138530-94-6 Usage
Description
Different sources of media describe the Description of 138530-94-6 differently. You can refer to the following data:
1. The mechanism of PPIs involves the irreversible binding to the hydrogen/potassium adenosine triphosphatase enzyme system, commonly
referred to as the gastric proton pump, of the gastric parietal cell. As
the last stage in gastric acid secretion, blockade of the gastric proton
pump is an effective treatment for a variety of diseases requiring acid suppression, such as heartburn, peptic ulcers, and GERD. Dexlansoprazole is the latest PPI to hit the market, joining the ranks of omeprazole,
rabeprazole, pantoprazole, esomeprazole, and lansoprazole, and is the Renantiomer of the racemic lansoprazole. Compared to its predecessors,
dexlansoprazole exhibits improved pharmacokinetics with slower clearance and longer terminal half-life. In addition, dexlansoprazole utilizes a
novel DDR technology; drug release is optimized through the use of
granules with different pH-dependent dissolution profiles, thereby providing an initial release in the proximal small intestine within 1-2 h of
administration followed by a subsequent release at distal regions of the
small intestine several hours later. With its longer duration of action
culminating in more effective acid suppression, dexlansoprazole may
have an advantage over conventional PPIs that possess single release
formulations (immediate or delayed).
Similar to all PPIs, dexlansoprazole
is a prodrug that consists of pyridine and benzimidazole rings with a
latent sulfenamide moiety. In order to form the disulfide bond with
cysteine residues of the proton pump, dexlansoprazole must be activated
through two protonations followed by a spontaneous rearrangement to
unmask the sulfenamide.
2. Lansoprazole is a proton pump inhibitor that irreversibly inactivates the H+/K+-stimulated ATPase pumps in parietal cells, inhibiting gastric acid secretion and increasing intragastric pH. It is a 1:1 racemic mixture of (R)-lansoprazole and (S)-lansoprazole, both of which are pharmacologically active. (R)-Lansoprazole is an enantiomerically pure form of lansoprazole. It can inhibit acid formation in isolated canine parietal cells with an IC50 value of 59 nM and inhibit the H+/K+-ATPase with an IC50 value of 4.2 μM.
Chemical Properties
Brown Solid
Originator
Takeda (Japan)
Uses
Different sources of media describe the Uses of 138530-94-6 differently. You can refer to the following data:
1. antiulcer, proton pump inhibitor
2. Acts as a gastric proton pump inhibitor and an antiulcerative
3. The R-enantiomer of Lansoprazole; a gastric proton pump inhibitor. An antiulcerative
Brand name
Kapidex
Clinical Use
Takeda Pharmaceuticals received approval of dexlansoprazole, a
dual release formulation of the (R)-isomer of lansoprazol proton
pump inhibitor (PPI) already in the market, from the FDA in January
2009. Dexlansoprazole is a delayed release capsule for the oncedaily,
oral treatment of heartburn associated with symptomatic
non-erosive gastroesophageal reflux disease (GERD), the healing
of erosive esophagitis (EE) and the maintenance of healed EE.
The dual release formulation is designed to provide two separate
releases of medication, one at 1–2 h and then another at 4–5 h after
treatment, for extended efficacy in the treatment of GERD.
Side effects
The most commonly recorded adverse reactions that occurred at a higher incidence than placebo were diarrhea, abdominal pain, nausea, vomiting, flatulence, and upper respiratory tract infection. As dexlansoprazole inhibits gastric acid secretion, its use is expected to interfere with the absorption of drugs with pH-dependent oral bioavailability. Since the HIV protease inhibitor atazanavir is dependent on gastric acid for absorption, dexlansoprazole should not be co-administered with atazanavir to avoid a loss of therapeutic efficacy. While co-administration of dexlansoprazole did not affect the pharmacokinetics of warfarin or INR (international normalized ratio: the ratio of a patient s prothrombin time to a normal sample), there have been reports of increased INR and prothrombin time in patients receiving concomitant treatment with PPIs and warfarin. Since increases in INR and prothrombin time may lead to abnormal bleeding and possibly death, concomitant use of dexlansoprazole and warfarin may necessitate monitoring for increases in INR and prothrombin time.
Synthesis
Similar
to the synthesis of the chiral sulfoxide of armodafinil vide supra, the
preparation of the chiral sulfoxide of lansoprazole utilized the catalytic
oxidation method developed by Kagan and co-workers
(the Scheme). Two routes have been reported that describe the
preparation of dexlansoprazole on large scale. The first route
developed by Takeda reacts commercially available thioether 29,
also used to make lansoprazole, under the Kagan asymmetric oxidation
conditions and the alternative route utilizes the cheaper commercial intermediate nitrosulfide 30 in the analogous asymmetric
oxidation by Kagan). Thus, the catalyst complex
consisting of (+)-DET, Ti(OiPr)4 and water was formed in the presence
of thioether 29 in toluene at 30–40°C. The reaction mixture
was then cooled to 5 °C and DIPEA and cumene hydroperoxide
(CMHP) were added to give, after aqueous work-up and in situ crystallization
from the organic layer, dexlansoprazole (VI) in 98% ee.
No yield was given in the patent. An alternate, but similar, sequence
was also described wherein the nitrosulfide intermediate 30 was
subjected to similar oxidative conditions that gave intermediate nitro
compound 31 in 80% yield and 98% ee. Compound 31 was treated
with KOH and trifluoroethanol to provide dexlansoprazole (VI).
Check Digit Verification of cas no
The CAS Registry Mumber 138530-94-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,3 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138530-94:
(8*1)+(7*3)+(6*8)+(5*5)+(4*3)+(3*0)+(2*9)+(1*4)=136
136 % 10 = 6
So 138530-94-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H14F3N3O2S/c1-10-13(20-7-6-14(10)24-9-16(17,18)19)8-25(23)15-21-11-4-2-3-5-12(11)22-15/h2-7H,8-9H2,1H3,(H,21,22)/t25-/m1/s1
138530-94-6Relevant articles and documents
Two-dimensional chromatography method applied to the enantiomeric determination of lansoprazole in human plasma by direct sample injection
Gomes, Ricardo F.,Cassiano, Neila M.,Pedrazzoli Jr.,Cass, Quezia B.
, p. 35 - 41 (2010)
A two-dimensional HPLC method based on the direct injection of biological samples has been developed and validated for the determination of lansoprazole enantiomers in human plasma. The lansoprazole enantiomers were extracted from the biological matrix using an octyl restricted access media bovine serum albumin column (C8 RAM BSA) and the enantioseparation was performed on an amylose tris(3,5-dimethoxyphenylcarbamate) chiral column using acetonitrile:water (35:65 v/v) and UV detection at 285 nm. Analysis time was 25 min with no time spent on sample preparation. The method was applied to the analysis of the plasma samples obtained from nine Brazilian volunteers who received a 30 mg oral dose of racemic lansoprazole and was able to quantify the enantiomers of lansoprazole in the clinical samples analyzed.
Preparation method of high-optical-purity anti-gastric-ulcer drug R-lansoprazole
-
Paragraph 0052-0057, (2018/08/03)
The invention belongs to the technical field of chiral synthesized chemical drugs and in particular relates to a preparation method of a high-optical-purity anti-gastric-ulcer drug R-lansoprazole. According to the preparation method, a molecular sieve is used as a carrier and tungsten trioxide is loaded on the surface of the molecular sieve in situ to prepare a tungsten loaded molecular sieve; L-hydroxyproline and tetraisopropyl titanate form a complex compound and the complex compound is deposited on the surface of the tungsten loaded molecular sieve and/or in a pore diameter to form a tungsten-titanium double-metal center catalyst; the catalyst can be used for catalyzing thioether2-[3-methyl-4-(2,2,2-trifluoroethoxy)pyridine-2-yl]-methylthio-1H-benzimidazole to be subjected to oxidization reaction to obtain the high-optical-purity R-lansoprazole; the chemical purity and optical purity of the prepared product reach requirements of medical-grade crude drugs.
Ti-Salan catalyzed asymmetric sulfoxidation of pyridylmethylthiobenzimidazoles to optically pure proton pump inhibitors
Talsi, Evgenii P.,Bryliakov, Konstantin P.
, p. 84 - 89 (2016/11/11)
The asymmetric sulfoxidation of two pyridylmethylthiobenzimidazoles to anti-ulcer drugs of the PPI family (S)-omeprazole and (R)-lansoprazole with hydrogen peroxide, mediated by a series of chiral titanium(IV) salan complexes is reported. High sulfoxide yields (up to?>95%) and enantioselectivities (up to 94% ee) have been achieved. The introduction of electron-withdrawing substituents leads to less active and less enantioselective catalysts. Like for the previously reported Ti-salalen catalyzed sulfoxidations, the temperature dependence of the sulfoxidation enantioselectivity in the presence of Ti-salan complexes is nonmonotonic, demonstrating isoinversion behavior with decreasing temperature. The oxidation is likely rate-limited by the formation of the active (presumably peroxotitanium(IV)) species, followed by a faster oxygen transfer to the substrate.
