[引用][C] Inhibitors of myo-inositol monophosphatase unrelated to the enzyme substrate

SR Fletcher, R Baker, PD Leeson, M Teall… - Bioorganic & medicinal …, 1992 - Elsevier
The enzyme myo-inositol monophosphatase plays a key role in controlling the
phosphoinositide (PI) secondary messenger system'. Uncompetitive inhibition of this …

Inhibitors of myo-inositol monophosphatase containing methylenebisphosphonic acid as a replacement for a phosphate group

JJ Kulagowski, R Baker, SR Fletcher - Journal of the Chemical Society …, 1991 - pubs.rsc.org
Inhibitors of myo-lnositol Monophosphatase containing Methylenebisphosphonic Acid as a
Replacement for a Phosphate Group Page 1 J. CHEM. SOC., CHEM. COMMUN., 1991 …

Inhibition of myo-inositol monophosphatase isoforms by aromatic phosphonates

AJ Ganzhorn, J Hoflack, PD Pelton, F Strasser… - Bioorganic & medicinal …, 1998 - Elsevier
α-Hydroxyphosphonates are moderately potent (Ki= 6–600μM) inhibitors of the enzyme myo-
inositol monophosphatase (McLeod et al., Med. Chem. Res. 1992, 2, 96). Hydroxy-[4-(5, 6 …

Synthesis of myo-inositol-1-phosphatase inhibitors in which the phosphate group is replaced by less polar groups

AMP Van Steijn, HAM Willems, T de Boer… - Bioorganic & Medicinal …, 1995 - Elsevier
The phosphate group in the inositol-1-phosphatase inhibitor (1) is replaced by less polar
phosphorus containing groups (substituted phosphate and phosphonates), by sulphur …

Identification of (1S)-phosphoryloxy-(2R, 4S)-dihydroxycyclohexane as a potent inhibitor of inositol monophosphatase

R Baker, PD Leeson, NJ Liverton… - Journal of the Chemical …, 1990 - pubs.rsc.org
The 3, 5, 6-trisdeoxy derivative of myo-Inositol 1-monophosphate,(1S)-phosphoryloxy-(2R,
4S)-dihydroxycyclohexane [(–)-(1)], derived from the parent substrate by a strategy of …

Design of potent and selective inhibitors of myo-inositol 1, 4, 5-trisphosphate 5-phosphatase

ST Safrany, SJ Mills, C Liu, D Lampe, NJ Noble… - Biochemistry, 1994 - ACS Publications
Revised Manuscript Received June 24, 1994® abstract: The interactions of synthetic
analogues of D-myo-inositol 1, 4, 5-trisphosphate [Ins (l, 4, 5) P3] with the Ins (l, 4, 5) P3 …

4-hydroxyphenoxymethylene bisphosphonic acid derivatives: potent, non-hydrolysable inhibitors of MYO-inositol monophosphatase

SR Fletcher, R Baker, T Ladduwahetty, A Sharpe… - Bioorganic & Medicinal …, 1993 - Elsevier
From a series of 4-hydroxyphenoxymethylene bisphosphonic acid derivatives 1-(4-
Hydroxyphenoxy)-1-(methyl) methylenebisphosphonic acid has been identified as a …

Stereochemistry at Phosphorus of the Reaction Catalyzed by myo-Inositol Monophosphatase

CMJ Fauroux, M Lee, PM Cullis… - Journal of medicinal …, 2002 - ACS Publications
myo-Inositol monophosphatase (IMPase), the proposed target for lithium therapy for manic
depression, is an important enzyme in the biosynthesis of second messengers. Earlier …

Synthesis of arylalkylmonofluorophosphonates as myo-inositol monophosphatase ligands

L Schmitt, N Cavusoglu, B Spiess, G Schlewer - Tetrahedron letters, 1998 - Elsevier
Arylalkylmonofluorophosphonates were prepared by condensation of arylalkylaldehydes
with the lithium salt of diethyl 1-fluoro-1-(trimethylsilyl)-methylphosphonate. Reduction and …

Modification of myo-inositol monophosphatase by the arginine-specific reagent phenylglyoxal

RG Jackson, NS Gee, CI Ragan - Biochemical Journal, 1989 - portlandpress.com
myo-Inositol monophosphatase is inhibited by the arginine-specific reagent phenylglyoxal.
The rate of inactivation is decreased in the presence of Pi, a competitive inhibitor of the …