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3-甲基-6-(3-[三氟甲基]苯基)-1,2,4-噻唑并-(4,3-b)吡嗪

更新时间:2025-08-22 20:52:42

3-甲基-6-(3-[三氟甲基]苯基)-1,2,4-噻唑并-(4,3-b)吡嗪结构式
3-甲基-6-(3-[三氟甲基]苯基)-1,2,4-噻唑并-(4,3-b)吡嗪结构式
品牌特惠专场
常用名 3-甲基-6-(3-[三氟甲基]苯基)-1,2,4-噻唑并-(4,3-b)吡嗪 英文名 CL 218872
CAS号 66548-69-4 分子量 278.23300
密度 1.43g/cm3 沸点 N/A
分子式 C13H9F3N4 熔点 N/A
MSDS N/A 闪点 N/A

 用途


CL 218872是一种选择性的口服活性苯二氮卓,其α1亚基含有GABAAR受体,Ki为130 nM。CL 218872在体内发挥抗焦虑和抗惊厥作用【1】。

 名称

中文名 3-甲基-6-(3-[三氟甲基]苯基)-1,2,4-噻唑并-(4,3-b)吡嗪
英文名 3-methyl-6-[3-(trifluoromethyl)phenyl]-[1,2,4]triazolo[4,3-b]pyridazine
英文别名 更多

 生物活性

描述 CL 218872是一种选择性的口服活性苯二氮卓,其α1亚基含有GABAAR受体,Ki为130 nM。CL 218872在体内发挥抗焦虑和抗惊厥作用【1】。
相关类别
参考文献

[1]. Squires RF, et al. Some properties of brain specific benzodiazepine receptors: new evidence for multiple receptors. Pharmacol Biochem Behav. 1979 May;10(5):825-30.

 物理化学性质

密度 1.43g/cm3
分子式 C13H9F3N4
分子量 278.23300
精确质量 278.07800
PSA 43.08000
LogP 3.11850
InChIKey GUOQUXNJZHGPQF-UHFFFAOYSA-N
SMILES Cc1nnc2ccc(-c3cccc(C(F)(F)F)c3)nn12
折射率 1.615
储存条件 -20°C

 靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident pro...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-p1-antagonist
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1266185
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:Rescue cell viability in cybrid cells with a genetic mutation in complex 1 of the mit...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1315
实验名称:In vitro binding affinity against benzodiazepine receptor using [3H]diazepam as radio...
来源:ChEMBL
靶标:Gamma-aminobutyric acid receptor subunit alpha-3
External Id:CHEMBL653129
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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 英文别名

CL 218,872
Tocris-1709
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