Fesoterodine fumarate
CAS No. 286930-03-8
Fesoterodine fumarate( PF-00695838 fumarate )
Catalog No. M13874 CAS No. 286930-03-8
Fesoterodine (PF-00695838) is a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 49 | In Stock |
|
| 2MG | 29 | In Stock |
|
| 5MG | 43 | In Stock |
|
| 10MG | 65 | In Stock |
|
| 25MG | 102 | In Stock |
|
| 50MG | 137 | In Stock |
|
| 100MG | 211 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 409 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameFesoterodine fumarate
-
NoteResearch use only, not for human use.
-
Brief DescriptionFesoterodine (PF-00695838) is a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties.
-
DescriptionFesoterodine (PF-00695838) is a competitive muscarinic receptor antagonist with muscle relaxant and urinary antispasmodic properties; binds and inhibits muscarinic receptors on the bladder detrusor muscle, prevents bladder contractions or spasms caused by acetylcholine.Other Indication Approved(In Vitro):FFesoterodine Fumarate decreases micturition frequency, urgency severity and urgency incontinence episodes and increases the volume voided with each micturition.After oral administration, Fesoterodine Fumarate is rapidly and extensively hydrolysed in plasma by nonspecific esterases to Desfesoterodine (5-hydroxymethyl tolterodine; SPM 7605; HY-76569; an active metabolite of Fesoterodine).(In Vivo):Fesoterodine Fumarate (0.01-1 mg/kg; IV) reduces the micturition pressure and increases bladder capacity and ICIs (intercontraction intervas) at the lowest dose tested of 0.01 mg/kg.
-
In VitroFFesoterodine Fumarate decreases micturition frequency, urgency severity and urgency incontinence episodes and increases the volume voided with each micturition.After oral administration, Fesoterodine Fumarate is rapidly and extensively hydrolysed in plasma by nonspecific esterases to Desfesoterodine (5-hydroxymethyl tolterodine; SPM 7605; HY-76569; an active metabolite of Fesoterodine).
-
In VivoFesoterodine Fumarate (0.01-1 mg/kg; IV) reduces the micturition pressure and increases bladder capacity and ICIs (intercontraction intervas) at the lowest dose tested of 0.01 mg/kg. Animal Model:Bladders from female Sprague-Dawley rats (225-275 g)Dosage:0.01, 0.1 and 1 mg/kg Administration:IV Result:Reduced the micturition pressure and increased bladder capacity and ICIs at the lowest dose tested of 0.01 mg/kg.
-
SynonymsPF-00695838 fumarate
-
PathwayGPCR/G Protein
-
TargetmAChR
-
RecptormAChR
-
Research AreaOther Indications
-
IndicationOther Disease
Chemical Information
-
CAS Number286930-03-8
-
Formula Weight527.658
-
Molecular FormulaC30H41NO7
-
Purity>98% (HPLC)
-
SolubilityDMSO: 93 mg/mL (176.3 mM); Ethanol: 93 mg/mL (176.3 mM); Water: 92 mg/mL (174.4 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
-
SMILESCC(C)C(=O)OC1=C(C=C(C=C1)CO)[C@H](CCN(C(C)C)C(C)C)C2=CC=CC=C2.C(=C/C(=O)O)\C(=O)O
-
Chemical Name[2-[(1R)-3-[di(propan-2-yl)amino]-1-phenylpropyl]-4-(hydroxymethyl)phenyl] 2-methylpropanoate fumarate
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Ney P, et al. BJU Int. 2008 Apr;101(8):1036-42.
2. Michel MC. Expert Opin Pharmacother. 2008 Jul;9(10):1787-96.
3. Chapple CR, et al. BJU Int. 2008 Nov;102(9):1128-32.
molnova catalog
related products
-
Glycopyrrolate
A muscarinic anticholinergic that blocks muscarinic receptors, thus inhibiting cholinergic transmission.
-
Revefenacin
A novel potent, long-acting, lung-selective inhaled muscarinic antagonist that has high affinity at M3 receptor.
-
Glycopyrronium bromi...
Glycopyrronium bromide (CHF 5259) is a peripherally-acting quaternary ammonium antimuscarinic agent with little or no central nervous system activity.
Cart
sales@molnova.com