            
CONECT   28   19                                                            
CONECT   29   20                                                            
CONECT   30   20                                                            
CONECT   31   10   18                                                       
CONECT   32   13                                                            
CONECT   33   14                                                            
CONECT   34   15                                                            
CONECT   35   18                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   72    0
END

COMPND    HMDB0060299
HETATM    1  N1  UNL     1       5.673  -3.093  -0.676  1.00  0.00           N  
HETATM    2  C1  UNL     1       5.868  -1.654  -0.708  1.00  0.00           C  
HETATM    3  C2  UNL     1       4.691  -0.944  -0.075  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.412  -1.270  -0.819  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.244  -0.574  -0.202  1.00  0.00           C  
HETATM    6  O1  UNL     1       1.993  -0.888   1.132  1.00  0.00           O  
HETATM    7  N2  UNL     1       1.565   0.238  -0.901  1.00  0.00           N  
HETATM    8  C5  UNL     1       0.424   0.999  -0.515  1.00  0.00           C  
HETATM    9  C6  UNL     1      -0.679   0.078  -0.028  1.00  0.00           C  
HETATM   10  S1  UNL     1      -2.136   1.016   0.468  1.00  0.00           S  
HETATM   11  C7  UNL     1      -3.434  -0.126   0.975  1.00  0.00           C  
HETATM   12  C8  UNL     1      -4.071  -0.844  -0.147  1.00  0.00           C  
HETATM   13  C9  UNL     1      -3.546  -0.776  -1.423  1.00  0.00           C  
HETATM   14  C10 UNL     1      -4.052  -1.623  -2.414  1.00  0.00           C  
HETATM   15  C11 UNL     1      -5.061  -2.501  -2.084  1.00  0.00           C  
HETATM   16  C12 UNL     1      -5.572  -2.547  -0.805  1.00  0.00           C  
HETATM   17  C13 UNL     1      -5.082  -1.711   0.183  1.00  0.00           C  
HETATM   18  C14 UNL     1      -5.779  -1.592   1.477  1.00  0.00           C  
HETATM   19  C15 UNL     1      -5.431  -0.619   2.302  1.00  0.00           C  
HETATM   20  C16 UNL     1      -4.380   0.363   1.970  1.00  0.00           C  
HETATM   21  O2  UNL     1      -3.775   0.845   3.141  1.00  0.00           O  
HETATM   22  C17 UNL     1       0.675   1.978   0.545  1.00  0.00           C  
HETATM   23  O3  UNL     1       1.119   1.543   1.782  1.00  0.00           O  
HETATM   24  N3  UNL     1       0.487   3.235   0.339  1.00  0.00           N  
HETATM   25  C18 UNL     1       0.029   3.696  -0.932  1.00  0.00           C  
HETATM   26  C19 UNL     1      -0.010   5.168  -0.954  1.00  0.00           C  
HETATM   27  O4  UNL     1      -0.397   5.771  -2.013  1.00  0.00           O  
HETATM   28  O5  UNL     1       0.371   5.869   0.173  1.00  0.00           O  
HETATM   29  C20 UNL     1       7.124  -1.261  -0.038  1.00  0.00           C  
HETATM   30  O6  UNL     1       7.909  -2.119   0.481  1.00  0.00           O  
HETATM   31  O7  UNL     1       7.443   0.082   0.020  1.00  0.00           O  
HETATM   32  H1  UNL     1       5.413  -3.388   0.288  1.00  0.00           H  
HETATM   33  H2  UNL     1       6.600  -3.536  -0.931  1.00  0.00           H  
HETATM   34  H3  UNL     1       5.960  -1.364  -1.788  1.00  0.00           H  
HETATM   35  H4  UNL     1       4.902   0.158  -0.172  1.00  0.00           H  
HETATM   36  H5  UNL     1       4.626  -1.241   0.978  1.00  0.00           H  
HETATM   37  H6  UNL     1       3.512  -1.002  -1.884  1.00  0.00           H  
HETATM   38  H7  UNL     1       3.268  -2.372  -0.758  1.00  0.00           H  
HETATM   39  H8  UNL     1       2.673  -0.717   1.876  1.00  0.00           H  
HETATM   40  H9  UNL     1       0.012   1.488  -1.436  1.00  0.00           H  
HETATM   41  H10 UNL     1      -0.277  -0.393   0.932  1.00  0.00           H  
HETATM   42  H11 UNL     1      -0.835  -0.730  -0.733  1.00  0.00           H  
HETATM   43  H12 UNL     1      -2.871  -1.000   1.518  1.00  0.00           H  
HETATM   44  H13 UNL     1      -2.772  -0.080  -1.709  1.00  0.00           H  
HETATM   45  H14 UNL     1      -3.626  -1.553  -3.407  1.00  0.00           H  
HETATM   46  H15 UNL     1      -5.440  -3.149  -2.848  1.00  0.00           H  
HETATM   47  H16 UNL     1      -6.372  -3.235  -0.523  1.00  0.00           H  
HETATM   48  H17 UNL     1      -6.541  -2.317   1.672  1.00  0.00           H  
HETATM   49  H18 UNL     1      -5.959  -0.565   3.261  1.00  0.00           H  
HETATM   50  H19 UNL     1      -4.909   1.266   1.511  1.00  0.00           H  
HETATM   51  H20 UNL     1      -4.361   1.548   3.531  1.00  0.00           H  
HETATM   52  H21 UNL     1       2.086   1.715   2.022  1.00  0.00           H  
HETATM   53  H22 UNL     1       0.709   3.375  -1.769  1.00  0.00           H  
HETATM   54  H23 UNL     1      -0.977   3.274  -1.197  1.00  0.00           H  
HETATM   55  H24 UNL     1      -0.325   6.469   0.606  1.00  0.00           H  
HETATM   56  H25 UNL     1       7.881   0.611  -0.702  1.00  0.00           H  
CONECT    1    2   32   33
CONECT    2    3   29   34
CONECT    3    4   35   36
CONECT    4    5   37   38
CONECT    5    6    7    7
CONECT    6   39
CONECT    7    8
CONECT    8    9   22   40
CONECT    9   10   41   42
CONECT   10   11
CONECT   11   12   20   43
CONECT   12   13   13   17
CONECT   13   14   44
CONECT   14   15   15   45
CONECT   15   16   46
CONECT   16   17   17   47
CONECT   17   18
CONECT   18   19   19   48
CONECT   19   20   49
CONECT   20   21   50
CONECT   21   51
CONECT   22   23   24   24
CONECT   23   52
CONECT   24   25
CONECT   25   26   53   54
CONECT   26   27   27   28
CONECT   28   55
CONECT   29   30   30   31
CONECT   31   56
END

HMDB0060299
     RDKit          3D
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene
 56 57  0  0  0  0  0  0  0  0999 V2000
    5.6731   -3.0934   -0.6763 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8681   -1.6540   -0.7080 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6915   -0.9440   -0.0752 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4124   -1.2698   -0.8189 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2438   -0.5739   -0.2025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9933   -0.8878    1.1321 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5646    0.2375   -0.9013 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4244    0.9990   -0.5145 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6789    0.0775   -0.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1356    1.0162    0.4679 S   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4342   -0.1258    0.9749 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0708   -0.8440   -0.1468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5460   -0.7755   -1.4231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0521   -1.6234   -2.4144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0609   -2.5007   -2.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5721   -2.5474   -0.8051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0823   -1.7113    0.1833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7793   -1.5922    1.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4312   -0.6195    2.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3801    0.3629    1.9703 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7751    0.8448    3.1410 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6746    1.9780    0.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1193    1.5425    1.7818 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4867    3.2351    0.3390 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0291    3.6955   -0.9322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0104    5.1679   -0.9536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3969    5.7707   -2.0131 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3712    5.8694    0.1727 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1236   -1.2609   -0.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9090   -2.1188    0.4812 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4431    0.0821    0.0204 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4132   -3.3875    0.2882 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6004   -3.5357   -0.9310 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9595   -1.3644   -1.7881 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9024    0.1582   -0.1717 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6264   -1.2407    0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5123   -1.0016   -1.8840 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2684   -2.3718   -0.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6729   -0.7171    1.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0124    1.4880   -1.4361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2768   -0.3932    0.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8354   -0.7301   -0.7333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8710   -1.0004    1.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7718   -0.0796   -1.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6259   -1.5531   -3.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4404   -3.1486   -2.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3723   -3.2354   -0.5229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5410   -2.3166    1.6722 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9591   -0.5652    3.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9090    1.2660    1.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3610    1.5480    3.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0857    1.7147    2.0225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7090    3.3751   -1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9772    3.2743   -1.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3248    6.4686    0.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8813    0.6114   -0.7017 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
  8 22  1  0
 22 23  1  0
 22 24  2  3
 24 25  1  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
  2 29  1  0
 29 30  2  0
 29 31  1  0
 20 11  1  0
 17 12  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  6
  3 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  6 39  1  0
  8 40  1  6
  9 41  1  0
  9 42  1  0
 11 43  1  1
 13 44  1  0
 14 45  1  0
 15 46  1  0
 16 47  1  0
 18 48  1  0
 19 49  1  0
 20 50  1  6
 21 51  1  0
 23 52  1  0
 25 53  1  0
 25 54  1  0
 28 55  1  0
 31 56  1  0
M  END

Synonyms

Not Available

Molecular Formula

C₂₀H₂₅N₃O₇S

Average Mass

451.493

Monoisotopic Mass

451.141320859

IUPAC Name

(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-{[(1R,2R)-2-hydroxy-1,2-dihydronaphthalen-1-yl]sulfanyl}ethyl]-C-hydroxycarbonimidoyl}butanoic acid

Traditional Name

(2S)-2-amino-4-{[(1R)-1-(carboxymethyl-C-hydroxycarbonimidoyl)-2-{[(1R,2R)-2-hydroxy-1,2-dihydronaphthalen-1-yl]sulfanyl}ethyl]-C-hydroxycarbonimidoyl}butanoic acid

CAS Registry Number

Not Available

SMILES

[H][C@](N)(CCC(O)=N[C@@]([H])(CS[C@]1([H])C2=CC=CC=C2C=C[C@@]1([H])O)C(O)=NCC(O)=O)C(O)=O

InChI Identifier

InChI=1S/C20H25N3O7S/c21-13(20(29)30)6-8-16(25)23-14(19(28)22-9-17(26)27)10-31-18-12-4-2-1-3-11(12)5-7-15(18)24/h1-5,7,13-15,18,24H,6,8-10,21H2,(H,22,28)(H,23,25)(H,26,27)(H,29,30)/t13-,14-,15+,18+/m0/s1

InChI Key

UWBZAZWPTVBBEL-OIPACUDHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Gamma-glutamyl alpha peptide
Glutamine or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
Alpha-amino acid amide
Cysteine or derivatives
Alpha-amino acid
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
Naphthalene
L-alpha-amino acid
Fatty acyl
N-acyl-amine
Fatty amide
Dicarboxylic acid or derivatives
Benzenoid
Secondary alcohol
Secondary carboxylic acid amide
Amino acid
Amino acid or derivatives
Carboxamide group
Dialkylthioether
Carboxylic acid
Sulfenyl compound
Thioether
Primary amine
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
Amine
Organic oxide
Primary aliphatic amine
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

peptide (CHEBI:33993 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.058 g/L	ALOGPS
logP	-1.6	ALOGPS
logP	-1.7	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	1.96	ChemAxon
pKa (Strongest Basic)	9.54	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	186.03 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	114.1 m³·mol⁻¹	ChemAxon
Polarizability	45 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-0002-3915700000-d663b106af5ff8f05ab5	2017-09-20	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (3 TMS) - 70eV, Positive	splash10-0gb9-6491156000-387722deb85a575c8d1f	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_2_4) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_3_3) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_3_6) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_3_10) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS ("(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,#4" TMS) - 70eV, Positive	Not Available	2021-10-14	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00e9-3126900000-e852fce9919b502e2de0	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00di-9226100000-8ad87012ef3d3e1f9b0b	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-00di-9221000000-4da054dda6edae051eb7	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0zir-0513900000-99965a9d9f77c397a0b8	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0a6r-0910000000-b0f870f10a0d4c614ccf	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-002f-1900000000-e7b810e5d1d7c3d02dd0	2015-09-15	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-24	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-24	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
MMDBp0192428	Glutathione S-transferase Mu 2	Enzyme	P28161	Homo sapiens
MMDBp0192431	Glutathione S-transferase Mu 1	Enzyme	P09488	Homo sapiens
MMDBp0192433	Glutathione S-transferase kappa 1	Enzyme	Q9Y2Q3	Homo sapiens
MMDBp0192434	Microsomal glutathione S-transferase 3	Enzyme	O14880	Homo sapiens
MMDBp0192435	Glutathione S-transferase Mu 3	Enzyme	P21266	Homo sapiens
MMDBp0192436	Glutathione S-transferase A1	Enzyme	P08263	Homo sapiens
MMDBp0192438	Microsomal glutathione S-transferase 1	Enzyme	P10620	Homo sapiens
MMDBp0192439	Glutathione S-transferase Mu 4	Enzyme	Q03013	Homo sapiens
MMDBp0192440	Glutathione S-transferase Mu 5	Enzyme	P46439	Homo sapiens
MMDBp0192441	Microsomal glutathione S-transferase 2	Enzyme	Q99735	Homo sapiens
MMDBp0192442	Glutathione S-transferase omega-1	Enzyme	P78417	Homo sapiens
MMDBp0192443	Glutathione S-transferase A5	Enzyme	Q7RTV2	Homo sapiens
MMDBp0192444	Glutathione S-transferase A2	Enzyme	P09210	Homo sapiens
MMDBp0192446	Glutathione S-transferase A3	Enzyme	Q16772	Homo sapiens
MMDBp0192447	Glutathione S-transferase A4	Enzyme	O15217	Homo sapiens
MMDBp0192451	Glutathione S-transferase omega-2	Enzyme	Q9H4Y5	Homo sapiens
MMDBp0192452	Glutathione S-transferase theta-1	Unknown	P30711	Homo sapiens
MMDBp0192454	Glutathione S-transferase P	Enzyme	P09211	Homo sapiens
MMDBp0196825	Glutathione S-transferase theta-2B	Unknown	P0CG30

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	Proteobacteria	1	Human ; Human feces; Human feces; pleural fluid plaque; bal; Human stool	Unknown

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

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

External Links

HMDB ID

HMDB0060299

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

10128341

KEGG Compound ID

C14793

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11954046

PDB ID

Not Available

ChEBI ID

33993

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Magrane M: UniProt Knowledgebase: a hub of integrated protein data. Database (Oxford). 2011 Mar 29;2011:bar009. doi: 10.1093/database/bar009. Print 2011. [PubMed:21447597 ]

Showing metabocard for (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene (MMDBc0029944)

MOL for #<Metabolite:0x00007fecdc619178>

3D MOL for #<Metabolite:0x00007fecdc619178>

3D SDF for #<Metabolite:0x00007fecdc619178>

3D-SDF for #<Metabolite:0x00007fecdc619178>

PDB for #<Metabolite:0x00007fecdc619178>

3D PDB for #<Metabolite:0x00007fecdc619178>

SMILES for #<Metabolite:0x00007fecdc619178>

INCHI for #<Metabolite:0x00007fecdc619178>

Structure for #<Metabolite:0x00007fecdc619178>

3D Structure for #<Metabolite:0x00007fecdc619178>