Diltiazem N-Oxide

Product Name Diltiazem N-Oxide
Alternate Names Diltiazem Impurities, Impurities of Diltiazem
CAT No. CS-T-90720
CAS No. 142843-04-7
Category Impurities
Stock IN-Stock
Mol. Wt. 430.52 g/mol
Mol. For. C22H26N2O5S
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Diltiazem
Smileys O=C1[C@H](OC(C)=O)[C@H](C2=CC=C(OC)C=C2)SC3=CC=CC=C3N1CC[N+](C)(C)[O-]
Canonical Smiles CC(=O)OC1C(SC2=CC=CC=C2[N+](C1=O)(CCN(C)C)[O-])C3=CC=C(C=C3)OC
InchIKey VMYITXJQDGPHNJ-JBAPTLGWSA-N
Inchl InChI=1S/C22H26N2O5S/c1-15(25)29-20-21(16-9-11-17(28-4)12-10-16)30-19-8-6-5-7-18(19)24(27,22(20)26)14-13-23(2)3/h5-12,20-21H,13-14H2,1-4H3/t20-,21+,24?/m1/s1
IUPAC [(2S,3S)-5-[2-(dimethylamino)ethyl]-2-(4-methoxyphenyl)-5-oxido-4-oxo-2,3-dihydro-1,5-benzothiazepin-5-ium-3-yl] acetate
Controlled No
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Diltiazem N-Oxide is a potent and selective inhibitor of L-type calcium channels. It is a derivative of diltiazem, which is commonly used to treat hypertension and angina. Diltiazem N-Oxide is used primarily as a research tool to study the role of L-type calcium channels in various physiological and pathological conditions. The chemical structure of Diltiazem N-Oxide includes an N-oxide group, which is responsible for its unique pharmacological properties. This group is known to undergo rapid reduction in vivo, leading to the formation of the parent compound diltiazem. This process is thought to contribute to the pharmacokinetics and pharmacodynamics of Diltiazem N-Oxide. In vitro studies have shown that Diltiazem N-Oxide is a potent inhibitor of L-type calcium channels, with an IC50 value in the low micromolar range. It has also been shown to have selectivity for this channel subtype over other calcium channels. This selectivity makes Diltiazem N-Oxide a valuable tool for investigating the specific roles of L-type calcium channels in various cellular processes. Overall, Diltiazem N-Oxide is a useful research tool for investigating the physiology and pharmacology of L-type calcium channels. Its unique chemical structure and pharmacological properties make it a valuable addition to the research arsenal of scientists studying cardiovascular and neurological diseases.

Related Compounds

Diltiazem Impurity 2 | Diltiazem related compound H | Diltiazem formamide impurity | O-Desmethyldiltiazem | Diltiazem Impurity 1 | N-Acetyl Diltiazem | Diltiazem EP Impurity C Hydrochloride (O-Desmethyl Diltiazem Hydrochloride) | N,N-Didesmethyl N-tert-Butoxycarbonyl Diltiazem | Diltiazem dihydrolysed impurity | rel-N-Desmethyl Desacetyl Diltiazem | Diltiazem Sulphone | Diltiazem-d3 Hydrochloride | Diltiazem Impurity G (N-Desmethyl Desacetyl Diltiazem Hydrochloride) | Deacetyl o-demethyl diltiazem | DTZ-II Diltiazem impurity | Diltiazem EP Impurity C | N,N-didesmethyl diltiazem | Diltiazem EP Impurity A | Diltiazem monohydrolysed impurity | Diltiazem Epoxide (2R,3S) Isomers | Not in use Diltiazem related compound G | N-desmethyl N-nitroso Diltiazem | Acetoxy Lactam Diltiazem | dl-cis-Diltiazem | N,N-Didesmethyl Diltiazem Hydrochloride | Diltiazem DTZ-I Impurity | Deacetyl Diltiazem N-Oxide |

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