5-hexylsulfanyl-1,3,4-thiadiazol-2-amine

• 常用名: 5-hexylsulfanyl-1,3,4-thiadiazol-2-amine
• 英文名: 5-hexylsulfanyl-1,3,4-thiadiazol-2-amine
• CAS号: 61516-63-0
• 分子量: 217.35500
• 密度: N/A
• 沸点: N/A
• 分子式: C₈H₁₅N₃S₂
• 熔点: N/A
• 闪点: N/A

5-hexylsulfanyl-1,3,4-thiadiazol-2-amine名称

• 英文名: 5-hexylsulfanyl-1,3,4-thiadiazol-2-amine

5-hexylsulfanyl-1,3,4-thiadiazol-2-amine物理化学性质

• 分子式: C₈H₁₅N₃S₂
• 分子量: 217.35500
• 精确质量: 217.07100
• PSA: 106.07000
• LogP: 2.72280
• InChIKey: NSOOBCMKNXDQHP-UHFFFAOYSA-N
• SMILES: CCCCCCSc1nnc(N)s1

5-hexylsulfanyl-1,3,4-thiadiazol-2-amine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：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：Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect... 来源：Broad Institute 靶标：N/A External Id：Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_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：Dicer-mediated maturation of pre-microRNA 来源：Center for Chemical Genomics, University of Michigan 靶标：N/A External Id：TargetID_659_CEMA

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5-hexylsulfanyl-1,3,4-thiadiazol-2-amine英文别名

• 5-hexylthio-1,3,4-thiadiazole-2-ylamine
• 2-amino-5-hexylthio-1,3,4-thiadiazole