Aurantiamide
CAS No. 58115-31-4
Aurantiamide( TMC-58B )
Catalog No. M20469 CAS No. 58115-31-4
Aurantiamide has anti-cancer anti-inflammatory and antinociceptive activities it may suppress the growth of malignant gliomas by blocking autophagic flux.Aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the NF-κB JNK and p38 pathways.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 374 | In Stock |
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10MG | 556 | In Stock |
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25MG | 887 | In Stock |
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50MG | 1197 | In Stock |
|
100MG | 1611 | In Stock |
|
200MG | Get Quote | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
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Biological Information
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Product NameAurantiamide
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NoteResearch use only, not for human use.
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Brief DescriptionAurantiamide has anti-cancer anti-inflammatory and antinociceptive activities it may suppress the growth of malignant gliomas by blocking autophagic flux.Aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the NF-κB JNK and p38 pathways.
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DescriptionAurantiamide has anti-cancer anti-inflammatory and antinociceptive activities it may suppress the growth of malignant gliomas by blocking autophagic flux.Aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the NF-κB JNK and p38 pathways.
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In Vitro——
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In Vivo——
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SynonymsTMC-58B
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PathwayApoptosis
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TargetNF-κB
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RecptorNF-κB|p38
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Research Area——
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Indication——
Chemical Information
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CAS Number58115-31-4
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Formula Weight402.5
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Molecular FormulaC25H26N2O3?
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Purity>98% (HPLC)
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Solubility——
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SMILESOC[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1
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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
1.Yoon C S Kim D C Lee D S et al. Anti-neuroinflammatory effect of aurantiamide acetate from the marine fungus Aspergillus sp. SF-5921: Inhibition of NF-κB and MAPK pathways in lipopolysaccharide-induced mouse BV2 microglial cells[J]. International Immunopharmacology 2014 23(2):568-574.
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