99624-67-6

Basic information

• Product Name: paeonimetabolin I
• Synonyms: paeonimetabolin I
• CAS NO: 99624-67-6
• Molecular Formula: C₁₀H₁₄O₄
• Molecular Weight: 198.2158
• Mol File: 99624-67-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 323.6°Cat760mmHg
• Flash Point: 129.2°C
• Appearance: /
• Density: 1.371g/cm³
• Vapor Pressure: 2.03E-05mmHg at 25°C
• Refractive Index: 1.566
• CAS DataBase Reference: paeonimetabolin I(CAS DataBase Reference)
• NIST Chemistry Reference: paeonimetabolin I(99624-67-6)
• EPA Substance Registry System: paeonimetabolin I(99624-67-6)

Safety Data

• Hazardous Substances Data: 99624-67-6(Hazardous Substances Data)

Usage

General Description

Paeonimetabolin I is a natural chemical compound isolated from the roots of Paeonia lactiflora, commonly known as peony. It belongs to the class of bioactive metabolites and has been found to exhibit various pharmacological properties, including anti-inflammatory, antioxidant, and neuroprotective activities. Paeonimetabolin I has been studied for its potential use in the treatment of inflammatory and neurological disorders. Its ability to modulate the immune response and reduce oxidative stress makes it a promising candidate for therapeutic applications. Further research is needed to fully understand the mechanisms of action and potential clinical uses of Paeonimetabolin I.

InChI:InChI=1/C10H14O4/c1-5-6-3-10(12)9(2,4-7(6)11)13-8(5)14-10/h5-6,8,12H,3-4H2,1-2H3

Upstream product

• 23180-57-6 paeoniflorin 
• 139685-64-6 (3aS,4aR,7S,7aR,8aR)-2,2,3a,7-Tetramethyl-hexahydro-furo[2',3':4,5]benzo[1,2-d][1,3]dioxol-6-one 
• 139685-66-8 (3aS,5R,6R,7aR)-2,2,3a-Trimethyl-6-((S)-1-methyl-allyl)-hexahydro-benzo[1,3]dioxol-5-ol 
• 139618-34-1 (3aS,5R,6R,7aR)-2,2,3a-Trimethyl-6-((R)-1-methyl-allyl)-hexahydro-benzo[1,3]dioxol-5-ol 
• 139685-67-9 (2S,5R)-2-Hydroxy-2-methyl-5-((S)-1-methyl-allyl)-cyclohexane-1,4-dione 
• 139618-30-7 (3aR,4R,6S,7aR)-6-Isopropenyl-2,2,3a-trimethyl-4-phenylselanyl-hexahydro-benzo[1,3]dioxole 
• 139618-33-0 (3aR,4R,4aS,7aR,8aR)-4-Iodo-2,2,3a-trimethyl-7-methylene-hexahydro-furo[2',3':4,5]benzo[1,2-d][1,3]dioxol-6-one 
• 139618-32-9 2-((3aR,5S,7aS)-2,2,7a-Trimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-5-yl)-prop-2-en-1-ol 
• 139685-63-5 (3aS,4aR,7aR,8aR)-2,2,3a-Trimethyl-7-methylene-hexahydro-furo[2',3':4,5]benzo[1,2-d][1,3]dioxol-6-one 
• 139618-31-8 (3aR,5S,7aS)-2,2,7a-Trimethyl-5-(2-methyl-oxiranyl)-3a,4,5,7a-tetrahydro-benzo[1,3]dioxole 
• 24120-79-4 (1R,2R,4S,6S)-(-)-1-methyl-4-(prop-1-en-2-yl)-7-oxabicyclo[4.1.0]heptan-2-ol 
• 139618-35-2 (2S,5R)-2-Hydroxy-2-methyl-5-((R)-1-methyl-allyl)-cyclohexane-1,4-dione 
• 23180-57-6 paeoniflorin 
• 38642-49-8 benzoylpaeoniflorin 

Downstream Products

• 111950-56-2 7S-paeonimetaboline-6-O-3,5-dinitrophenyl carbamate 

Relevant articles and documents

Enantiospecific syntheses of paeonilactone A, paeonilactone B, 7S-paeonimetabolin-I, and 7R-paeonimetabolin-I from R-(-)-carvone

The first enantiospecific syntheses of the title monoterpenes have been accomplished starting with R-(-)-carvone, which made their absolute structures unequivocal.

Metabolism of paeoniflorin and related compounds by human intestinal bacteria

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