Pages that link to "Q71674354"
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The following pages link to Development of bioactive functions in hydrangeae dulcis folium. III. On the antiallergic and antimicrobial principles of hydrangeae dulcis folium. (1). Thunberginols A, B, and F (Q71674354):
Displaying 50 items.
- resveratrol (Q407329) (← links)
- umbelliferone (Q416196) (← links)
- thunberginol E (Q3526036) (← links)
- dihydroresveratrol (Q5276414) (← links)
- phyllodulcin (Q5961163) (← links)
- thunberginol A (Q7798878) (← links)
- thunberginol B (Q7798879) (← links)
- thunberginol C (Q7798880) (← links)
- thunberginol D (Q7798881) (← links)
- thunberginol F (Q7798884) (← links)
- hydrangeic acid (Q15411033) (← links)
- hydramacrophyllol B (Q27136627) (← links)
- hydramacrophyllol A (Q27136628) (← links)
- isoarborinol (Q27149876) (← links)
- Solution-phase synthesis of a diverse isocoumarin library (Q33509589) (← links)
- Plant products as antimicrobial agents (Q33749123) (← links)
- Effects of phyllodulcin, hydrangenol, and their 8-O-glucosides, and thunberginols A and F from Hydrangea macrophylla SERINGE var. thunbergii MAKINO on passive cutaneous anaphylaxis reaction in rats (Q33845894) (← links)
- Development of bioactive functions in hydrangeae dulcis folium. V. On the antiallergic and antimicrobial principles of hydrangeae dulcis folium. (2). Thunberginols C, D, and E, thunberginol G 3'-O-glucoside, (-)-hydrangenol 4'-o-glucoside, and (+)-h (Q34063200) (← links)
- Synthesis of 3-substituted isocoumarins via a cascade intramolecular Ullmann-type coupling-rearrangement process (Q34296175) (← links)
- Inhibitory effects of thunberginols A and B isolated from Hydrangeae Dulcis Folium on mRNA expression of cytokines and on activation of activator protein-1 in RBL-2H3 cells (Q34704313) (← links)
- Phthalides: Distribution in Nature, Chemical Reactivity, Synthesis, and Biological Activity (Q39119157) (← links)
- Total synthesis and cytotoxic activity of stellatin (Q39600480) (← links)
- Synthesis of 3-substituted isocoumarins and their inhibitory effects on degranulation of RBL-2H3 cells induced by antigen (Q39945433) (← links)
- Inhibitory effects of thunberginols A, B, and F on degranulations and releases of TNF-alpha and IL-4 in RBL-2H3 cells (Q40176415) (← links)
- Differentiation inducing activities of isocoumarins from Hydrangea Dulcis Folium (Q40883695) (← links)
- Inhibitory effect of oleanene-type triterpene oligoglycosides on ethanol absorption: the structure-activity relationships (Q41258958) (← links)
- Synthesis of isocoumarins with different substituted patterns via Passerini-aldol sequence (Q42545769) (← links)
- Stilbenecarboxylate biosynthesis: a new function in the family of chalcone synthase-related proteins (Q42594518) (← links)
- New type of anti-diabetic compounds from the processed leaves of Hydrangea macrophylla var. thunbergii (Hydrangeae Dulcis Folium). (Q42826881) (← links)
- Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra (Q43888630) (← links)
- Multicomponent one-pot reactions: synthesis of some new 6-oxopyrano [2,3-c]isochromenes by condensation of homophthalic anhydride, dialkyl acetylenedicarboxylate, and isocyanides. (Q45973024) (← links)
- Synthesis of isocoumarins and alpha-pyrones via tandem Stille reaction/heterocyclization. (Q46645682) (← links)
- Efficient synthesis of isobenzofuran-1(3H)-ones (phthalides) and selected biological evaluations (Q46809778) (← links)
- Medicinal foodstuffs. II. On the bioactive constituents of the tuber of Sagittaria trifolia L. (Kuwai, Alismataceae): absolute stereostructures of trifoliones A, B, C, and D, sagittariosides a and b, and arabinothalictoside (Q47179623) (← links)
- Synthesis of azulene-substituted benzofurans and isocoumarins via intramolecular cyclization of 1-ethynylazulenes, and their structural and optical properties (Q47225935) (← links)
- Bioactive constituents of Chinese natural medicines. IV. Rhodiolae radix. (2).: On the histamine release inhibitors from the underground part of Rhodiola sacra (Prain ex Hamet) S. H. Fu (Crassulaceae): chemical structures of rhodiocyanoside D and sa (Q47779102) (← links)
- p-Coumaroyltriacetic acid synthase, a new homologue of chalcone synthase, from Hydrangea macrophylla var. thunbergii (Q47933312) (← links)
- Coumarin to Isocoumarin: One-Pot Synthesis of 3-Substituted Isocoumarins from 4-Hydroxycoumarins and Benzyne Precursors. (Q50707092) (← links)
- Cp*Co(III)-Catalyzed Annulation of Carboxylic Acids with Alkynes. (Q53329204) (← links)
- Immunomodulatory activity of thunberginol a and related compounds isolated from hydrangeae dulcis folium on splenocyte proliferation activated by mitogens (Q56765441) (← links)
- Solid-Phase Synthesis of Isocoumarins: A Traceless Halocyclization Approach (Q58101968) (← links)
- Diselenide- and Disulfide-Mediated Synthesis of Isocoumarins (Q60368615) (← links)
- EZ-resveratrol (Q60998680) (← links)
- Synthesis of 3-arylisocoumarins, including thunberginols A and B, unsymmetrical 3,4-disubstituted isocoumarins, and 3-ylidenephthalides via iodolactonization of methyl 2-ynylbenzoates or the corresponding carboxylic acids (Q63309435) (← links)
- (3R)-8-hydroxy-3-(4-hydroxyphenyl)-3,4-dihydroisochromen-1-one (Q63392623) (← links)
- Medicinal foodstuffs. I. Hypoglycemic constituents from a garnish foodstuff "taranome," the young shoot of Aralia elata SEEM.: elatosides G, H, I, J, and K (Q70934563) (← links)
- Bioactive saponins and glycosides. I. Senegae radix. (1): E-senegasaponins a and b and Z-senegasaponins a and b, their inhibitory effect on alcohol absorption and hypoglycemic activity (Q70952431) (← links)
- Development of bioactive functions in Hydrangeae dulcis folium. VI. Syntheses of thunberginols A and F and their 3'-deoxy-derivatives using regiospecific lactonization of stilbene carboxylic acid: structures and inhibitory activity on histamine rele (Q71751551) (← links)
- Rhodiocyanosides A and B, new antiallergic cyanoglycosides from chinese natural medicine "Si Lie Hong Jing Tian", the underground part of Rhodiola quadrifida (Pall.) Fisch. et Mey (Q71806924) (← links)
- Chemical Constituents of Chinese Natural Medicine, Morindae Radix, the Dried Roots of Morinda officinalis How.: Structures of Morindolide and Morofficinaloside (Q71806941) (← links)