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SML2322

Sigma-Aldrich

Ilaprazole

≥98% (HPLC)

Synonym(e):

2-[[(4-Methoxy-3-methyl-2-pyridinyl)methyl]sulfinyl]-6-(1H-pyrrol-1-yl)-1H-benzimidazole, IY 81149, IY-81149

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About This Item

Empirische Formel (Hill-System):
C19H18N4O2S
CAS-Nummer:
172152-36-2
Molekulargewicht:
366.44
MDL-Nummer:
MFCD00942538
UNSPSC-Code:
12352200
NACRES:
NA.77

Assay

≥98% (HPLC)

Form

powder

Farbe

white to beige

Löslichkeit

DMSO: 2 mg/mL, clear

Lagertemp.

−20°C

SMILES String

[S](=O)(Cc4nccc(c4C)OC)c1[nH]c2c(n1)cc(cc2)[n]3cccc3

InChI

1S/C19H18N4O2S/c1-13-17(20-8-7-18(13)25-2)12-26(24)19-21-15-6-5-14(11-16(15)22-19)23-9-3-4-10-23/h3-11H,12H2,1-2H3,(H,21,22)

InChIKey

HRRXCXABAPSOCP-UHFFFAOYSA-N

Biochem./physiol. Wirkung

Ilaprazole is a proton pump inhibitor (H+/K+ ATPase inhibitor) that suppresses acids secretion. Ilaprazole is a potent and selective inhibitor of T-cell-originated protein kinase (TOPK) that suppresses cancer growth.
proton pump inhibitor (H+/K+ ATPase inhibitor)

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

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Analysenzertifikate (COA)

Lot/Batch Number

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Mengzhu Zheng et al.
Oncotarget, 8(24), 39143-39153 (2017-04-08)
T-cell-originated protein kinase (TOPK) is highly and frequently expressed in various cancer tissues and plays an indispensable role in the mitosis of cancer cells, and therefore, it is an important target for drug treatment of tumor. Ilaprazole was identified to
J S Shin et al.
Alimentary pharmacology & therapeutics, 40(5), 548-561 (2014-07-22)
Ilaprazole, a proton pump inhibitor (PPI) currently in clinical use, may provide improved acid suppression vs. other PPIs. To compare the pharmacodynamic and pharmacokinetic profiles of ilaprazole and esomeprazole. A phase 1, randomised, open-label, single-centre, 4-period crossover study was conducted
D Kwon et al.
Arzneimittel-Forschung, 51(3), 204-213 (2001-04-18)
The inhibitory effects of IY-81149 (2-[[(4-methoxy-3-methyl)-2- pyridinyl]methyl-sulfinyl]-5-(1H-pyrol-1-yl)-1H-benzimidazole, CAS 172152-36-2), a newly developed proton pump inhibitor (PPI) on gastric acid secretion were investigated in vitro and in vivo. In rabbit parietal cell preparation, IY-81149 irreversibly inhibited H+/K(+)-ATPase in dose-dependent manner with

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