99624-67-6 Usage
Description
Paeonimetabolin I is a natural chemical compound derived from the roots of Paeonia lactiflora, also known as peony. It is a bioactive metabolite that has demonstrated various pharmacological properties, such as anti-inflammatory, antioxidant, and neuroprotective activities. Its potential therapeutic applications in treating inflammatory and neurological disorders make it a promising candidate for further research and development.
Uses
Used in Pharmaceutical Industry:
Paeonimetabolin I is used as a therapeutic agent for its anti-inflammatory properties, targeting the treatment of inflammatory disorders. Its ability to modulate the immune response and reduce oxidative stress contributes to its potential as a treatment option for various inflammatory conditions.
Used in Neurological Applications:
Paeonimetabolin I is used as a neuroprotective agent for its potential to treat neurological disorders. Its neuroprotective activities may help in mitigating the effects of neurodegenerative diseases and promoting the health of the nervous system.
Further research is necessary to fully understand the mechanisms of action and explore the potential clinical uses of Paeonimetabolin I in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 99624-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,2 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99624-67:
(7*9)+(6*9)+(5*6)+(4*2)+(3*4)+(2*6)+(1*7)=186
186 % 10 = 6
So 99624-67-6 is a valid CAS Registry Number.
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
99624-67-6Relevant articles and documents
Enantiospecific syntheses of paeonilactone A, paeonilactone B, 7S-paeonimetabolin-I, and 7R-paeonimetabolin-I from R-(-)-carvone
Hatakeyama,Kawamura,Shimanuki,Takano
, p. 333 - 336 (2007/10/02)
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
Hattori,Shu,Shimizu,Hayashi,Morita,Kobashi,Xu,Namba
, p. 3838 - 3846 (2007/10/02)
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