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Chemical compound
Umbelliferone, also known as 7-hydroxycoumarin, hydrangine, skimmetine, and beta-umbelliferone, is a natural product of the coumarin family. It absorbs
Umbelliferone
Chemical compound
combination of the shikimate pathway, which produces umbelliferone, and the mevalonate pathway. Umbelliferone is a phenylpropanoid and as such is synthesized
Methoxsalen
Chemical compound
isomer of caffeic acid. It is a precursor in the umbelliferone biosynthesis pathway. Umbelliferone is a phenylpropanoid and as such is synthesized from
Umbellic_acid
Indian spice derived from Ferula roots
along with coumarins and various terpenoids, asaresinotannols A and B, umbelliferone, and four unidentified compounds. The gum fraction is composed of simple
Asafoetida
Species of flowering plant in the celery family
recipe/module on Dill Apiole and dillapiole Carvone Limonene Myristicin Umbelliferone Fresh and dried dill leaves (sometimes called "dill weed" or "dillweed"
Dill
Species of flowering plant
North America and Europe. It contains herniarin, a methoxy analog of umbelliferone. Herniarin on www.liberherbarum.com Media related to Herniaria glabra
Herniaria_glabra
Chemical compound
addition of a fused furan ring, and may be considered as a derivative of umbelliferone. Psoralen occurs naturally in the seeds of Psoralea corylifolia, as
Psoralen
Chemical compound
lactonizes to yield umbeliferone. Subsequently, umbelliferone 6-prenyltransferase (PT) couples umbelliferone with prenyl diphosphate to give osthenol and
Angelicin
Species of flowering plant
tribe Hyoscyameae of the nightshade family Solanaceae. The coumarins umbelliferone and scopoletin have been isolated from the roots of Scopolia japonica
Scopolia_japonica
Any organic aromatic compound with a structure based on a phenylpropane skeleton
which can be further modified into hydroxylated derivatives such as umbelliferone. Another use of p-coumaric acid via its thioester with coenzyme A, i
Phenylpropanoid
Chemical compound
considered a methoxy derivative of coumarin or a methyl derivative of umbelliferone. Herniarin is found in Herniaria glabra, Ayapana triplinervis and in
Herniarin
Gum resin
gum; and a very small quantity of the colorless crystalline substance umbelliferone. It also contains α-pinene, β-pinene, limonene, cadinene, 3-carene,
Galbanum
Class of phyto-photo toxic compounds
coupling of dimethylallyl pyrophosphate (DMAPP) and 7-hydroxycoumarin (umbelliferone). Many furanocoumarin compounds are toxic. The phytochemicals enter
Furanocoumarin
Species of flowering plant in the hydrangea family
roots of H. macrophylla. Hydrangine is another name for the coumarin umbelliferone, and may be responsible for the possible toxicity of the plant. Amacha
Hydrangea_macrophylla
Named reaction for synthesis of coumarins
performed under much milder conditions. This provides a useful route to umbelliferone derivatives: For coumarins unsubstituted at the 4-position, the method
Pechmann_condensation
Flowering plant in the daisy family
lactucopicrin. Other components are aesculetin, aesculin, cichoriin, umbelliferone, scopoletin, 6,7-dihydrocoumarin, and further sesquiterpene lactones
Chicory
Chemical compound
younghusbandii, and Zanthoxylum americanum mill. It is biosynthesized from umbelliferone, a coumarin derivative. The procedure for the isolation of imperatorin
Imperatorin
Genus of flowering plants in the passion flower family
compounds found in passion flowers are coumarins (e.g. scopoletin and umbelliferone), maltol, phytosterols (e.g. lutenin) and cyanogenic glycosides (e.g
Passiflora
Species of flowering plant
coumarin, which it produces in plenty, and which in combination with umbelliferone is responsible for many of its notable properties. It is also admixed
Dianthera_pectoralis
Species of flowering plant
of Gmelina arborea. The parent compounds are arboreol or gmelanone. Umbelliferone 7-apiosylglucoside can be isolated from the root. Five constituents
Gmelina_arborea
Genus of flowering plants
cuscohygrine, hyoscyamine, and atroscine. The coumarin phenylpropanoids umbelliferone and scopoletin have been isolated from the roots of Scopolia japonica
Scopolia
Chemical compound
which is formed via the alkylation of the umbelliferone (2) compound. The alkylation of the umbelliferone is initiated with the use of dimethylallyl
Bergamottin
Chemical compound
Skimmin is a glucoside of umbelliferone. Austin, D.J.; Meyers, M.B. (1965). "Studies on glucoside intermediates in umbelliferone biosynthesis". Phytochemistry
Skimmin
Species of flowering plant
alpha-terneol, ayapanin, ayapin, borneol, coumarin, sabinene, and umbelliferone, among many others.[citation needed] Phytochemical analysis of a methanolic
Ayapana_triplinervis
Organic compounds derived from coumarin
coumarin itself. Some naturally occurring coumarin derivatives include umbelliferone (7-hydroxycoumarin), aesculetin (6,7-dihydroxycoumarin), herniarin (7-methoxycoumarin)
Coumarin_derivatives
Aromatic chemical compound
of Justicia pectoralis Jacq. and its main constituents: coumarin and umbelliferone". Phytotherapy Research. 11 (3): 211–215. doi:10
Coumarin
Chemical compounds that absorb and re-emit light
2′-stilbenedisulfonic acid. Older, non-commercial fluorescent compounds include umbelliferone, which absorbs in the UV portion of the spectrum and re-emit it in the
Optical_brightener
Species of flowering plant in the daisy family Asteraceae
through stone as easily as through wood. The mouse-ear hawkweed contains umbelliferone, a compound similar to coumarin. The plant produces triterpenoids, mainly
Pilosella_officinarum
Chemical compound
point of 194–195 °C. It is soluble in methanol and glacial acetic acid. Umbelliferone Coumarin Yang Y, Hamaguchi K (April 1980). "Hydrolysis of 4-methylumbelliferyl
Hymecromone
Species of flowering plant
Chemical compounds isolated from E. alsinoides include scopoletin, umbelliferone, scopolin, and 2-methyl-1,2,3,4-butanetetrol. "Evolvulus alsinoides
Evolvulus_alsinoides
4-bromoisoquinoline 1532–97–4 C9H6N2 5-cyanoindole 15861–24–2 C9H6O3 umbelliferone 93–35–6 C9H6OS thiochromone 491–39–4 C9H7NO 8-hydroxyquinoline 148–24–3
Glossary_of_chemical_formulae
Index of chemical compounds with the same molecular formula
(molar mass: 162.14 g/mol, exact mass: 162.031694 u) may refer to: Umbelliferone, also known as 7-hydroxycoumarin or hydrangine 4-Hydroxycoumarin This
C9H6O3
Dye used as a laser medium
Polyphenyl ("polyphenyl 1") Rhodamine 6G Rhodamine B Rhodamine 123 Umbelliferone (also known as 7-hydroxycoumarin) Organic laser Solid state dye laser
Laser_dye
Index of chemical compounds with the same name
Hydroxycoumarin may refer to: 4-Hydroxycoumarin 7-Hydroxycoumarin (umbelliferone) This set index article lists chemical compounds articles associated
Hydroxycoumarin
Chemical compound
dimethylallyl pyrophosphate (DMAPP) to a modified coumarate known as umbelliferone. The biosynthesis is shown below: Kleiner, Heather E.; Suryanarayana
Isopimpinellin
Equipment using an organic dye to emit coherent light
530–560 nm), coumarin (blue 490–620 nm), stilbene (violet 410–480 nm), umbelliferone (blue, 450–470 nm), tetracene, malachite green, and others. While some
Dye_laser
6-prenyltransferase EC 2.5.1.138: coumarin 8-geranyltransferase EC 2.5.1.139: umbelliferone 6-dimethylallyltransferase EC 2.5.1.140: N-(2-amino-2-carboxyethyl)-L-glutamate
List_of_EC_numbers_(EC_2)
Enzyme for controlling the production of melanin
Sollai F, Zucca P, Sanjust E, Steri D, Rescigno A (December 2008). "Umbelliferone and esculetin: inhibitors or substrates for polyphenol oxidases?". Biological
Tyrosinase
Chemical compound
hydroxyhydroquinone triacetate with malic acid in concentrated sulfuric acid. Umbelliferone "Aesculetin". Sigma-Aldrich. Dey, P. M.; Harborne, J. B., eds. (1997)
Aesculetin
others 154.026608 C8H10O3 Hydroxytyrosol, others 154.062993 C9H6O3 Umbelliferone, others 162.031694 C9H8O3 Coumaric acid 164.047344 C10H12O2 Chavibetol
List of natural phenols and polyphenols molecular formulas
List_of_natural_phenols_and_polyphenols_molecular_formulas
Chemical compound
asafoetida and galbanum (from which, however, it differs in yielding no umbelliferone) both in regard to the plant which yields it and its putative effects
Ammoniacum
Species of flowering plant
salicylic acid, and its derivatives. Anthocyanidins and coumarins, such as umbelliferone, were also detected in V. tricolor. Extracts from the plant are anti-microbial
Viola_tricolor
Species of flowering plant
acid and arbutin have been identified within the plant. Furthermore, umbelliferone and phlorizin were found. An unknown triterpenoid known as 7α-hydroxybaruol
Adenostoma_fasciculatum
Class of enzymes
hydroxylation of the pharmacologically interesting phenylpropanoids umbelliferone and resveratrol. However, these approaches are not currently used commercially
4-Hydroxyphenylacetate 3-monooxygenase
4-Hydroxyphenylacetate_3-monooxygenase
Index of chemical compounds with the same molecular formula
exact mass: 176.0473 u) may refer to: Herniarin, a methoxy analog of umbelliferone Hymecromone This set index page lists chemical structure articles associated
C10H8O3
Chemical compound
L-phenylalanine. The precursor molecule then is converted into umbelliferone. After that, the umbelliferone molecule go through two pathways: either being converted
Calanolide_A
Genus of flowering plants
the coumarins: sfondine, isobergapten, pimpinellin, isopimpinellin, umbelliferone, daphniretin, bicoumastechamin and daphnetin; diterpenes (unspecified);
Stellera
Group of chemical compounds
Isocoumarins, Chromones Caffeic, ferulic acids, Myristicin, Eugenol, Umbelliferone. 10 C6-C4 1 Naphthoquinones Juglone, Plumbagin 13 C6-C1-C6 2 Xanthonoids
Naturally_occurring_phenols
Genus of flowering plants in the nightshade family
liquiritigenin, guaiaverine, coumarin, scopolin, fabriatrin, scopoletin, umbelliferone, and also β-sitosterol, 3-O-β-D-glucopyranoside-β-sitosterol and the
Physochlaina
MeSH D03.438.150.446.853 – pyranocoumarins MeSH D03.438.150.446.912 – umbelliferones MeSH D03.438.150.446.912.326 – coumaphos MeSH D03.438.150.446.912.531
List_of_MeSH_codes_(D03)
UMBELLIFERONE
UMBELLIFERONE
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UMBELLIFERONE
UMBELLIFERONE
UMBELLIFERONE
UMBELLIFERONE
UMBELLIFERONE
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