Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C24H30N2O4S |
Molecular Weight | 442.571 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1)[C@@H]2SC3=C(C=CC=C3)N(CCN(C)C(C)C)C(=O)[C@@H]2OC(C)=O
InChI
InChIKey=VVZILLNNYUUOIY-PKTZIBPZSA-N
InChI=1S/C24H30N2O4S/c1-16(2)25(4)14-15-26-20-8-6-7-9-21(20)31-23(22(24(26)28)30-17(3)27)18-10-12-19(29-5)13-11-18/h6-13,16,22-23H,14-15H2,1-5H3/t22-,23+/m1/s1
Siratiazem [LRA 113] is a calcium channel antagonist that is structurally similar to diltiazem but has a branched alkyl group on the basic nitrogen. Siratiazem has been developed in an attempt to limit the in vivo N-demethylation that is known to occur with diltiazem. Preliminary binding and functional studies in cardiac and vascular tissues indicate that it not only binds to diltiazem binding sites but also exhibits Ca2+ channel blocking
properties comparable to diltiazem. Siratiazem has a similar profile of activity to its parent compound, diltiazem, in that it blocks calcium channels in vascular, intestinal smooth muscle and cardiac tissue, and is least potent in cardiac muscle. At higher concentrations, siratiazem may also block cardiac sodium channels.
Originator
Approval Year
PubMed
Title | Date | PubMed |
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Pharmacokinetics of diltiazem and a new analogue, LR-A/113, in the conscious rat. | 1992 Oct-Dec |
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Comparison of antiarrhythmic and electrophysiologic effects of diltiazem and its analogue siratiazem. | 1993 Nov |
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Antiarrhythmic effects of LR-A/113 a new calcium antagonistic drug. | 1996 Aug |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1301356
Conscious rats, with the jugular vein cannulated, received Siratiazem by intravenous (3 mg/kg body weight) or oral (50 mg/kg body weight) route.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7615573
Siratiazem inhibited, in a concentration-dependent manner, the maximum contraction produced by cumulative addition of calcium chloride to rabbit mesenteric artery (IC25 = 0.75 uM), ileum (IC25 = 0.33 uM) and paced atria (IC25 = 10 uM) in vitro. Siratiazem inhibited calcium concentration-response curves in sheep cerebral arteries and in this tissue the IC25 value was 1.18 uM.
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C333
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ACTIVE MOIETY