881673-95-6

Basic information

• Product Name: 1H-Pyrrole-3-methanol, 5-phenyl-
• CAS NO: 881673-95-6
• Molecular Formula: C11H11NO
• Molecular Weight: 173.214
• Mol File: 881673-95-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-3-methanol, 5-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-3-methanol, 5-phenyl-(881673-95-6)
• EPA Substance Registry System: 1H-Pyrrole-3-methanol, 5-phenyl-(881673-95-6)

Safety Data

• Hazardous Substances Data: 881673-95-6(Hazardous Substances Data)

Usage

Structure

A derivative of pyrrole, which is a five-membered aromatic ring with one nitrogen atom, with a phenyl group attached to the 5th position of the pyrrole ring.

Physical state

Colorless liquid at room temperature.

Usage

Commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and biologically active compounds.

Pharmacological properties

Studied for its potential anti-inflammatory and anti-cancer activities.

Upstream product

• 158692-57-0 Ethyl 2-chloro-5-phenyl-1H-pyrrole-3-carboxylate 
• 70-11-1 α-bromoacetophenone 
• 22984-74-3 Ethyl 2-cyano-4-oxo-4-phenylbutanoate 
• 161958-61-8 ethyl 5-phenyl-1H-pyrrole-3-carboxylate 

Downstream Products

• 881676-94-4 1-(6-chloropyridin-3-ylsulfonyl)-5-phenyl-1H-pyrrole-3-carbaldehyde 
• 881676-87-5 1-[(3-nitrophenyl)sulfonyl]-5-phenyl-1H-pyrrole-3-carbaldehyde 
• 881676-84-2 1-[(3-acetylphenyl)sulfonyl]-5-phenyl-1H-pyrrole-3-carbaldehyde 
• 881676-81-9 1-{[4-(methylsulfonyl)phenyl]sulfonyl}-5-phenyl-1H-pyrrole-3-carbaldehyde 
• 881676-78-4 1-(1-benzothien-2-ylsulfonyl)-5-phenyl-1H-pyrrole-3-carbaldehyde 
• 881681-44-3 5-phenyl-1-(3-thienylsulfonyl)-1H-pyrrole-3-carbaldehyde 
• 881681-42-1 5-phenyl-1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde 
• 881681-28-3 5-phenyl-1-({4-[(trifluoromethyl)sulfonyl]phenyl}sulfonyl)-1H-pyrrole-3-carbaldehyde 
• 881680-86-0 N-methyl-1-{1-[(3-nitrophenyl)sulfonyl]-5-phenyl-1H-pyrrol-3-yl}methanamine hydrochloride 
• 1381767-21-0 {4-[(methylamino)methyl]-2-phenyl-1H-pyrrol-1-yl}-(phenyl)methanone fumarate 

Relevant articles and documents

Proton pump inhibitors

A proton pump inhibitor containing a compound represented by the formula (I) wherein X and Y are the same or different and each is a bond or a spacer having 1 to 20 carbon atoms in the main chain, R 1 is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, R 2 , R 3 and R 4 are the same or different and each is a hydrogen atom, an optionally substituted hydrocarbon group, an optionally substituted thienyl group, an optionally substituted benzo[b]thienyl group, an optionally substituted furyl group, an optionally substituted pyridyl group, an optionally substituted pyrazolyl group, an optionally substituted pyrimidinyl group, an acyl group, a halogen atom, a cyano group or a nitro group, R 5 and R 6 are the same or different and each is a hydrogen atom or an optionally substituted hydrocarbon group, which has a superior proton pump action and shows an antiulcer activity and the like after conversion to a proton pump inhibitor in the body, or a salt thereof. or a prodrug thereof is provided.

Discovery, synthesis, and biological evaluation of novel pyrrole derivatives as highly selective potassium-competitive acid blockers

To discover a gastric antisecretory agent more potent than existing proton pump inhibitors, novel pyrrole derivatives were synthesized, and their H +,K+-ATPase inhibitory activities and inhibitory action on histamine-stimulated gastric acid secretion in rats were evaluated. Among the compounds synthesized, compound 17a exhibited selective and potent H +,K+-ATPase inhibitory activity through reversible and K+-competitive ionic binding; furthermore, compound 17c exhibited potent inhibitory action on histamine-stimulated gastric acid secretion in rats and Heidenhain pouch dogs.

PROTON PUMP INHIBITORS

A proton pump inhibitor containing a compound represented by the formula (I) wherein X and Y are the same or different and each is a bond or a spacer having 1 to 20 carbon atoms in the main chain, R1 is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, R2, R3 and R4 are the same or different and each is a hydrogen atom, an optionally substituted hydrocarbon group, an optionally substituted thienyl group, an optionally substituted benzo[b]thienyl group, an optionally substituted furyl group, an optionally substituted pyridyl group, an optionally substituted pyrazolyl group, an optionally substituted pyrimidinyl group, an acyl group, a halogen atom, a cyano group or a nitro group, R5 and R6 are the same or different and each is a hydrogen atom or an optionally substituted hydrocarbon group, which has a superior proton pump action and shows an antiulcer activity and the like after conversion to a proton pump inhibitor in the body, or a salt thereof. or a prodrug thereof is provided.