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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
79 Results for "
Pinus pumila (Pall.) Regel
" in MedChemExpress (MCE) Product Catalog:
Products (79)
79 Results for "Pinus pumila (Pall.) Regel" in MCE Product Catalog:
29
Category:
Rosaceae Plants Dihydrochalcones Endogenous metabolite Human Gut Microbiota Metabolites Flavonoids Microorganisms Malus pumila Mill. Phenols Polyphenols Disease Research Fields Cancer
Target:
3
3 Cited Publications
Cat. No.: HY-N5080
CAS No.: 20013-23-4
Category:
Flavonoids Gentianaceae Phenols Polyphenols Plants Gentiana algida Pall. Disease Research Fields Inflammation/Immunology Isoflavones
Target:
1
Category:
Infection other families Microorganisms Anti-aging Terpenoids Diterpenoids Plants Disease Research Fields Inflammation/Immunology
Target:
1
Category:
Cardiacglycosides Ranunculaceae Adonis amurensis Regel et Radde Plants Disease Research Fields Inflammation/Immunology Steroids
Target:
1
1 Cited Publications
Cat. No.: HY-N1854
CAS No.: 52117-69-8
Category:
Flavanonols Flavonoids Animals Other Diseases Scrophulariaceae Eremophila alternifolia Plants Disease Research Fields
Target:
1
1
Target:
1
1 Cited Publications
Cat. No.: HY-N3035
CAS No.: 38853-67-7
Category:
Infection Alkaloids Ranunculaceae Coptis chinensis Franch. Plants Disease Research Fields Isoquinoline Alkaloids
Target:
Cat. No.: HY-N2387
CAS No.: 22139-77-1
Category:
other families Lignans Phenols Polyphenols Phenylpropanoids Plants Disease Research Fields Inflammation/Immunology
Target:
o-Vanillin (2-Vanillin) is a nature product, could be extracted from Vanilla planifolia, Pinus koraiensis fruit. o-Vanillin is a potent antifungal agent. o-Vanillin inhibits the growth of mycelia by disrupting the integrity of cell walls and cell membranes. o-Vanillin inhibits Doxorubicin (HY-15142A)- and 4-hydroperoxycyclophosphamide-induced NF-κB activation .
Synonyms: PNLA
Target:
Cat. No.: HY-N14039
CAS No.: 90082-75-0
Category:
Cat. No.: HY-N5049
CAS No.: 124151-38-8
Category:
Cardiovascular Disease Flavonols Flavonoids Zygophyllaceae Phenols Polyphenols Plants Disease Research Fields Nitraria sibirica Pall
Target:
Target:
Cat. No.: HY-W278867
CAS No.: 21956-56-9
Synonyms: trans-Pinosylvin dimethyl ether
Category:
Stilbenes Leguminosae Plants Disease Research Fields Inflammation/Immunology Astragalus membranaceus (Fisch.) Bunge
Target:
trans-3,5-Dimethoxystilbene (trans-Pinosylvin dimethyl ether) is a natural stilbenoid metabolite. trans-3,5-Dimethoxystilbene acts as an acetylcholinesterase inhibitor with a IC50 of 9 μM against Electrophorus electricus acetylcholinesterase. trans-3,5-Dimethoxystilbene binds to acetylcholinesterase and blocks acetylcholine hydrolysis, thereby increasing acetylcholine levels in the cholinergic synaptic cleft. trans-3,5-Dimethoxystilbene can be used in the research of neurodegenerative diseases such as Alzheimer's disease .
Target:
Research Areas:
7-Oxodehydroabietic acid is a diterpene resin acid isolated from the roots of the pine Pinus densiflora. 7-Oxodehydroabietic acid play a defensive role against herbivorous insects via insect endocrine-disrupting activity .
Category:
Triterpenes Anemone cathayensis Kitag. Terpenoids Ranunculaceae Anemone raddeana Regel Other Diseases Plants Disease Research Fields
Target:
Cat. No.: HY-133592R
CAS No.: 471-77-2
Target:
Research Areas:
Neoabietic acid (Standard) is the analytical standard of Neoabietic acid. This product is intended for research and analytical applications. Neoabietic acid, an abietic-type acid, is a nature product that could be isolated from the oleoresin and rosin of Pinus palustris. Neoabietic acid is highly susceptible to mineral acid. Neoabietic acid has antibacterial activity .
Synonyms: Ethyl pinolenate
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
