Hmdb loader

Showing metabocard for (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene (HMDB0060299)

Jump To Section:
IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesenzymes (19) Show 19 proteinsXML
enzymes (19) Show 19 proteins
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2013-05-17 00:50:28 UTC
Update Date2022-03-07 03:17:42 UTC
HMDB IDHMDB0060299
Secondary Accession Numbers
  • HMDB60299
Metabolite Identification
Common Name(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene
Description(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene 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 (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene is a very strong basic compound (based on its pKa) (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene exists in all living organisms, ranging from bacteria to humans. 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.
Structure
Data?1563866040
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0060299 ((1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene)


  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
Download

3D MOL for HMDB0060299 ((1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene)

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
Download

3D SDF for HMDB0060299 ((1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene)


  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>
HMDB0060299

> <DATABASE_NAME>
hmdb

> <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

$$$$
Download

3D-SDF for HMDB0060299 ((1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene)

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
Download

PDB for HMDB0060299 ((1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene)

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
Download

3D PDB for HMDB0060299 ((1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene)

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
Download

SMILES for HMDB0060299 ((1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene)

[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
Download

INCHI for HMDB0060299 ((1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene)

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
Download
View in JSmolView NMR AssignmentsView Stereo Labels
SynonymsNot Available
Chemical FormulaC20H25N3O7S
Average Molecular Weight451.493
Monoisotopic Molecular Weight451.141320859
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 NumberNot 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 KeyUWBZAZWPTVBBEL-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.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentOligopeptides
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 FrameworkAromatic homopolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
DispositionNot Available
Process
Naturally occurring process
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.058 g/LALOGPS
logP-1.6ALOGPS
logP-1.7ChemAxon
logS-3.9ALOGPS
pKa (Strongest Acidic)1.96ChemAxon
pKa (Strongest Basic)9.54ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area186.03 ŲChemAxon
Rotatable Bond Count11ChemAxon
Refractivity114.1 m³·mol⁻¹ChemAxon
Polarizability45 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+203.63931661259
DarkChem[M-H]-195.93331661259
DeepCCS[M+H]+195.7730932474
DeepCCS[M-H]-193.87530932474
DeepCCS[M-2H]-227.11630932474
DeepCCS[M+Na]+201.44630932474
AllCCS[M+H]+199.532859911
AllCCS[M+H-H2O]+197.732859911
AllCCS[M+NH4]+201.132859911
AllCCS[M+Na]+201.632859911
AllCCS[M-H]-194.432859911
AllCCS[M+Na-2H]-195.132859911
AllCCS[M+HCOO]-196.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene[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)=O4909.7Standard polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene[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)=O3620.6Standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene[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)=O4068.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TMS,isomer #1C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O3982.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TMS,isomer #2C[Si](C)(C)O[C@@H]1C=CC2=CC=CC=C2[C@H]1SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O3942.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TMS,isomer #3C[Si](C)(C)OC(=NCC(=O)O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O3945.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O3953.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TMS,isomer #5C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O3910.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TMS,isomer #6C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)C(=O)O4036.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)O[Si](C)(C)C3826.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #10C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O3819.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #11C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C3794.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #12C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O3908.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #13C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C3815.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #14C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O3904.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #15C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C3879.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #16C[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C4077.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #2C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O3862.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #3C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C3861.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C3866.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O3924.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O3800.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #7C[Si](C)(C)OC(=NCC(=O)O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O3827.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O3831.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O3915.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C3737.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #10C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3849.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #11C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O3941.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C3705.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #13C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C3731.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #14C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C3804.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #15C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O3718.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #16C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O3838.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #17C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O3834.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #18C[Si](C)(C)O[C@@H]1C=CC2=CC=CC=C2[C@H]1SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O)=NCC(=O)O3941.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #19C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C3708.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #2C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C3738.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #20C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3809.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #21C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3790.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #22C[Si](C)(C)OC(=NCC(=O)O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3918.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #23C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3812.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #24C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3939.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C3947.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3766.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #4C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3814.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #5C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C3744.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #6C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C3767.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #7C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O3855.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C3762.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3840.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C3655.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #10C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3790.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #11C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O3877.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #12C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3755.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #13C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C3873.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #14C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3884.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #15C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C3629.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #16C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3729.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #17C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3748.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #18C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C3871.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #19C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3747.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #2C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3687.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #20C[Si](C)(C)OC(=NCC(=O)O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3853.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #21C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3868.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #22C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3715.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #23C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3852.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3853.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #25C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3891.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #3C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3752.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3660.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3746.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #6C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3764.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #7C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3875.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C3672.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,4TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3781.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3616.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #10C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3847.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #11C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3840.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #12C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3682.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #13C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3810.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #14C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3836.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #15C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3805.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #16C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3808.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #2C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3701.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #3C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3725.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #4C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3842.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3685.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3832.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #7C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3853.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #8C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3719.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,5TMS,isomer #9C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C3845.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #1C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3681.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #1C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3555.1Standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #1C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C4729.5Standard polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3831.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3595.3Standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4908.0Standard polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3838.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3677.7Standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C5032.5Standard polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3814.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3713.8Standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C4941.6Standard polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3833.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3643.9Standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C4868.8Standard polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #6C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3794.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #6C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3650.1Standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,6TMS,isomer #6C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4903.7Standard polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O4153.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@@H]1C=CC2=CC=CC=C2[C@H]1SC[C@H](N=C(O)CC[C@H](N)C(=O)O)C(O)=NCC(=O)O4131.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O4123.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O4178.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O4132.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)C(=O)O4201.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C4232.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O4243.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4207.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O4285.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C4286.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O4331.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C4295.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C4449.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O4251.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4224.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C4278.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O4311.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O4243.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O4225.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O4278.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)C(=O)O4293.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C4353.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4435.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O4584.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4313.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C4394.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C4412.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)N=C(O)CC[C@H](N)C(=O)O4336.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O4395.9Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O4438.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)O[C@@H]1C=CC2=CC=CC=C2[C@H]1SC[C@H](N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O4592.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C4321.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4309.3Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4404.0Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4375.7Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4565.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4435.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4606.4Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4590.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4358.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4408.2Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4329.8Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C4381.6Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O[Si](C)(C)C(C)(C)C)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O4427.5Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C4335.1Semi standard non polar33892256
(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CS[C@@H]1C2=CC=CC=C2C=C[C@H]1O)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O4399.9Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene GC-MS (Non-derivatized) - 70eV, Positivesplash10-0002-3915700000-d663b106af5ff8f05ab52017-09-20Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene GC-MS (3 TMS) - 70eV, Positivesplash10-0gb9-6491156000-387722deb85a575c8d1f2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene GC-MS (TBDMS_2_4) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene GC-MS (TBDMS_3_3) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene GC-MS (TBDMS_3_6) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene GC-MS (TBDMS_3_10) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene GC-MS ("(1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene,2TBDMS,#4" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene 10V, Positive-QTOFsplash10-00e9-3126900000-e852fce9919b502e2de02015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene 20V, Positive-QTOFsplash10-00di-9226100000-8ad87012ef3d3e1f9b0b2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene 40V, Positive-QTOFsplash10-00di-9221000000-4da054dda6edae051eb72015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene 10V, Negative-QTOFsplash10-0zir-0513900000-99965a9d9f77c397a0b82015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene 20V, Negative-QTOFsplash10-0a6r-0910000000-b0f870f10a0d4c614ccf2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalene 40V, Negative-QTOFsplash10-002f-1900000000-e7b810e5d1d7c3d02dd02015-09-15Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID10128341
KEGG Compound IDC14793
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound11954046
PDB IDNot Available
ChEBI ID33993
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. 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 ]

Only showing the first 10 proteins. There are 19 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details
1. Glutathione S-transferase Mu 2
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTM2
Uniprot ID:
P28161
Molecular weight:
25744.395
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails
Enzyme Details
2. Glutathione S-transferase Mu 1
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTM1
Uniprot ID:
P09488
Molecular weight:
25711.555
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails
Enzyme Details
3. Glutathione S-transferase kappa 1
General function:
Involved in protein disulfide oxidoreductase activity
Specific function:
Significant glutathione conjugating activity is found only with the model substrate, 1-chloro-2,4-dinitrobenzene (CDNB).
Gene Name:
GSTK1
Uniprot ID:
Q9Y2Q3
Molecular weight:
31565.605
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails
Enzyme Details
4. Microsomal glutathione S-transferase 3
General function:
Involved in glutathione transferase activity
Specific function:
Also functions as a glutathione peroxidase.
Gene Name:
MGST3
Uniprot ID:
O14880
Molecular weight:
16516.185
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails
Enzyme Details
5. Glutathione S-transferase Mu 3
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. May govern uptake and detoxification of both endogenous compounds and xenobiotics at the testis and brain blood barriers.
Gene Name:
GSTM3
Uniprot ID:
P21266
Molecular weight:
26559.32
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails
Enzyme Details
6. Glutathione S-transferase A1
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTA1
Uniprot ID:
P08263
Molecular weight:
25630.785
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails
Enzyme Details
7. Microsomal glutathione S-transferase 1
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. Has a wide substrate specificity.
Gene Name:
MGST1
Uniprot ID:
P10620
Molecular weight:
17598.45
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails
Enzyme Details
8. Glutathione S-transferase Mu 4
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. Active on 1-chloro-2,4-dinitrobenzene.
Gene Name:
GSTM4
Uniprot ID:
Q03013
Molecular weight:
25561.095
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails
Enzyme Details
9. Glutathione S-transferase Mu 5
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTM5
Uniprot ID:
P46439
Molecular weight:
25674.455
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails
Enzyme Details
10. Microsomal glutathione S-transferase 2
General function:
Involved in enzyme activator activity
Specific function:
Can catalyze the production of LTC4 from LTA4 and reduced glutathione. Can catalyze the conjugation of 1-chloro-2,4-dinitrobenzene with reduced glutathione.
Gene Name:
MGST2
Uniprot ID:
Q99735
Molecular weight:
16620.4
Reactions
(1S,2R)-Naphthalene 1,2-oxide + Glutathione → (1R)-Glutathionyl-(2R)-hydroxy-1,2-dihydronaphthalenedetails

Only showing the first 10 proteins. There are 19 proteins in total.

Show all enzymes and transporters