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Gene Set: D4 : CTD - Suramin


Collection D4 : CTD
Chemical Name Suramin ( From PubChem : SURAMIN )
FDA NPC WHO Indian Australia China Traditional
Herbal
Clinical
Trail
NotNotApprovedNotNotNotNotNot
Molecular
Weight
Hydrogen Bond
Donor Count
Hydrogen Bond
Acceptor Count
cLogP Lipinski Rule
1297.28 g/mol 12 29 13.666 False(0/4)
Structure
InChI InChI=1S/C51H40N6O23S6/c1-25-9-11-29(49(60)54-37-13-15-41(83(69,70)71)35-21-33(81(63,64)65)23-43(45(35)37)85(75,76)77)19-39(25)56-47(58)27-5-3-7-31(17-27)52-51(62)53-32-8-4-6-28(18-32)48(59)57-40-20-30(12-10-26(40)2)50(61)55-38-14-16-42(84(72,73)74)36-22-34(82(66,67)68)24-44(46(36)38)86(78,79)80/h3-24H,1-2H3,(H,54,60)(H,55,61)(H,56,58)(H,57,59)(H2,52,53,62)(H,63,64,65)(H,66,67,68)(H,69,70,71)(H,72,73,74)(H,75,76,77)(H,78,79,80)
InChIKey FIAFUQMPZJWCLV-UHFFFAOYSA-N
Links

Gene (34 / 67)


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Source Type Unit Value Gene PMID Assay Other
CTDdecreases(reaction)CASP3
D013498
CTDincreases(expression)CASP3
D013498
CTDdecreases(reaction)CREB1
D013498
CTDincreases(phosphorylation)CREB1
D013498
CTDdecreases(activity)CYP1A2
D013498
CTDdecreases(reaction)CYP1B1
D013498
CTDincreases(expression)CYP1B1
D013498
CTDdecreases(activity)CYP2C19
D013498
CTDincreases(expression)FGF2
D013498
CTDincreases(expression)FGF5
D013498
CTDaffects(localization)FGF7
D013498
CTDaffects(binding)FGF7
D013498
CTDdecreases(reaction)FGF7
D013498
CTDaffects(binding)FGFR2
D013498
CTDdecreases(reaction)FGFR2
D013498
CTDdecreases(reaction)IL10
D013498
CTDincreases(activity)IL10
D013498
CTDincreases(expression)IL10
D013498
CTDdecreases(activity)IL10
D013498
CTDincreases(expression)IL12B
D013498
CTDdecreases(reaction)IL6
D013498
CTDincreases(expression)IL6
D013498
CTDdecreases(reaction)MAPK1
D013498
CTDincreases(activity)MAPK1
D013498
CTDdecreases(reaction)MAPK1
D013498
CTDincreases(phosphorylation)MAPK1
D013498
CTDdecreases(reaction)MAPK1
D013498
CTDincreases(phosphorylation)MAPK1
D013498
CTDdecreases(reaction)MAPK3
D013498
CTDincreases(activity)MAPK3
D013498
CTDdecreases(reaction)MAPK3
D013498
CTDincreases(phosphorylation)MAPK3
D013498
CTDdecreases(reaction)MAPK3
D013498
CTDincreases(phosphorylation)MAPK3
D013498
CTDdecreases(reaction)PTGS2
D013498
CTDincreases(expression)PTGS2
D013498
CTDincreases(reaction)PTGS2
D013498
CTDdecreases(acetylation)SIRT1
D013498
CTDdecreases(activity)SIRT1
D013498
CTDincreases(expression)TNF
D013498
CTDdecreases(acetylation)TP53
D013498
CTDdecreases(activity)TP53
D013498
CTDdecreases(reaction)VDR
D013498
CTDincreases(expression)VDR
D013498
PubChem PotencyuM1.413EHMT2-GI(Protien) :
PubChem PotencyuM8.912GLS-GI(Protien) :
PubChem PotencyuM14.125KMT2A-GI(Protien) :
PubChem PotencyuM0.032POLK-GI(Protien) :
PubChem PotencyuM7.943USP1-GI(Protien) :
PubChem PotencyuM35.481VDR-GI(Protien) :
ChEMBLPotencynM1995.300CBX1
-Target : CHEMBL1741193
ChEMBLPotencynM1412.500EHMT2
-Target : CHEMBL6032
ChEMBLPotencynM281.800EHMT2
-Target : CHEMBL6032
ChEMBLPotencynM335.900FEN1
-Target : CHEMBL5027
ChEMBLPotencynM7943.300HSD17B10
-Target : CHEMBL4159
ChEMBLPotencynM14125.400KMT2A
-Target : CHEMBL1293299
ChEMBLPotencynM1888.800MPHOSPH8
-Target : CHEMBL1741210
ChEMBLPotencynM425.600PIN1
-Target : CHEMBL2288
ChEMBLPotencynM2511.900RECQL
-Target : CHEMBL1293236
ChEMBLPotencynM19952.600RECQL
-Target : CHEMBL1293236
ChEMBLInhibition-SIRT1
-Target : CHEMBL4506
ChEMBLInhibition-SIRT3
-Target : CHEMBL4461
ChEMBLInhibition-SIRT5
-Target : CHEMBL2163183
ChEMBLPotencynM11220.200TDP1
-Target : CHEMBL1075138
ChEMBLPotencynM4466.800TDP1
-Target : CHEMBL1075138
ChEMBLPotencynM2511.900TDP1
-Target : CHEMBL1075138
ChEMBLPotencynM3288.500USP2
-Target : CHEMBL1293227
Download gene sets gmt, text, Detailed text
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