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Aporphine Alkaloids
Aporphine alkaloids are naturally occurring chemical compounds from the group of alkaloids. After the benzylisoquinoline alkaloids they are the second largest group of isoquinoline alkaloids. At least 85 aporphine alkaloids have been isolated from plants of 15 families. The best known representative is apomorphine. The aporphine alkaloids are of interest mainly because of their similarity to morphine. Occurrence The aporphine alkaloids are most commonly found in plants. For example, isoboldine can be found in the plants in the genera ''Beilschmiedia'', ''Nandina'' (''Nandina domestica''), ''Glaucium'' (horn poppy), and other plants. As the name suggests, glaucine was first found in the horn poppy and usually the name of the alkaloids is derived from the plants in which they were first found. Corydin as a further representative of the aporphine alkaloids is found in ''Corydalis'' (larkspurs) ''Dicentra'' (heart flowers), and also in the horn poppy. Examples Apoglaziovin ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Aporphine
Aporphine is an alkaloid with the chemical formula . It is the core chemical substructure of the aporphine alkaloids, a subclass of quinoline alkaloids. It can exist in either of two enantiomeric forms, (''R'')-aporphine and (''S'')-aporphine. Derivatives Many different derivatives of aporphine have been isolated from plants. For example, many water lilies (''Nymphaea'' species) produce aporphine alkaloids such as Nuciferine, nymphaeine, nymphaline, nupharine, α- and β-nupharidine. ''In vitro,'' tests of some aporphine derivatives isolated from '' Cassytha filiformis'', namely, actinodaphnine, cassythine, and dicentrine, showed antiparasitic activity against ''Trypanosoma brucei''. Investigation of possible mechanisms revealed that the compounds bind to DNA and act as intercalating agents, in addition to inhibiting topoisomerase activity. Aporphine natural products occur with either the (R)- or (S)- isomeric forms, or they can be achiral. Furthermore, morphine-based nat ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dicentra
''Dicentra'' (Ancient Greek, Greek ''dís'' "twice", ''kéntron'' "spur"), known collectively as the bleeding-hearts, is a genus containing eight species of herbaceous plant, herbaceous Flowering plant, flowering perennial plants with unique, "heart"-shaped Flower, flowers and finely divided Leaf, foliage. The species are, primarily, native plant, native to North America, although several are found in temperate East Asia. Description and growth requirements Flowers have two tiny sepals and four petals. The flowers are bisymmetric: the two outer petals are spur (botany), spurred or pouched at the base and curved outwards or backwards at the tip, and the two inner ones with or without a crest at the tip. In ''Dicentra'', all leaves are in a basal rosette (botany), rosette, and flowers are on leafless pedicel (botany), stalks. In other genera with bisymmetric heart-shaped flowers (''Lamprocapnos'', ''Dactylicapnos'', ''Ichtyoselmis'', ''Ehrendorferia''), leaves grow on stems as well ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cyclization Reaction
A cyclic compound (or ring compound) is a term for a compound in the field of chemistry in which one or more series of atoms in the compound is connected to form a ring. Rings may vary in size from three to many atoms, and include examples where all the atoms are carbon (i.e., are carbocycles), none of the atoms are carbon (inorganic cyclic compounds), or where both carbon and non-carbon atoms are present (heterocyclic compounds with rings containing both carbon and non-carbon). Depending on the ring size, the bond order of the individual links between ring atoms, and their arrangements within the rings, carbocyclic and heterocyclic compounds may be aromatic or non-aromatic; in the latter case, they may vary from being fully saturated to having varying numbers of multiple bonds between the ring atoms. Because of the tremendous diversity allowed, in combination, by the valences of common atoms and their ability to form rings, the number of possible cyclic structures, even of smal ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Reticuline
Reticuline is an alkaloid found in opium and a variety of plants including ''Lindera aggregata'', ''Annona squamosa'', and ''Ocotea#Selected species, Ocotea fasciculata'' (also known as ''Ocotea duckei''). Experiments in rodents suggest reticuline possesses potent central nervous system depressant, depressing effects. It is the precursor of morphine and many other alkaloids. It is also toxic to dopaminergic neurons causing a form of Parkinson plus syndrome, atypical parkinsonism known as Guadeloupean Parkinsonism. Metabolism 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase uses S-Adenosyl methionine, ''S''-adenosyl methionine and 3'-hydroxy-''N''-methyl-(''S'')-coclaurine to produce S-Adenosyl-L-homocysteine, ''S''-adenosylhomocysteine and (''S'')-reticuline. Reticuline oxidase uses (''S'')-reticuline and O2 to produce (''S'')-scoulerine and H2O2. Salutaridine synthase uses (''R'')-reticuline, NADPH, H+, and O2 to produce salutaridine, NADP+, and H2O. Salutaridine ca ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Biosynthesis
Biosynthesis, i.e., chemical synthesis occurring in biological contexts, is a term most often referring to multi-step, enzyme-Catalysis, catalyzed processes where chemical substances absorbed as nutrients (or previously converted through biosynthesis) serve as enzyme substrate (chemistry), substrates, with conversion by the living organism either into simpler or more complex Product (chemistry), products. Examples of biosynthetic pathways include those for the production of amino acids, lipid membrane components, and nucleotides, but also for the production of all classes of biological macromolecules, and of acetyl-coenzyme A, adenosine triphosphate, nicotinamide adenine dinucleotide and other key intermediate and transactional molecules needed for metabolism. Thus, in biosynthesis, any of an array of Chemical compound, compounds, from simple to complex, are converted into other compounds, and so it includes both the catabolism and anabolism (building up and breaking down) of comple ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bulbocapnine
Bulbocapnine is an alkaloid found in ''Corydalis'' (notably the European species C. cava) and ''Dicentra'', genera of the plant family Fumariaceae which have caused (notably the American species ''Corydalis caseana'') the fatal poisoning of sheep and cattle. It has been shown to act as an acetylcholinesterase inhibitor, and inhibits biosynthesis of dopamine via inhibition of the enzyme tyrosine hydroxylase. Like apomorphine, it is reported to be an inhibitor of amyloid beta protein (Aβ) fiber formation, whose presence is a hallmark of Alzheimer's disease (AD). Bulbocapnine is thus a potential therapeutic under the amyloid hypothesis. According to the ''Dorlands Medical Dictionary'', it "inhibits the reflex and motor activities of striated muscle. It has been used in the treatment of muscular tremors and vestibular nystagmus". A psychiatrist at Tulane University named Robert Heath carried out experiments on prisoners at the Louisiana State Penitentiary using bulbocapnine to ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Substituent
In organic chemistry, a substituent is one or a group of atoms that replaces (one or more) atoms, thereby becoming a moiety in the resultant (new) molecule. The suffix ''-yl'' is used when naming organic compounds that contain a single bond replacing one hydrogen; ''-ylidene'' and ''-ylidyne'' are used with double bonds and triple bonds, respectively. In addition, when naming hydrocarbons that contain a substituent, positional numbers are used to indicate which carbon atom the substituent attaches to when such information is needed to distinguish between isomers. Substituents can be a combination of the inductive effect and the mesomeric effect. Such effects are also described as electron-rich and electron withdrawing. Additional steric effects result from the volume occupied by a substituent. The phrases ''most-substituted'' and ''least-substituted'' are frequently used to describe or compare molecules that are products of a chemical reaction. In this terminology, ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Nuciferine
Nuciferine is an alkaloid found within the plants ''Nymphaea caerulea'' and ''Nelumbo nucifera''. Preliminary psychopharmacological research in 1978 was unable to conclusively determine the compound's classification regarding dopamine-receptor activity. On one hand, investigative studies found evidence of behavior traditionally associated with ''dopamine-receptor'' ''stimulation'': stereotypy, increase in spontaneous motor activity, inhibition of conditioned avoidance response, and an increase in pain sensitivity resulting in an inhibition of morphine analgesia. On the other hand, these early investigative studies also found evidence of behavior traditionally associated with ''dopamine-receptor'' ''blockade'': decrease of spontaneous motor activity, chills, catalepsy, trance-like states of consciousness. Nuciferine exhibits a receptor profile similar to atypical antipsychotics, demonstrating antipsychotic-like effects in rodent models without inducing catalepsy. Pharmacology ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Glaucine
Glaucine (also known as 1,2,9,10-tetramethoxyaporphine, bromcholitin, glauvent, tusidil, and tussiglaucin) is an aporphine alkaloid found in several different plant species in the family Papaveraceae, such as '' Glaucium flavum'', '' Glaucium oxylobum'', and '' Corydalis yanhusuo'', and in other plants such as '' Croton lechleri'' in the family Euphorbiaceae. It has bronchodilator, neuroleptic and antiinflammatory effects, acting as a PDE4 inhibitor and calcium channel blocker, and is used medically as an antitussive in some countries. TLRs plays role in its anti inflammatory effects. Glaucine may produce side effects such as sedation, fatigue, and a hallucinogenic effect characterised by colourful visual images, and has been detected as a novel psychoactive drug. In a 2019 publication,Heng, HL, Chee, CF, Thy, CK, et al. In vitro functional evaluation of isolaureline, dicentrine and glaucine enantiomers at 5‐HT2 and α1 receptors. Chem Biol Drug Des. 2019; 93: 132– 13 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Domesticine
Domesticine is an alpha-1D adrenergic receptor, α1D-adrenergic receptor receptor antagonist, antagonist. The compound belongs to the group of aporphine alkaloids. References Alpha-1 blockers Aporphine alkaloids {{pharma-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
