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4-甲基-N1-(3-苯丙基)-1,2-苯二胺

NFκB转录活性抑制剂
规格或纯度: ≥98% (HPLC)
有货

库存信息

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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
M134534-25mg
25mg 现货 Stock Image
M134534-100mg
100mg 现货 Stock Image
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含氮化合物 非杂环砌块

基本描述

别名 4-甲基-N1-(3-苯丙基)-1,2-苯二胺
英文别名 JSH-23|749886-87-1|4-Methyl-N1-(3-phenylpropyl)benzene-1,2-diamine|JSH 23|4-Methyl-1-N-(3-phenylpropyl)benzene-1,2-diamine|JSH23|NFKB-activation-inhibitor-II|4-Methyl-N~1~-(3-phenylpropyl)benzene-1,2-diamine|4-Methyl-N1-(3-phenylpropyl)-1,2-phenylenediami
规格或纯度 ≥98% (HPLC)
英文名称 JSH-23
生化机理 NF-κB Activation Inhibitor II, JSH-23 is an inhibitor of NF-κB transcriptional activity (IC50 = 7.1 μM). JSH-23 is described to interfere with lipopolysaccharide-induced nuclear translocation of the factor, inhibiting the mechanism of transcription, without affecting the process of IκB degradation.NFκB transcriptional activity inhibitor (IC 50 = 7.1 μM). Inhibits LPS-induced nuclear translocation of NFκB. Does not affect IκB degradation. Potentiates the antitumor effects of cisplatin . Shows neuroprotective effects in vivo.
储存温度 -20°C储存
运输条件 超低温冰袋运输
备注 有毒,请参阅SDS以获取更多信息。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。
产品介绍

JSH-23是一种NF-κB转录活性抑制剂,在RAW 264.7细胞系中IC50为7.1 μM。

JSH-23 is an inhibitor of NF-κB transcriptional activity with IC50 of 7.1 μM in RAW 264.7 cell line.

名称和标识符

IUPAC Name 4-methyl-1-N-(3-phenylpropyl)benzene-1,2-diamine
INCHI InChI=1S/C16H20N2/c1-13-9-10-16(15(17)12-13)18-11-5-8-14-6-3-2-4-7-14/h2-4,6-7,9-10,12,18H,5,8,11,17H2,1H3
InChi Key YMFNPBSZFWXMAD-UHFFFAOYSA-N
Canonical SMILES CC1=CC(=C(C=C1)NCCCC2=CC=CC=C2)N
Isomeric SMILES CC1=CC(=C(C=C1)NCCCC2=CC=CC=C2)N
WGK Germany 3
PubChem CID 16760588
分子量 240.34
Reaxy-Rn 24398255

化学和物理性质

溶解性 Soluble in DMSO (>10 mg/mL)
敏感性 对光敏感、对热敏感
熔点 103 °C

安全和危险性(GHS)

象形图
ghs09

Environmental Hazard

ghs05

Corrosive

ghs07

Harmful

信号词 Danger
危险声明 H302: Harmful if swallowed
H318: Causes serious eye damage
H400: Very toxic to aquatic life
预防措施声明 P273,P280,P501,P264,P270,P391,P330,P264+P265,P301+P317,P305+P354+P338,P317
WGK Germany 3
Reaxy-Rn 24398255

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参考文献

1. Cursano S et al..  (2020)  A CRHR1 antagonist prevents synaptic loss and memory deficits in a trauma-induced delirium-like syndrome..  Mol Psychiatry,    ():  ().  [PMID:32051550]
2. Lai J et al..  (2019)  Activation of NFKB-JMJD3 signaling promotes bladder fibrosis via boosting bladder smooth muscle cell proliferation and collagen accumulation..  Biochim Biophys Acta Mol Basis Dis,  1865  (9):  (2403-2410).  [PMID:31102789]
3. Barbero G et al..  (2019)  An Autocrine Wnt5a Loop Promotes NF-?B Pathway Activation and Cytokine/Chemokine Secretion in Melanoma..  Cells,  (9):  ().  [PMID:31510045]
4. Kubota M et al..  (2019)  Autophagy deficiency exacerbates colitis through excessive oxidative stress and MAPK signaling pathway activation..  PLoS One,  14  (11):  (e0225066).  [PMID:31703091]
5. Battaglia CR et al..  (2020)  Corticotropin-releasing hormone (CRH) alters mitochondrial morphology and function by activating the NF-kB-DRP1 axis in hippocampal neurons..  Cell Death Dis,  11  (11):  (1004).  [PMID:33230105]
6. Smaldone G et al..  (2021)  KCTD15 deregulation is associated with alterations of the NF-?B signaling in both pathological and physiological model systems..  Sci Rep,  11  ():  (18237).  [PMID:34521919]
7. Mantsounga CS et al..  (2022)  Macrophage IL-1ß promotes arteriogenesis by autocrine STAT3- and NF-?B-mediated transcription of pro-angiogenic VEGF-A..  Cell Rep,  38  (5):  (110309).  [PMID:35108537]
8. Nadeem L et al..  (2021)  Pro-inflammatory signals induce 20a-HSD expression in myometrial cells: A key mechanism for local progesterone withdrawal..  J Cell Mol Med,  25  (14):  (6773-6785).  [PMID:34114342]