Chaetoglobosin Fex
CAS No. 149457-95-4
Chaetoglobosin Fex( —— )
Catalog No. M23645 CAS No. 149457-95-4
Chaetoglobosin Fex from the marine-derived endophytic fungus inhibits induction of inflammatory mediators via Toll-like receptor 4 signaling in macrophages.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 1728 | In Stock |
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| 10MG | 2880 | 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 NameChaetoglobosin Fex
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NoteResearch use only, not for human use.
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Brief DescriptionChaetoglobosin Fex from the marine-derived endophytic fungus inhibits induction of inflammatory mediators via Toll-like receptor 4 signaling in macrophages.
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DescriptionChaetoglobosin Fex from the marine-derived endophytic fungus inhibits induction of inflammatory mediators via Toll-like receptor 4 signaling in macrophages.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptorinflammation
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Research Area——
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Indication——
Chemical Information
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CAS Number149457-95-4
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Formula Weight530.65
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Molecular FormulaC32H38N2O5
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Purity>98% (HPLC)
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SolubilityDMSO:10 mM
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SMILESO=C1[C@]([C@](/C=C/C[C@@H](/C=C2/C)C)([H])[C@H](O)C3=C)(C(CC[C@@H](C2=O)O)=O)[C@]([C@@H]3C)([H])[C@H](CC4=CNC5=C4C=CC=C5)N1
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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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Isorhamnetin 3-O-gal...
Isorhamnetin 3-O-galactoside shows antioxidant, anti-inflammatory, neuroprotective,and barrier protective activities, it could be used as a candidate therapeutic for treatment of severe vascular inflammatory diseases.
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Flurbiprofen Axetil
Flurbiprofen Axetil is an anti-inflammatory used as an analgesic.
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OD1
Potent rat Nav1.7, human Nav1.4 and rat Nav1.6 channel activator (EC50 values are 7, 10 and 47 nM, respectively). Exhibits minimal activation at mammalian Nav1.2, Nav1.3 and Nav1.5 (EC50 values >3 μM). Inhibits fast inactivation on all channels. Increases peak currents at all voltages and stimulates a persistent Na+ current at hNav1.7 channel. Increases hyperpolarization at Nav1.4 and Nav1.6 channels. Induces spontaneous pain in vivo.
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