null

SMILES C\C1=C\CC[C@@]2(C)O[C@H]2[C@H]2OC(=O)C(=C)[C@@H]2CC1

InChI Key InChIKey=KTEXNACQROZXEV-QLIGOWBFSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50194429   

Target5-hydroxytryptamine receptor 1A(RABBIT)
University of Montana

Curated by PDSP Ki Database
LigandPNGBDBM50194429((-)-parthenolide | (1aR,7aS,10aS,10bS,Z)-1a,5-dime...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6HWKPubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
University of Montana

Curated by ChEMBL
LigandPNGBDBM50194429((-)-parthenolide | (1aR,7aS,10aS,10bS,Z)-1a,5-dime...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+5nMAssay Description:Displacement of [3H]ketanserin from rat 5HT2A receptor expressed in mouse NIH3T3 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC83R7PubMed
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
University of Montana

Curated by ChEMBL
LigandPNGBDBM50194429((-)-parthenolide | (1aR,7aS,10aS,10bS,Z)-1a,5-dime...)copy SMILEScopy InChI
Affinity DataKi:  2.50E+5nMAssay Description:Displacement of [3H]ketanserin from 5HT2A receptor in rat brain membraneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZC83R7PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50194429((-)-parthenolide | (1aR,7aS,10aS,10bS,Z)-1a,5-dime...)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of COX2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PN5PubMed
TargetUDP-N-acetylglucosamine 1-carboxyvinyltransferase(Pseudomonas aeruginosa (G-proteobacteria))
Saarland University

Curated by ChEMBL
LigandPNGBDBM50194429((-)-parthenolide | (1aR,7aS,10aS,10bS,Z)-1a,5-dime...)copy SMILEScopy InChI
Affinity DataIC50: 2.78E+4nMAssay Description:Inhibition of Pseudomonas aeruginosa PAO1293 MurA in presence of UNAGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20Z742GPubMed
TargetUDP-N-acetylglucosamine 1-carboxyvinyltransferase(Escherichia coli K-12 (Enterobacteria))
Saarland University

Curated by ChEMBL
LigandPNGBDBM50194429((-)-parthenolide | (1aR,7aS,10aS,10bS,Z)-1a,5-dime...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of Escherichia coli K12 Mur A in presence of UNAGMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20Z742GPubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
The University of Mississippi

Curated by ChEMBL
LigandPNGBDBM50194429((-)-parthenolide | (1aR,7aS,10aS,10bS,Z)-1a,5-dime...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of iNOS in LPS-induced mouse RAW264.7 cells assessed as inhibition of nitric acid at measured after 24 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1N83PubMed