计算溶液所需的质量、体积或浓度。
活性类型 | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
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N137206-25mg |
25mg |
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N137206-100mg |
100mg |
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N137206-500mg |
500mg |
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N137206-1g |
1g |
现货 ![]() |
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别名 | N-甲基-4-苯基吡啶鎓碘化物 |
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英文别名 | HY-W008719 | MPP+ iodide | FT-0672164 | Q27284640 | SCHEMBL2203363 | MPP iodide | CS-W009435 | UNII-N708D004VE | N-Methyl-4-phenylpyridiniumIodide | D95477 | MPP+ (iodide) | Cyperquat iodide | N-Methyl-4-phenylpyridinium iodide | Pyridinium, 1-methyl-4-ph |
规格或纯度 | ≥98% |
英文名称 | MPP+ iodide |
生化机理 | MPP+ 碘化物是多巴胺能神经毒素 MPTP 的活性代谢物。活性 MPTP 代谢物。干扰氧化磷酸化,诱导线粒体功能障碍。消耗细胞 ATP。在体内显示帕金森效应。 |
应用 | An active metabolite of the dopaminergic neurotoxin MPTP. |
运输条件 | 常规运输 |
备注 | Unstable; make up solutions fresh and use immediately. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
产品介绍 |
1-甲基-4-苯基吡啶(MPP+)可通过抑制纹状体突触体中的线粒体氧化还原功能而诱发神经毒性。它是一种潜在的神经毒素并可在动物模型中诱导帕金森症。它可通过在小脑颗粒神经元和神经母细胞瘤细胞中产生活性氧来介导细胞凋亡。MPP+可调控多巴胺的分布。它可通过激活神经元一氧化氮合酶(nNOS)而引起神经毒性,产生过量的一氧化氮。 产品应用: MPP+碘化物已用于: 在斑马鱼胚胎中诱导氧化应激 抑制星形胶质细胞线粒体中谷氨酸的摄入 在小胶质细胞(BV2)中使用MTT(3(4,5-二甲基噻唑)-2-基-2,5-二苯基四唑溴化物)检测细胞活力 Product Describtion: Product Application: MPP+ iodide has been used: to induce oxidative stress in zebrafish embryos for the inhibition of glutamate uptake in mitochondria of astrocytes in testing cell viability using MTT (3 (4,5-dimethylthiazol)-2-yl-2,5-diphenyltetrazolium bromide) in microglia (BV2) cells |
活性类型 | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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活性类型 | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
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PubChem SID | 504765742 |
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分子类型 | 小分子 |
IUPAC Name | 1-methyl-4-phenylpyridin-1-ium;iodide |
INCHI | InChI=1S/C12H12N.HI/c1-13-9-7-12(8-10-13)11-5-3-2-4-6-11;/h2-10H,1H3;1H/q+1;/p-1 |
InChi Key | RFDFRDXIIKROAI-UHFFFAOYSA-M |
Canonical SMILES | C[N+]1=CC=C(C=C1)C2=CC=CC=C2.[I-] |
Isomeric SMILES | C[N+]1=CC=C(C=C1)C2=CC=CC=C2.[I-] |
WGK Germany | 3 |
RTECS | UU6580000 |
PubChem CID | 10924457 |
UN Number | 2811 |
Packing Group | II |
分子量 | 297.13 |
溶解性 | H2O: >10 mg/mL, soluble |
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敏感性 | 对光线和湿度敏感 |
分子量 | 297.130 g/mol |
XLogP3 | |
氢键供体数Hydrogen Bond Donor Count | 0 |
氢键受体数Hydrogen Bond Acceptor Count | 1 |
可旋转键计数Rotatable Bond Count | 1 |
精确质量Exact Mass | 297.001 Da |
单同位素质量Monoisotopic Mass | 297.001 Da |
拓扑极表面积Topological Polar Surface Area | 3.900 Ų |
重原子数Heavy Atom Count | 14 |
形式电荷Formal Charge | 0 |
复杂度Complexity | 141.000 |
同位素原子数Isotope Atom Count | 0 |
定义的原子立体中心计数Defined Atom Stereocenter Count | 0 |
未定义的原子立体中心计数Undefined Atom Stereocenter Count | 0 |
定义的键立体中心计数Defined Bond Stereocenter Count | 0 |
未定义的键立体中心计数Undefined Bond Stereocenter Count | 0 |
所有立体化学键的总数The total count of all stereochemical bonds | 0 |
共价键合单元计数Covalently-Bonded Unit Count | 2 |
象形图 | GHS06, GHS07 |
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信号词 | Danger |
危险声明 |
H315: 引起皮肤刺激 H319: 引起严重眼睛刺激 H335: 可能引起呼吸道刺激 H301: 吞咽会中毒 H311: 皮肤接触有毒 H331: 吸入会中毒 |
预防措施声明 |
P261: 避免吸入灰尘/烟雾/气体/雾/蒸汽/喷雾 P305+P351+P338: 如进入眼睛:用水小心冲洗几分钟。如戴隐形眼镜并可方便地取出,取出隐形眼镜。继续冲洗。 P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。 P302+P352: 如皮肤沾染:用水充分清洗。 P321: 特殊处理(请参阅此标签上的...)。 P405: 密闭存放 P501: 将内容物/容器处理到。。。 P264: 处理后要彻底洗手。 P271: 仅在室外或通风良好的地方使用。 P270: 使用本产品时,请勿进食、饮水或吸烟。 P304+P340: 如误吸入:将人转移到空气新鲜处,保持呼吸舒适体位。 P403+P233: 存放在通风良好的地方。保持容器密闭。 P362+P364: 脱掉沾污的衣服,清洗后方可重新使用。 P330: 漱口 P361+P364: 立即脱掉所有沾染的衣服,清洗后方可重新使用。 P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。 P301+P316: 如果吞咽:立即寻求紧急医疗救助。 P337+P317: 如果眼睛刺激持续:寻求医疗帮助。 P332+P317: 如果出现皮肤刺激:请寻求医疗帮助。 P316: 立即寻求紧急医疗救助。 P319: 如果你感到不适,请寻求医疗帮助。 |
WGK Germany | 3 |
RTECS | UU6580000 |
Class | 6.1 |
个人防护装备 | Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges |
Appearance(N137206) | White to beige powder or soild |
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Proton NMR spectrum | Conforms to Structure |
Purity(Titration by AgNO3) | 97.5-102.5(%) |
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批号(Lot Number) | 证书类型 | 日期 | 货号 |
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分析证书 | 24-09-18 | N137206 |
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分析证书 | 24-09-18 | N137206 |
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分析证书 | 24-09-18 | N137206 |
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分析证书 | 24-09-18 | N137206 |
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分析证书 | 24-09-18 | N137206 |
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分析证书 | 24-01-04 | N137206 |
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分析证书 | 24-01-04 | N137206 |
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分析证书 | 22-09-29 | N137206 |
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分析证书 | 22-09-29 | N137206 |
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分析证书 | 22-09-29 | N137206 |
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分析证书 | 22-09-29 | N137206 |
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分析证书 | 22-09-29 | N137206 |
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分析证书 | 22-01-05 | N137206 |
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分析证书 | 22-01-05 | N137206 |
1. Chao Guo, Junrong Zhu, Jingwen Wang, Jialin Duan, Shanbo Ma, Ying Yin, Wei Quan, Wei Zhang, Yue Guan, Yi Ding, Aidong Wen, Yingdong Zhang. (2019) Neuroprotective effects of protocatechuic aldehyde through PLK2/p-GSK3β/Nrf2 signaling pathway in both in vivo and in vitro models of Parkinson's disease. Aging-US, 11 (21): ( 9424–9441). [PMID:31697645] [10.18632/aging.102394] |
2. Yun Yu, Xiu-Yuan Lang, Xi-Xi Li, Run-Ze Gu, Qing-Shan Liu, Rongfeng Lan, Xiao-Yan Qin. (2019) 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside attenuates MPP+/MPTP-induced neurotoxicity in vitro and in vivo by restoring the BDNF-TrkB and FGF2-Akt signaling axis and inhibition of apoptosis. Food & Function, 10 (9): (6009-6019). [PMID:31482900] [10.1039/C9FO01309A] |
1. Zhou P et al.. (2020) A Three-Way Combinatorial CRISPR Screen for Analyzing Interactions among Druggable Targets.. Cell Rep, 32 (6): (108020). [PMID:32783942] |
2. Liu W et al.. (2018) MiR-19b alleviates MPP+-induced neuronal cytotoxicity via targeting the HAPLN4/MAPK pathway in SH-SY5Y cells.. RSC Adv, 8 (19): (10706-10714). [PMID:35540477] |
3. Chao Guo, Junrong Zhu, Jingwen Wang, Jialin Duan, Shanbo Ma, Ying Yin, Wei Quan, Wei Zhang, Yue Guan, Yi Ding, Aidong Wen, Yingdong Zhang. (2019) Neuroprotective effects of protocatechuic aldehyde through PLK2/p-GSK3β/Nrf2 signaling pathway in both in vivo and in vitro models of Parkinson's disease. Aging-US, 11 (21): ( 9424–9441). [PMID:31697645] [10.18632/aging.102394] |
4. Yun Yu, Xiu-Yuan Lang, Xi-Xi Li, Run-Ze Gu, Qing-Shan Liu, Rongfeng Lan, Xiao-Yan Qin. (2019) 2,3,5,4′-Tetrahydroxystilbene-2-O-β-D-glucoside attenuates MPP+/MPTP-induced neurotoxicity in vitro and in vivo by restoring the BDNF-TrkB and FGF2-Akt signaling axis and inhibition of apoptosis. Food & Function, 10 (9): (6009-6019). [PMID:31482900] [10.1039/C9FO01309A] |