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Results for "

ranitidine

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Bacterial (1) Biochemical Assay Reagents (3) COX (2) Drug Derivative (1) Drug Intermediate (11) Drug Metabolite (2) Endogenous Metabolite (1) Histamine Receptor (8) Isotope-Labeled Compounds (4) Reference Standards (3) SARS-CoV (1)
By Research Areas:	Cancer (8) Endocrinology (1) Infection (1) Inflammation/Immunology (4) Metabolic Disease (7)

Inhibitors & Agonists

Biochemical Assay Reagents

Natural
Products

Isotope-Labeled Compounds

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-B0693

*Ranitidine* 3 Publications Verification	Histamine Receptor	Metabolic Disease Cancer
Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA₂ values of 7.2 and 6.95, respectively. Ranitidine inhibits breast tumor development and spread in mice .

HY-B0281A

Ranitidine hydrochloride 3 Publications Verification	Histamine Receptor	Metabolic Disease Cancer
Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine hydrochloride antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA₂ values of 7.2 and 6.95, respectively. Ranitidine hydrochloride inhibits breast tumor development and spread in mice .

HY-W040203

Decyl β-D-maltopyranoside	Biochemical Assay Reagents	Others
Decyl β-D-maltopyranoside is an epithelial permeability enhancer. Decyl β-D-maltopyranoside regulates the paracellular transport pathway and increases the permeability of molecules and proteins transported via the paracellular route. Decyl β-D-maltopyranoside enhances the transepithelial paracellular permeability of EPO across cell monolayers .

HY-Y0543

5-Methylfurfural 1 Publications Verification	Biochemical Assay Reagents COX	Inflammation/Immunology Cancer
5-Methylfurfural is a chemical that can be utilized as food additive, intermediate in the production of agrochemicals, and precursor of certain anti-cancer natural products. 5-Methylfurfural is formed during the photoexposition of ranitidine hydrochloride. 5-Methylfurfural is an organic compound. 5-Methylfurfural has a strong tendency to be further hydrogenated to 2,5-dimethylfuran (DMF). 5-Methylfurfural can predominantly evoke skin inflammation and barrier disintegration. 5-Methylfurfural degrades native DNA through the formation of single-strand breaks .

HY-B0693A

Ranitidine bismuth citrate	Histamine Receptor SARS-CoV Bacterial	Infection Metabolic Disease Cancer
Ranitidine bismuth citrate is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine bismuth citrate antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA₂ values of 7.2 and 6.95, respectively. Ranitidine bismuth citrate has selectivity for SARS-CoV-2-infected cells. Ranitidine bismuth citrate also has anti-Helicobacter pylori infection. Ranitidine bismuth citrate inhibits breast tumor development and spread in mice .

HY-W011245

Ranitidine S-oxide	Drug Metabolite	Metabolic Disease
Ranitidine S-oxide is the metabolite of Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist with an IC₅₀ of 3.3 μM that inhibits gastric secretion .

HY-W011245R

Ranitidine S-oxide (Standard)	Reference Standards Drug Metabolite	Metabolic Disease
Ranitidine S-oxide (Standard) is the analytical standard of Ranitidine S-oxide. This product is intended for research and analytical applications. Ranitidine S-oxide is the metabolite of Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist with an IC50 of 3.3 μM that inhibits gastric secretion .

HY-B0281AR

Ranitidine hydrochloride (Standard)	Reference Standards Histamine Receptor	Metabolic Disease Cancer
Ranitidine hydrochloride (Standard) is the analytical standard of Ranitidine hydrochloride (HY-B0281A). This product is intended for research and analytical applications. Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine hydrochloride antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA₂ values of 7.2 and 6.95, respectively. Ranitidine hydrochloride inhibits breast tumor development and spread in mice.

HY-B0281AS

Ranitidine-d6 hydrochloride	Isotope-Labeled Compounds Histamine Receptor	Metabolic Disease Cancer
Ranitidine-d₆ hydrochloride is the deuterium labeled Ranitidine hydrochloride (HY-B0281A) . Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine hydrochloride antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA₂ values of 7.2 and 6.95, respectively. Ranitidine hydrochloride inhibits breast tumor development and spread in mice .

HY-B0693S

Ranitidine-d6	Isotope-Labeled Compounds Histamine Receptor	Cancer
Ranitidine-d₆ is the deuterium labeled Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA2 values of 7.2 and 6.95, respectively. Ranitidine inhibits breast tumor development and spread in mice .

HY-Z8387

Ranitidine impurity 2 ranitidine impurity I	Drug Intermediate	Others
Ranitidine impurity 2 (Ranitidine impurity I) is an impurity of Ranitidine.

HY-Z8388

Ranitidine impurity 3 ranitidine impurity J	Drug Intermediate	Others
Ranitidine impurity 3 (Ranitidine impurity J) is an impurity of Ranitidine.

HY-W013109

Ranitidine impurity 15	Drug Intermediate	Others
Ranitidine impurity 15 is an impurity of Ranitidine.

HY-W015620

Ranitidine impurity 14	Drug Intermediate	Others
Ranitidine impurity 14 is an impurity of Ranitidine.

HY-Z6359

Ranitidine impurity 4 hydrochloride	Drug Intermediate	Others
Ranitidine impurity 4 hydrochloride is an impurity of Ranitidine hydrochloride.

HY-Z2616

Ranitidine impurity 4	Drug Intermediate	Others
Ranitidine impurity 4 is an impurity of Ranitidine.

HY-W702661

Ranitidine impurity 13	Drug Intermediate	Others
Ranitidine impurity 13 is an impurity of Ranitidine.

HY-Z2517

Ranitidine impurity 8	Drug Intermediate	Others
Ranitidine impurity 8 is an impurity of Ranitidine.

HY-126875

Ranitidine impurity 12	Drug Intermediate	Others
Ranitidine impurity 12 is an impurity of Ranitidine.

HY-Z1899

Ranitidine impurity 11	Drug Intermediate	Others
Ranitidine impurity 11 is an impurity of Ranitidine.

HY-Y0543R

5-Methylfurfural (Standard)	Biochemical Assay Reagents Reference Standards COX	Inflammation/Immunology Cancer
5-Methylfurfural (Standard) is the analytical standard of 5-Methylfurfural. This product is intended for research and analytical applications. 5-Methylfurfural is a chemical that can be utilized as food additive, intermediate in the production of agrochemicals, and precursor of certain anti-cancer natural products. 5-Methylfurfural is formed during the photoexposition of ranitidine hydrochloride. 5-Methylfurfural is an organic compound. 5-Methylfurfural has a strong tendency to be further hydrogenated to 2,5-dimethylfuran (DMF). 5-Methylfurfural can predominantly evoke skin inflammation and barrier disintegration. 5-Methylfurfural degrades native DNA through the formation of single-strand breaks .

HY-136818

DA 4643 dihydrochloride	Histamine Receptor	Endocrinology
DA 4643 (hydrochloride) is an H2 receptor antagonist with the chemical name 2-guanidino-4 (3-methylaminomethyleneiminophenyl) thiazole dihydrochloride. It has a weak interaction with cytochrome P-450 and has a less inhibitory effect on P-450 than cimetidine and tiotidine. DA 4643 (hydrochloride) is able to inhibit both enzymatic and non-enzymatic lipid peroxidation reactions. This inhibition may not be achieved by inhibiting agent metabolizing enzymes, but rather due to the antioxidant properties of the compound itself. Compared with other H2 receptor antagonists such as cimetidine, ranitidine and tiotidine, DA 4643 (hydrochloride) shows a unique effect in lipid peroxidation inhibition. These properties make DA 4643 (hydrochloride) a potential H2 receptor antagonist with multiple mechanisms of action.

HY-Z8386

Ranitidine impurity 1 N-Methylnitroacetamide	Drug Intermediate	Others
Ranitidine impurity 1 (N-Methylnitroacetamide) is an impurity of Ranitidine.

HY-W739861

α-Hydroxytriazolam 1'-Hydroxytriazolam	Endogenous Metabolite	Others
α-Hydroxytriazolam (1'-Hydroxytriazolam) is a major metabolite of ranitidine (HY-B0693) .

HY-W711197

*2,2'-Methylene Bis[Ranitidine]-d12*	Isotope-Labeled Compounds	Others
2,2'-Methylene Bis[Ranitidine]-d₁₂ is the deuterium labeled (1Z,4Z)-N1,N5-Bis(2-(((5-((dimethylamino)methyl)furan-2-yl)methyl)thio)ethyl)-N1,N5-dimethyl-2,4-dinitropenta-1,4-diene-1,1,5,5-tetraamine (Ranitidine Impurity) (HY-Z8387).

HY-W1040921

AY-31574	Drug Derivative	Inflammation/Immunology
AY-31574 is a 3, 5-difluoro derivative and selective mucosal protectant. AY-31574 is equipotent with Ranitidine (HY-B0693) against gastric injury caused by stress .

HY-W700730

5-[(Dimethyl-amino)methyl]-2-furanmethanol-d6	Isotope-Labeled Compounds	Others
5-[(Dimethyl-amino)methyl]-2-furanmethanol-d₆ is the deuterium labeled (5-((dimethylamino)methyl)furan-2-yl)methanol (Ranitidine Impurity） (HY-Z2616).

HY-182427

ORF 17583	Histamine Receptor	Inflammation/Immunology
ORF 17583 is a Ranitidine (HY-B0693) analogue and H2 receptor antagonist. ORF 17583 exhibits typical reversible competitive antagonism in the guinea pig right atria model, causing a dose-dependent rightward shift of the histamine concentration-response curve without reducing the maximum effect, and its action is fully reversible upon washing. ORF 17583 can be used for research on peptic ulcers and hyperacidity .

Decyl β-D-maltopyranoside	Biochemical Assay Reagents
Decyl β-D-maltopyranoside is an epithelial permeability enhancer. Decyl β-D-maltopyranoside regulates the paracellular transport pathway and increases the permeability of molecules and proteins transported via the paracellular route. Decyl β-D-maltopyranoside enhances the transepithelial paracellular permeability of EPO across cell monolayers .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-Y0543

5-Methylfurfural 1 Publications Verification	Cornaceae Classification of Application Fields Cornus officinalis Sieb. et Zucc. Ketones, Aldehydes, Acids Other Diseases Plants Disease Research Fields Source Classification	Biochemical Assay Reagents COX
5-Methylfurfural is a chemical that can be utilized as food additive, intermediate in the production of agrochemicals, and precursor of certain anti-cancer natural products. 5-Methylfurfural is formed during the photoexposition of ranitidine hydrochloride. 5-Methylfurfural is an organic compound. 5-Methylfurfural has a strong tendency to be further hydrogenated to 2,5-dimethylfuran (DMF). 5-Methylfurfural can predominantly evoke skin inflammation and barrier disintegration. 5-Methylfurfural degrades native DNA through the formation of single-strand breaks .

HY-Y0543R

5-Methylfurfural (Standard)	Structural Classification Microorganisms Cornaceae Cornus officinalis Sieb. et Zucc. Ketones, Aldehydes, Acids Plants Source Classification	Biochemical Assay Reagents Reference Standards COX
5-Methylfurfural (Standard) is the analytical standard of 5-Methylfurfural. This product is intended for research and analytical applications. 5-Methylfurfural is a chemical that can be utilized as food additive, intermediate in the production of agrochemicals, and precursor of certain anti-cancer natural products. 5-Methylfurfural is formed during the photoexposition of ranitidine hydrochloride. 5-Methylfurfural is an organic compound. 5-Methylfurfural has a strong tendency to be further hydrogenated to 2,5-dimethylfuran (DMF). 5-Methylfurfural can predominantly evoke skin inflammation and barrier disintegration. 5-Methylfurfural degrades native DNA through the formation of single-strand breaks .

Cat. No.	Product Name	Chemical Structure

HY-B0281AS

Ranitidine-d6 hydrochloride
Ranitidine-d₆ hydrochloride is the deuterium labeled Ranitidine hydrochloride (HY-B0281A) . Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine hydrochloride antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA₂ values of 7.2 and 6.95, respectively. Ranitidine hydrochloride inhibits breast tumor development and spread in mice .

Ranitidine-d6 hydrochloride

Ranitidine-d₆ hydrochloride is the deuterium labeled Ranitidine hydrochloride (HY-B0281A) . Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine hydrochloride antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA₂ values of 7.2 and 6.95, respectively. Ranitidine hydrochloride inhibits breast tumor development and spread in mice .

HY-B0693S

Ranitidine-d6
Ranitidine-d₆ is the deuterium labeled Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA2 values of 7.2 and 6.95, respectively. Ranitidine inhibits breast tumor development and spread in mice .

Ranitidine-d6

Ranitidine-d₆ is the deuterium labeled Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA2 values of 7.2 and 6.95, respectively. Ranitidine inhibits breast tumor development and spread in mice .

HY-W711197

*2,2'-Methylene Bis[Ranitidine]-d12*
2,2'-Methylene Bis[Ranitidine]-d₁₂ is the deuterium labeled (1Z,4Z)-N1,N5-Bis(2-(((5-((dimethylamino)methyl)furan-2-yl)methyl)thio)ethyl)-N1,N5-dimethyl-2,4-dinitropenta-1,4-diene-1,1,5,5-tetraamine (Ranitidine Impurity) (HY-Z8387).

HY-W700730

5-[(Dimethyl-amino)methyl]-2-furanmethanol-d6
5-[(Dimethyl-amino)methyl]-2-furanmethanol-d₆ is the deuterium labeled (5-((dimethylamino)methyl)furan-2-yl)methanol (Ranitidine Impurity） (HY-Z2616).

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