Isolinderalactone
CAS No. 957-66-4
Isolinderalactone( —— )
Catalog No. M25015 CAS No. 957-66-4
Isolinderalactone shows anti-inflammatory and anticancer capacity, and it exhibits moderate iNOS inhibitory activity, with the IC50 value of 0.30 uM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 143 | In Stock |
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| 5MG | 155 | In Stock |
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| 10MG | 258 | In Stock |
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| 25MG | 436 | In Stock |
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| 50MG | 612 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 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 NameIsolinderalactone
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NoteResearch use only, not for human use.
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Brief DescriptionIsolinderalactone shows anti-inflammatory and anticancer capacity, and it exhibits moderate iNOS inhibitory activity, with the IC50 value of 0.30 uM.
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DescriptionIsolinderalactone shows anti-inflammatory and anticancer capacity, and it exhibits moderate iNOS inhibitory activity, with the IC50 value of 0.30 uM.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayImmunology/Inflammation
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TargetNOS
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RecptorSTAT3|iNOS
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Research Area——
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Indication——
Chemical Information
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CAS Number957-66-4
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Formula Weight244.29
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Molecular FormulaC15H16O3
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESCC1=COC2=C1[C@H]3[C@H](C(=C)C(=O)O3)[C@@](C2)(C)C=C
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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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Neotuberostemonine
Neotuberostemonine (NTS) is one of the main antitussive alkaloids in the root of Stemona tuberosa Lour it has a significant protective effect on bleomycin (BLM)-induced pulmonary fibrosis through suppressing the recruitment and M2 polarization of macrophages. Neotuberostemonine demonstrates antitussive properties in guinea pigs.
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3,4-O-Isopropylidene...
3,4-Oxo- isopropylidene-shikimic acid has significant anti-inflammatory, anti-thrombosis, antioxidant, analgesic effects, it has protective effects on experimental colitis induced by trinitrobenzenesulfonic acid in rats, probably due to antioxidant action.
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ABT-702 dihydrochlor...
ABT-702 dihydrochloride is a potent adenosine kinase (AK) inhibitor.
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