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2-(2,6-dimethylpyran-4-ylidene)indene-1,3-dione

更新时间:2025-10-06 16:49:20

2-(2,6-dimethylpyran-4-ylidene)indene-1,3-dione结构式
2-(2,6-dimethylpyran-4-ylidene)indene-1,3-dione结构式
品牌特惠专场
常用名 2-(2,6-dimethylpyran-4-ylidene)indene-1,3-dione 英文名 2-(2,6-dimethylpyran-4-ylidene)indene-1,3-dione
CAS号 71107-31-8 分子量 252.26500
密度 1.296g/cm3 沸点 364.7ºC at 760 mmHg
分子式 C16H12O3 熔点 N/A
MSDS N/A 闪点 160.8ºC

 名称

英文名 2-(2,6-dimethylpyran-4-ylidene)indene-1,3-dione
英文别名 更多

 物理化学性质

密度 1.296g/cm3
沸点 364.7ºC at 760 mmHg
分子式 C16H12O3
分子量 252.26500
闪点 160.8ºC
精确质量 252.07900
PSA 43.37000
LogP 3.20000
InChIKey DPCHHWLRXZZPAI-UHFFFAOYSA-N
SMILES CC1=CC(=C2C(=O)c3ccccc3C2=O)C=C(C)O1
折射率 1.634

 合成线路

~69%

2-(2,6-dimethylpyran-4-ylidene)indene-1,3-dione结构式

2-(2,6-dimethyl...

71107-31-8

文献:Clairc; Le Baut; Ploquin; et al. European Journal of Medicinal Chemistry, 1981 , vol. 16, # 6 p. 529 - 532

 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:Confirmed allosteric antagonists of M1 Muscarinic receptor
来源:1043
靶标:Muscarinic acetylcholine receptor M1
External Id:SAID_435034
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 英文别名

<4-(2,6-Dimethyl-pyrylo)>-<2-indandion-(1,3)>-apomerocyanin
HMS1652D13
2-(2,6-dimethyl-pyran-4-ylidene)-indan-1,3-dione
(dimethyl-2,6 4 H-pyrannylidene-4 yl)-2 indanedione-1,3
HMS2545N17
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