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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
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 Mon Mar 31 18:17:24 GMT 2025
Edited
by admin
on Mon Mar 31 18:17:24 GMT 2025
Record UNII
CHJ1X6AG9F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SIRATIAZEM
INN  
INN  
Official Name English
LR-A 113
Preferred 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 Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
Code System Code Type Description
INN
7034
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
EVMPD
SUB10536MIG
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
PUBCHEM
65989
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
MESH
C085176
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
NCI_THESAURUS
C90823
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
ChEMBL
CHEMBL2107305
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
FDA UNII
CHJ1X6AG9F
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
EPA CompTox
DTXSID101350914
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
CAS
138778-28-6
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
SMS_ID
100000083539
Created by admin on Mon Mar 31 18:17:24 GMT 2025 , Edited by admin on Mon Mar 31 18:17:24 GMT 2025
PRIMARY
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