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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
Structure of SIRATIAZEM

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

HIDE SMILES / InChI

Molecular Formula C24H30N2O4S
Molecular Weight 442.571
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacokinetics of diltiazem and a new analogue, LR-A/113, in the conscious rat.
1992 Oct-Dec
Comparison of antiarrhythmic and electrophysiologic effects of diltiazem and its analogue siratiazem.
1993 Nov
Effects of diltiazem and its analogue siratiazem on contraction and 45Ca2+ uptake in sheep coronary artery rings.
1995 Oct
Antiarrhythmic effects of LR-A/113 a new calcium antagonistic drug.
1996 Aug
Patents

Patents

Sample Use Guides

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
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.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:02:55 GMT 2023
Edited
by admin
on Fri Dec 15 16:02:55 GMT 2023
Record UNII
CHJ1X6AG9F
Record Status Validated (UNII)
Record Version
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Name Type Language
SIRATIAZEM
INN  
INN  
Official Name English
siratiazem [INN]
Common Name English
(+)-(2S,3S)-2,3-DIHYDRO-3-HYDROXY-5-(2-(ISOPROPYLMETHYLAMINO)ETHYL)-2-(P-METHOXYPHENYL)-1,5-BENZOTHIAZEPIN-4(5H)-ONE ACETATE (ESTER)
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C333
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
Code System Code Type Description
INN
7034
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
PRIMARY
EVMPD
SUB10536MIG
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
PRIMARY
PUBCHEM
65989
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
PRIMARY
MESH
C085176
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
PRIMARY
NCI_THESAURUS
C90823
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107305
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
PRIMARY
FDA UNII
CHJ1X6AG9F
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
PRIMARY
CAS
138778-28-6
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
PRIMARY
SMS_ID
100000083539
Created by admin on Fri Dec 15 16:02:55 GMT 2023 , Edited by admin on Fri Dec 15 16:02:55 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY