Reaction Details |
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Target | Dopamine beta-hydroxylase |
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Ligand | BDBM50286812 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_59304 |
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Ki | 1060000±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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BDBM50286812 |
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n/a |
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Name | BDBM50286812 |
Synonyms: | 6,6a-Dihydro-1aH-1-oxa-cyclopropa[a]indene | CHEMBL170741 |
Type | Small organic molecule |
Emp. Form. | C9H8O |
Mol. Mass. | 132.1592 |
SMILES | C1C2OC2c2ccccc12 |
Structure |
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