ETAZOLATE
ETAZOLATE Basic information
- Product Name:
- ETAZOLATE
- Synonyms:
-
- 1-ethyl-4-[(1-methylethylidene)hydrazino]1h-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester hydrochloride
- SQ20009, 1-Ethyl-4-[(1-methylethylidene)hydrazino]1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester hydrochloride
- 1H-Pyrazolo[3,4-B]pyridine-5-carboxylic acid, 1-ethyl-4-[(1-methylethylidene)hydrazino]-, ethyl ester, monohydrochloride
- Ethyl 1-ethyl-4-(isopropylidenehydrazino)-1H-pyrazolo[3,4-B]pyridine-5-carboxylate monohydrochloride
- Nsc163611
- Etazolate hydrochloride solid
- CAS:
- 35838-58-5
- MF:
- C14H18N5O2HCl
- MW:
- 0
- Mol File:
- 35838-58-5.mol
ETAZOLATE Chemical Properties
- Melting point:
- 193-194 °C
- storage temp.
- room temp
- solubility
- H2O: >20mg/mL (Solutions should be freshly prepared.)
- form
- solid
- color
- white
ETAZOLATE Usage And Synthesis
Uses
Antipsychotic.
Uses
Etazolate Hydrochloride is an acyclic nucleotide phosphodiesterase 4 inhibitor, which also exhibits antidepressant-like activity in acute and chronic mouse and rat model of depression.
Biological Activity
etazolate hydrochloride is a pde-4 inhibitor and selective gaba-a receptor modulator [3].pde-4 modulates the release of inflammatory mediators through camp-dependent and -independent mechanisms. selective targeting pde-4 is a novel therapeutic approach in the treatment of inflammation-associated respiratory diseases, such as asthma and copd (chronic obstructive pulmonary disease) [1].in rat neuronal cortical cells, etazolate hydrochloride (0.2 μm) induced sappα through the stimulation of the α-secretase pathway, and exerted a neuroprotective effect against aβ which was associated with sappα induction via the gaba-a receptor [2].in 159 alzheimer’s disease patients, etazolate hydrochloride in combination with one achei (acetycholinesterase inhibitor) was shown to be safe and generally well tolerated in the phase iia study over a 3-month treatment period [3].
Biochem/physiol Actions
Selective inhibitor of cAMP-specific phosphodiesterase.
References
[1] dastidar s g, rajagopal d, ray a. therapeutic benefit of pde4 inhibitors in inflammatory diseases.[j]. current opinion in investigational drugs, 2007, 8(5):364-72.
[2] marcade m, bourdin j, loiseau n, et al. etazolate, a neuroprotective drug linking gaba(a) receptor pharmacology to amyloid precursor protein processing.[j]. journal of neurochemistry, 2008, 106(1):392-404.
[3] vellas b; sol o; snyder pj; ousset pj; haddad r; maurin m; lemarié jc; désiré l; pando mp; eht0202/002 study group. eht0202 in alzheimer's disease: a 3-month, randomized, placebo-controlled, double-blind study.[j]. current alzheimer research, 2011, 8(2):203-12.
ETAZOLATESupplier
- Tel
- 021-61415566 800-8193336
- orderCN@merckgroup.com
- Tel
- 021-65675885 18964387627
- info@efebio.com
- Tel
- 0931-8235634 13321316780
- 1455540579@qq.com
- Tel
- info@bocsci.com
- Tel
- +86-0371-86658258 +8613203830695
- laboratory@coreychem.com
ETAZOLATE(35838-58-5)Related Product Information
- ZARDAVERINE
- RO 20-1724
- BRL 50481
- Vinpocetine
- ZAPRINAST
- ROLIPRAM
- Cilostazol
- (4S)-4-[3-(CYCLOPENTYLOXY)-4-METHOXYPHENYL]PYRROLIDIN-2-ONE
- CILOSTAMIDE
- Irsogladine maleate
- QUAZINONE
- 3-ISOBUTYL-1-METHYLXANTHINE
- SIGUAZODAN
- Pentoxifylline
- AG 1295
- S- (+)-Rolipram
- 4-[[3,4-(METHYLENEDIOXY)BENZYL]AMINO]-6-CHLOROQUINAZOLINE
- EHNA HYDROCHLORIDE