19275-44-6 Usage
Description
1-Isomangostin is an organic heterotetracyclic compound characterized by its unique structure, which includes 3,4-dihydro-2H,12H-pyrano[2,3-a]xanthen-12-one substituted by hydroxy groups at positions 5 and 9, a methoxy group at position 10, two methyl groups at position 2, a prenyl group at position 11, and an oxo group at position 12. 1-Isomangostin is known for its potential biological activities and applications in various fields.
Uses
Used in Pharmaceutical Industry:
1-Isomangostin is used as a pharmaceutical agent for its potential anti-inflammatory, antioxidant, and anticancer properties. Its ability to modulate various biological pathways and target specific enzymes makes it a promising candidate for the development of new drugs to treat various diseases.
Used in Cosmetic Industry:
1-Isomangostin is used as an active ingredient in cosmetic products for its potential skin-whitening and anti-aging effects. Its antioxidant and anti-inflammatory properties contribute to the protection and rejuvenation of the skin, making it a valuable component in skincare formulations.
Used in Food Industry:
1-Isomangostin is used as a natural preservative and antioxidant in the food industry. Its ability to inhibit the growth of microorganisms and prevent oxidation of food products helps to extend their shelf life and maintain their quality.
Used in Agricultural Industry:
1-Isomangostin is used as a biopesticide in the agricultural industry due to its potential insecticidal and antimicrobial properties. It can help protect crops from pests and diseases, promoting sustainable agriculture practices.
Check Digit Verification of cas no
The CAS Registry Mumber 19275-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,7 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19275-44:
(7*1)+(6*9)+(5*2)+(4*7)+(3*5)+(2*4)+(1*4)=126
126 % 10 = 6
So 19275-44-6 is a valid CAS Registry Number.
InChI:InChI=1/C24H26O6/c1-12(2)6-7-14-19-17(11-16(26)22(14)28-5)29-18-10-15(25)13-8-9-24(3,4)30-23(13)20(18)21(19)27/h6,10-11,25-26H,7-9H2,1-5H3
19275-44-6Relevant articles and documents
Stout et al.
, p. 211 (1968)
Design, synthesis and structure-activity relationships of mangostin analogs as cytotoxic agents
Chi, Xiao-Qian,Zi, Cheng-Ting,Li, Hong-Mei,Yang, Liu,Lv, Yong-Feng,Li, Jin-Yu,Hou, Bo,Ren, Fu-Cai,Hu, Jiang-Miao,Zhou, Jun
, p. 41377 - 41388 (2019/01/03)
In order to better understand the structure-activity relationship of mangostin, a series of xanthone derivatives based on α-mangostin were designed and synthesized. All the compounds were evaluated for their cytotoxicity against a panel of five human canc
Bicyclomangostin: A new acid-catalysed cyclization product from mangostin
Mahabusarakam, Wilawan,Pakawatchai, Chaveng,Wiriyachitra, Pichaet,Taylor, Walter C.,Skelton, Brian W.,White, Allan H.
, p. 249 - 254 (2007/10/03)
Cyclization of mangostin with p-toluenesulfonic acid gave 1-isomangostin, 3-isomangostin, and a new cyclization product, bicyclomangostin (4). The structure of bicyclomangostin was determined by spectroscopic and X-ray crystallographic studies. The methyl ether derivatives (8) and (9) or (10) were produced on methylation of bicyclomangostin, depending on the method used.
