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

BRENDA support

5.4.99.8: cycloartenol synthase

This is an abbreviated version!
For detailed information about cycloartenol synthase, go to the full flat file.

Word Map on EC 5.4.99.8

Reaction

(3S)-2,3-epoxy-2,3-dihydrosqualene
=
Cycloartenol

Synonyms

(S)-2,3-epoxysqualene mutase, 2,3-Epoxysqualene cycloartenol-cyclase, 2,3-epoxysqualene--cycloartenol cyclase, 2,3-Epoxysqualene-cycloartenol cyclase, 2,3-Oxidosqualene cycloartenol cyclase, 2,3-Oxidosqualene-cycloartenol cyclase, 2,3-Oxidosqualene:cycloartenol cyclase, ACX, AtCAS1, AthCAS1, CaCYS, CAS, CAS1, Cyclase, 2,3-oxidosqualene-cycloartenol, cycloartenol synthase, cycloartenol synthase 1, LdCAS, NbCAS, NtCAS, OSC, OSC/CS, Oxidosqualene cyclase, PNX, PtCAS1, PtCAS2, SgCAS, WsCAS

ECTree

     5 Isomerases
         5.4 Intramolecular transferases
             5.4.99 Transferring other groups
                5.4.99.8 cycloartenol synthase

Inhibitors

Inhibitors on EC 5.4.99.8 - cycloartenol synthase

Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
2-Aza-2,3-dihydro-squalene-N-oxide
-
-
2-Aza-2,3-dihydrosqualene
2-hydroxyethyl jasmonate
downregulation of gene expression at 200 mM, diethydithiocarbamate depresses the down-regulation of CAS gene expression by 2-hydroxyethyl jasmonate
3beta-(2-Diethylaminoethoxy)androstenone
-
-
8-Azadecalin
-
-
Carbenium ion intermediate analogue inhibitors
-
-
-
methyl jasmonate
-
inhibits CaCYS transcription
Monocyclic 4-hydroxypiperidine
-
-
N-Lauryl-N-dimethylamino-N-oxide
-
-
N-[(1,5,9)-Trimethyl-decyl]-4alpha,10-dimethyl-8-aza-trans-decal-3beta-ol
-
-
p-chloromercuribenzene sulfonic acid
-
-
p-hydroxymercuribenzoate
Ochromonas malhamensis
-
-
Ro 48-8071
a potent inhibitor of oxidosqualene cyclization, the site of RO 48-8071 inhibition is CAS
sodium deoxycholate
Ochromonas malhamensis
-
stimulates at low concentrations, optimal activation at 0.1%. Inhibition at levels greater than 0.5%
additional information
-