Phytochemical investigation of Anaphalis lactea

Four new compounds, 2',6'-dihydroxy-3'-(2-hydroxy-3-methyl-3-butenyl)-4'-methoxychalcone ( 1), 4,6-dihydroxy-7-isobutyryl-5-prenyl-2(3 H)-benzofuranone ( 4), 7- O-(beta- D-glucopyranosyloxy)-5-hydroxy-1(3 H)-isobenzofuranone ( 6) and (2 R,3 S)-3-methyl-2-(5-oxo-2-isopropenylhexyl)-cyclopentanone ( 7), along with thirteen known compounds were isolated from the whole plant of Anaphalis lactea. Their structures were established based on spectroscopic methods including IR, UV, MS, CD, 1 D NMR and 2 D NMR techniques. Compounds 2, 4 - 6 and 8 - 16 were tested for free-radical scavenging properties in the DPPH assays.     

Phytochemical investigation of Perovskia abrotanoides

The phytochemical investigation of the n-hexane, the EtOAc, and the n-BuOH soluble fractions of the methanolic extract of the arial parts of Perovskia abrotanoides Karelin furnished ten compounds including the two new tetracyclic diterpenes abrotandiol (7) and abrotanone (8) besides the known cirsimaritin (9), hespiridin (10), rosmarinic acid (11), stigmast-5-en-3beta-ol (12), stigmast-5,22-dien-3beta-ol (13), stigmast-5-en-3beta,7alpha-diol (14), ursolic acid (15) and betulinic acid (16). Compounds 7 and 8 both show a 6,5,6,6 ring skeleton with a trans-1,1-dimethylcyclohexano[e,b]tetrahydrofuran element perpendicular to a benzodihydropyran system. The complete structure elucidation of these compounds has been achieved with NMR techniques.     

Phytochemical investigation of Tiarella polyphylla

Seven flavonoids (1–7), two triterpenoids (8 and 9) and four steroids (10, 11, 12 and 13) were isolated from the whole plant of Tiarella polyphylla. Based on the physicochemical and spectroscopic analyses, their structures were identified as myricetin (1), astragalin (2), afzelin (3), quercitrin (4), myricitin (5), nicotiflorin (6), isoquercitrin (7), tiarellic acid (8), 3β-hydroxy-20(29)lupen-27-oic acid (9), β-sitosterol-3-O-β-D-glucoside (10), stigmasterol-3-O-β-D-glucoside (11), β-sitosterol (12) and ergosterol endoperoxide (13). All 13 compounds, with the exception of tiarellic acid were isolated for the first time from T. polyphylla. In the anti-complementary assay, the steroids (12 and 13) exhibited potent activities; whereas, the flavonoids (1 to 7) showed weak or no activities, but even the triterpenoids (8 and 9) and steroidal saponins (10 and 11) evoked hemolysis.     

Anti-HIV-1 integrase effect of compounds from Aglaia andamanica leaves and molecular docking study with acute toxicity test in mice

Context: Acquired immunodeficiency syndrome (AIDS) is a serious health problem worldwide. It has been reported that Aglaia andamanica Hiern (Meliaceae) leaves possessed an antiviral effect. Therefore, a search of anti-HIV-1 integrase (HIV-1 IN) agents from A. andamanica is a promising target.

Objective: The objective of this study is to evaluate anti-HIV-1 IN activity of isolated compounds from A. andamanica using an in vitro assay and molecular docking study as well as testing acute toxicity in mice using the up and down method.

Materials and methods: The leaves and compounds (3–100?μg/mL) from A. andamanica were determined for the anti-HIV-1 IN effect using the multiplate integration assay (MIA) by detection the absorbance of the final product, p-nitrophenol, at 405?nm. The molecular docking with the HIV-1 IN of the active compound N-methyl-trans-4-hydroxy-l-proline (10) was also studied. The Swiss albino mice were used for an acute toxicity test.

Results and discussion: Among the isolated compounds, 10 showed marked anti-HIV-1 IN effect with an IC₅₀ value of 11.8?μg/mL, whereas other compounds were inactive (IC₅₀ value?>?100?μg/mL). The molecular docking of compound 10 with an HIV-1 IN enzyme was also studied. The result revealed that this compound formed the hydrogen bonding with the Thr66, Asn155, and Lys159 of the HIV-1 IN binding site. The acute toxicity of the A. andamanica extract was not observed at the dose 2000?mg/kg mice. This is the first report of A. andamanica for anti-HIV-1 IN activity.     

Phytochemical investigation of Cassia multijuga seeds

From the seeds of CASSIA MULTIJUGA 1,3,8-trihydroxy-2-methyl anthraquinone, 1:3-dihydroxy 6,8-dimethoxy-2-methyl anthraquinone and two glycosides 3-hydroxy-6,8-dimethoxy-2-methyl anthraquinone-1-O-beta- D(+) glucopyranoside and 3-hydroxy 6,8-dimethoxy-2-methyl anthraquinone 1-O-rhamnopyranosyl (1 --> 6) glucopyranoside (rutinoside) have been isolated and their structures elucidated. The last three compounds are new and have not been isolated previously from any plant source.