5-戊基-1,3,4-噻二唑-2-胺

• 常用名: 5-戊基-1,3,4-噻二唑-2-胺
• 英文名: 4-thiadiazole,2-amino-5-pentyl-3
• CAS号: 52057-90-6
• 分子量: 171.26300
• 密度: 1.141g/cm3
• 沸点: 302.6ºC at 760mmHg
• 分子式: C₇H₁₃N₃S
• 熔点: N/A
• 闪点: 136.8ºC

5-戊基-1,3,4-噻二唑-2-胺名称

• 中文名: 5-戊基-1,3,4-噻二唑-2-胺
• 英文名: 5-Pentyl-1,3,4-thiadiazol-2-amine

5-戊基-1,3,4-噻二唑-2-胺物理化学性质

• 密度: 1.141g/cm3
• 沸点: 302.6ºC at 760mmHg
• 分子式: C₇H₁₃N₃S
• 分子量: 171.26300
• 闪点: 136.8ºC
• 精确质量: 171.08300
• PSA: 80.04000
• LogP: 2.43420
• InChIKey: ZTUVGDVRIPDQSI-UHFFFAOYSA-N
• SMILES: CCCCCc1nnc(N)s1
• 折射率: 1.56

5-戊基-1,3,4-噻二唑-2-胺毒性和生态

5-戊基-1,3,4-噻二唑-2-胺安全信息

• 海关编码: 2934999090

5-戊基-1,3,4-噻二唑-2-胺海关

• 海关编码: 2934999090
• 中文概述: 2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
• 申报要素: 品名, 成分含量, 用途
• Summary: 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

5-戊基-1,3,4-噻二唑-2-胺靶点实验

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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：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：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：A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus 来源：ICCB-Longwood/NSRB Screening Facility, Harvard Medical School External Id：HMS979

实验名称：High throughput fluorescence intensity-based biochemical assay to screen for small mo... 来源：University of Pittsburgh Molecular Library Screening Center 靶标：furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens] External Id：MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.

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

实验名称：Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste... 来源：Broad Institute 靶标：N/A External Id：7124-01_Inhibitor_SinglePoint_HTS_Activity

实验名称：Fluorescence-based cell-based primary high throughput screening assay to identify pos... 来源：The Scripps Research Institute Molecular Screening Center 靶标：muscarinic acetylcholine receptor M1 [Homo sapiens] External Id：CHRM1_PAM_FLUO8_1536_1X%ACT PRUN

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5-戊基-1,3,4-噻二唑-2-胺英文别名

• 5-Pentyl-[1,3,4]thiadiazol-2-ylamine
• 5-Pentyl-2-amino-1,3,4-thiadiazole
• 1,3,4-Thiadiazole,2-amino-5-pentyl
• 5-Pentyl-[1,3,4]thiadiazol-2-ylamin
• 2-amino-5-n-pentyl-1,3,4-thiadiazole
• 5-pentyl-1,3,4-thiadiazole-2-ylamine