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ACRIDONE

Acridone

Chemical compound

Acridone is an organic compound based on the acridine skeleton, with a carbonyl group at the 9 position. The molecule is planar. Optical spectra reveal

Acridone

Acridone alkaloids

Acridone alkaloids are natural products derived from acridone. Acridone alkaloids are found in bark, wood, leaves and roots of rue plants, especially

Acridone alkaloids

Acridone_alkaloids

Fenamic acid

Chemical compound

can be synthesized from 2-chlorobenzoic acid and can be converted into acridone. Gupta, PK. Drug NomenclatureUnited States Adopted Names. Ch 27 in Remington:

Fenamic acid

Fenamic_acid

Acridine

Organic compound used in dyes

chloride or by distilling acridone (9-position a carbonyl group) over zinc dust. Another classic method for the synthesis of acridones is the Lehmstedt-Tanasescu

Acridine

Ruta graveolens

Species of plant

mechanism of action is currently unknown. A series of furanoacridones and two acridone alkaloids (arborinine and evoxanthine) have been isolated from R. graveolens

Ruta graveolens

Ruta_graveolens

Lehmstedt–Tanasescu reaction

Method in organic chemistry

reaction is a method in organic chemistry for the organic synthesis of acridone derivatives (3) from a 2-nitrobenzaldehyde (1) and an arene compound (2):

Lehmstedt–Tanasescu reaction

Lehmstedt–Tanasescu_reaction

Acridone synthase

Class of enzymes

Acridone synthase (EC 2.3.1.159) is an enzyme that catalyzes the chemical reaction N-methylanthraniloyl-CoA + 3 malonyl-CoA 3 CO2 1

Acridone synthase

Acridone_synthase

Cridanimod

Pharmaceutical compound

Cridanimod, also known as cycloferon or meglumine acridone acetate, is a low molecular weight immunomodulatory drug known to trigger the production of

Cridanimod

Lucigenin

Chemical compound

biology, for its chemiluminescent properties. It may be prepared from acridone. There's also a route from toluene: Amiet, R. Gary (February 1982). "The

Lucigenin

Sarcomelicope glauca

Species of flowering plant

"Quinoline, quinazoline, and acridone alkaloids". Natural Product Reports (3): 293–307. "In vitro activities of furoquinoline and acridone alkaloids against Plasmodium

Sarcomelicope glauca

Sarcomelicope_glauca

Quinacridone

Organic compound used as a pigment

[citation needed] The name indicates that the compounds are a fusion of acridone and quinoline, although they are not made that way. Classically the parent

Quinacridone

Aminoaldehydes and aminoketones

Class of organic compounds

the ketone is located on a ring, e.g. 4-piperidinone, triacetonamine, acridone. Most members of this class are unstable towards self-condensation, however

Aminoaldehydes and aminoketones

Aminoaldehydes_and_aminoketones

Ullmann condensation

Copper-promoted cross-coupling reactions

doi:10.15227/orgsyn.082.0069. C. F. H. Allen, G. H. W. McKee (1939). "Acridone". Organic Syntheses. 19: 6. doi:10.15227/orgsyn.019.0006. H.B. Goodbrand;

Ullmann condensation

Ullmann_condensation

C13H9NO

Index of chemical compounds with the same molecular formula

C13H9NO (molar mass: 195.22 g/mol, exact mass: 195.0684 u) may refer to: Acridone CR gas, or dibenzoxazepine This set index page lists chemical structure

C13H9NO

Noncovalent solid-phase organic synthesis

setup the hydrophobic matrix is RP silica gel (C18) and the anchor is acridone. Acridone is N-alkylated and the terminal alkene group is converted into an

Noncovalent solid-phase organic synthesis

Noncovalent_solid-phase_organic_synthesis

Zanthoxylum gilletii

Species of tree

the stem bark. The lignan sesamin, the N-isobutylamide γ-sanshool, the acridone alkaloids 1-hydroxy-3-methoxy-N-methylacridone, arborinine, xanthoxoline

Zanthoxylum gilletii

Zanthoxylum_gilletii

Anthranilate—CoA ligase

pathways: carbazole degradation, benzoate degradation via coa ligation, and acridone alkaloid biosynthesis. Altenschmidt U, Eckerskorn C, Fuchs G (1990). "Evidence

Anthranilate—CoA ligase

Anthranilate—CoA_ligase

I-motif DNA

Cytosine-rich quadruplex DNA structure

biological functions. These include IMC-48, IMC-76, Nitidine, NSC309874, acridone derivative, and PBP1. IMC-48 stabilizes the bcl-2 structure of i-motif

I-motif DNA

I-motif_DNA

Zanthoxylum

Genus of shrubs and trees

tembetarine, magnoflorine, M-methyl-corydine), canthinones (6-canthinone), acridones (1-hydroxy-3-methoxy-10-methylacridon-9-one, 1-hydroxy-10-methylacridon-9-one

Zanthoxylum

Furoquinoline alkaloid

Group of chemical compounds

Koch, M; Le Bras, J (1994). "In vitro activities of furoquinoline and acridone alkaloids against Plasmodium falciparum". Antimicrobial Agents and Chemotherapy

Furoquinoline alkaloid

Furoquinoline_alkaloid

Evoxine

Chemical compound

Coombes, PH; Crouch, NR; Mulholland, DA; El Amin, SM; Smith, PJ (2007). "Acridone and furoquinoline alkaloids from Teclea gerrardii (Rutaceae: Toddalioideae)

Evoxine

List of EC numbers (EC 2)

EC 2.3.1.158: phospholipid:diacylglycerol acyltransferase EC 2.3.1.159: acridone synthase EC 2.3.1.160: vinorine synthase EC 2.3.1.161: lovastatin nonaketide

List of EC numbers (EC 2)

List_of_EC_numbers_(EC_2)

Diethylsuccinoylsuccinate

Chemical compound

required) Smith, J. Anthony; West, Richard M.; Allen, Malcolm (2004). "Acridones and Quinacridones: Novel Fluorophores for Fluorescence Lifetime Studies"

Diethylsuccinoylsuccinate

Anthranilate N-methyltransferase

Class of enzymes

N-methyltransferase. The reaction is the first step specific to the biosynthesis of acridone alkaloids. Eilert U, Wolters B (1989). "Elicitor induction of

Anthranilate N-methyltransferase

Anthranilate_N-methyltransferase

Elizabeth Hardy (chemist)

Canadian-American chemist (1915–2008)

Hardy, Bound Brook. Patented: November 30, 1948 Soluble vat dyes of the acridone series. William B. Hardy and Elizabeth M. Hardy, Bound Brook. Patented:

Elizabeth Hardy (chemist)