DRAinh-A250
CAS No. 858747-13-4
DRAinh-A250( DRAinhA250 | DRAinh A250 | DRAinh-A250 )
Catalog No. M16225 CAS No. 858747-13-4
DRAinh-A250 is a specific inhibitor of Cl-/anion exchanger SLC26A3 (DRA).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 873 | Get Quote |
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| 50MG | 1782 | Get Quote |
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| 100MG | 2250 | 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 NameDRAinh-A250
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NoteResearch use only, not for human use.
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Brief DescriptionDRAinh-A250 is a specific inhibitor of Cl-/anion exchanger SLC26A3 (DRA).
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DescriptionDRAinh-A250 is a specific inhibitor of Cl-/anion exchanger SLC26A3 (DRA), fully and reversibly inhibits SLC26A3-mediated Cl- exchange with HCO3-, I-, and thiocyanate (SCN-) with IC50 of ~0.2 uM; does not inhibit the homologous anion exchangers SLC26A4 (pendrin) or SLC26A6 (PAT-1), as well as other related proteins or intestinal ion channels; blocked fluid absorption in closed colonic loops but not in jejunal loops in mice, while the NHE3 (SLC9A3) inhibitor tenapanor blocked absorption only in the jejunum; reduces signs of constipation in loperamide-treated mice after oral treatment.
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In Vitro——
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In Vivo——
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SynonymsDRAinhA250 | DRAinh A250 | DRAinh-A250
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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 Number858747-13-4
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Formula Weight417.255
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Molecular FormulaC20H17BrO5
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO=C(O)CC(C1=O)=C(C)C2=C(O1)C(C)=C(OCC3=CC=CC(Br)=C3)C=C2
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Chemical Name2-(7-((3-bromobenzyl)oxy)-4,8-dimethyl-2-oxo-2H-chromen-3-yl)acetic acid
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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DCPIB
DCPIB, a known specific and potent inhibitor of volume-regulated anion channels (VRAC),DCPIB displayed superior selectivity toward TRESK with an IC50 of 0.14 μM, demonstrating at least 100-fold higher affinity over TREK1/TRAAK channels.?DCPIB, a known specific and potent inhibitor of volume-regulated anion channels (VRAC), has been reported to activate TREK1 and TREK2 in astrocytes and in vitro recently.?
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Caftaric acid
Caftaric acid is an inhibitor of the protein-protein interactions mediated by the Src-family kinases.
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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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