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SQ 22799

更新时间:2025-08-21 16:55:08

SQ 22799结构式
SQ 22799结构式
委托求购
常用名 SQ 22799 英文名 SQ 22799
CAS号 7051-86-7 分子量 239.27600
密度 1.34g/cm3 沸点 486.6ºC at 760 mmHg
分子式 C13H13N5 熔点 N/A
MSDS N/A 闪点 248.1ºC

 SQ 22799名称

英文名 9-(2-phenylethyl)purin-6-amine
英文别名 更多

 SQ 22799物理化学性质

密度 1.34g/cm3
沸点 486.6ºC at 760 mmHg
分子式 C13H13N5
分子量 239.27600
闪点 248.1ºC
精确质量 239.11700
PSA 69.62000
LogP 2.23240
InChIKey MALQBKDZBRRFOM-UHFFFAOYSA-N
SMILES Nc1ncnc2c1ncn2CCc1ccccc1
折射率 1.713

 SQ 22799合成线路

~81%

SQ 22799结构式

SQ 22799

7051-86-7

文献:Lambertucci, Catia; Antonini, Ippolito; Buccioni, Michela; Dal Ben, Diego; Kachare, Dhuldeo D.; Volpini, Rosaria; Klotz, Karl-Norbert; Cristalli, Gloria Bioorganic and Medicinal Chemistry, 2009 , vol. 17, # 7 p. 2812 - 2822

~40%

SQ 22799结构式

SQ 22799

7051-86-7

文献:Borrmann, Thomas; Abdelrahman, Aliaa; Volpini, Rosaria; Lambertucci, Catia; Alksnis, Edgars; Gorzalka, Simone; Knospe, Melanie; Schiedel, Anke C.; Cristalli, Gloria; Mueller, Christa E. Journal of Medicinal Chemistry, 2009 , vol. 52, # 19 p. 5974 - 5989

~64%

SQ 22799结构式

SQ 22799

7051-86-7

文献:Petrov; Ozerov; Novikov; Pannecouque; Balzarini; De Clercq Chemistry of Heterocyclic Compounds, 2003 , vol. 39, # 9 p. 1218 - 1226

~79%

SQ 22799结构式

SQ 22799

7051-86-7

文献:Rad, Mohammad Navid Soltani; Khalafi-Nezhad, Ali; Behrouz, Somayeh; Asrari, Zeinab; Behrouz, Marzieh; Aminia, Zohreh Synthesis, 2009 , # 18 p. 3067 - 3076

~%

SQ 22799结构式

SQ 22799

7051-86-7

文献:Leese; Timmis Journal of the Chemical Society, 1958 , p. 4107,4108

~%

SQ 22799结构式

SQ 22799

7051-86-7

文献:Leese; Timmis Journal of the Chemical Society, 1958 , p. 4107,4108

 SQ 22799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: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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 SQ 22799英文别名

9-(2-phenylethyl)adenine
9-(2-Phenethyl)-adenin
9-Phenethyladenine
9-Phenylethyl-9H-adenine
9-(Phenylethyl)-adenin
9-Phenaethyl-9H-purin-6-ylamin
9-phenethylpurin-6-amine
9-phenethyl-9H-purin-6-ylamine
9-phenethyl-9H-purin-6-amine
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