BDBM50241487 2,3,6,23-tetrahydroxyurs-12-en-28-oic acid::Asiatic acid::CHEMBL404313::asiantic acid

SMILES C[C@@H]1CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](O)[C@@](C)(CO)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C)C(O)=O

InChI Key InChIKey=JXSVIVRDWWRQRT-UYDOISQJSA-N

Data  13 IC50  1 EC50

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 14 hits for monomerid = 50241487   

TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of PTP1B (unknown origin) by pNPP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of TCPTP (unknown origin) by pNPP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen phosphorylase, muscle form(Oryctolagus cuniculus (rabbit))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibition of rabbit muscle glycogen phosphorylase A assessed as release of phosphate from glucose-1-phosphate after 25 mins by microplate reader bas...More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Gifu Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50:  3.40E+4nMAssay Description:Inhibition of reductase activity of N-terminal 6His-tagged human recombinant AKR1B1 expressed in Escherichia coli BL21(DE3) assessed as assessed as p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
Gifu Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50:  5.90E+3nMAssay Description:Inhibition of reductase activity of N-terminal 6His-tagged human AKR1B10 expressed in Escherichia coli BL21(DE3) assessed as pyridine-3-aldehyde redu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenylate cyclase(Spirulina platensis)
Ruhr-University Bochum

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50:  1.00E+5nMAssay Description:Inhibition of Spirulina platensis adenylyl cyclase assessed as cAMP level by cAMP immunogenic assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
Osaka University

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50: >4.00E+4nMAssay Description:Inhibition of human recombinant 5-LOX expressed in insect cells assessed as decrease in production of 5-HPETE and 5-HETE using arachidonic acid as su...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPancreatic alpha-amylase(Sus scrofa (Pig))
Dalian University Of Technology

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50: >2.00E+5nMAssay Description:Inhibition of porcine pancreatic alpha-amylase using starch as substrate preincubated for 15 mins followed by substrate addition measured after 10 mi...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
Osaka University

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50: >4.00E+4nMAssay Description:Inhibition of human recombinant 5-LOX expressed in insect cells assessed as decrease in production of 5-HPETE and 5-HETE using arachidonic acid as su...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Osaka University

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50: >4.00E+4nMAssay Description:Inhibition of human recombinant COX2 expressed in baculovirus infected sf21 cells assessed as decrease in PGE2 formation using arachidonic acid as su...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Ovis aries (Sheep))
Osaka University

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50: >4.00E+4nMAssay Description:Inhibition of ovine recombinant COX1 assessed as decrease in formation of PGE2 using arachidonic acid as substrate preincubated for 10 mins followed ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Osaka University

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50: >4.00E+4nMAssay Description:Inhibition of human recombinant COX2 expressed in baculovirus infected sf21 cells assessed as decrease in PGE2 formation using arachidonic acid as su...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Ovis aries (Sheep))
Osaka University

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataIC50: >4.00E+4nMAssay Description:Inhibition of ovine recombinant COX1 assessed as decrease in formation of PGE2 using arachidonic acid as substrate preincubated for 10 mins followed ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetG-protein coupled bile acid receptor 1(Homo sapiens (Human))
Universite Louis Pasteur

Curated by ChEMBL
LigandPNGBDBM50241487(2,3,6,23-tetrahydroxyurs-12-en-28-oic acid | Asiat...)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at TGR5 expressed in CHO cells by CRE-driven luciferase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed