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Luciferase-IN-1

更新时间:2025-08-25 22:49:03

Luciferase-IN-1结构式
Luciferase-IN-1结构式
品牌特惠专场
常用名 Luciferase-IN-1 英文名 Benzenamine,4-(2-benzothiazolyl)-N,N-dimethyl
CAS号 10205-56-8 分子量 254.35000
密度 1.213g/cm3 沸点 414.1ºC at 760mmHg
分子式 C15H14N2S 熔点 N/A
MSDS N/A 闪点 204.2ºC

 Luciferase-IN-1用途


荧光素酶-IN-1是一种荧光素酶抑制剂[1]。

 Luciferase-IN-1名称

英文名 4-(1,3-benzothiazol-2-yl)-N,N-dimethylaniline
英文别名 更多

 Luciferase-IN-1生物活性

描述 荧光素酶-IN-1是一种荧光素酶抑制剂[1]。
相关类别
体外研究 荧光素酶-IN-1是一种荧光素酶抑制剂[1]。
参考文献

[1]. Auld DS, et al. A basis for reduced chemical library inhibition of firefly luciferase obtained from directed evolution. J Med Chem. 2009;52(5):1450-1458.

 Luciferase-IN-1物理化学性质

密度 1.213g/cm3
沸点 414.1ºC at 760mmHg
分子式 C15H14N2S
分子量 254.35000
闪点 204.2ºC
精确质量 254.08800
PSA 44.37000
LogP 4.02930
InChIKey HYKGLCSXVAAXNC-UHFFFAOYSA-N
SMILES CN(C)c1ccc(-c2nc3ccccc3s2)cc1
蒸汽压 4.58E-07mmHg at 25°C
折射率 1.683
储存条件 2-8°C,干燥,密封

 Luciferase-IN-1毒性和生态

 Luciferase-IN-1安全信息

危害码 (欧洲) Xi
海关编码 2934999090

 Luciferase-IN-1合成线路

 Luciferase-IN-1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%

 Luciferase-IN-1靶点实验

查看更多实验

实验名称:A screen for compounds that inhibit cell wall-associated teichoic acid synthesis in S...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS704
实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
实验名称:Firefly luciferase (FLuc-C-HiBiT) enzymatic inhibition screen - Functional assay
来源:NCGC
External Id:adst_SDR_Fluc-Fluc_Km
实验名称:Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of VER...
来源:ChEMBL
靶标:Severe acute respiratory syndrome coronavirus 2
External Id:CHEMBL4513082
实验名称:Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:ORF 73 [Human herpesvirus 8 type M]
External Id:HMS791
实验名称:Binding affinity for Amyloid beta 1-40 aggregates in competition with [N-methyl-3H] B...
来源:ChEMBL
靶标:Amyloid-beta precursor protein
External Id:CHEMBL649400
实验名称:Firefly luciferase (FLuc-C-HiBiT) SDR gain of signal screen - plus ATP
来源:NCGC
External Id:adst_SDR_Fluc-HiBit_ATP
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:Firefly luciferase (FLuc-C-HiBiT) SDR gain of signal screen - without ATP
来源:NCGC
External Id:adst_SDR_Fluc-HiBit_NoATP
实验名称:SARS-CoV-2 3CL-Pro protease inhibition percentage at 20µM by FRET kind of response f...
来源:ChEMBL
靶标:Replicase polyprotein 1ab
External Id:CHEMBL4495582
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 Luciferase-IN-1英文别名

MFCD00937700
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