Reaction Details |
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Target | Dopamine beta-hydroxylase |
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Ligand | BDBM50286815 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_59304 |
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Ki | 150000±n/a nM |
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Citation | Eydoux, F; Chlenov, MA; Réglier, M Synthesis of indane derivatives as mechanism-based inhibitors of dopamine β-hydroxylase Bioorg Med Chem Lett5:941-944 (1995) Article |
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More Info.: | Get all data from this article, Assay Method |
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Dopamine beta-hydroxylase |
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Name: | Dopamine beta-hydroxylase |
Synonyms: | DBH | DOPO_BOVIN |
Type: | PROTEIN |
Mol. Mass.: | 68136.39 |
Organism: | Bos taurus |
Description: | ChEMBL_50738 |
Residue: | 610 |
Sequence: | MQVPSPSVREAASMYGTAVAVFLVILVAALQGSAPAESPFPFHIPLDPEGTLELSWNISY
AQETIYFQLLVRELKAGVLFGMSDRGELENADLVVLWTDRDGAYFGDAWSDQKGQVHLDS
QQDYQLLRAQRTPEGLYLLFKRPFGTCDPNDYLIEDGTVHLVYGFLEEPLRSLESINTSG
LHTGLQRVQLLKPSIPKPALPADTRTMEIRAPDVLIPGQQTTYWCYVTELPDGFPRHHIV
MYEPIVTEGNEALVHHMEVFQCAAEFETIPHFSGPCDSKMKPQRLNFCRHVLAAWALGAK
AFYYPEEAGLAFGGPGSSRFLRLEVHYHNPLVITGRRDSSGIRLYYTAALRRFDAGIMEL
GLAYTPVMAIPPQETAFVLTGYCTDKCTQLALPASGIHIFASQLHTHLTGRKVVTVLARD
GRETEIVNRDNHYSPHFQEIRMLKKVVSVQPGDVLITSCTYNTEDRRLATVGGFGILEEM
CVNYVHYYPQTQLELCKSAVDPGFLHKYFRLVNRFNSEEVCTCPQASVPEQFASVPWNSF
NREVLKALYGFAPISMHCNRSSAVRFQGEWNRQPLPEIVSRLEEPTPHCPASQAQSPAGP
TVLNISGGKG
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BDBM50286815 |
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n/a |
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Name | BDBM50286815 |
Synonyms: | 1,1a,6,6a-Tetrahydro-cyclopropa[a]inden-3-ol | CHEMBL368520 |
Type | Small organic molecule |
Emp. Form. | C10H10O |
Mol. Mass. | 146.1858 |
SMILES | Oc1ccc2CC3CC3c2c1 |
Structure |
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