Found 4 hits in this display Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Lanosterol synthase
(Homo sapiens (Human)) | BDBM50433365
(CHEMBL2377450)Show SMILES CNCCCC1=C2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CCC1 |r,c:5| Show InChI InChI=1S/C22H41N/c1-17(2)9-6-10-18(3)20-13-14-21-19(12-8-16-23-5)11-7-15-22(20,21)4/h17-18,20,23H,6-16H2,1-5H3/t18-,20-,22-/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ludwig-Maximilians-Universit£t M£nchen
Curated by ChEMBL
| Assay Description Inhibition of human lanosterol synthase expressed in Saccharomyces cerevisiae SMY8[pSOB1.1] using [14C]-(3S)-2,3-oxidosqualene as substrate |
Eur J Med Chem 63: 758-64 (2013)
Article DOI: 10.1016/j.ejmech.2013.03.002 BindingDB Entry DOI: 10.7270/Q2FB54B4 |
More data for this Ligand-Target Pair | |
Lanosterol synthase ERG7
(Saccharomyces cerevisiae) | BDBM50433365
(CHEMBL2377450)Show SMILES CNCCCC1=C2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CCC1 |r,c:5| Show InChI InChI=1S/C22H41N/c1-17(2)9-6-10-18(3)20-13-14-21-19(12-8-16-23-5)11-7-15-22(20,21)4/h17-18,20,23H,6-16H2,1-5H3/t18-,20-,22-/m1/s1 | Reactome pathway KEGG
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ludwig-Maximilians-Universit£t M£nchen
Curated by ChEMBL
| Assay Description Inhibition of wild type yeast lanosterol synthase expressed in Saccharomyces cerevisiae SMY8[pSM61.21] using [14C]-(3S)-2,3-oxidosqualene as substrat... |
Eur J Med Chem 63: 758-64 (2013)
Article DOI: 10.1016/j.ejmech.2013.03.002 BindingDB Entry DOI: 10.7270/Q2FB54B4 |
More data for this Ligand-Target Pair | |
Lanosterol synthase
(Pneumocystis carinii) | BDBM50433365
(CHEMBL2377450)Show SMILES CNCCCC1=C2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CCC1 |r,c:5| Show InChI InChI=1S/C22H41N/c1-17(2)9-6-10-18(3)20-13-14-21-19(12-8-16-23-5)11-7-15-22(20,21)4/h17-18,20,23H,6-16H2,1-5H3/t18-,20-,22-/m1/s1 | UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ludwig-Maximilians-Universit£t M£nchen
Curated by ChEMBL
| Assay Description Inhibition of Pneumocystis carinii lanosterol synthase expressed in Saccharomyces cerevisiae SMY8[pBJ4.21] using [14C]-(3S)-2,3-oxidosqualene as subs... |
Eur J Med Chem 63: 758-64 (2013)
Article DOI: 10.1016/j.ejmech.2013.03.002 BindingDB Entry DOI: 10.7270/Q2FB54B4 |
More data for this Ligand-Target Pair | |
Cycloartenol synthase
(Arabidopsis thaliana) | BDBM50433365
(CHEMBL2377450)Show SMILES CNCCCC1=C2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CCC1 |r,c:5| Show InChI InChI=1S/C22H41N/c1-17(2)9-6-10-18(3)20-13-14-21-19(12-8-16-23-5)11-7-15-22(20,21)4/h17-18,20,23H,6-16H2,1-5H3/t18-,20-,22-/m1/s1 | Reactome pathway KEGG
UniProtKB/SwissProt
GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ludwig-Maximilians-Universit£t M£nchen
Curated by ChEMBL
| Assay Description Inhibition of Arabidopsis thaliana cycloartenol synthase expressed in Saccharomyces cerevisiae SMY8[pSM60.21] using [14C]-(3S)-2,3-oxidosqualene as s... |
Eur J Med Chem 63: 758-64 (2013)
Article DOI: 10.1016/j.ejmech.2013.03.002 BindingDB Entry DOI: 10.7270/Q2FB54B4 |
More data for this Ligand-Target Pair | |