Results 121 to 130 of about 10,368 (177)

A study on the antibacterial efficacy and action mechanism of clove against <i>Helicobacter pylori</i>. [PDF]

Front Pharmacol
Kang X, Fan Y, Meng X, Jiang Z, Wang C, Zhu J, Nian Y.   +6 more
europepmc   +1 more source

Divergent Conversion Efficiencies of <i>Mycobacterium</i> sp. 191574 for Various Phytosterols and Their Underlying Mechanisms. [PDF]

Biomolecules
Ni Z, Bi Y, Wang Z, Han Y, Bi Y, Zhang L, Sun S.   +6 more
europepmc   +1 more source

Volatile compounds formed during heating of asymmetric distigmasterol-modified acylglycerols as indicators of thermo-oxidative degradation. [PDF]

Sci Rep
Grygier A, Rudzińska M, Kmiecik D, Grudniewska A.   +3 more
europepmc   +1 more source

Network pharmacology, molecular docking, and dynamics reveal the mechanisms of Hejie Shengfa Decoction against alopecia areata. [PDF]

Medicine (Baltimore)
Zhao L, Mi H, Aikeda T, Diao Z, Mou L, Zhang P, Zhang C.   +6 more
europepmc   +1 more source

In-Silico Screening of HMG-CoA Reductase Inhibition Potential from <i>Anredera cordifolia</i> (Ten.) Steenis and <i>Elephantopus scaber</i> Linn. [PDF]

Acta Med Philipp
Khotimah S.
europepmc   +1 more source

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Stigmasterol hemihydrate

Acta Crystallographica Section C Crystal Structure Communications, 2002
The title compound, stigmasta-5,22-dien-3beta-ol hemihydrate, C(29)H(48)O x 0.5H(2)O, previously thought to be the monohydrate, has two sterol molecules and one water molecule in the asymmetric unit. In both sterol molecules, the methyl group of the ethyl substituent at the end of the hydrocarbon chain is disordered over two sites.
Gloria A, Benavides, Frank R, Fronczek, Nikolaus H, Fischer   +2 more
openaire   +2 more sources

Synthesis and Characterization of Stigmasterol Oxidation Products

Journal of Agricultural and Food Chemistry, 2010
The synthesis and structural characterization of a series of oxides of stigmasterol is described providing a valuable series of reference standards for these oxides, analogous to the cholesterol oxidation products (COPs) which have been shown to have detrimental biological effects.
Florence Mccarthy, Anita Maguire, Nora O'Brien   +2 more
exaly   +3 more sources

Absolute configuration assignment of stigmasterol oxiranes

Chirality, 2021
AbstractDiastereoisomeric stigmasterol oxiranes 4, 5, 8, and 9 are known phytosterol oxidation products (POPs) that have been evaluated for their cytotoxicity, although the results are of limited significance since, in most cases, they were evaluated as mixtures.
Miguel Á. Fuentes‐Figueroa, Pedro Joseph‐Nathan, Eleuterio Burgueño‐Tapia   +2 more
openaire   +2 more sources

Polyamine conjugates of stigmasterol

Steroids, 2012
Three new polyamine conjugates with stigmasterol [(3β,22E)-stigmasta-5,22-dien-3-ol] were synthesized and subjected to basic antimicrobial and cytotoxic tests. The conjugate derived from spermine, (3β,22E)-stigmasta-5,22-dien-3-yl 4(12-amino-4,9-diaza-dodecylamino)-4-oxobutanoate (5c), displayed considerable antimicrobial activity on Staphylococcus ...
Vida, Norbert, Svobodová, Hana, Rárová, Lucie, Drašar, Pavel, Šaman, David, Cvačka, Josef, Wimmer, Zdeněk   +6 more
openaire   +4 more sources