Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 1.1.1.149 extracted from

  • El-Kabbani, O.; Scammells, P.J.; Gosling, J.; Dhagat, U.; Endo, S.; Matsunaga, T.; Soda, M.; Hara, A.
    Structure-guided design, synthesis, and evaluation of salicylic acid-based inhibitors targeting a selectivity pocket in the active site of human 20alpha-hydroxysteroid dehydrogenase (AKR1C1) (2009), J. Med. Chem., 52, 3259-3264.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
expressed in Escherichia coli JM109 cells Homo sapiens

Inhibitors

Inhibitors Comment Organism Structure
3,5-dibromosalicylic acid
-
Homo sapiens
3-bromo-5-phenylsalicylic acid
-
Homo sapiens
3-phenyl-5-bromosalicylic acid
-
Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
Homo sapiens

Synonyms

Synonyms Comment Organism
20-alpha-HSD
-
Homo sapiens
AKR1C1
-
Homo sapiens

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
0.000004
-
3-bromo-5-phenylsalicylic acid
-
Homo sapiens
0.000009
-
3,5-dibromosalicylic acid
-
Homo sapiens
0.00014
-
3-phenyl-5-bromosalicylic acid
-
Homo sapiens