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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H24N2O3S
Molecular Weight 372.481
Optical Activity ( + )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEACETYLDILTIAZEM

SMILES

COC1=CC=C(C=C1)[C@@H]2SC3=CC=CC=C3N(CCN(C)C)C(=O)[C@@H]2O

InChI

InChIKey=NZHUXMZTSSZXSB-MOPGFXCFSA-N
InChI=1S/C20H24N2O3S/c1-21(2)12-13-22-16-6-4-5-7-17(16)26-19(18(23)20(22)24)14-8-10-15(25-3)11-9-14/h4-11,18-19,23H,12-13H2,1-3H3/t18-,19+/m1/s1

HIDE SMILES / InChI

Molecular Formula C20H24N2O3S
Molecular Weight 372.481
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of diltiazem and low-dose aspirin on platelet aggregation and ATP release induced by paired agonists.
1993 Aug 2
Anaphylatoxin C3a induces rapid protein phosphorylation in guinea pig platelets.
1994 Sep-Oct
Ca2+ channel blockers modulate metabolism of collagens within the extracellular matrix.
1996 May 28
Effects of diltiazem on down-regulation of lymphocyte beta-adrenoceptors in patients with chronic congestive heart failure.
2000 Oct
Pharmacokinetic interaction between tacrolimus and diltiazem: dose-response relationship in kidney and liver transplant recipients.
2002
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:17:11 UTC 2023
Edited
by admin
on Fri Dec 15 16:17:11 UTC 2023
Record UNII
849UT193YJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DEACETYLDILTIAZEM
Common Name English
DILTIAZEM HYDROCHLORIDE IMPURITY F [EP IMPURITY]
Common Name English
1,5-BENZOTHIAZEPIN-4(5H)-ONE, 5-(2-(DIMETHYLAMINO)ETHYL)-2,3-DIHYDRO-3-HYDROXY-2-(4-METHOXYPHENYL)-, (2S,3S)-
Systematic Name English
(+)-DESACETYLDILTIAZEM
Common Name English
DEACETYL-D-DILTIAZEM
Common Name English
Desacetyldiltiazem [WHO-DD]
Common Name English
DESACETYLDILTIAZEM [WHO-IP]
Common Name English
DESACETYLDILTIAZEM
WHO-DD  
Common Name English
Code System Code Type Description
PUBCHEM
91638
Created by admin on Fri Dec 15 16:17:11 UTC 2023 , Edited by admin on Fri Dec 15 16:17:11 UTC 2023
PRIMARY
EVMPD
SUB112491
Created by admin on Fri Dec 15 16:17:11 UTC 2023 , Edited by admin on Fri Dec 15 16:17:11 UTC 2023
PRIMARY
MESH
C037769
Created by admin on Fri Dec 15 16:17:11 UTC 2023 , Edited by admin on Fri Dec 15 16:17:11 UTC 2023
PRIMARY
CAS
91602-22-1
Created by admin on Fri Dec 15 16:17:11 UTC 2023 , Edited by admin on Fri Dec 15 16:17:11 UTC 2023
SUPERSEDED
SMS_ID
100000142066
Created by admin on Fri Dec 15 16:17:11 UTC 2023 , Edited by admin on Fri Dec 15 16:17:11 UTC 2023
PRIMARY
CAS
42399-40-6
Created by admin on Fri Dec 15 16:17:11 UTC 2023 , Edited by admin on Fri Dec 15 16:17:11 UTC 2023
PRIMARY
ECHA (EC/EINECS)
255-795-9
Created by admin on Fri Dec 15 16:17:11 UTC 2023 , Edited by admin on Fri Dec 15 16:17:11 UTC 2023
PRIMARY
EPA CompTox
DTXSID00881093
Created by admin on Fri Dec 15 16:17:11 UTC 2023 , Edited by admin on Fri Dec 15 16:17:11 UTC 2023
PRIMARY
FDA UNII
849UT193YJ
Created by admin on Fri Dec 15 16:17:11 UTC 2023 , Edited by admin on Fri Dec 15 16:17:11 UTC 2023
PRIMARY
Related Record Type Details
BINDER->LIGAND
SALT/SOLVATE -> PARENT
Related Record Type Details
PARENT -> METABOLITE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP