Z3777
ZD7288 水合物
≥98% (HPLC), cation channel Ih blocker, powder
别名:
4-（N-苯乙烯-N-苯氨基）-1,2-二甲基-6-（甲氨基）甲苯氯化物, ICI-D7288, N-苯乙烯-1,6-二氢-1,2-二甲基-6-（甲亚胺基）-N-苯基-4-甲苯酚胺盐酸盐, ZD 7288
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关于此项目
经验公式（希尔记法）:
C15H20N4 · HCl · xH2O
分子量:
292.81 (anhydrous basis)
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
产品名称
ZD7288 水合物, ≥98% (HPLC)
SMILES string
O.Cl.CCN(c1ccccc1)C2=CC(=N/C)\N(C)C(C)=N2
InChI key
NCEDDDWQLCMZQG-UPONXUSQSA-N
InChI
1S/C15H20N4.ClH.H2O/c1-5-19(13-9-7-6-8-10-13)15-11-14(16-3)18(4)12(2)17-15;;/h6-11H,5H2,1-4H3;1H;1H2/b16-14+;;
assay
≥98% (HPLC)
form
powder
storage condition
desiccated
color
white to beige
solubility
DMSO: 10 mg/mL, clear
originator
AstraZeneca
storage temp.
2-8°C
Quality Level
相关类别
Application
ZD7288水合物已被用作 Ih 阻滞剂，用于研究其对
新皮层组织的作用。它还被用作超极化激活和环状核苷酸门控 (HCN) 通道阻滞剂，用于测试HCN通道是否参与光转导途径。
新皮层组织的作用。它还被用作超极化激活和环状核苷酸门控 (HCN) 通道阻滞剂，用于测试HCN通道是否参与光转导途径。
Biochem/physiol Actions
ZD7288可以抑制海马突触可塑性。
阳离子通道 Ih 的选择性阻断剂；如果是阻断剂和窦房结功能调节剂，则阻断超极化激活和环状核苷酸门控（HCN）通道。
阳离子通道 Ih 的选择性阻断剂；如果是阻断剂和窦房结功能调节剂，则阻断超极化激活和环状核苷酸门控（HCN）通道。
Features and Benefits
该化合物在受体分类和信号转导手册的环核苷酸门控（CNG）和超极化激活的环核苷酸门控（HCN）通道页面上有详细描述。想要浏览手册的其他页面， 请单击此处。
该化合物由 AstraZeneca 公司开发。若要浏览其他制药公司研发的化合物和批准的药物/候选药物列表，请单击此处。
这种化合物是环核苷酸研究的特色产品。点击此处发现更多特色环核苷酸产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Proneural transcription factors (TFs) drive highly efficient differentiation of pluripotent stem cells to lineage-specific neurons. However, current strategies mainly rely on genome-integrating viruses. Here, we used synthetic mRNAs coding two proneural TFs (Atoh1 and Ngn2) to differentiate induced pluripotent stem
Marcin Siwiec et al.
Neuropharmacology, 177, 108248-108248 (2020-08-01)
Accumulating evidence suggests a widespread role of serotonin 5-HT7 receptors (5-HT7Rs) in the physiology of cognitive and affective processing. However, we still lack insights into 5-HT7R electrophysiology. Studies analyzing the 5-HT7R-mediated changes in CA1 pyramidal neuron activity revealed that 5-HT7R
ZD7288, a selective hyperpolarization-activated cyclic nucleotide-gated channel blocker, inhibits hippocampal synaptic plasticity
Zhang XX, et al.
Neural Regeneration Research, 11(5), 779-779 (2016)
Barbara Beiderbeck et al.
Nature communications, 9(1), 1771-1771 (2018-05-04)
The integration of excitatory and inhibitory synaptic inputs is fundamental to neuronal processing. In the mammalian auditory brainstem, neurons compare excitatory and inhibitory inputs from the ipsilateral and contralateral ear, respectively, for sound localization. However, the temporal precision and functional
Janna Lehnhoff et al.
Neuropharmacology, 144, 58-69 (2018-10-14)
Alterations of the hyperpolarization activated nonselective cation current (Ih) are associated with epileptogenesis. Accordingly, the second-generation antiepileptic drug lamotrigine (LTG) enhances Ih in rodent hippocampus. We directly evaluated here whether LTG fails to enhance Ih in neocortical slices from patients
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