Thioperamide maleate
CAS No. 148440-81-7
Thioperamide maleate( MR-12842 maleate )
Catalog No. M28347 CAS No. 148440-81-7
Thioperamide maleate is an effective and selective antagonist of H3 receptor (Ki = 4.3 nM) for inhibition of [3H]histamine synthesis (Ki = 31 nM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 393 | Get Quote |
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| 10MG | 581 | Get Quote |
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| 25MG | 888 | Get Quote |
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| 50MG | 1242 | Get Quote |
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| 100MG | 1674 | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameThioperamide maleate
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NoteResearch use only, not for human use.
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Brief DescriptionThioperamide maleate is an effective and selective antagonist of H3 receptor (Ki = 4.3 nM) for inhibition of [3H]histamine synthesis (Ki = 31 nM).
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DescriptionThioperamide maleate is an effective and selective antagonist of H3 receptor (Ki = 4.3 nM) for inhibition of [3H]histamine synthesis (Ki = 31 nM).(In Vitro):Thioperamide maleate (0.01, 0.1, 1, 10, 100 μM) promotes the viability of NE-4C stem cells in a concentration-dependent manner. Thioperamide maleate displays similar potencies at human H4 and H3 receptors with Kis of 43 and 60 nM, respectively. Thioperamide maleate inhibits [3H]-(R)α-MeHA binding rat brain and guinea-pig lung with Kis of 2.1 nM and 2.0 nM, respectively. Thioperamide maleate competitively blocks H3-autoreceptors regulating [3H]histamine release with a mean apparent Ki of 4 nM.(In Vivo):In C57BL/6J mice, Thioperamide (5-20 mg/kg; i.p.) facilitates reconsolidation of a contextually-conditioned fear memory.
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In VitroThioperamide inhibits [3H]-(R)α-MeHA binding rat brain and guinea-pig lung with Kis of 2.1 nM and 2.0 nM, respectively. Thioperamide competitively blocks H3-autoreceptors regulating [3H]histamine release with a mean apparent Ki of 4 nM.Thioperamide (0.01-100 μM; 24 hours) promotes the viability of NE-4C stem cells in a concentration-dependent manner.Thioperamide displays similar potencies at human H4 and H3 receptors (Ki=43 and 60 nM, respectively).Cell Viability Assay Cell Line:NE-4C stem cells Concentration:0.01, 0.1, 1, 10, 100 μM Incubation Time:24 hours Result:The viability of NE-4C stem cells increased significantly to 150.83±6.91% when (1 μM) was administrated, and increased to 145.11±14.52% and 132.02%±25.65% when 10 μM and 100 μM were administrated respectively.
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In VivoThioperamide (5-20 mg/kg; i.p.) is able to facilitate reconsolidation of a contextually-conditioned fear memory in C57BL/6J mice. Animal Model:Naive female C57BL/6J mice Dosage:5, 10 or 20 mg/kg Administration:Injections (i.p.)Result:Facilitated reconsolidation of a contextually-conditioned fear memory.
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SynonymsMR-12842 maleate
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PathwayGPCR/G Protein
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TargetHistamine Receptor
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number148440-81-7
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Formula Weight408.52
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Molecular FormulaC19H28N4O4S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 100 mg/mL
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SMILESOC(=O)\C=C/C(O)=O.S=C(NC1CCCCC1)N1CCC(CC1)c1cnc[nH]1
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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.Wang R, et al. Capsaicinoids from hot pepper (Capsicum annuum L.) and their phytotoxic effect on seedling growth of lettuce (Lactuca sativa L.). Nat Prod Res. 2020 Jun;34(11):1597-1601.
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