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3-Phenylacetylamino-2,6-piperidinedione

更新时间:2026-06-30 19:13:25

3-Phenylacetylamino-2,6-piperidinedione结构式
3-Phenylacetylamino-2,6-piperidinedione结构式
品牌特惠专场
常用名 3-Phenylacetylamino-2,6-piperidinedione 英文名 (rac)-Antineoplaston A10
CAS号 77658-84-5 分子量 246.26
密度 1.27 g/cm3 沸点 571.2ºC at 760 mmHg
分子式 C13H14N2O3 熔点 N/A
MSDS N/A 闪点 N/A

 用途


(rac)-Antineoplaston A10 是(rac)-Antineoplaston A10 的消旋体。Antineoplaston A10是 Ras 的一个抑制剂,可用于治疗胶质瘤、淋巴瘤、星形细胞瘤和乳腺癌。

 3-Phenylacetylamino-2,6-piperidinedione名称

中文名 1,1'-二甲基-4,4'-联吡啶翁盐
英文名 Antineoplaston A10
中文别名 3-苯基乙酰氨基-2,6-哌啶二酮 | 抗瘤酮 A10
英文别名 更多

 3-Phenylacetylamino-2,6-piperidinedione生物活性

描述 (rac)-Antineoplaston A10 是(rac)-Antineoplaston A10 的消旋体。Antineoplaston A10是 Ras 的一个抑制剂,可用于治疗胶质瘤、淋巴瘤、星形细胞瘤和乳腺癌。
相关类别
参考文献

[1]. Qu XJ, et al. Induction of apoptosis in human hepatocellular carcinoma cells by synthetic antineoplaston A10. Anticancer Res. 2007 Jul-Aug;27(4B):2427-31.

 3-Phenylacetylamino-2,6-piperidinedione物理化学性质

密度 1.27 g/cm3
沸点 571.2ºC at 760 mmHg
分子式 C13H14N2O3
分子量 246.26
精确质量 246.10000
PSA 75.27000
LogP 0.87020
InChIKey OQGRFQCUGLKSAV-UHFFFAOYSA-N
SMILES O=C1CCC(NC(=O)Cc2ccccc2)C(=O)N1
外观性状 固体
折射率 1.584
储存条件 2-8°C,密封,干燥

 3-Phenylacetylamino-2,6-piperidinedione安全信息

危害码 (欧洲) Xi

 3-Phenylacetylamino-2,6-piperidinedione靶点实验

查看更多实验

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:Luminescence-based cell-based primary high throughput screening assay to identify act...
来源:The Scripps Research Institute Molecular Screening Center
靶标:TTR [Homo sapiens]
External Id:TTR_ACT_LUMI_1536_1X%ACT PRUN
实验名称:Counterscreen for inhibitors of 5-meCpG-binding domain protein 2 (MBD2): TRFRET-based...
来源:The Scripps Research Institute Molecular Screening Center
靶标:E3 ubiquitin-protein ligase UHRF1 isoform 1 [Homo sapiens]
External Id:UHRF1-CPGDNA_INH_TRFRET_1536_1X%INH CSRUN for MBD2-CPGDNA INH
实验名称:Luminescence-based cell-based primary high throughput screening assay for inhibitors ...
来源:The Scripps Research Institute Molecular Screening Center
靶标:nuclear receptor subfamily 0 group B member 1 [Homo sapiens]
External Id:DAX1-FULL_INH_LUMI_1536_1X%INH PRUN
实验名称:uHTS identification of small molecule modulators of Rev-erb Alpha.
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:SBCCG-A1016-RevErbaLBD-Primary-Assay
实验名称:HTS for Bacterial rRNA inhibitors Measured in Microorganism-Based System Using Plate ...
来源:Broad Institute
靶标:N/A
External Id:7056-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Fluorescence-based biochemical high throughput primary assay to identify inhibitors o...
来源:The Scripps Research Institute Molecular Screening Center
靶标:Phospholipase C, beta 3 (phosphatidylinositol-specific) [Homo sapiens]
External Id:PLCB3_INH_QFRET_1536_1X%INH 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:ADAM10 [Homo sapiens]
External Id:ADAM10_INH_QFRET_1536_1X%INH PRUN
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:Protein DAF-12, isoform a [Caenorhabditis elegans]
External Id:HGDAF12_AG_LUMI_1536_1X%ACT PRUN
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
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 3-Phenylacetylamino-2,6-piperidinedione英文别名

3-Phenylacetylamino-2,6-piperidinedione
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