Sarpogrelate hydrochloride

Sarpogrelate hydrochloride
Item number Size Datasheet Manual SDS Delivery time Quantity Price
TGM-T4978-5mg 5 mg

7 - 10 business days*

42.00€
TGM-T4978-1mL 1 ml

7 - 10 business days*

46.00€
TGM-T4978-10mg 10 mg

7 - 10 business days*

65.00€
TGM-T4978-25mg 25 mg

7 - 10 business days*

120.00€
TGM-T4978-50mg 50 mg

7 - 10 business days*

194.00€
TGM-T4978-100mg 100 mg

7 - 10 business days*

287.00€
TGM-T4978-500mg 500 mg

7 - 10 business days*

687.00€
 
Description: Sarpogrelate hydrochloride (MCI-9042) , a selective 5-HT2 antagonist, has been... more
Product information "Sarpogrelate hydrochloride"
Description: Sarpogrelate hydrochloride (MCI-9042) , a selective 5-HT2 antagonist, has been widely used as an anti-platelet agent for the treatment of PAD. Target: 5-HT2 Recepter Sarpogrelate is a drug which acts as an antagonist at the 5HT2A and 5-HT2B receptors. Sarpogrelate hydrochloride was shown to have the same affinity as ritanserin for 5-HT2A receptors, with a Ki value of 8.39 nM. Sarpogrelate hydrochloride lacked prominent 5-HT1-like, 5-HT3, beta, H1, H2 and M3 antagonist activity and weakly blocked alpha 1-adrenoceptors (pKB = 6.30). (S)-M-1 showed weak affinity for 5-HT1-like receptors (pKB = 6.30), alpha 1- (pKB = 6.80) and beta- (pKB = 6.54) adrenoceptors, while (R)-M-1 was a weak antagonist at histamine H1 receptors (pKB = 6.49). After 12 weeks of sarpogrelate administration, FBF and LBF responses during RH showed significant increases from 13.2 +/- 1.7 to 18.1 +/- 2.2 mL/min per 100 mL tissue (P < 0.01) and from 8.2 +/- 0.9 to 14.2 +/- 2.1 mL/min per 100 mL tissue (P < 0.05), respectively. Sarpogrelate hydrochloride -induced augmentation of FBF and LBF responses to RH was maintained at 24 weeks. Long-term oral administration of sarpogrelate improves vascular function in patients with PAD. Target: 5-HT Receptor. Smiles: Cl.COc1cccc(CCc2ccccc2OCC(CN(C)C)OC(=O)CCC(O)=O)c1. References: Pertz, H. and S. Elz, In-vitro pharmacology of sarpogrelate and the enantiomers of its major metabolite: 5-HT2A receptor specificity, stereoselectivity and modulation of ritanserin-induced depression of 5-HT contractions in rat tail artery. J Pharm Pharma
Keywords: MCI-9042
Supplier: TargetMol
Supplier-Nr: T4978

Properties

Application: Targets 5-hydroxytryptamine receptor 2 (HTR2)
MW: 465.97 D
Formula: C24H32ClNO6

Database Information

CAS : 135159-51-2| Matching products
KEGG ID : K04157 | Matching products
Protein Atlas Nr. : GPCR Modulators/A(nta)gonists

Handling & Safety

Storage: -20°C
Shipping: +4°C (International: +4°C)
Signal Word: Warning
GHS Hazard Pictograms:
H Phrases: H302, H400
P Phrases: P264, P270, P273, P330, P391, P301+P310, P501
Caution
Our products are for laboratory research use only: Not for administration to humans!
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