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Anisomycin/茴香霉素 {[allProObj[0].p_purity_real_show]}

货号:A646979 同义名: Flagecidin; Wuningmeisu C

Anisomycin是一种天然抗生素,既能作为应激活化蛋白激酶(JNK/SAPK 和 p38 MAPK)的强效激活剂,也能通过阻断翻译抑制蛋白质合成。

Anisomycin/茴香霉素 化学结构 CAS号:22862-76-6
Anisomycin/茴香霉素 化学结构
CAS号:22862-76-6
Anisomycin/茴香霉素 3D分子结构
CAS号:22862-76-6
Anisomycin/茴香霉素 化学结构 CAS号:22862-76-6
Anisomycin/茴香霉素 3D分子结构 CAS号:22862-76-6
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Anisomycin/茴香霉素 纯度/质量文件 产品仅供科研

货号:A646979 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 JNK JNK1 JNK2 JNK3 其他靶点 纯度
Mulberroside A 99%+
Loureirin B Calcium Channel,Potassium Channel 99%+
Ginsenoside Re NF-κB 98%
(+)-(3R,8S)-Falcarindiol ERK,STAT 99%+
trans-Zeatin ERK,p38 MAPK 95+%
Urolithin B ERK,NF-κB 95%
Cucurbitacin IIb NF-κB 99%
Astragaloside IV Akt,mTOR,NF-κB 98%
m-PEG25-NHS ester 95%
NDMC101 99%+
DB07268 ++++

JNK1, IC50: 9 nM

99%+
SP600125 +

MKK4, IC50: 0.4 μM

+++

JNK1, IC50: 40 nM

+++

JNK2, IC50: 40 nM

+++

JNK3, IC50: 90 nM

98%
JNK-IN-7 ++++

JNK1, IC50: 1.5 nM

++++

JNK2, IC50: 2 nM

++++

JNK3, IC50: 0.7 nM

99%
JNK-IN-8 ++++

JNK1, IC50: 4.7 nM

+++

JNK2, IC50: 18.7 nM

++++

JNK3, IC50: 1 nM

99%+
3,3',5-Triiodo-L-thyronine ++

JNK1, Kd: 240 nM

++

JNK2, Kd: 290 nM

+++

JNK3, Kd: 66 nM

98%
IQ-1S free acid +

JNK1, IC50: 390 nM

++

JNK2, IC50: 360 nM

+++

JNK3, IC50: 87 nM

99%
BI-78D3 ++

JNK, IC50: 280 nM

++

JNK, IC50: 280 nM

++

JNK, IC50: 280 nM

++

JNK, IC50: 280 nM

99%+
Bentamapimod +++

JNK1, IC50: 80 nM

+++

JNK2, IC50: 90 nM

++

JNK3, IC50: 230 nM

98%
Resveratrol +

JNK1, IC50: 50 μM

98%
Indirubin-3′-oxime 99%+
SU3327 +

JNK, IC50: 0.7 μM

+

JNK, IC50: 0.7 μM

+

JNK, IC50: 0.7 μM

+

JNK, IC50: 0.7 μM

99%+
JNK Inhibitor VIII ++++

JNK1, Ki: 2 nM

JNK1, IC50: 45 nM

++++

JNK2, IC50: 160 nM

JNK2, Ki: 4 nM

+++

JNK3, Ki: 52 nM

98%
Doramapimod 99%+
RPI-1 99%
TCS JNK 5a ++

JNK2, pIC50: 6.5

++

JNK3, pIC50: 6.7

98%
SP 600125, negative control +

JNK2, IC50: 18 μM

+

JNK3, IC50: 24 μM

97%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Anisomycin/茴香霉素 生物活性

描述 c-Jun N-terminal kinase (JNK) is a member of the mitogen-activated protein kinases (MAPK) family. Anisomycin is an activator of both JNK and p38[3]. The incubation of HL-1 myocytes with 50ng/mL anisomycin for 24 h markedly increased the protein level of CaMKIIδ by ∼60% relative to the control group. The c-jun phosphorylation in total cell lysates and nuclear extracts was also increased by the treatment of 50ng/mL HL-1 myocytes with anisomycin for 24 h[4]. The intraperitoneal injection of wild-type, TNFR p55/p75-/-, and Nox2-/- mice with 0.1mg/kg anisomycin resulted in the activation of p38, an increase in the production of TNF-α and Nox2, and the phosphorylation of Nox2 compared with the control group[5].

Anisomycin/茴香霉素 细胞实验

Cell Line
Concentration Treated Time Description References
HeLa cells 50μM 20 minutes To investigate the role of p38 in EphA2 Ser-897 phosphorylation, results showed anisomycin induced EphA2 phosphorylation via the p38 pathway. J Biol Chem. 2023 May;299(5):104699
AML12 cells 10 μM 2 h Activated JNK signaling pathway, increased TG accumulation, and partially deprived the therapeutic role of Tamoxifen Signal Transduct Target Ther. 2023 Mar 3;8(1):94.
Cell monolayers derived from pig jejunum organoids 1 µM 24 h Anisomycin disrupted the epithelial barrier integrity but failed to induce a significant increase in paracellular permeability. Butyrate (BUT) prevented the disruption of epithelial barrier integrity induced by ANI. Gut Microbes. 2024 Jan-Dec;16(1):2430424.
SK-MES-1 0.5 µM 24 h Anisomycin pre-treatment activated p38 and HSP27 and induced apoptosis. Int J Biol Sci. 2020 Sep 2;16(15):2883-2894.
NCI-H520 0.5 µM 24 h Anisomycin pre-treatment activated p38 and HSP27 and induced apoptosis. Int J Biol Sci. 2020 Sep 2;16(15):2883-2894.
murine neonatal cardiomyocytes 25 ng/mL 1 hour Pretreatment with anisomycin partially abolished the protective effects of NG-R1 against H/R-induced cardiomyocyte apoptosis. Acta Pharmacol Sin. 2023 Jul;44(7):1366-1379.

Anisomycin/茴香霉素 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
Mice MCD diet-induced NASH model Intraperitoneal injection 50 mg/kg 5 consecutive days Activated JNK signaling pathway and partially abolished the therapeutic effect of Tamoxifen on hepatic steatosis Signal Transduct Target Ther. 2023 Mar 3;8(1):94.
Rats Fear memory model Bilateral infusion into the basolateral amygdala 125 mg/ml Single administration To evaluate the effect of Anisomycin on fear memory reconsolidation blockade, results showed that Anisomycin effectively blocked memory reconsolidation in rats trained with 1P, but had no effect in rats trained with 10P. Elife. 2020 May 18;9:e57010
Mice Depressive-like behavior model Intraperitoneal injection 100 mg/kg Single injection, behavioral tests performed 3 hours later To evaluate the effect of Anisomycin on depressive-like behavior in mice, results showed that Anisomycin increased immobility time in TST and latency to feed in NSF. Transl Psychiatry. 2024 Oct 1;14(1):397

Anisomycin/茴香霉素 参考文献

[1]Dubue JD, McKinney TL, et al. Intrahippocampal Anisomycin Impairs Spatial Performance on the Morris Water Maze. J Neurosci. 2015 Aug 5;35(31):11118-24.

[2]Dubue JD, McKinney TL, et al. Intrahippocampal Anisomycin Impairs Spatial Performance on the Morris Water Maze. J Neurosci. 2015 Aug 5;35(31):11118-24.

[3]Nikaido M, Otani T, Kitagawa N, et al. Anisomycin, a JNK and p38 activator, suppresses cell-cell junction formation in 2D cultures of K38 mouse keratinocyte cells and reduces claudin-7 expression, with an increase of paracellular permeability in 3D cultures. Histochem Cell Biol. 2019;151(5):369-384. doi:10.1007/s00418-018-1736-z

[4]Gao X, Wu X, Yan J, et al. Transcriptional regulation of stress kinase JNK2 in pro-arrhythmic CaMKIIδ expression in the aged atrium. Cardiovasc Res. 2018;114(5):737-746. doi:10.1093/cvr/cvy011

[5]Zhao TC, Zhang L, Liu JT, Guo TL. Disruption of Nox2 and TNFRp55/p75 eliminates cardioprotection induced by anisomycin. Am J Physiol Heart Circ Physiol. 2012;303(10):H1263-H1272. doi:10.1152/ajpheart.00306.2012

Anisomycin/茴香霉素 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.77mL

0.75mL

0.38mL

18.85mL

3.77mL

1.88mL

37.69mL

7.54mL

3.77mL

Anisomycin/茴香霉素 技术信息

CAS号22862-76-6
分子式C14H19NO4
分子量 265.31
SMILES Code O[C@@H]1[C@@H](OC(C)=O)[C@@H](CC2=CC=C(OC)C=C2)NC1
MDL No. MFCD00077650
别名 Flagecidin; Wuningmeisu C; AI3-50846; NSC 76712
运输蓝冰
InChI Key YKJYKKNCCRKFSL-RDBSUJKOSA-N
Pubchem ID 253602
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Inert atmosphere, store in freezer, under -20°C

溶解方案

DMSO: 50 mg/mL(188.46 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 4 mg/mL(15.08 mM),配合低频超声,并水浴加热至45℃助溶

配制的工作液建议现用现配,短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案 一
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