SM-6586


Catalog No. Size PriceQuantity
M21785-C Contact sales@xcessbio.com for quotation $100Unavailable

Description

SM-6586 is a calcium channel antagonist and inhibitor of Na+/H+ and Na+/Ca2+ exchange transport, potentially for the treatment of cerebrovasular diseases and hypertension.

Product information

CAS Number: 103898-38-0

Molecular Weight: 489.52

Formula: C26H27N5O5

Chemical Name: methyl 5-(3-{[benzyl(methyl)amino]methyl}-1,2,4-oxadiazol-5-yl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

Smiles: COC(=O)C1C(C(C2=NC(CN(C)CC3C=CC=CC=3)=NO2)=C(C)NC=1C)C1C=C(C=CC=1)[N+]([O-])=O

InChiKey: HHVCXSOKQHQGFB-UHFFFAOYSA-N

InChi: InChI=1S/C26H27N5O5/c1-16-22(25-28-21(29-36-25)15-30(3)14-18-9-6-5-7-10-18)24(23(17(2)27-16)26(32)35-4)19-11-8-12-20(13-19)31(33)34/h5-13,24,27H,14-15H2,1-4H3

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vivo:

In SM-6586-treated spontaneously hypertensive rats, the survival rate after bilateral common carotid artery ligation is higher, the brain water content is lower, and the ATP level is higher and lactate level. In focal ischemia models, the SM-treated group shows a reduction of T1 relaxation time. The brain water content is significantly decreased in the SM-treated group.

Products are for research use only. Not for human use.

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