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Gene Set: D4 : CTD - Amphotericin B


Collection D4 : CTD
Chemical Name Amphotericin B ( From PubChem : AMPHOTERICIN B )
FDA NPC WHO Indian Australia China Traditional
Herbal
Clinical
Trail
ApprovedNotApprovedApprovedNotNotNotNot
Molecular
Weight
Hydrogen Bond
Donor Count
Hydrogen Bond
Acceptor Count
cLogP Lipinski Rule
924.079 g/mol 12 18 1.412 False(1/4)
Structure
InChI InChI=1S/C47H73NO17/c1-27-17-15-13-11-9-7-5-6-8-10-12-14-16-18-34(64-46-44(58)41(48)43(57)30(4)63-46)24-38-40(45(59)60)37(54)26-47(61,65-38)25-33(51)22-36(53)35(52)20-19-31(49)21-32(50)23-39(55)62-29(3)28(2)42(27)56/h5-18,27-38,40-44,46,49-54,56-58,61H,19-26,48H2,1-4H3,(H,59,60)/b6-5+,9-7+,10-8+,13-11+,14-12+,17-15+,18-16+/t27-,28-,29-,30+,31+,32+,33-,34-,35+,36+,37-,38?,40+,41-,42+,43+,44-,46-,47+/m0/s1
InChIKey APKFDSVGJQXUKY-ZCGADPMASA-N
Links

Gene (39 / 60)


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Source Type Unit Value Gene PMID Assay Other
CTDincreases(expression)ARHGEF26
D000666
CTDaffects(binding)ARNT
D000666
CTDdecreases(reaction)ARNT
D000666
CTDdecreases(expression)ATG3
D000666
CTDincreases(expression)EDNRB
D000666
CTDdecreases(reaction)ENO1
D000666
CTDincreases(expression)ENO1
D000666
CTDaffects(binding)EP300
D000666
CTDdecreases(reaction)EP300
D000666
CTDincreases(reaction)EP300
D000666
CTDaffects(binding)EPO
D000666
CTDdecreases(reaction)EPO
D000666
CTDincreases(expression)EPO
D000666
CTDdecreases(expression)EPO
D000666
CTDdecreases(expression)GLOD4
D000666
CTDincreases(expression)GPR20
D000666
CTDdecreases(reaction)GSTP1
D000666
CTDincreases(metabolic processing)GSTP1
D000666
CTDaffects(binding)HIF1A
D000666
CTDdecreases(reaction)HIF1A
D000666
CTDincreases(reaction)HIF1A
D000666
CTDdecreases(activity)HIF1A
D000666
CTDincreases(hydroxylation)HIF1A
D000666
CTDaffects(binding)HIF1AN
D000666
CTDdecreases(activity)HIF1AN
D000666
CTDincreases(hydroxylation)HIF1AN
D000666
CTDincreases(reaction)HIF1AN
D000666
CTDincreases(expression)HLA-F
D000666
CTDaffects(cotreatment)IFNG
D000666
CTDincreases(expression)IFNG
D000666
CTDincreases(expression)IFNGR1
D000666
CTDdecreases(expression)IGFBP5
D000666
CTDaffects(cotreatment)IL10
D000666
CTDdecreases(expression)IL10
D000666
CTDdecreases(expression)KCNQ4
D000666
CTDdecreases(expression)LSG1
D000666
CTDdecreases(expression)NPRL2
D000666
CTDincreases(expression)NT5C2
D000666
CTDdecreases(expression)PAIP1
D000666
CTDdecreases(expression)PARD3
D000666
CTDdecreases(reaction)PGK1
D000666
CTDincreases(expression)PGK1
D000666
CTDincreases(expression)POLM
D000666
CTDdecreases(expression)RUNX3
D000666
CTDdecreases(expression)SLIT1
D000666
CTDaffects(cotreatment)TGFB1
D000666
CTDdecreases(expression)TGFB1
D000666
CTDincreases(expression)USP36
D000666
CTDdecreases(expression)ZNF671
D000666
PubChem Ratio Potency (uM)uM61.131NFE2L2-GI(Protien) :
PubChem Ratio Potency (uM)uM54.954NR1H4-GI(Protien) :
PubChem Potency-Replicate_1uM48.978NR3C1-GI(Protien) :
PubChem NoneuMNR3C1-GI(Protien) :
PubChem PotencyuM42.163TNF-GI(Protien) :
ChEMBLInhibition-CYP1A2
-Target : CHEMBL3356
ChEMBLInhibition-CYP2C9
-Target : CHEMBL3397
ChEMBLInhibition-CYP2D6
-Target : CHEMBL289
ChEMBLInhibition-CYP3A4
-Target : CHEMBL340
ChEMBLInhibition-CYP3A4
-Target : CHEMBL340
ChEMBLPotencynM31622.800HSD17B10
-Target : CHEMBL4159
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