Reaction Details |
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Target | Lanosterol synthase |
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Ligand | BDBM50542443 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1987069 (CHEMBL4620616) |
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IC50 | 70±n/a nM |
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Citation | Hitge, R; Smit, S; Petzer, A; Petzer, JP Evaluation of nitrocatechol chalcone and pyrazoline derivatives as inhibitors of catechol-O-methyltransferase and monoamine oxidase. Bioorg Med Chem Lett30:0 (2020) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Lanosterol synthase |
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Name: | Lanosterol synthase |
Synonyms: | LSS_RAT | Lss | Osc |
Type: | PROTEIN |
Mol. Mass.: | 83302.12 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_12083 |
Residue: | 733 |
Sequence: | MTEGTCLRRRGGPYKTEPATDLTRWRLHNELGRQRWTYYQAEEDPGREQTGLEAHSLGLD
TTSYFKNLPKAQTAHEGALNGVTFYAKLQAEDGHWAGDYGGPLFLLPGLLITCHIAHIPL
PAGYREEMVRYLRSVQLPDGGWGLHIEDKSTVFGTALSYVSLRILGIGPDDPDLVRARNI
LHKKGGAVAIPSWGKFWLAVLNVYSWEGINTLFPEMWLLPEWFPAHPSTLWCHCRQVYLP
MSYCYATRLSASEDPLVQSLRQELYVEDYASIDWPAQKNNVCPDDMYTPHSWLLHVVYGL
LNLYERFHSTSLRKWAIQLLYEHVAADDRFTKCISIGPISKTVNMLIRWSVDGPSSPAFQ
EHVSRIKDYLWLGLDGMKMQGTNGSQTWDTSFAVQALLEAGAHRRPEFLPCLQKAHEFLR
LSQVPDNNPDYQKYYRHMHKGGFPFSTLDCGWIVADCTAEALKAVLLLQERCPSITEHVP
RERLYDAVAVLLSMRNSDGGFATYETKRGGYLLELLNPSEVFGDIMIDYTYVECTSAVMQ
ALRHFREYFPDHRATESRETLNQGLDFCRKKQRADGSWEGSWGVCFTYGTWFGLEAFACM
GHIYQNRTACAEVAQACHFLLSRQMADGGWGEDFESCEQRRYVQSAGSQVHSTCWALLGL
MAVRHPDISAQERGIRCLLGKQLPNGDWPQENISGVFNKSCAISYTNYRNIFPIWALGRF
SSLYPDNTLAGHI
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BDBM50542443 |
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n/a |
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Name | BDBM50542443 |
Synonyms: | CHEMBL4639358 |
Type | Small organic molecule |
Emp. Form. | C16H13NO6 |
Mol. Mass. | 315.2775 |
SMILES | COc1cccc(\C=C\C(=O)c2cc(O)c(O)c(c2)[N+]([O-])=O)c1 |
Structure |
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