Pomolic acid, a pentacyclic triterpene, is a bioactive natural compound commonly derived from plants such as Euscaphis japonica, Centella asiatica, Picramnia sellowii, and Cecropia pachystachya. Current research suggests that this metabolite acts as an inhibitor and may exhibit diverse biological activities, including anticancer, anti-inflammatory, antiviral, apoptotic, and antihypertensive properties.
Application
Pomolic acid is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.
Biochem/physiol Actions
Pomolic acid is highly effective in inhibiting cell growth and inducing apoptosis.
Features and Benefits
Suitable for Biochemical and Biomedical research
Versatile and adaptable for wide variety of laboratory and research applications
Other Notes
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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The dichloromethane extract and pomolic acid ( 5) obtained from leaves of Cecropia pachystachya both reduced carrageenan-induced paw oedema in mice. Interestingly, while the triterpenoid inhibited the in vivo production of interleukin-1beta by 39 %, it had no effect on
A new ursane-type triterpenoid, weigelic acid (1), and seven known compounds, ursolic acid (2), ilekudinol A (3), corosolic acid (4), ilekudinol B (5), esculentic acid (6), pomolic acid (7), and asiatic acid (8) were isolated from the leaf and stem
Studies on constituents of medicinal plants. XIII. Constituents of the pericarps of the capsules of Euscaphis japonica Pax.
K Takahashi et al.
Chemical & pharmaceutical bulletin, 22(3), 650-653 (1974-03-01)
Journal of natural products, 61(9), 1090-1095 (1998-09-28)
Oleanolic acid (1) was identified as an anti-HIV principle from several plants, including Rosa woodsii (leaves), Prosopis glandulosa (leaves and twigs), Phoradendron juniperinum (whole plant), Syzygium claviflorum (leaves), Hyptis capitata (whole plant), and Ternstromia gymnanthera (aerial part). It inhibited HIV-1
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