Securinine
CAS No. 5610-40-2
Securinine( (-)-Securinine )
Catalog No. M21463 CAS No. 5610-40-2
(-)-Securinine is plant-derived alkaloid and also a GABAA receptor antagonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 45 | In Stock |
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| 10MG | 75 | In Stock |
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| 25MG | 156 | In Stock |
|
| 50MG | 229 | In Stock |
|
| 100MG | 343 | In Stock |
|
| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameSecurinine
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NoteResearch use only, not for human use.
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Brief Description(-)-Securinine is plant-derived alkaloid and also a GABAA receptor antagonist.
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Description(-)-Securinine is plant-derived alkaloid and also a GABAA receptor antagonist.(In Vitro):(-)-Securinine is a major plant-derived alkaloid and also a GABAA receptor antagonist. (-)-Securinine is significantly potent on HeLa cells growth inhibition with IC50 values of 7.02±0.52 μg/mL (32.3 μM). (-)-Securinine induces apoptosis in a dose-dependent manner in the tested cells, increases the percentage of ROS positive cells and depolarized cells as well as stimulates the activity of ERK1/2, caspase-9 and -3/7. (-)-Securinine also induces cell cycle arrest in S phase. Real-time PCR analysis shows high expression of tumor necrosis factor receptor superfamily (TNFRSF) genes in the cells stimulated with (-)-Securinine.(In Vivo):In this tumor model, tumor growth is significantly impaired with (-)-Securinine treatment indicating that (-)-Securinine has potential as an Acute Myeloid Leukemia (AML) therapeutic. (-)-Securinine treated mice (n=5 mice, bilateral tumors), exhibit an average of more than 75% smaller tumors than vehicle treated mice at the end of the study period.
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In Vitro(-)-Securinine is a major plant-derived alkaloid and also a GABAA receptor antagonist. (-)-Securinine is significantly potent on HeLa cells growth inhibition with IC50 values of 7.02±0.52 μg/mL (32.3 μM). (-)-Securinine induces apoptosis in a dose-dependent manner in the tested cells, increases the percentage of ROS positive cells and depolarized cells as well as stimulates the activity of ERK1/2, caspase-9 and -3/7. (-)-Securinine also induces cell cycle arrest in S phase. Real-time PCR analysis shows high expression of tumor necrosis factor receptor superfamily(TNFRSF) genes in the cells stimulated with (-)-Securinine.
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In VivoIn this tumor model, tumor growth is significantly impaired with (-)-Securinine treatment indicating that (-)-Securinine has potential as an Acute Myeloid Leukemia (AML) therapeutic. (-)-Securinine treated mice (n=5 mice, bilateral tumors), exhibit an average of more than 75% smaller tumors than vehicle treated mice at the end of the study period.
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Synonyms(-)-Securinine
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PathwayOthers
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TargetOther Targets
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RecptorGABAA
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Research Area——
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Indication——
Chemical Information
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CAS Number5610-40-2
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Formula Weight217.26
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Molecular FormulaC13H15NO2
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Purity>98% (HPLC)
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SolubilityDMSO:2 mg/mL (9.21 mM)
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SMILESO=C1O[C@](C2)([C@@H](CCCC3)N3[C@@H]2C=C2)C2=C1
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Chemical Name(6S11aR11bS)-9101111a-tetrahydro-8H-611b-methanofuro[23-c]pyrido[12-a]azepin-2(6H)-one
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Stefanowicz-Hajduk J et al. Securinine from Phyllanthus glaucus Induces Cell Cycle Arrest and Apoptosis in Human Cervical Cancer HeLa Cells. PLoS One. 2016 Oct 28;11(10):e0165372.
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