andrographolide and labdane

andrographolide has been researched along with labdane* in 2 studies

Other Studies

2 other study(ies) available for andrographolide and labdane

ArticleYear
Discovery and development of labdane-oxindole hybrids as small-molecule inhibitors against chikungunya virus infection.
    European journal of medicinal chemistry, 2022, Feb-15, Volume: 230

    Chikungunya virus (CHIKV) infection, a febrile illness caused by a mosquito-transmitted alphavirus, has afflicted millions of people worldwide. There is currently no approved effective antiviral treatment for CHIKV infection. In this study, we report a new class of small-molecule CHIKV inhibitors, the oxindole-labdanes, that potently block the replication of CHIKV with good selectivity. Andrographolide, a previously reported inhibitor of CHIKV infection, was used as the lead compound for our initial structure-activity relationship (SAR) study. From a focused library of 72 andrographolide analogues, we identified the lead compound (E)-2 with improved antiviral activities. Further optimization of (E)-2 led to the discovery of the normal-labdane 7-chloro-oxindole (E)-42 as potent inhibitor against two low-passage CHIKV isolates from human patients with an EC

    Topics: Animals; Antiviral Agents; Chikungunya Fever; Diterpenes; Humans; Oxindoles; RNA, Viral; Virus Replication

2022
ent-Labdane diterpenoids from Andrographis paniculata.
    Journal of natural products, 2006, Volume: 69, Issue:3

    Six new ent-labdane diterpenoids, 3-O-beta-D-glucopyranosyl-14,19-dideoxyandrographolide (1), 14-deoxy-17-hydroxyandrographolide (2), 19-O-[beta-D-apiofuranosyl(1-->2)-beta-D-glucopyranoyl]-3,14-dideoxyandrographolide (3), 3-O-beta-d-glucopyranosylandrographolide (4), 12S-hydroxyandrographolide (5), and andrographatoside (6), together with 17 known analogues, were isolated from the aerial parts of Andrographis paniculata. The structures of 1-6 were determined by spectroscopic data analysis. All compounds isolated were evaluated for their inhibitory activity against several bacterial and fungal strains.

    Topics: Andrographis; Anti-Bacterial Agents; Bacillus subtilis; Diterpenes; Drugs, Chinese Herbal; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plants, Medicinal; Stereoisomerism

2006