| Company Name: |
Nanjing Shizhou Biology Technology Co.,Ltd
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| Tel: |
025-85560043 13675144456 |
| Email: |
sean.lv@synzest.com |
| Products Intro: |
Product Name:1H-Indole-3-carbaldehyde(3,7-dimethyl-2-quinolinyl)hydrazone CAS:364361-68-2 Purity:95%HPLC Package:500mg;1g;5g;10g
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| Company Name: |
Cayman Chemical Company
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| Tel: |
800-364-9897 |
| Email: |
sales@caymanchem.com |
| Products Intro: |
Product Name:Endosidin 5 CAS:364361-68-2
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| | 1H-Indole-3-carboxaldehyde, 2-(3,7-dimethyl-2-quinolinyl)hydrazone Basic information |
| | 1H-Indole-3-carboxaldehyde, 2-(3,7-dimethyl-2-quinolinyl)hydrazone Chemical Properties |
| Boiling point | 559.8±50.0 °C(Predicted) | | density | 1.22±0.1 g/cm3(Predicted) | | solubility | Acetonitrile: Slightly soluble: 0.1-1 mg/ml DMSO: Sparingly soluble: 1-10 mg/ml | | pka | 10.97±0.70(Predicted) |
| | 1H-Indole-3-carboxaldehyde, 2-(3,7-dimethyl-2-quinolinyl)hydrazone Usage And Synthesis |
| Uses | Endosidine 5 (ES5) inhibits EPS (extracellular polymeric substance) secretion and cell wall expansion. Endosidine 5 alters secretion of ECM (extracellular matrix) material in Penium margaritaceum by affecting the Golgi apparatus. Endosidine 5 interferes with recycling endosomes through Annexin A6, thereby promoting the release and expression of mRNA into the cytoplasm[1][2]. | | References | [1] LoRicco JG, et al. Endosidin 5 disruption of the Golgi apparatus and extracellular matrix secretion in the unicellular charophyte Penium margaritaceum. Ann Bot. 2023 Jul 10;131(6):967-983. DOI:10.1093/aob/mcad054 [2] Shin J, et al. Targeting Recycling Endosomes to Potentiate mRNA Lipid Nanoparticles. Nano Lett. 2024 May 1;24(17):5104-5109. DOI:10.1021/acs.nanolett.3c04415 [3] GEORGIA DRAKAKAKI. Clusters of bioactive compounds target dynamic endomembrane networks in vivo.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2011, 108 43: 17850-17855. DOI: 10.1073/pnas.1108581108 [4] SABIN LLONA-MINGUEZ . Diverse heterocyclic scaffolds as dCTP pyrophosphatase 1 inhibitors. Part 1: Triazoles, triazolopyrimidines, triazinoindoles, quinoline hydrazones and arylpiperazines[J]. Bioorganic & Medicinal Chemistry Letters, 2017, 27 16: Pages 3897-3904. DOI: 10.1016/j.bmcl.2017.06.038 |
| | 1H-Indole-3-carboxaldehyde, 2-(3,7-dimethyl-2-quinolinyl)hydrazone Preparation Products And Raw materials |
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