beta-Eudesmol
CAS No. 473-15-4
beta-Eudesmol( —— )
Catalog No. M18588 CAS No. 473-15-4
β-Eudesmol is a noncompetitive antagonist of nicotinic acetylcholine receptors (nAChRs). It is a sesquiterpene that has been found in a variety of plants, including Cannabis, and has diverse biological activities.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 112 | In Stock |
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| 5MG | 107 | In Stock |
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| 10MG | 170 | In Stock |
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| 25MG | 282 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product Namebeta-Eudesmol
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NoteResearch use only, not for human use.
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Brief Descriptionβ-Eudesmol is a noncompetitive antagonist of nicotinic acetylcholine receptors (nAChRs). It is a sesquiterpene that has been found in a variety of plants, including Cannabis, and has diverse biological activities.
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Descriptionβ-Eudesmol is a noncompetitive antagonist of nicotinic acetylcholine receptors (nAChRs). It is a sesquiterpene that has been found in a variety of plants, including Cannabis, and has diverse biological activities.
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In VitroWestern Blot Analysis Cell Line:HL-60Concentration:40 μM, 80 μM Incubation Time:4 h Result:Increased the expression of caspase-3 protein at 80 μM.Cell Viability Assay Cell Line:HL-60 Concentration:10 μM, 20 μM, 40 μM, 60 μM, 80 μM, 120 μM Incubation Time:4 h Result:Didn’t affect cell activity at a dose of 40 μM, but decreased cell activity at a dose of 80 μM, and cell viability decreased by 51.6%.Apoptosis Analysis Cell Line:HL-60 Concentration:40 μM, 80 μM Incubation Time:4 hResult:Had no effect on apoptosis at the dose of 40 μM, but induced apoptosis at the dose of 80 μM, and the apoptosis rate was 31.7%.
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In VivoAnimal Model:Male KM mice modelDosage:1.25 mg/kg, 2.5mg/kg, 5 mg/kg Administration:Intraperitoneal injection (i.p.); Once daily for 7 days Result:Inhibited the growth of H22 tumor cells with inhibition rates of 39.9% (2.5 mg/kg) and 49.3%(5 mg/kg), respectively.Inhibited the growth of S108 tumor cells with inhibition rates of 22.4% (2.5 mg/kg) and 42.2%(5 mg/kg), respectively.Significantly decreased vascular index with inhibition rates of 34.4% (2.5 mg/kg) and 44.3% (5 mg/kg).Animal Model: Male C57BL/6 mice model Dosage:50 mg/kg, 100 mg/kg Administration:Intraperitoneal injection (i.p.); Single dose. 2 h before the cecal ligation and puncture (CLP) operation. Result:Increased the expression of TNF-α, IL-1β and IL-6 in a dose-dependent manner.Increased the levels of superoxide dismutase (SOD) and glutathione (GSH), and decreased the levels of malondialdehyde (MDA) and myeloperoxidase (MPO).Inhibit the phosphorylation of p65.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptornAChR| TRPA1| TRPV3| TRPM8
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Research Area——
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Indication——
Chemical Information
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CAS Number473-15-4
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Formula Weight222.37
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Molecular FormulaC15H26O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (449.70 mM)
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SMILESCC(C)(O)[C@@H]1CC[C@@]2(C)CCCC(=C)[C@@H]2C1
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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. Kimura M, et al. Mechanism of the blocking action of beta-eudesmol on the nicotinic acetylcholine receptor channel in mouse skeletal muscles[J]. Neuropharmacology, 1991, 30(8):835-41.
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