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Gene Set: D4 : CTD - S-Nitrosoglutathione


Collection D4 : CTD
Chemical Name S-Nitrosoglutathione ( From PubChem : GSNO )
FDA NPC WHO Indian Australia China Traditional
Herbal
Clinical
Trail
NotNotNotNotNotNotNotNot
Molecular
Weight
Hydrogen Bond
Donor Count
Hydrogen Bond
Acceptor Count
cLogP Lipinski Rule
336.322 g/mol 5 11 -0.2392 False(3/4)
Structure
InChI InChI=1S/C10H16N4O7S/c11-5(10(19)20)1-2-7(15)13-6(4-22-14-21)9(18)12-3-8(16)17/h5-6H,1-4,11H2,(H,12,18)(H,13,15)(H,16,17)(H,19,20)/t5-,6+/m0/s1
InChIKey HYHSBSXUHZOYLX-NTSWFWBYSA-N
Links

Gene (31 / 71)


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Source Type Unit Value Gene PMID Assay Other
CTDincreases(reduction)ADH5
D026422
CTDdecreases(reaction)ADH5
D026422
CTDincreases(reduction)ADH5
D026422
CTDincreases(oxidation)ADH5
D026422
CTDincreases(reaction)ADH5
D026422
CTDincreases(response to substance)ATM
D026422
CTDincreases(abundance)BAX
D026422
CTDincreases(expression)BAX
D026422
CTDdecreases(expression)BCL2
D026422
CTDincreases(abundance)BCL2
D026422
CTDdecreases(activity)CASP3
D026422
CTDincreases(abundance)CASP3
D026422
CTDincreases(metabolic processing)CASP3
D026422
CTDincreases(activity)CASP3
D026422
CTDaffects(cotreatment)CASP3
D026422
CTDdecreases(reaction)CASP3
D026422
CTDincreases(activity)CASP8
D026422
CTDincreases(reduction)CBR1
D026422
CTDdecreases(reaction)CBR1
D026422
CTDaffects(binding)CBR1
D026422
CTDdecreases(activity)CBR1
D026422
CTDincreases(activity)CBR1
D026422
CTDdecreases(reaction)CBR1
D026422
CTDincreases(metabolic processing)CBR1
D026422
CTDincreases(reaction)CBR1
D026422
CTDdecreases(secretion)CCL5
D026422
CTDdecreases(reaction)CCT7
D026422
CTDincreases(abundance)CCT7
D026422
CTDdecreases(expression)CD86
D026422
CTDdecreases(reaction)CFTR
D026422
CTDincreases(expression)CFTR
D026422
CTDincreases(stability)CFTR
D026422
CTDdecreases(activity)CFTR
D026422
CTDdecreases(expression)CFTR
D026422
CTDdecreases(secretion)CXCL10
D026422
CTDdecreases(reaction)FASLG
D026422
CTDincreases(abundance)FASLG
D026422
CTDincreases(activity)FASLG
D026422
CTDdecreases(reaction)GUCY1A3
D026422
CTDincreases(abundance)GUCY1A3
D026422
CTDincreases(expression)HIF1A
D026422
CTDincreases(expression)HMOX1
D026422
CTDaffects(localization)HTRA2
D026422
CTDaffects(cotreatment)HTRA2
D026422
CTDdecreases(reaction)HTRA2
D026422
CTDincreases(secretion)IFNG
D026422
CTDdecreases(secretion)IL10
D026422
CTDdecreases(expression)IL12B
D026422
CTDdecreases(secretion)IL5
D026422
CTDdecreases(response to substance)NOS2
D026422
CTDincreases(chemical synthesis)NOS2
D026422
CTDaffects(binding)PARK2
D026422
CTDdecreases(reaction)PARK2
D026422
CTDdecreases(expression)PARK2
D026422
CTDaffects(localization)PARK2
D026422
CTDincreases(nitrosation)PARK2
D026422
CTDincreases(metabolic processing)RELA
D026422
CTDincreases(reaction)RELA
D026422
CTDincreases(activity)SP1
D026422
CTDdecreases(activity)SP3
D026422
CTDincreases(activity)SP3
D026422
CTDincreases(secretion)TNF
D026422
CTDaffects(binding)TP53
D026422
CTDdecreases(reaction)TP53
D026422
CTDdecreases(expression)TP53
D026422
CTDincreases(nitrosation)TP53
D026422
PubChem PotencyuM44.668BAZ2B-GI(Protien) :
PubChem PotencyuM1.122EHMT2-GI(Protien) :
ChEMBLPotencynM44668.400BAZ2B
-Target : CHEMBL1741220
ChEMBLPotencynM1122.000EHMT2
-Target : CHEMBL6032
ChEMBLPotencynM8912.500KDM4A
-Target : CHEMBL5896
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