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2-氨基-5-N-丙基硫代-1,3,4-噻二唑

更新时间:2025-08-27 04:16:39

2-氨基-5-N-丙基硫代-1,3,4-噻二唑结构式
2-氨基-5-N-丙基硫代-1,3,4-噻二唑结构式
品牌特惠专场
常用名 2-氨基-5-N-丙基硫代-1,3,4-噻二唑 英文名 2-AMINO-5-N-PROPYLTHIO-1,3,4-THIADIAZOLE
CAS号 30062-49-8 分子量 175.27500
密度 N/A 沸点 N/A
分子式 C5H9N3S2 熔点 N/A
MSDS N/A 闪点 N/A

 2-氨基-5-N-丙基硫代-1,3,4-噻二唑名称

中文名 2-氨基-5-N-丙基硫代-1,3,4-噻二唑
英文名 5-propylsulfanyl-1,3,4-thiadiazol-2-amine
英文别名 更多

 2-氨基-5-N-丙基硫代-1,3,4-噻二唑物理化学性质

分子式 C5H9N3S2
分子量 175.27500
精确质量 175.02400
PSA 105.34000
LogP 2.20360
InChIKey UWXTXBIBHSFVCG-UHFFFAOYSA-N
SMILES CCCSc1nnc(N)s1

 2-氨基-5-N-丙基硫代-1,3,4-噻二唑MSDS

 2-氨基-5-N-丙基硫代-1,3,4-噻二唑安全信息

海关编码 2934999090

 2-氨基-5-N-丙基硫代-1,3,4-噻二唑合成线路

~83%

2-氨基-5-N-丙基硫代-1,3,4-噻二唑结构式

2-氨基-5-N-丙基硫代-1...

30062-49-8

文献:Marin; Valls; Berenguer; Alonso; Martinez; Elguero Farmaco, 1992 , vol. 47, # 1 p. 63 - 75

~55%

2-氨基-5-N-丙基硫代-1,3,4-噻二唑结构式

2-氨基-5-N-丙基硫代-1...

30062-49-8

文献:Clerici; Pocar; Guido; Loche; Perlini; Brufani Journal of Medicinal Chemistry, 2001 , vol. 44, # 6 p. 931 - 936

 2-氨基-5-N-丙基硫代-1,3,4-噻二唑上下游产品

2-氨基-5-N-丙基硫代-1,3,4-噻二唑上游产品  3

2-氨基-5-N-丙基硫代-1,3,4-噻二唑下游产品  0

 2-氨基-5-N-丙基硫代-1,3,4-噻二唑海关

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%

 2-氨基-5-N-丙基硫代-1,3,4-噻二唑靶点实验

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: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: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
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 2-氨基-5-N-丙基硫代-1,3,4-噻二唑英文别名

5-(Propylsulfanyl)-1,3,4-thiadiazol-2-amine
2-Amino-5-propylthio-1,3,4-thiadiazole
2-Amino-5-n-propylthio-1,3,4-thiadiazole
5-propylthio-1,3,4-thiadiazole-2-ylamine
1,3,4-Thiadiazol-2-amine,5-(propylthio)
5-propylsulfanyl-[1,3,4]thiadiazol-2-ylamine
5-(propylthio)-1,3,4-thiadiazol-2-amine
2-amino-5-n-propyl-mercapto-1,3,4-thiadiazole
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