302924-75-0Relevant academic research and scientific papers
First stereoselective total synthesis of ophiocerins B and C
Yadav,Naga Lakshmi,Harshavardhan,Subba Reddy
, p. 1945 - 1947 (2007)
An elegant synthesis of ophiocerins B and C is accomplished for the first time with 3R,4R,6R and 3S,4S,6R-configuration. Of these three stereogenic centers, the C-3/C-4 vic-diol was created by Sharpless asymmetric dihydroxylation, while the C-6 stereocent
ACTIVE AGENTS AND METHODS OF THEIR USE FOR THE TREATMENT OF METABOLIC DISORDERS AND NONALCOHOLIC FATTY LIVER DISEASE
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Page/Page column 67; 78, (2019/12/28)
Disclosed herein are active agents, compositions containing them, unit dosage forms containing them, and methods of their use, e.g., for treating a metabolic disorder or nonalcoholic fatty liver disease or for modulating a metabolic marker or nonalcoholic fatty liver disease marker.
ACYLATED CATECHIN POLYPHENOLS AND METHODS OF THEIR USE FOR THE TREATMENT OF CANCER
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Page/Page column 59, (2019/12/28)
Disclosed herein are acylated active agents and methods of their use, e.g., for modulating a cancer marker or for treating cancer.
MULTIBIOTIC AGENTS AND METHODS OF USING THE SAME
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Page/Page column 157, (2019/01/06)
Multibiotic agents are disclosed. The multibiotic agents may contain two or more moieties linked through bonds cleavable in vivo. The bonds cleavable in vivo can be ester bonds, amide bonds, azo bonds, glycosidic bonds, carbonate linkers, or carbamate linkers. The moieties can be alcohol cores, amine cores, and/or acyls. Also disclosed are compositions containing multibiotic agents and methods of using the multibiotic agents.
First Synthesis and Characterization of Stereoisomers of Choleretic Drug Dihydroxydibutylether
Yue, Qiming,Zhao, Yi,Sun, Baohou,Hai, Li,Guo, Li,Wu, Yong
, p. 1145 - 1152 (2015/11/02)
Dihydroxydibutylether (DHBE) is a choleretic drug used for the treatment of gallstone and hepatic disorders due to its choleretic activity and hepatoprotective action. The drug is a mixture of three regioisomers. The main regioisomer 3-(3-hydroxylbutoxy)-
First stereoselective total synthesis of Neocosmosin A: A facile approach
Dachavaram, Soma Shekar,Kalyankar, Kondbarao Balasaheb,Das, Saibal
, p. 5629 - 5631 (2014/12/11)
First stereoselective concise synthesis of Neocosmosin A, with in vitro binding affinity for human opioid and cannabinoid receptors, has been reported using readily available starting materials such as methylacetoacetate, cyclohexanone, and homoallyl alco
Acceleration of hetero-Michael reaction by symmetrical pentacyclic guanidines
Nagasawa, Kazuo,Georgieva, Angelina,Takahashi, Hiroki,Nakata, Tadashi
, p. 8959 - 8964 (2007/10/03)
Symmetrical pentacyclic guanidines 1a-c and 2 which contain the core skeleton of 13,14,15-isocrmbescidine 800, have been synthesized. In the presence of catalytic amounts of these guanidines 1, the reaction rate of the conjugate addition of pyrrolidine (9) to γ-crotonolactone (10) could be enhanced depending upon the size of the cavities and substituents on tetrahydropyran rings of 1 and 2.
