TETRAHYDROPIPERINE
CAS No. 23434-88-0
TETRAHYDROPIPERINE( Cosmoperine )
Catalog No. M20421 CAS No. 23434-88-0
TETRAHYDROPIPERINE is a natural product derived from piperine can be used to treat convulsion epilepsy relieve pain and control insects.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | 33 | In Stock |
|
| 50MG | 48 | In Stock |
|
| 100MG | 68 | In Stock |
|
| 200MG | 99 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameTETRAHYDROPIPERINE
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NoteResearch use only, not for human use.
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Brief DescriptionTETRAHYDROPIPERINE is a natural product derived from piperine can be used to treat convulsion epilepsy relieve pain and control insects.
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DescriptionTETRAHYDROPIPERINE is a natural product derived from piperine can be used to treat convulsion epilepsy relieve pain and control insects.
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In Vitro——
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In Vivo——
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SynonymsCosmoperine
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PathwayMembrane Transporter/Ion Channel
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TargetTRP/TRPV Channel
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RecptorHtrpv1|CYP450
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Research Area——
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Indication——
Chemical Information
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CAS Number23434-88-0
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Formula Weight289.37
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Molecular FormulaC17H23NO3
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Purity>98% (HPLC)
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SolubilityDMSO:57 mg/mL (196.97 mM)
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SMILESO=C(CCCCc1ccc2OCOc2c1)N1CCCCC1
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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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Pyr6
Pyr6 is a selective TRPC3 inhibitor with IC50 of 0.49 uM(Ca2+ influx inhibition in thapsigargin depleted native RBL-2H3 cells).Pyr6 is an inhibitor of Ca2+ entry, which displays higher potency to inhibit Ca2+ entry mediated by CRAC channel than by TRPC3.Pyr3 is selective inhibitor of TRPC3, inhibited Orai1- and TRPC3-mediated Ca(2+) entry and currents as well as mast cell activation with similar potency.?
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Methyl Kakuol
Methyl Kakuol is an agonist of TRPA1 with an EC50 of 0.27 μM and can be used in studies about acting as an active ingredient in MBST constituent Asiasari Radix.
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AMG-9810
A potent, selective and competitive TRPV1 antagonist with IC50 of 24.5 and 85.6 nM for human and rat TRPV1, repectively.
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