Phytochemical Name : PH-1 (4-methyl-5-oxo-tetrahydrofuran-3-yl acetate)

Properties Information
PhytoCAT-ID PhytoCAT-1328
Phytochemical name or plant extracts PH-1 (4-methyl-5-oxo-tetrahydrofuran-3-yl acetate)
PMID 34560864
Literature evidence This study was aimed to isolate potential anticancer compounds from its most potent fractions and evaluate their anticancer potentials.
IUPAC name (4-methyl-5-oxooxolan-3-yl) acetate
Phytochemicals’ class or type of plant extracts Esters and cyclic ether
Source of phytochemicals or plant Extracts Polygonum hydropiper
Geographical availability Afghanistan, Albania, Algeria, Altay, Amur, Andaman Is., Assam, Austria, Azores, Baltic States, Bangladesh, Belarus, Belgium, Bulgaria, Buryatiya, Central European Russia, China South-Central, China Southeast, Chita, Corse, Czechoslovakia, Denmark, East European Russia, East Himalaya, Finland, France, Germany, Great Britain, Greece, Hainan, Hungary, India, Inner Mongolia, Iran, Ireland, Irkutsk, Italy, Japan, Jawa, Kazakhstan, Khabarovsk, Kirgizstan, Korea, Krasnoyarsk, Krym, Kuril Is., Madeira, Malaya, Manchuria, Mongolia, Morocco, Myanmar, Nansei-shoto, Nepal, Netherlands, New South Wales, Nicobar Is., North Caucasus, North European Russia, Northwest European Russia, Norway, Ogasawara-shoto, Pakistan, Philippines, Poland, Portugal, Primorye, Qinghai, Queensland, Romania, Sakhalin, Sardegna, Sicilia, South Australia, South European Russia, Spain, Sri Lanka, Sumatera, Sweden, Switzerland, Tadzhikistan, Taiwan, Tasmania, Thailand, Tibet, Transcaucasus, Turkey, Turkey-in-Europe, Tuva, Ukraine, Uzbekistan, Victoria, Vietnam, West Himalaya, West Siberia, Western Australia, Xinjiang, Yakutskiya, Yugoslavia
Plant parts NA
Other cancers Breast cancer, Cervical cancer
Target gene or protein NA
Gene or Protein evidence NA
Target pathways NA
IC50 340 µgm/L
Potency LD50 of 340 µgL-1 (Anti-tumor assay)
Cell line/ mice model MCF-7, HeLA, NIH/3T3
Additional information  The compound cause considerable cytotoxicity against cancer cells. The anti-angiogenic and anti-tumor results suggests additional tumor suppressive properties.
PubChem ID 15743484
Additional PMIDs NA
Additional sources of information https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:77069479-1
Safety In anti-tumor assay, PH-1 and PH-2 exhibited 81.15 and 76.09% inhibitions with LD50 of 340 and 550 µgL-1 respectively.