Basic information Safety Supplier Related

ETAZOLATE

Basic information Safety Supplier Related

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
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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
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
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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

Sigma-Aldrich
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021-61415566 800-8193336
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orderCN@merckgroup.com
Shanghai EFE Biological Technology Co., Ltd.
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021-65675885 18964387627
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Lanzhou Angeli Biochemical Technology Co., Ltd.
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0931-8235634 13321316780
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BOC Sciences
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Career Henan Chemica Co
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+86-0371-86658258 +8613203830695
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laboratory@coreychem.com