Hydroxy-?α-?sanshool
CAS No. 83883-10-7
Hydroxy-?α-?sanshool( —— )
Catalog No. M21545 CAS No. 83883-10-7
Hydroxy- α- sanshool is an alkyl amide isolated from the pepper. It acts as a TRPA1 covalent and TRPV1 non-covalent agonist (EC50s: 69 and 1.1 μM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
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| 10MG | 357 | In Stock |
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| 25MG | 587 | In Stock |
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| 50MG | 822 | In Stock |
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| 100MG | 1107 | In Stock |
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| 200MG | Get Quote | In Stock |
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Biological Information
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Product NameHydroxy-?α-?sanshool
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NoteResearch use only, not for human use.
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Brief DescriptionHydroxy- α- sanshool is an alkyl amide isolated from the pepper. It acts as a TRPA1 covalent and TRPV1 non-covalent agonist (EC50s: 69 and 1.1 μM).
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DescriptionHydroxy- α- sanshool is an alkyl amide isolated from the pepper. It acts as a TRPA1 covalent and TRPV1 non-covalent agonist (EC50s: 69 and 1.1 μM).
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In VitroHydroxy-α-sanshool (0-10 mM; 20 s) induces inward currents in cultured DRG neuron.Hydroxy-α-sanshool (1 mM; 0-1 min) increases intracellular Ca2+ in cultured DRG neuron. Cell Viability Assay Cell Line:Dorsal root ganglion (DRG) neurons Concentration:0-10 mM Incubation Time:20 s Result:Induced small but robust inward currents for DRG neuron with an EC50 of 66.2 μM.Cell Viability Assay Cell Line:Dorsal root ganglion (DRG) neurons Concentration:1 mM Incubation Time:0-1 min Result:Led to an intracellular Ca2+ increase in the majority of DRG neurons tested (98 of 100).
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In VivoHydroxy-α-sanshool (intradermal injection; 4 mg per mouse; once) shows paw-licking response in wild-type and TRPV1-deficient mice.Hydroxy-α-sanshool (1 mM) ismarkedly aversive to WT mice, but in TRPV1 KO mice, the aversion is almost entirely eliminated (P<0.001). Animal Model:Wild-type and TRPV1-deficient mice Dosage:4 mg per mouse Administration:Intradermal injection; 4 mg per mouse; once Result:Reduced paw-licking response in TRPV1-deficient mice (160 times, P < 0.05).Showed paw-licking response in wild-type mice (mean 284.8 times) in 20 min.
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Synonyms——
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PathwayMembrane Transporter/Ion Channel
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TargetTRP/TRPV Channel
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RecptorTRPA1| TRPV1
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Research Area——
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Indication——
Chemical Information
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CAS Number83883-10-7
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Formula Weight263.37
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Molecular FormulaC16H25NO2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (379.68 mM)
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SMILESCC(C)(CNC(/C=C/CC/C=C\C=C\C=C\C)=O)O
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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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EIPA
EIPA (L593754, MH 12-43) is a TRPP3 channel inhibitor (IC50: 10.5 μM). It also inhibits Na+/H+-exchanger (NHE) and macropinocytosis.It is found that EIPA, benzamil, and phenamil rapidly and reversibly block Ca2+-activated TRPP3 channel activation at -50 mV, with IC50s of 143, 10.5, 1.1, and 0.14 μM, respectively.
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Pyr10
Pyr10 is a pyrazole derivative and a selective TRP cation 3 inhibitor. Pyr10 has the ability to distinguish between receptor-operated TRPC3 and native stromal interaction molecule 1 (STIM1)/Orai1 channels. Pyr10 inhibits Ca2+ influx in carbachol-stimulated TRPC3-transfected HEK293 cells (IC50: 0.72 μM) (IC50 of 13.08 μM for store-operated Ca2+ entry in BRL-2H3 cells) .
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JNJ-38893777 sulfate
JNJ-38893777 is a potent and selective transient receptor potential vanilloid 1 (TRPV1) channel antagonist for treatment of ociceptive and neuropathic pain.
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