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ChEMBL ligand: CHEMBL168 (NSC-114945) |
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DB | Assay description | Assay Type | Standard value | Standard parameter | Original value | Original units | Original parameter | Reference |
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acetyl-CoA acetyltransferase 1/Acetyl-CoA acetyltransferase, mitochondrial in Rat (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3393] [GtoPdb: 2435] [UniProtKB: P17764] | ||||||||
ChEMBL | Inhibition of rat liver microsomal ACAT | B | 4.11 | pIC50 | 77900 | nM | IC50 | Eur J Med Chem (2017) 139: 201-213 [PMID:28802120] |
carboxylesterase 1/Acyl coenzyme A:cholesterol acyltransferase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2265] [GtoPdb: 2592] [UniProtKB: P23141] | ||||||||
ChEMBL | Inhibition of CES1A1 in human liver microsomes using D-luciferin methyl ester as substrate preincubated for 10 mins followed by substrate addition and measured after 10 mins by fluorescence assay | B | 7 | pIC50 | 100 | nM | IC50 | J Nat Prod (2020) 83: 2940-2949 [PMID:32951423] |
Aldo-keto reductase family 1 member B10 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5983] [UniProtKB: O60218] | ||||||||
ChEMBL | Competitive inhibition of dehydrogenase activity of N-terminal 6His-tagged human AKR1B10 W220Y mutant expressed in Escherichia coli BL21(DE3) assessed as NADP+-linked geraniol oxidation | B | 5.45 | pKi | 3560 | nM | Ki | J Nat Prod (2011) 74: 1201-1206 [PMID:21561086] |
ChEMBL | Competitive inhibition of dehydrogenase activity of N-terminal 6His-tagged human AKR1B10 V301L mutant expressed in Escherichia coli BL21(DE3) assessed as NADP+-linked geraniol oxidation | B | 6.03 | pKi | 940 | nM | Ki | J Nat Prod (2011) 74: 1201-1206 [PMID:21561086] |
ChEMBL | Competitive inhibition of dehydrogenase activity of N-terminal 6His-tagged human AKR1B10 Q303S mutant expressed in Escherichia coli BL21(DE3) assessed as NADP+-linked geraniol oxidation | B | 6.18 | pKi | 660 | nM | Ki | J Nat Prod (2011) 74: 1201-1206 [PMID:21561086] |
ChEMBL | Competitive inhibition of dehydrogenase activity of N-terminal 6His-tagged human AKR1B10 K125L mutant expressed in Escherichia coli BL21(DE3) assessed as NADP+-linked geraniol oxidation | B | 6.8 | pKi | 160 | nM | Ki | J Nat Prod (2011) 74: 1201-1206 [PMID:21561086] |
ChEMBL | Competitive inhibition of dehydrogenase activity of N-terminal 6His-tagged human AKR1B10 expressed in Escherichia coli BL21(DE3) assessed as NADP+-linked geraniol oxidation | B | 7.14 | pKi | 72 | nM | Ki | J Nat Prod (2011) 74: 1201-1206 [PMID:21561086] |
ChEMBL | Inhibition of N-terminal 6His-tagged human AKR1B10 overexpressed in human HeLa cells assessed as inhibition of [1-14C]farnesol reduction pretreated for 2 hrs before [1-14C]farnesol challenge measured after 6 hrs | B | 5.4 | pIC50 | 4000 | nM | IC50 | J Nat Prod (2011) 74: 1201-1206 [PMID:21561086] |
ChEMBL | Inhibition of reductase activity of N-terminal 6His-tagged human AKR1B10 expressed in Escherichia coli BL21(DE3) assessed as pyridine-3-aldehyde reduction | B | 7.05 | pIC50 | 90 | nM | IC50 | J Nat Prod (2011) 74: 1201-1206 [PMID:21561086] |
coagulation factor III, tissue factor/Coagulation factor III in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4081] [GtoPdb: 3192] [UniProtKB: P13726] | ||||||||
ChEMBL | Inhibition of LPS-induced tissue factor procoagulant activity in human THP1 cells preincubated for 1 hr followed by LPS addition measured after 5 hrs using factor 10a chromogenic substrate in presence of prothrombin complex | B | 8.3 | pIC50 | 4.97 | nM | IC50 | Bioorg Med Chem Lett (2017) 27: 1026-1030 [PMID:28109788] |
Cyclooxygenase-1 in Sheep (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2949] [UniProtKB: P05979] | ||||||||
ChEMBL | Inhibition of ovine recombinant COX1 assessed as decrease in formation of PGE2 using arachidonic acid as substrate preincubated for 10 mins followed by substrate addition measured after 45 mins by LC-MS analysis | B | 4.38 | pIC50 | 42000 | nM | IC50 | J Nat Prod (2019) 82: 3311-3320 [PMID:31774676] |
COX-2 /Cyclooxygenase-2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL230] [GtoPdb: 1376] [UniProtKB: P35354] | ||||||||
ChEMBL | Inhibition of COX2 by scintillation proximity assay | B | 4.06 | pIC50 | 87000 | nM | IC50 | J Nat Prod (2002) 65: 1517-1521 [PMID:12444669] |
ChEMBL | Inhibition of human recombinant COX2 expressed in baculovirus infected sf21 cells assessed as decrease in PGE2 formation using arachidonic acid as substrate preincubated for 10 mins followed by substrate addition measured after 45 mins by LC-MS analysis | B | 4.4 | pIC50 | >40000 | nM | IC50 | J Nat Prod (2019) 82: 3311-3320 [PMID:31774676] |
DNA polymerase beta in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2392] [GtoPdb: 3231] [UniProtKB: P06746] | ||||||||
ChEMBL | Inhibition of lyase activity of DNA polymerase beta | B | 4.58 | pIC50 | 26250 | nM | IC50 | Bioorg Med Chem (2008) 16: 4331-4340 [PMID:18343122] |
ChEMBL | Inhibition of polymerase activity of DNA polymerase beta | B | 4.6 | pIC50 | 24980 | nM | IC50 | Bioorg Med Chem (2008) 16: 4331-4340 [PMID:18343122] |
ChEMBL | Inhibition of DNA polymerase beta lyase activity | B | 5.06 | pIC50 | 8800 | nM | IC50 | J Nat Prod (2004) 67: 964-967 [PMID:15217274] |
ChEMBL | Inhibition of DNA polymerase beta lyase activity by deoxyribose phosphate excision assay | B | 5.06 | pIC50 | 8800 | nM | IC50 | J Nat Prod (2003) 66: 1463-1465 [PMID:14640519] |
ChEMBL | Inhibition of DNA polymerase beta | B | 5.52 | pIC50 | 3000 | nM | IC50 | J Nat Prod (2011) 74: 1201-1206 [PMID:21561086] |
GtoPdb | Inhibition of POLB polymerase activity | - | 5.6 | pIC50 | 2498 | nM | IC50 | Bioorg Med Chem (2008) 16: 4331-40 [PMID:18343122] |
DNA polymerase beta in Rat (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4343] [GtoPdb: 3231] [UniProtKB: P06766] | ||||||||
ChEMBL | Inhibition of rat DNA polymerase beta in presence of BSA | B | 5.12 | pIC50 | 7500 | nM | IC50 | J Nat Prod (1999) 62: 1624-1626 [PMID:10654412] |
ChEMBL | Inhibition of rat DNA polymerase beta in absence of BSA | B | 5.43 | pIC50 | 3700 | nM | IC50 | J Nat Prod (1999) 62: 1624-1626 [PMID:10654412] |
Dual specificity phosphatase Cdc25B in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4804] [UniProtKB: P30305] | ||||||||
ChEMBL | Inhibition of CDC25B (unknown origin) using pNPP as substrate by spectrophotometry | B | 6.01 | pIC50 | 980 | nM | IC50 | Bioorg Med Chem (2015) 23: 38-45 [PMID:25497963] |
Dual specificity protein phosphatase 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2635] [UniProtKB: P51452] | ||||||||
ChEMBL | Inhibition of human VHR expressed in Escherichia coli using pNPP as substrate preincubated for 10 mins followed by substrate addition measured after 30 mins | B | 5.27 | pIC50 | 5400 | nM | IC50 | Bioorg Med Chem Lett (2017) 27: 1159-1161 [PMID:28189419] |
epidermal growth factor receptor/Epidermal growth factor receptor erbB1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL203] [GtoPdb: 1797] [UniProtKB: P00533] | ||||||||
ChEMBL | Inhibition of C-terminal His-tagged/ N-terminal GST-tagged recombinant human EGFR (668 to 1210 residues) expressed in a Baculovirus infected Sf9 cell expression system using poly-EY as substrate incubated for 30 mins by ADP-Glo kinase assay | B | 4.7 | pIC50 | >20000 | nM | IC50 | J Nat Prod (2019) 82: 3065-3073 [PMID:31718182] |
ChEMBL | Inhibition of C-terminal His-tagged/ N-terminal GST-tagged recombinant human EGFR L858R/T790M double mutant (668 to 1210 residues) expressed in a Baculovirus infected Sf9 cell expression system using poly-EY as substrate incubated for 30 mins by ADP-Glo kinase assay | B | 4.7 | pIC50 | >20000 | nM | IC50 | J Nat Prod (2019) 82: 3065-3073 [PMID:31718182] |
ChEMBL | Inhibition of C-terminal His-tagged/ N-terminal GST-tagged recombinant human EGFR L858R/T790M/C797S mutant (668 to 1210 residues) expressed in a Baculovirus infected Sf9 cell expression system using poly-EY as substrate incubated for 30 mins by ADP-Glo kinase assay | B | 4.7 | pIC50 | >20000 | nM | IC50 | J Nat Prod (2019) 82: 3065-3073 [PMID:31718182] |
Glycogen phosphorylase, muscle form in Rabbit (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4696] [UniProtKB: P00489] | ||||||||
ChEMBL | Inhibition of rabbit muscle glycogen phosphorylase a assessed as release of phosphate from glucose-1-phosphate after 25 mins using malachite green staining | B | 4.64 | pIC50 | 22900 | nM | IC50 | Bioorg Med Chem Lett (2012) 22: 1036-1039 [PMID:22204907] |
ChEMBL | Inhibition of rabbit muscle glycogen phosphorylase assessed as release of phosphate from glucose-1-phosphate after 25 mins | B | 4.66 | pIC50 | 22100 | nM | IC50 | J Nat Prod (2009) 72: 1414-1418 [PMID:19642687] |
ChEMBL | Inhibition of rabbit muscle glycogen phosphorylase A assessed as release of phosphate from glucose-1-phosphate after 25 mins by microplate reader based method | B | 4.85 | pIC50 | 14125.38 | nM | IC50 | Eur J Med Chem (2011) 46: 2011-2021 [PMID:21439694] |
ChEMBL | Inhibition of rabbit muscle GPa | B | 4.85 | pIC50 | 14000 | nM | IC50 | Bioorg Med Chem Lett (2006) 16: 2915-2919 [PMID:16546381] |
ChEMBL | Inhibition of rabbit muscle glycogen phosphorylase A assessed as phosphate release from glucose-1-phosphate | B | 4.85 | pIC50 | 14000 | nM | IC50 | J Med Chem (2008) 51: 3540-3554 [PMID:18517260] |
ChEMBL | Inhibition of rabbit muscle glycogen phosphorylase A assessed as release of phosphate from glucose-1-phosphate after 25 mins by microplate reader based method | B | 4.85 | pIC50 | 14000 | nM | IC50 | Eur J Med Chem (2011) 46: 2011-2021 [PMID:21439694] |
GP41 in Human immunodeficiency virus 1 (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3559676] [UniProtKB: Q76270] | ||||||||
ChEMBL | Inhibition of HIV1 gp41-induced cell-cell fusion between viral envelope expressing human HL2/3 cells to CD4/CCR5 receptor expressing TZM-bl cells after 6 to 8 hrs by luciferase assay | B | 4 | pEC50 | >100000 | nM | EC50 | J Med Chem (2014) 57: 7342-7354 [PMID:25156906] |
GPBA receptor/G-protein coupled bile acid receptor 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5409] [GtoPdb: 37] [UniProtKB: Q8TDU6] | ||||||||
ChEMBL | Agonist activity at TGR5 expressed in CHO cells by CRE-driven luciferase reporter gene assay | F | 5.65 | pEC50 | 2250 | nM | EC50 | J Med Chem (2010) 53: 178-190 [PMID:19911773] |
GtoPdb | - | - | 5.65 | pEC50 | 2250 | nM | EC50 | Biochem Biophys Res Commun (2007) 362: 793-8 [PMID:17825251] |
Hemagglutinin in Influenza A virus (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3559640] [UniProtKB: B4URE7] | ||||||||
ChEMBL | Binding affinity to recombinant influenza A hemagglutinin assessed as dissociation constant by SPR assay | B | 4.96 | pKd | 10900 | nM | Kd | J Med Chem (2022) 65: 7154-7169 [PMID:35579113] |
RTP Type C/Leukocyte common antigen in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3243] [GtoPdb: 1852] [UniProtKB: P08575] | ||||||||
ChEMBL | Inhibition of human CD45 cytoplasmic domain (584 to 1281 residues) expressed in yeast using pNPP as substrate preincubated for 10 mins followed by substrate addition measured after 30 mins | B | 6 | pIC50 | 1000 | nM | IC50 | Bioorg Med Chem Lett (2017) 27: 1159-1161 [PMID:28189419] |
Low molecular weight phosphotyrosine protein phosphatase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4903] [UniProtKB: P24666] | ||||||||
ChEMBL | Inhibition of human recombinant LMW-PTP2 expressed in Escherichia coli TB1 using p-nitrophenyl phosphate as substrate after 1 hr | B | 4.64 | pIC50 | 22900 | nM | IC50 | Eur J Med Chem (2011) 46: 2243-2251 [PMID:21453996] |
ChEMBL | Inhibition of human LMW-PTP IF2 using p-nitrophenylphosphate as substrate by spectrophotometry | B | 4.64 | pIC50 | 22900 | nM | IC50 | Eur J Med Chem (2014) 87: 316-327 [PMID:25264584] |
ChEMBL | Inhibition of human recombinant LMW-PTP1 expressed in Escherichia coli TB1 using p-nitrophenyl phosphate as substrate after 1 hr | B | 4.67 | pIC50 | 21200 | nM | IC50 | Eur J Med Chem (2011) 46: 2243-2251 [PMID:21453996] |
ChEMBL | Inhibition of human LMW-PTP IF1 using p-nitrophenylphosphate as substrate by spectrophotometry | B | 4.67 | pIC50 | 21200 | nM | IC50 | Eur J Med Chem (2014) 87: 316-327 [PMID:25264584] |
sirtuin 5/NAD-dependent protein deacylase sirtuin-5, mitochondrial in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2163183] [GtoPdb: 2711] [UniProtKB: Q9NXA8] | ||||||||
ChEMBL | Inhibition of SIRT5 (unknown origin) | B | 4.15 | pIC50 | 70000 | nM | IC50 | Eur J Med Chem (2022) 236: 114363-114363 [PMID:35436671] |
Inducible NOS/Nitric oxide synthase, inducible in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4481] [GtoPdb: 1250] [UniProtKB: P35228] | ||||||||
ChEMBL | Inhibition of inducible nitric oxide synthase in activated macrophages | B | 4.4 | pIC50 | >40000 | nM | IC50 | Bioorg Med Chem Lett (2005) 15: 2215-2219 [PMID:15837296] |
nuclear factor, erythroid 2 like 2/Nuclear factor erythroid 2-related factor 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1075094] [GtoPdb: 3057] [UniProtKB: Q16236] | ||||||||
ChEMBL | Activation of Nrf2 (unknown origin) expressed in human HaCaT-ARE-luc cells after 6 hrs by luciferase reporter gene assay | B | 4.72 | pEC50 | >=18900 | nM | EC50 | J Nat Prod (2017) 80: 2276-2283 [PMID:28753294] |
RELA proto-oncogene, NF-kB subunit/Nuclear factor NF-kappa-B p65 subunit in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5533] [GtoPdb: 3280] [UniProtKB: Q04206] | ||||||||
ChEMBL | Inhibition of biotinylated consensus sequence binding to NF-kB p65 in human HeLa nuclear extracts after 3 hrs by ELISA | B | 5.62 | pIC50 | 2400 | nM | IC50 | Bioorg Med Chem (2018) 26: 4452-4460 [PMID:30057155] |
Pancreatic alpha-amylase in Pig (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5730] [UniProtKB: P00690] | ||||||||
ChEMBL | Non-competitive inhibition of porcine pancreatic alpha-amylase assessed as inhibitor-enzyme complex using starch as substrate by Lineweaver-Burk plot analysis | B | 4.02 | pKi | 95.8 | uM | Kii | Bioorg Med Chem Lett (2017) 27: 5065-5070 [PMID:28964635] |
ChEMBL | Inhibition of porcine pancreatic alpha-amylase using starch as substrate preincubated for 15 mins followed by substrate addition measured after 10 mins by dinitrosalicylic acid reagent based assay | B | 4.03 | pIC50 | 94100 | nM | IC50 | Bioorg Med Chem Lett (2017) 27: 5065-5070 [PMID:28964635] |
sPLA2-1B/Phospholipase A2 group 1B in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4426] [GtoPdb: 1416] [UniProtKB: P04054] | ||||||||
ChEMBL | Inhibition of phospholipase A2 | B | 5.52 | pIC50 | 3000 | nM | IC50 | J Nat Prod (2011) 74: 1201-1206 [PMID:21561086] |
Phosphotyrosine protein phosphatase in Mycobacterium tuberculosis (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4295521] [UniProtKB: A0A045ISB3] | ||||||||
ChEMBL | Inhibition of Mycobacterium tuberculosis H37Ra PTPB expressed in Escherichia coli BL21 (DE3) using p-nitrophenyl phosphate as substrate preincubated for 10 mins followed by substrate addition measured for 5 mins by spectrophotometric analysis | B | 4.66 | pIC50 | 22100 | nM | IC50 | J Nat Prod (2018) 81: 1376-1383 [PMID:29792702] |
ChEMBL | Inhibition of Mycobacterium tuberculosis H37Ra PTPB expressed in Escherichia coli BL21 (DE3) using p-nitrophenyl phosphate as substrate preincubated for 10 mins followed by substrate addition and measured for 5 mins by spectrophotometric analysis | B | 4.66 | pIC50 | 22000 | nM | IC50 | J Nat Prod (2019) 82: 2268-2278 [PMID:31365251] |
ChEMBL | Inhibition of Mycobacterium tuberculosis H37Rv ptpB expressed in Escherichia coli BL21 (DH3) cells using 6,8-difluoromethylumbelliferyl phosphate as substrate incubated for 30 mins by fluorescence based assay | B | 4.85 | pIC50 | 14000 | nM | IC50 | J Nat Prod (2019) 82: 3440-3449 [PMID:31799843] |
Plasmodium falciparum (target type: ORGANISM) [ChEMBL: CHEMBL364] | ||||||||
ChEMBL | Antiplasmodial activity against Plasmodium falciparum W2 | F | 4.58 | pIC50 | 26240 | nM | IC50 | Bioorg Med Chem Lett (2013) 23: 3088-3095 [PMID:23562058] |
ChEMBL | Antiplasmodial activity against Plasmodium falciparum D6 | F | 4.62 | pIC50 | 23810 | nM | IC50 | Bioorg Med Chem Lett (2013) 23: 3088-3095 [PMID:23562058] |
Protease in Human immunodeficiency virus 1 (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2366517] [UniProtKB: Q9YQ12] | ||||||||
ChEMBL | Inhibition of HIV1 recombinant protease expressed in Escherichia coli using Abz-Ala-Arg-Val-Nle-Tyr(NO2)-Glu-Ala-Nle-NH2 as substrate by FRET assay | B | 4.24 | pIC50 | 57700 | nM | IC50 | Eur J Med Chem (2014) 74: 278-301 [PMID:24480359] |
ChEMBL | Inhibition of HIV1 protease expressed in Escherichia coli using Abz-Ala-Arg-Val-Nle-Tyr(NO2)-Glu-Ala-Nle-NH2 peptide as substrate by FRET assay | B | 4.24 | pIC50 | 57700 | nM | IC50 | J Nat Prod (2019) 82: 2886-2896 [PMID:31617361] |
ChEMBL | Inhibition of HIV1 protease activity | B | 5.1 | pIC50 | 8000 | nM | IC50 | Bioorg Med Chem (2009) 17: 5238-5246 [PMID:19515569] |
protein tyrosine phosphatase non-receptor type 1/Protein-tyrosine phosphatase 1B in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL335] [GtoPdb: 2976] [UniProtKB: P18031] | ||||||||
ChEMBL | Mixed type inhibition of human recombinant PTP-1B expressed in Escherichia coli TB1 using p-nitrophenyl phosphate as substrate | B | 5.22 | pKi | 6000 | nM | Ki | Eur J Med Chem (2011) 46: 2243-2251 [PMID:21453996] |
ChEMBL | Mixed-type inhibition of purified human GST-tagged PTP-1B using p-nitrophenylphosphate as substrate by double-reciprocal plot method | B | 5.22 | pKi | 6000 | nM | Ki | Eur J Med Chem (2014) 87: 316-327 [PMID:25264584] |
ChEMBL | Inhibition of PTP1B (unknown origin) using pNPP as substrate incubated for 30 mins by ELISA | B | 4.39 | pIC50 | 40700 | nM | IC50 | J Nat Prod (2019) 82: 3267-3278 [PMID:31738062] |
ChEMBL | Inhibition of purified human GST-tagged PTP-1B using p-nitrophenylphosphate as substrate by spectrophotometry | B |