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Sofpironium bromide
CAS No. 1628106-94-4
Sofpironium bromide ( BBI-4000; BBI4000; BBI 4000 )
Catalog No. M23722 CAS No. 1628106-94-4
Sofpironium bromide belongs to a class of drugs called anticholinergics, which exert their effect by blocking the action of acetylcholine.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 177 | In Stock |
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| 10MG | 295 | In Stock |
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| 25MG | 502 | In Stock |
|
| 50MG | 709 | In Stock |
|
| 100MG | 1008 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameSofpironium bromide
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NoteResearch use only, not for human use.
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Brief DescriptionSofpironium bromide belongs to a class of drugs called anticholinergics, which exert their effect by blocking the action of acetylcholine.
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DescriptionSofpironium bromide belongs to a class of drugs called anticholinergics, which exert their effect by blocking the action of acetylcholine.
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SynonymsBBI-4000; BBI4000; BBI 4000
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PathwayOthers
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TargetOther Targets
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Recptorothers
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Research Area——
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Indication——
Chemical Information
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CAS Number1628106-94-4
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Formula Weight470.4
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Molecular FormulaC22H32BrNO5
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Purity>98% (HPLC)
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SolubilityDMSO:95 mg/mL?(201.95 mM;?Need ultrasonic)
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SMILESCCOC(C[N+](C)(CC1)C[C@@H]1OC([C@@](C2CCCC2)(C3=CC=CC=C3)O)=O)=O.[Br-]
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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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Thioredoxin reductas...
Thioredoxin reductase peptide corresponds to residues 53–67 in thioredoxin reductase (TrxR), used in thioredoxin reductase research.Mammalian thioredoxin reductase (TR) catalyzes the reduction of the redox-active disulfide bond of thioredoxin (Trx) and is similar in structure and mechanism to glutathione reductase except for a C-terminal 16-amino acid extension containing a rare vicinal selenylsulfide bond.
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AOB2796
AOB2796 is a novel PAR2 agonist; activated PAR2 signaling in cellular proliferation assays, phosphatidylinositol hydrolysis assays, and Ca(2+) mobilization assays, with potencies ranging from 200 to 1000 nM.
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Chlorobenzothiazolin...
Inhibition of recombinant human chymase using bis(succinoyl-L-alanyl-L-prolyl-L-phenylalanylamide) as substrate after 1 hr by fluorescence assay with activity value of 90μM
