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Cyclopentolate Hydrochloride
CAS No. 5870-29-1
Cyclopentolate Hydrochloride( —— )
Catalog No. M21588 CAS No. 5870-29-1
Cyclopentolate Hydrochloride is a muscarinic acetylcholine receptors antagonist with Kis of 1.62 27.5 and 2.63 nM for M1 M2 and M3 receptors respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 29 | Get Quote |
|
| 25MG | 59 | Get Quote |
|
| 50MG | 87 | Get Quote |
|
| 100MG | 156 | 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 NameCyclopentolate Hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionCyclopentolate Hydrochloride is a muscarinic acetylcholine receptors antagonist with Kis of 1.62 27.5 and 2.63 nM for M1 M2 and M3 receptors respectively.
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DescriptionCyclopentolate Hydrochloride is a muscarinic acetylcholine receptors antagonist with Kis of 1.62 27.5 and 2.63 nM for M1 M2 and M3 receptors respectively.(In Vivo):Survival in rats pretreated with cyclopentolate (20 mg/kg) is 90%.
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In Vitro——
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In VivoSurvival in rats pretreated with cyclopentolate (20 mg/kg) is 90%. Animal Model:Eighty Sprague-Dawley rats (acute, lethal organophosphate pesticide (OP) poisoning model)Dosage:20 mg/kg (Ophthalmic cyclopentolate)Administration:i.p.Result:Survival in rats pretreated with ophthalmic cyclopentolate (20 mg/kg) is 90%.
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Synonyms——
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PathwayEndocrinology/Hormones
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TargetAChR
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RecptorM5 mAChR
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Research Area——
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Indication——
Chemical Information
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CAS Number5870-29-1
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Formula Weight327.85
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Molecular FormulaC17H26ClNO3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (762.54 mM)
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SMILESCl.CN(C)CCOC(=O)C(c1ccccc1)C1(O)CCCC1
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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.Ishikawa H Desantis L Patil P N . Selectivity of Muscarinic Agonists Including (±)-Aceclidine and Antimuscarinics on the Human Intraocular Muscles[J]. Journal of Ocular Pharmacology & Therapeutics 1998 14(4):363-373.
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