Reaction Details |
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Target | Lanosterol synthase |
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Ligand | BDBM50051375 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_149028 (CHEMBL759503) |
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Ki | 400±n/a nM |
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Citation | Barth, MM; Binet, JL; Thomas, DM; de Fornel, DC; Samreth, S; Schuber, FJ; Renaut, PP Structural and stereoelectronic requirements for the inhibition of mammalian 2,3-oxidosqualene cyclase by substituted isoquinoline derivatives. J Med Chem39:2302-12 (1996) [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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BDBM50051375 |
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n/a |
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Name | BDBM50051375 |
Synonyms: | (6S,8aS)-5,5,8a-Trimethyl-2-((E)-1,5,9-trimethyl-deca-4,8-dienyl)-1,2,3,5,6,7,8,8a-octahydro-isoquinolin-6-ol | CHEMBL76239 |
Type | Small organic molecule |
Emp. Form. | C25H43NO |
Mol. Mass. | 373.615 |
SMILES | [#6]-[#6](-[#6]-[#6]\[#6]=[#6](/[#6])-[#6]-[#6]\[#6]=[#6](\[#6])-[#6])-[#7]-1-[#6]-[#6]=[#6]2C([#6])([#6])[#6@@H](-[#8])-[#6]-[#6][C@]2([#6])[#6]-1 |t:15| |
Structure |
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