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Phenolic constituents from the aerial parts ofArtemisia stolonifera
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/chin.197812360openalex-snapshot
ChemInform Abstract: SYNTHESIS OF DOMESTICOSIDE, A NEW GLUCOSIDE
inferredcites →https://doi.org/10.1007/bf02974179openalex-snapshot
Antitumor and immunomodulating activities of the polysaccharide fractions fromArtemisia selengensis andArtemisia iwayomogi
inferredcites →https://doi.org/10.1016/0022-2860(92)80230-fopenalex-snapshot
Basic one- and two-dimensional NMR spectroscopy
inferredcites →https://doi.org/10.1016/0031-9422(79)80167-3openalex-snapshot
Sesquiterpene lactones and systematics of the genus Artemisia
inferredcites →https://doi.org/10.1016/0031-9422(91)85044-zopenalex-snapshot
Seco- and Nor-sesquiterpene lactones with a new carbon skeleton from Artemisia santolinifolia
inferredcites →https://doi.org/10.1016/0031-9422(94)85092-5openalex-snapshot
An anthrone, an anthraquinone and two oxanthrones from Kniphofia foliosa
inferredcites →https://doi.org/10.1016/0192-0561(93)90062-4openalex-snapshot
Poly I:C-induced antiviral and cytotoxic activities are mediated by different mechanisms
inferredcites →https://doi.org/10.1016/0924-2031(92)87024-aopenalex-snapshot
Spectrometric Identification of Organic Compounds
inferredcites →https://doi.org/10.1016/b978-0-444-89366-6.70001-0openalex-snapshot
Studies in Natural Products Chemistry
inferredcites →https://doi.org/10.1016/s0031-9422(00)85883-5openalex-snapshot
The spectroscopic identification of coniferin
inferredcites →https://doi.org/10.1021/ed039p546openalex-snapshot
Spectrometric identification of organic compounds
inferredcites →https://doi.org/10.1021/jm01240a020openalex-snapshot
Some New Synthetic Flavonoid Glycosides Related in Structure to Phlorizin
inferredcites →https://doi.org/10.1248/cpb.19.207openalex-snapshot
Constituents of Three Thai Medicinal Plants : Ardisia polycephala (Myrsinaceae), Rhabdia lycioides (Boraginaceae), and Balanophora polyandra (Balanophoraceae)
inferredcites →https://doi.org/10.5860/choice.43-2213openalex-snapshot
Basic one- and two-dimensional NMR spectroscopy
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4691606openalex-extracted
Discovery of New Sesquiterpenoids And Jasmonic Acid Derivative From Artemisia Stolonifera And Their Anti-Inflammation Activity
inferred← citeshttps://doi.org/10.1007/1-4020-2291-3_1openalex-snapshot
Compounds derived from acetic acid
inferred← citeshttps://doi.org/10.1007/978-1-4020-9787-4_9openalex-snapshot
Compounds Derived from Acetic Acid
inferred← citeshttps://doi.org/10.1007/bf02975098openalex-snapshot
Phytochemical constituents ofArtemisia stolonifera
inferred← citeshttps://doi.org/10.1007/bf02975504openalex-snapshot
Cytotoxic peroxides fromArtemisia stolonifera
inferred← citeshttps://doi.org/10.1007/s11418-016-0974-4openalex-snapshot
New potent accelerator of neurite outgrowth from Lawsonia inermis flower under non-fasting condition
inferred← citeshttps://doi.org/10.1007/s11418-018-1221-yopenalex-snapshot
Comparison of lawsone contents among Lawsonia inermis plant parts and neurite outgrowth accelerators from branches
inferred← citeshttps://doi.org/10.1016/j.bse.2021.104356openalex-snapshot
Chemical constituents from the fruits of Zanthoxylum bungeanum and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.foodchem.2010.08.060openalex-snapshot
Antioxidant constituents from Lawsonia inermis leaves: Isolation, structure elucidation and antioxidative capacity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112437openalex-snapshot
Antiproliferative diterpenoids and acetophenone glycoside from the roots of Euphorbia fischeriana
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114120openalex-snapshot
Anti-inflammatory discovery of sesquiterpenoids and a jasmonic acid derivative from Artemisia stolonifera
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01013-4openalex-snapshot
A new route to 3-(2-vinylphenyl)-2-methyl-2H-isoquinolin-1-ones and benzo[c]phenanthridines: total synthesis of fagaronine
inferred← citeshttps://doi.org/10.1039/d2ob01358dopenalex-snapshot
A synthetically benign one-pot construction of enamino-xanthene dyes
inferred← citeshttps://doi.org/10.1080/10575630290020640openalex-snapshot
Structural Distinction between Sabandins A and B from Artemisia Scoparia Waldst. (Asteraceae)
inferred← citeshttps://doi.org/10.1248/cpb.50.605openalex-snapshot
Constituents from Polygonum cuspidatum.
inferred← citeshttps://doi.org/10.3389/fphar.2017.00337openalex-snapshot
Characterization of Antileishmanial Compounds from Lawsonia inermis L. Leaves Using Semi-High Resolution Antileishmanial Profiling Combined with HPLC-HRMS-SPE-NMR
inferred← citeshttps://doi.org/10.3402/ljm.v5i0.4891openalex-snapshot
Potent hepatoprotective effect in CCl4-induced hepatic injury in mice of phloroacetophenone fromMyrcia multiflora
inferred← citeshttps://doi.org/10.3839/jabc.2023.034openalex-snapshot
Quantitative analysis of coumarins in Artemisia keiskeana and A. stolonifera using HPLC/PDA
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