Dehydrocrenatine

• 常用名: Dehydrocrenatine
• 英文名: 1-Vinyl-4-methoxy-β-carboline
• CAS号: 26585-13-7
• 分子量: 224.258
• 密度: 1.3±0.1 g/cm3
• 沸点: 461.2±40.0 °C at 760 mmHg
• 分子式: C₁₄H₁₂N₂O
• 熔点: N/A
• 闪点: 151.1±17.0 °C

Dehydrocrenatine用途

去氢克雷那定,一种β-卡宾生物碱,可从类蛇皮草中分离出来。脱氢克雷那定通过激活ERK和JNK诱导细胞凋亡。脱氢克雷那定抑制癌细胞的侵袭和迁移,它还抑制神经元兴奋性以发挥镇痛作用[1][2]。

Dehydrocrenatine名称

• 中文名: 1-乙烯基-4-甲氧基-9H-吡啶并[3,4-b]吲哚
• 英文名: 1-ethenyl-4-methoxy-9H-pyrido[3,4-b]indole

Dehydrocrenatine生物活性

• 描述: 去氢克雷那定,一种β-卡宾生物碱,可从类蛇皮草中分离出来。脱氢克雷那定通过激活ERK和JNK诱导细胞凋亡。脱氢克雷那定抑制癌细胞的侵袭和迁移,它还抑制神经元兴奋性以发挥镇痛作用[1][2]。
• 相关类别:
  信号通路 >> 细胞凋亡 >> 细胞凋亡
  信号通路 >> MAPK/ERK信号通路 >> ERK
  研究领域 >> 神经疾病
  信号通路 >> MAPK/ERK信号通路 >> JNK
  信号通路 >> 干细胞及 Wnt 通路 >> ERK
• 参考文献:

  [1]. Ho HY, et al. Apoptotic effects of dehydrocrenatidine via JNK and ERK pathway regulation in oral squamous cell carcinoma. Biomed Pharmacother. 2021 May;137:111362.

  [2]. Hsieh MC, et al. Dehydrocrenatidine extracted from Picrasma quassioidesinduces the apoptosis of nasopharyngeal carcinoma cells through the JNK and ERK signaling pathways. Oncol Rep. 2021 Aug;46(2):166.

Dehydrocrenatine物理化学性质

• 密度: 1.3±0.1 g/cm3
• 沸点: 461.2±40.0 °C at 760 mmHg
• 分子式: C₁₄H₁₂N₂O
• 分子量: 224.258
• 闪点: 151.1±17.0 °C
• 精确质量: 224.094955
• PSA: 37.91000
• LogP: 3.79
• InChIKey: HJVIUZHNRJYUTG-UHFFFAOYSA-N
• SMILES: C=Cc1ncc(OC)c2c1[nH]c1ccccc12
• 外观性状: 黄色粉末
• 蒸汽压: 0.0±1.1 mmHg at 25°C
• 折射率: 1.737
• 储存条件: 2-8℃，干燥，密闭

Dehydrocrenatine安全信息

• 危害码 (欧洲): Xi
• 海关编码: 2933990090

Dehydrocrenatine海关

• 海关编码: 2933990090
• 中文概述: 2933990090. 其他仅含氮杂原子的杂环化合物. 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, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期
• Summary: 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Dehydrocrenatine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：qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2 来源：NCGC 靶标：eyes absent homolog 2 isoform a [Homo sapiens] External Id：EYA2477

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：qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in... 来源：NCGC 靶标：TDP1 protein [Homo sapiens] External Id：TDP1100

实验名称：qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in... 来源：NCGC 靶标：TDP1 protein [Homo sapiens] External Id：TDP1101

实验名称：Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas... 来源：Broad Institute 靶标：N/A External Id：2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2

实验名称：Primary cell-based high-throughput screening for identification of compounds that all... 来源：Johns Hopkins Ion Channel Center 靶标：MAS-related GPR member X1 [Homo sapiens] External Id：JHICC_MrgX1_AlloAgonist_Primary

实验名称：Primary cell-based high-throughput screening for identification of compounds that ant... 来源：Johns Hopkins Ion Channel Center 靶标：MAS-related GPR member X1 [Homo sapiens] External Id：JHICC_MrgX1_Antagonist_Primary

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Dehydrocrenatine英文别名

• 1-Vinyl-4-methoxy-β-carboline
• dehydrocrenatine
• HMS2271N07
• TOB-10
• Dehydrocrenation
• 4-Methoxy-1-vinyl-9H-β-carboline