E1896
Etazolate hydrochloride
solid
别名:
1-Ethyl-4-[(1-methylethylidene)hydrazino]1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester hydrochloride, SQ 20009
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关于此项目
经验公式（希尔记法）:
C14H18N5O2 · HCl
化学文摘社编号:
分子量:
324.79
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
方案
≥98% (TLC)
表单
solid
颜色
white
mp
193-194 °C
溶解性
H2O: >20 mg/mL (Solutions should be freshly prepared.)
储存温度
room temp
SMILES字符串
Cl.CCOC(=O)c1cnc2n(CC)ncc2c1N\N=C(\C)C
InChI
1S/C14H19N5O2.ClH/c1-5-19-13-10(8-16-19)12(18-17-9(3)4)11(7-15-13)14(20)21-6-2;/h7-8H,5-6H2,1-4H3,(H,15,18);1H
InChI key
GQJUGJHJUZSJLZ-UHFFFAOYSA-N
基因信息
human ... GABRB3(2562), PRKAR1A(5573), PRKAR1AP(5574), PRKAR1B(5575), PRKAR2A(5576), PRKAR2B(5577)
相关类别
生化/生理作用
Selective inhibitor of cAMP-specific phosphodiesterase.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
R W Olsen et al.
Journal of neurochemistry, 44(4), 1074-1082 (1985-04-01)
The anthelminthic natural product avermectin B1a (AVM) modulates the binding of gamma-aminobutyric acid (GABA) and benzodiazepine (BZ) receptor ligands to membrane homogenates of mammalian brain. The potent (EC50 = 40 nM) enhancement by AVM of [3H]diazepam binding to rat or
E H Wong et al.
European journal of pharmacology, 102(2), 205-212 (1984-07-13)
Barbiturates and the related depressant drugs, etazolate and etomidate, inhibited both the binding of [3H]bicuculline methochloride (BMC) to gamma-aminobutyric acid (GABA) receptor sites and the binding of [3H] beta-carboline-3-carboxylic acid methyl ester (beta CCM) to benzodiazepine receptor sites in mammalian
Ankur Jindal et al.
European journal of pharmacology, 689(1-3), 125-131 (2012-06-16)
Etazolate, a pyrazolopyridine class derivative is selective inhibitor of type 4 phosphodiesterase (PDE4), an enzyme catalyzes the hydrolysis of cyclic nucleotide viz. cAMP & regulates cAMP signal transduction. Enhancing cAMP signal transduction by inhibition of PDE4 is known to be
Distinction of benzodiazepine receptor agonists and inverse agonists by binding studies in vitro.
M Karobath et al.
Advances in biochemical psychopharmacology, 38, 37-45 (1983-01-01)
G Maksay et al.
Journal of neurochemistry, 44(2), 480-486 (1985-02-01)
The dissociation of [35S]t-butylbicyclophosphorothionate ([35S]TBPT) from binding sites on membranes from rat cerebral cortex, after addition of saturating concentrations of convulsant and depressant drugs, was studied. The addition of unlabeled TBPT, picrotoxinin, or pentamethylenetetrazol resulted in dissociation patterns that were
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