Reaction Details |
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Target | Lanosterol synthase |
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Ligand | BDBM50167085 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1573537 (CHEMBL3801492) |
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IC50 | 50±n/a nM |
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Citation | Zhao, Z; Harrison, ST; Schubert, JW; Sanders, JM; Polsky-Fisher, S; Zhang, NR; McLoughlin, D; Gibson, CR; Robinson, RG; Sachs, NA; Kandebo, M; Yao, L; Smith, SM; Hutson, PH; Wolkenberg, SE; Barrow, JC Synthesis and optimization of N-heterocyclic pyridinones as catechol-O-methyltransferase (COMT) inhibitors. Bioorg Med Chem Lett26:2952-2956 (2016) [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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BDBM50167085 |
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n/a |
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Name | BDBM50167085 |
Synonyms: | CHEMBL3799623 |
Type | Small organic molecule |
Emp. Form. | C20H16N4O2 |
Mol. Mass. | 344.3666 |
SMILES | Oc1cn(ccc1=O)-c1cc(ccn1)-c1cnn(Cc2ccccc2)c1 |
Structure |
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