eupatilin: isolated from Artemisia argyi
eupatilin : A trimethoxyflavone that is flavone substituted by hydroxy groups at C-5 and C-7 and methoxy groups at C-6, C-3' and C-4' respectively. Isolated from Citrus reticulata and Salvia tomentosa, it exhibits anti-inflammatory, anti-ulcer and antineoplastic activities.
Flora | Rank | Flora Definition | Family | Family Definition |
---|---|---|---|---|
Salvia | genus | A genus in the mint family (LAMIACEAE).[MeSH] | Lamiaceae | The mint plant family. They are characteristically aromatic, and many of them are cultivated for their oils. Most have square stems, opposite leaves, and two-lipped, open-mouthed, tubular corollas (united petals), with five-lobed, bell-like calyxes (united sepals).[MeSH] |
Citrus | genus | A plant genus of the family RUTACEAE. They bear the familiar citrus fruits including oranges, grapefruit, lemons, and limes. There are many hybrids which makes the nomenclature confusing.[MeSH] | Rutaceae | A plant family in the order Sapindales that grows in warmer regions and has conspicuous flowers.[MeSH] |
Artemisia | genus | A plant genus of the family ASTERACEAE with strong-smelling foliage. It is a source of SANTONIN and other cytotoxic TERPENES.[MeSH] | Asteraceae | A large plant family of the order Asterales, subclass Asteridae, class Magnoliopsida. The family is also known as Compositae. Flower petals are joined near the base and stamens alternate with the corolla lobes. The common name of daisy refers to several genera of this family including Aster; CHRYSANTHEMUM; RUDBECKIA; TANACETUM.[MeSH] |
Salvia tomentosa | species | [no description available] | Lamiaceae | The mint plant family. They are characteristically aromatic, and many of them are cultivated for their oils. Most have square stems, opposite leaves, and two-lipped, open-mouthed, tubular corollas (united petals), with five-lobed, bell-like calyxes (united sepals).[MeSH] |
Artemisia argyi | species | [no description available] | Asteraceae | A large plant family of the order Asterales, subclass Asteridae, class Magnoliopsida. The family is also known as Compositae. Flower petals are joined near the base and stamens alternate with the corolla lobes. The common name of daisy refers to several genera of this family including Aster; CHRYSANTHEMUM; RUDBECKIA; TANACETUM.[MeSH] |
ID Source | ID |
---|---|
PubMed CID | 5273755 |
CHEMBL ID | 312750 |
CHEBI ID | 4932 |
SCHEMBL ID | 1033509 |
MeSH ID | M0131867 |
Synonym |
---|
AC-7926 |
chebi:4932 , |
CHEMBL312750 , |
euptailin |
nsc-122413 |
nsc122413 |
2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxy-chromen-4-one |
2-(3,4-dimethoxy-phenyl)-5,7-dihydroxy-6-methoxy-chromen-4-one |
22368-21-4 |
eupatilin |
5,7-dihydroxy-3',4',6-trimethoxyflavone |
2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxychromen-4-one |
bdbm50060926 |
LMPK12111228 |
4h-1-benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxy- |
nsc 122413 |
unii-4d58o05490 |
4d58o05490 , |
AKOS015917432 |
S3846 |
FT-0686610 |
AM84796 |
eupatilin [who-dd] |
SCHEMBL1033509 |
5,7-dihydroxy-3',4',6-trimethoxy flavone |
HB3894 |
2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxy-4h-chromen-4-one # |
2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxy-4h-chromen-4-one |
DTXSID30176904 |
mfcd13194819 |
CS-5407 |
HY-N0783 |
eupatilin, >=98% (hplc) |
2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxy-4h-1-benzopyran-4-one, 9ci |
Q3060385 |
BCP09703 |
CCG-267966 |
4-(2-methacryloxy-ethyl-1-oxy)benzoicacid |
2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxy-4h-1-benzopyran-4-one; 5,7-dihydroxy-3',4',6-trimethoxyflavone; 2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxychromen-4-one; 4h-1-benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-5,7-dihydroxy-6-methoxy- |
A878565 |
SC3971 |
AS-56084 |
E1409 |
SY231676 |
EX-A7726 |
Eupatilin is a major component extracted from the traditional herbal medicine Artemisia asiatica Nakai. It has shown potential anti-tumor activity in some cancers, but its potential in prostate cancer treatment has not yet been evaluated.
Eupatilin has been reported to have anti-apoptotic, anti-oxidative and anti-inflammatory activities. It has been known to possess anti-peptic,. anti-cancer, andAnti-allergy activity.
Eupatilin could inhibit the hyperproliferation of LPS-stimulated HaCaT cells through p38 MAPK/NF-κB signaling pathway in vitro. Eupatils could increase the efficacy of IPF treatment to curative levels.
Excerpt | Reference | Relevance |
---|---|---|
"Eupatilin could inhibit the hyperproliferation of LPS-stimulated HaCaT cells through p38 MAPK/NF-κB signaling pathway in vitro. " | ( Eupatilin inhibits keratinocyte proliferation and ameliorates imiquimod-induced psoriasis-like skin lesions in mice via the p38 MAPK/NF-κB signaling pathway. Bai, D; Cheng, X; Hao, J; Li, Q; Lu, F; Sun, T; Zhang, B; Zhang, Y, 2023) | 3.8 |
"Eupatilin could increase the efficacy of IPF treatment to curative levels." | ( Reversion of in vivo fibrogenesis by novel chromone scaffolds. Kim, HS; Kim, IH; Lee, JE; Lee, JY; Lee, TH; Meang, MK; Park, YE; Yoon, YM; Youn, BS, 2019) | 1.24 |
Treatment with eupatilin significantly decreased neutrophil gelatinase-associated lipocalin and kidney injury molecule-1 levels in urine, blood urea nitrogen level, and serum creatinine levels. Eup atilin treatment also reduced the levels of IL-1β, IL-6, and TNF-α, and repressed the expression levels of MyD88, TLR4, and p-NF-κB p65.
Excerpt | Relevance | Reference |
---|---|---|
"Eupatilin (5,7-dihydroxy-3',4',6-trimethoxyflavone) was isolated from Artemisia princeps to investigate the dose-response effects on blood glucose regulation and pancreatic beta-cell function in type 2 diabetic mice." | ( Eupatilin, isolated from Artemisia princeps Pampanini, enhances hepatic glucose metabolism and pancreatic beta-cell function in type 2 diabetic mice. Baek, NI; Choi, MS; Chung, HG; Jeon, SM; Jeong, TS; Jung, UJ; Kang, YJ; Kim, HJ; Lee, KT; Lee, MK; Park, YB, 2008) | 3.23 |
" Therefore, the GR system of DA-9601 could be a substitute dosage form for the treatment of gastritis, while reducing the dosing frequency and thus improving patient compliance." | ( In vivo gastric residence and gastroprotective effect of floating gastroretentive tablet of DA-9601, an extract of Artemisia asiatica, in beagle dogs. Cha, KH; Choi, HJ; Jang, SW; Kang, MJ; Kang, SY; Kim, JS; Lee, YW; Son, M; Son, MH; Won, D, 2016) | 0.43 |
Role | Description |
---|---|
metabolite | Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites. |
anti-ulcer drug | One of various classes of drugs with different action mechanisms used to treat or ameliorate peptic ulcer or irritation of the gastrointestinal tract. |
EC 1.13.11.34 (arachidonate 5-lipoxygenase) inhibitor | A lipoxygenase inhibitor that interferes with the action of arachidonate 5-lipoxygenase (EC 1.13.11.34). |
antineoplastic agent | A substance that inhibits or prevents the proliferation of neoplasms. |
anti-inflammatory agent | Any compound that has anti-inflammatory effects. |
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Class | Description |
---|---|
trimethoxyflavone | A methoxyflavone that is flavone substituted by three methoxy groups. |
dihydroxyflavone | Any hydroxyflavone in which two ring hydrogens are replaced by hydroxy substituents. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Tubulin beta-4A chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9680 | 10.0000 | AID214006 |
Tubulin beta chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 2.0529 | 10.0000 | AID214006 |
Tubulin alpha-3C chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9555 | 10.0000 | AID214006 |
Tubulin alpha-1B chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9555 | 10.0000 | AID214006 |
Tubulin alpha-4A chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9555 | 10.0000 | AID214006 |
Tubulin beta-4B chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9680 | 10.0000 | AID214006 |
Tubulin beta-3 chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.8945 | 10.0000 | AID214006 |
Tubulin beta-2A chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9680 | 10.0000 | AID214006 |
Tubulin beta-8 chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9680 | 10.0000 | AID214006 |
Tubulin alpha-3E chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9555 | 10.0000 | AID214006 |
Tubulin alpha-1A chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9555 | 10.0000 | AID214006 |
Tubulin alpha-1C chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9555 | 10.0000 | AID214006 |
Tubulin beta-6 chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9680 | 10.0000 | AID214006 |
Tubulin beta-2B chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9680 | 10.0000 | AID214006 |
Tubulin beta-1 chain | Homo sapiens (human) | IC50 (µMol) | 40.0000 | 0.0005 | 1.9870 | 10.0000 | AID214006 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1892316 | Inhibition of ERK activity in human MM121224 cells harboring BRAF V600E/NRAS Q61K mutant derived from melanoma patient by high-content screening microscopic analysis | 2022 | Journal of natural products, 06-24, Volume: 85, Issue:6 | Combining Activity Profiling with Advanced Annotation to Accelerate the Discovery of Natural Products Targeting Oncogenic Signaling in Melanoma. |
AID1230324 | Displacement of [3H]DPDPE from delta opioid receptor (unknown origin) transfected into HEK293 cells at 10 uM by microplate scintillation counting | 2015 | Journal of natural products, Jun-26, Volume: 78, Issue:6 | Flavonoids from Perovskia atriplicifolia and Their in Vitro Displacement of the Respective Radioligands for Human Opioid and Cannabinoid Receptors. |
AID1190339 | Displacement of [3H]DPDPE from delta opioid receptor in CD1 mouse whole brain minus cerebellum membranes by liquid scintillation counting | 2015 | Journal of natural products, Jan-23, Volume: 78, Issue:1 | Methoxyflavones from Stachys glutinosa with binding affinity to opioid receptors: in silico, in vitro, and in vivo studies. |
AID1627198 | Cytotoxicity against human MCF7 cells assessed as reduction in cell growth incubated for 48 hrs by MTT assay | 2016 | Bioorganic & medicinal chemistry letters, 08-15, Volume: 26, Issue:16 | Cytotoxic prenylated flavones from the stem and root bark of Daphne giraldii. |
AID214006 | In vitro inhibitory activity against tubulin polymerization (10 uM) | 1998 | Journal of medicinal chemistry, Jun-18, Volume: 41, Issue:13 | Structure-activity requirements for flavone cytotoxicity and binding to tubulin. |
AID1230329 | Displacement of [3H]-CP55940 from human CB2 receptor transfected into HEK293 cells at 10 uM by microplate scintillation counting | 2015 | Journal of natural products, Jun-26, Volume: 78, Issue:6 | Flavonoids from Perovskia atriplicifolia and Their in Vitro Displacement of the Respective Radioligands for Human Opioid and Cannabinoid Receptors. |
AID1420552 | Antiangiogenic activity in HUVEC assessed as inhibition of tube formation at 3.125 uM after 24 hrs by light microscopic analysis relative to control | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1546499 | Antiproliferative activity against human SNU638 cells assessed as reduction in cell viability after 24 hrs by CCK8 assay | 2020 | Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1 | Artemisia: a promising plant for the treatment of cancer. |
AID1420555 | Downregulation of HIF-1 alpha protein level in HUVEC at 3.125 uM after 24 hrs by Western blot analysis relative to control | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID144650 | In vitro cytotoxic potency against NCI-60 human tumor cell line | 1998 | Journal of medicinal chemistry, Jun-18, Volume: 41, Issue:13 | Structure-activity requirements for flavone cytotoxicity and binding to tubulin. |
AID1546497 | Antiproliferative activity against human SNU484 cells assessed as reduction in cell viability after 24 hrs by CCK8 assay | 2020 | Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1 | Artemisia: a promising plant for the treatment of cancer. |
AID1230326 | Displacement of [3H]DAMGO from mu opioid receptor (unknown origin) transfected into HEK293 cells at 10 uM by microplate scintillation counting | 2015 | Journal of natural products, Jun-26, Volume: 78, Issue:6 | Flavonoids from Perovskia atriplicifolia and Their in Vitro Displacement of the Respective Radioligands for Human Opioid and Cannabinoid Receptors. |
AID1546495 | Antiproliferative activity against human MKN1 cells assessed as reduction in cell viability after 24 hrs by CCK8 assay | 2020 | Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1 | Artemisia: a promising plant for the treatment of cancer. |
AID1420546 | Antiproliferative activity against human HepG2 cells after 24 hrs by MTT assay | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1627196 | Cytotoxicity against human A549 cells assessed as reduction in cell growth incubated for 48 hrs by MTT assay | 2016 | Bioorganic & medicinal chemistry letters, 08-15, Volume: 26, Issue:16 | Cytotoxic prenylated flavones from the stem and root bark of Daphne giraldii. |
AID1546496 | Antiproliferative activity against human AGS cells assessed as reduction in cell viability after 24 hrs by CCK8 assay | 2020 | Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1 | Artemisia: a promising plant for the treatment of cancer. |
AID1420549 | Downregulation of MMP9 mRNA levels in human SNU182 cells at 20 uM after 24 hrs by quantitative real-time qPCR analysis | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1627197 | Cytotoxicity against human HepG2 cells assessed as reduction in cell growth incubated for 48 hrs by MTT assay | 2016 | Bioorganic & medicinal chemistry letters, 08-15, Volume: 26, Issue:16 | Cytotoxic prenylated flavones from the stem and root bark of Daphne giraldii. |
AID1230328 | Displacement of [3H]-CP55940 from human CB1 receptor transfected into HEK293 cells at 10 uM by microplate scintillation counting | 2015 | Journal of natural products, Jun-26, Volume: 78, Issue:6 | Flavonoids from Perovskia atriplicifolia and Their in Vitro Displacement of the Respective Radioligands for Human Opioid and Cannabinoid Receptors. |
AID1190340 | Selectivity ratio of Ki for delta opioid receptor in CD1 mouse whole brain minus cerebellum membranes to Ki for mu opioid receptor in CD1 mouse whole brain minus cerebellum membranes | 2015 | Journal of natural products, Jan-23, Volume: 78, Issue:1 | Methoxyflavones from Stachys glutinosa with binding affinity to opioid receptors: in silico, in vitro, and in vivo studies. |
AID1420554 | Antiangiogenic activity in HUVEC assessed as inhibition of tube formation at 6.25 uM after 24 hrs by light microscopic analysis relative to control | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1420559 | Inhibition of Akt phosphorylation in HUVEC at 6.25 uM after 24 hrs by Western blot analysis relative to control | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1420557 | Downregulation of VEGF protein level in HUVEC at 3.125 uM after 24 hrs by Western blot analysis relative to control | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1546498 | Antiproliferative activity against human SNU601 cells assessed as reduction in cell viability after 24 hrs by CCK8 assay | 2020 | Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1 | Artemisia: a promising plant for the treatment of cancer. |
AID214172 | In vitro inhibition of binding of [3H]colchicine to tubulin at 50 mM. | 1998 | Journal of medicinal chemistry, Jun-18, Volume: 41, Issue:13 | Structure-activity requirements for flavone cytotoxicity and binding to tubulin. |
AID1594833 | Immunosuppressant activity in human T lymphocytes assessed as inhibition of anti-human CD3 and anti-human CD28 monoclonal antibody-induced T lymphocyte proliferation incubated for 72 hrs by FACS analysis | 2019 | Journal of natural products, 06-28, Volume: 82, Issue:6 | Sesquiterpene Lactones from Artemisia argyi: Absolute Configuration and Immunosuppressant Activity. |
AID1892315 | Inhibition of AKT activity in human MM121224 cells harboring BRAF V600E/NRAS Q61K mutant derived from melanoma patient by high-content screening microscopic analysis | 2022 | Journal of natural products, 06-24, Volume: 85, Issue:6 | Combining Activity Profiling with Advanced Annotation to Accelerate the Discovery of Natural Products Targeting Oncogenic Signaling in Melanoma. |
AID1627199 | Cytotoxicity against human Bcap37 cells assessed as reduction in cell growth incubated for 48 hrs by MTT assay | 2016 | Bioorganic & medicinal chemistry letters, 08-15, Volume: 26, Issue:16 | Cytotoxic prenylated flavones from the stem and root bark of Daphne giraldii. |
AID1420561 | Cytotoxicity against human SNU182 cells assessed as decrease in cell viability up to 20 uM after 48 hrs by MTT assay | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1420556 | Downregulation of HIF-1 alpha protein level in HUVEC at 6.25 uM after 24 hrs by Western blot analysis relative to control | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1420560 | Downregulation of VEGF level in HUVEC at 6.25 uM after 24 hrs by Western blot analysis relative to control | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1420553 | Cytotoxicity activity against HUVEC assessed as decrease in cell viability at 12.5 to 100 uM after 24 hrs by MTT assay | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1546501 | Antiproliferative activity against human HL60 cells assessed as cell viability at 150 uM by MTT assay relative to control | 2020 | Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1 | Artemisia: a promising plant for the treatment of cancer. |
AID1420548 | Downregulation of MMP2 mRNA levels in human SNU182 cells at 20 uM after 24 hrs by quantitative real-time qPCR analysis | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1420547 | Antiproliferative activity against human HepG2 cells at 200 uM after 24 hrs by MTT assay | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1420558 | Inhibition of Akt phosphorylation in HUVEC at 3.125 uM after 24 hrs by Western blot analysis relative to control | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1230325 | Displacement of [3H]U69593 from kappa opioid receptor (unknown origin) transfected into HEK293 cells at 10 uM by microplate scintillation counting | 2015 | Journal of natural products, Jun-26, Volume: 78, Issue:6 | Flavonoids from Perovskia atriplicifolia and Their in Vitro Displacement of the Respective Radioligands for Human Opioid and Cannabinoid Receptors. |
AID1546500 | Induction of apoptosis in human U87MG cells assessed as increase in apoptotic cells at 50 uM after 24 hrs by Annexin V-FITC/propidium iodide staining based flow cytometric analysis relative to control | 2020 | Bioorganic & medicinal chemistry, 01-01, Volume: 28, Issue:1 | Artemisia: a promising plant for the treatment of cancer. |
AID1420550 | Cytotoxicity activity against HUVEC assessed as decrease in cell viability up to 6.25 uM after 24 hrs by MTT assay | 2018 | Bioorganic & medicinal chemistry letters, 10-15, Volume: 28, Issue:19 | Eupatilin inhibits angiogenesis-mediated human hepatocellular metastasis by reducing MMP-2 and VEGF signaling. |
AID1190338 | Displacement of [3H]DAMGO from mu opioid receptor in CD1 mouse whole brain minus cerebellum membranes by liquid scintillation counting | 2015 | Journal of natural products, Jan-23, Volume: 78, Issue:1 | Methoxyflavones from Stachys glutinosa with binding affinity to opioid receptors: in silico, in vitro, and in vivo studies. |
AID1627195 | Cytotoxicity against human U251 cells assessed as reduction in cell growth incubated for 48 hrs by MTT assay | 2016 | Bioorganic & medicinal chemistry letters, 08-15, Volume: 26, Issue:16 | Cytotoxic prenylated flavones from the stem and root bark of Daphne giraldii. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 1 (0.98) | 18.7374 |
1990's | 3 (2.94) | 18.2507 |
2000's | 23 (22.55) | 29.6817 |
2010's | 51 (50.00) | 24.3611 |
2020's | 24 (23.53) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.
| This Compound (37.01) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 3 (2.91%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 100 (97.09%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |