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Kansuinine E
CAS No. 672945-84-5
Kansuinine E ( )
Catalog No. M31347 CAS No. 672945-84-5
Kansuinine E, a jatrophane-type diterpenoid, is a plant-derived compound isolated from the roots of E. kansui. It functions as a nitric oxide inhibitor, with an inhibitory concentration of 6.3 μM (IC50).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 873 | In Stock |
|
| 50MG | Get Quote | In Stock |
|
| 100MG | Get Quote | In Stock |
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Biological Information
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Product NameKansuinine E
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NoteResearch use only, not for human use.
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Brief DescriptionKansuinine E, a jatrophane-type diterpenoid, is a plant-derived compound isolated from the roots of E. kansui. It functions as a nitric oxide inhibitor, with an inhibitory concentration of 6.3 μM (IC50).
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DescriptionKansuinine E, a jatrophane-type diterpenoid, is a plant-derived compound isolated from the roots of E. kansui. It functions as a nitric oxide inhibitor, with an inhibitory concentration of 6.3 μM (IC50).
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Synonyms
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number672945-84-5
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Formula Weight777.8
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Molecular FormulaC41H47NO14
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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Chemical Name
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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CID1375606
CID 1375606 is a surrogate agonist of orphan G protein-coupled receptor?GPR27. characterized by a high level of conservation among vertebrates and a predominant expression in the central nervous system.
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Orexin A (human, rat...
Orexin A human, rat, mouse, a 33 amino acid excitatory neuropeptide, orchestrates diverse central and peripheral processes. Orexin A human, rat, mouse has been used to study its effect on the functioning of porcine pancreatic islets. It has also been used as an orexin receptor 1 (OX1R) antagonist to study the effect of orexin systems in the effect of etonogestrel on respiratory response to prolonged metabolic acidosis.
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WAY-620057
WAY-620057 is an inhibitor that target protein-protein interactions in RAD51 family of recombinases.
