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 |
|
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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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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NS1652
NS1652 is an anion conductance inhibitor. NS1652 blocks chloride channel has an IC50 of 1.6 μM in human and mouse red blood cells.NS1652 (20 μM) fully and reversibly inhibits the red cell Cl-conductance. NS1652 effectively inhibits the chloride conductance (IC50, 1.6 μM) in human and mouse red blood cells, but only weakly inhibits VRAC (IC50, 125 μM) in HEK293 cells. NS1652 markedly blocks the NO production (IC50: 3.1 μM in BV2 cells).
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OADS
OADS is a specific, reversible, small-molecule inhibitor directs against CLC (Chloride Channel) antiporter with Ki of 29 uM.
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