恩镰孢菌素B

• 常用名: 恩镰孢菌素B
• 英文名: Enniatin B
• CAS号: 917-13-5
• 分子量: 639.820
• 密度: 1.0±0.1 g/cm3
• 沸点: 827.0±65.0 °C at 760 mmHg
• 分子式: C₃₃H₅₇N₃O₉
• 熔点: N/A
• 闪点: 454.0±34.3 °C
• 符号: GHS06
• 信号词: Danger

恩镰孢菌素B用途

Enniatin B 是一种镰刀菌毒素。在大鼠肝微粒体酶实验中,Enniatin B 抑制酰基辅酶 A：胆固醇酰基转移酶 (ACAT) 活性,IC50 为 113 μM。Enniatins B 可降低 ERK (p44/p42) 活化。

恩镰孢菌素B名称

• 中文名: 恩镰孢菌素 B
• 英文名: enniatin B

恩镰孢菌素B生物活性

• 描述: Enniatin B 是一种镰刀菌毒素。在大鼠肝微粒体酶实验中,Enniatin B 抑制酰基辅酶 A：胆固醇酰基转移酶 (ACAT) 活性,IC50 为 113 μM。Enniatins B 可降低 ERK (p44/p42) 活化。
• 相关类别:
  研究领域 >> 癌症
  研究领域 >> 心血管疾病
  研究领域 >> 感染
  信号通路 >> MAPK/ERK信号通路 >> ERK
  信号通路 >> 代谢酶/蛋白酶 >> 酰基转移酶
  信号通路 >> 干细胞及 Wnt 通路 >> ERK
• 靶点实验:

  ACAT

  ERK

• 参考文献:

  [1]. Tomoda H, et al. Inhibition of acyl-CoA: cholesterol acyltransferase activity by cyclodepsipeptide antibiotics. J Antibiot (Tokyo). 1992 Oct;45(10):1626-32.

  [2]. Wätjen W, et al. Enniatins A1, B and B1 from an endophytic strain of Fusarium tricinctum induce apoptotic cell death in H4IIE hepatoma cells accompanied by inhibition of ERK phosphorylation. Mol Nutr Food Res. 2009 Apr;53(4):431-40.

恩镰孢菌素B物理化学性质

• 密度: 1.0±0.1 g/cm3
• 沸点: 827.0±65.0 °C at 760 mmHg
• 分子式: C₃₃H₅₇N₃O₉
• 分子量: 639.820
• 闪点: 454.0±34.3 °C
• 精确质量: 639.409485
• PSA: 139.83000
• LogP: 3.05
• InChIKey: MIZMDSVSLSIMSC-VYLWARHZSA-N
• SMILES: CC(C)C1OC(=O)C(C(C)C)N(C)C(=O)C(C(C)C)OC(=O)C(C(C)C)N(C)C(=O)C(C(C)C)OC(=O)C(C(C)C)N(C)C1=O
• 外观性状: 粉末
• 蒸汽压: 0.0±3.0 mmHg at 25°C
• 折射率: 1.460
• 储存条件: ?20°C
• 水溶解性: DMSO: soluble10mg/mL

恩镰孢菌素B安全信息

• 符号: GHS06
• 信号词: Danger
• 危害声明: H301-H311-H331
• 警示性声明: P261-P280-P301 + P310-P311
• 危害码 (欧洲): T
• 风险声明 (欧洲): 23/24/25
• 安全声明 (欧洲): 45
• 危险品运输编码: UN 2811
• 包装等级: I
• 危险类别: 6.1(a)

恩镰孢菌素B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：USP8 deubiquitinase inhibition: Primary qHTS 来源：24642 靶标：ubiquitin specific peptidase 8 External Id：USP8 FAST DUB HTS Primary

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：USP17 deubiquitinase inhibition: Primary qHTS 来源：24642 靶标：ubiquitin specific peptidase 17 like family member 5 External Id：USP17 FAST DUB HTS Primary

实验名称：USP7 deubiquitinase inhibition: Primary qHTS 来源：24642 靶标：ubiquitin specific peptidase 7 External Id：USP7 FAST DUB HTS Primary

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：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：Counterscreen for inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1): Lum... 来源：The Scripps Research Institute Molecular Screening Center 靶标：transactivating tegument protein VP16 [Human herpesvirus 1] External Id：VP16_INH_LUMI_1536_3X%INH CSRUN for SRC1

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恩镰孢菌素B英文别名

• enniatin b
• (3S,6R,9S,12R,15S,18R)-3,6,9,12,15,18-Hexaisopropyl-4,10,16-trimethyl-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone