
T16Ainh-A01
CAS No. 552309-42-9
T16Ainh-A01( —— )
Catalog No. M14998 CAS No. 552309-42-9
T16Ainh-A01 is an inhibitor of the calcium-activated chloride channel TMEM16A.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 60 | In Stock |
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10MG | 97 | In Stock |
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25MG | 194 | In Stock |
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50MG | 357 | In Stock |
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100MG | 530 | In Stock |
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200MG | 759 | 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 NameT16Ainh-A01
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NoteResearch use only, not for human use.
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Brief DescriptionT16Ainh-A01 is an inhibitor of the calcium-activated chloride channel TMEM16A.
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DescriptionT16Ainh-A01 is an inhibitor of the calcium-activated chloride channel TMEM16A, inhibits Ca2+-activated Cl? channel (CACC) activity in TMEM16A-transfected FRT cells with IC50 of 1 uM; T16Ainh-A01 (1-30 uM) inhibited single calcium (Ca2+)-activated chloride (Cl?) channels and whole cell currents activated by 500 nM free Ca2+; T16Ainh-A01 relaxed mouse thoracic aorta pre-contracted with methoxamine with an IC50 of 1.6 uM and suppressed the methoxamine concentration-effect curve; blocks calcium-activated chloride channels in vascular smooth muscle cells and relaxes murine and human blood vessels.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayMembrane Transporter/Ion Channel
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TargetChloride Channel
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RecptorChloride Channel
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Research Area——
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Indication——
Chemical Information
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CAS Number552309-42-9
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Formula Weight416.514
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Molecular FormulaC19H20N4O3S2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 83.33 mg/mL (200.06 mM)
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SMILESCCC1=C(N=C(NC1=O)SCC(=O)NC2=NC(=CS2)C3=CC=C(C=C3)OC)C
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Chemical Name2-[(5-Ethyl-1,6-dihydro-4-methyl-6-oxo-2-pyrimidinyl)thio]-N-[4-(4-methoxyphenyl)-2-thiazolyl]acetamide
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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Fenamic acid
Fenamic acid is a chloride channel blocker that causes renal papillary necrosis in rats. Fenamic acid serves as a parent structure for several nonsteroidal anti-inflammatory drugs (NSAIDs), including flufenamic acid, tolfenamic acid, mefenamic acid, and meclofenamic acid.
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Eact
Eact is a selective and potent TMEM16A activator. It directly activates the TRPV1 channels in sensory nociceptors. Which also produces itch, acute nociception and thermal hypersensitivity.
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Ani9
Ani9 is a high selective blocker of Anoctamin1 (ANO1)/transmembrane protein 16A (TMEM16A) with an IC50 of 77 nM and can be used in studies about ANO1 and the treatment of ancer, hypertension, pain, diarrhea and asthma.