| Schumanniophyton problematicum | |
|---|---|
Scientific classification  | |
| Kingdom: | Plantae |
| Clade: | Tracheophytes |
| Clade: | Angiosperms |
| Clade: | Eudicots |
| Clade: | Asterids |
| Order: | Gentianales |
| Family: | Rubiaceae |
| Genus: | Schumanniophyton |
| Species: | S. problematicum |
| Binomial name | |
| Schumanniophyton problematicum | |
| Synonyms | |
Assidora problematicaA.Chev. | |
Schumanniophyton problematicum is a species of plant in the family Rubiaceae. It is found in Ivory Coast, Ghana, and Sierra Leone. It is threatened by habitat loss. [1]
The plant has been found to contain the alkaloids rohitukine and rohitukine N-oxide, and the iridoid glycosides scyphiphorin A1–A2 and scyphiphorin B1–B2. [2] Alvocidib is a synthetic analog of rohitukine that acts as a CDK9 kinase inhibitor and is under clinical development for the treatment of acute myeloid leukemia. It has also been studied for the treatment of arthritis [3] and atherosclerotic plaque formation [4]
Rohitukine was initially extracted from Aphanamixis polystachya (the alkaloid name being derived from the synonym Amoora rohituka) and later from Dysoxylum binectariferum . [5] [6] - both of which plant species belong to the family Meliaceae.
The scyphiphorins were first isolated from (and subsequently named for) Scyphiphora hydrophylacea , which, like Schumanniophyton, belongs to the plant family Rubiaceae. [7]
Cardiac glycosides are a class of organic compounds that increase the output force of the heart and decrease its rate of contractions by inhibiting the cellular sodium-potassium ATPase pump. Their beneficial medical uses are as treatments for congestive heart failure and cardiac arrhythmias; however, their relative toxicity prevents them from being widely used. Most commonly found as secondary metabolites in several plants such as foxglove plants, these compounds nevertheless have a diverse range of biochemical effects regarding cardiac cell function and have also been suggested for use in cancer treatment.
In chemistry, a glycoside is a molecule in which a sugar is bound to another functional group via a glycosidic bond. Glycosides play numerous important roles in living organisms. Many plants store chemicals in the form of inactive glycosides. These can be activated by enzyme hydrolysis, which causes the sugar part to be broken off, making the chemical available for use. Many such plant glycosides are used as medications. Several species of Heliconius butterfly are capable of incorporating these plant compounds as a form of chemical defense against predators. In animals and humans, poisons are often bound to sugar molecules as part of their elimination from the body.
Junonia coenia, known as the common buckeye or buckeye, is a butterfly in the family Nymphalidae. Its range covers much of North America and some of Central America, including most of the eastern half of the US, the lower to middle Midwest, the Southwest, southern Canada, and Mexico. Its habitat is open areas with low vegetation and some bare ground. Its original ancestry has been traced to Africa, which then experiences divergence in Asia. The species Junonia grisea, the gray buckeye, is found west of the Rocky Mountains and was formerly a subspecies of Junonia coenia.
Dysoxylum is a genus of rainforest trees and shrubs in the flowering plant family Meliaceae. About 34 species are recognised in the genus, distributed from India and southern China, through southeast Asia to New Guinea, Solomon Islands, and Australia. The name Dysoxylum derives from the Greek word ‘Dys’ meaning "bad" referring to "ill-smelling" and ‘Xylon’ meaning "wood".
Triosteum, commonly known in American English as horse-gentian or, less commonly, feverwort, and, in Standard Chinese as 莛子藨属, is a genus of flowering plants belonging to the family Caprifoliaceae. A genus of six species in total, it has three species native to North America, and three more in eastern Asia.
Chelerythrine is a benzophenanthridine alkaloid present in the plant Chelidonium majus. It is a potent, selective, and cell-permeable protein kinase C inhibitor in vitro. And an efficacious antagonist of G-protein-coupled CB1 receptors. This molecule also exhibits anticancer qualities and it has served as a base for many potential novel drugs against cancer. Structurally, this molecule has two distinct conformations, one being a positively charged iminium form, and the other being an uncharged form, a pseudo-base.
Swainsonine is an indolizidine alkaloid. It is a potent inhibitor of Golgi alpha-mannosidase II, an immunomodulator, and a potential chemotherapy drug. As a toxin in locoweed it also is a significant cause of economic losses in livestock industries, particularly in North America. It was first isolated from Swainsona canescens.
Iridoids are a type of monoterpenoids in the general form of cyclopentanopyran, found in a wide variety of plants and some animals. They are biosynthetically derived from 8-oxogeranial. Iridoids are typically found in plants as glycosides, most often bound to glucose.
Staurosporine is a natural product originally isolated in 1977 from the bacterium Streptomyces staurosporeus. It was the first of over 50 alkaloids to be isolated with this type of bis-indole chemical structure. The chemical structure of staurosporine was elucidated by X-ray analysis of a single crystal and the absolute stereochemical configuration by the same method in 1994.
Aphanamixis polystachya, the pithraj tree, is a species of tree in the family Meliaceae. It is native to India, Pakistan, Nepal, Bhutan, Bangladesh, Myanmar and Sri Lanka. It is a widely used as a medicinal plant in Ayurveda.
Swietenia macrophylla, commonly known as mahogany, Honduran mahogany, Honduras mahogany, or big-leaf mahogany is a species of plant in the Meliaceae family. It is one of three species that yields genuine mahogany timber (Swietenia), the others being Swietenia mahagoni and Swietenia humilis. It is native to South America, Mexico and Central America, but naturalized in the Philippines, Singapore, Malaysia and Hawaii, and cultivated in plantations and wind-breaks elsewhere.
Cornus officinalis, the Japanese cornel or Japanese cornelian cherry, is a species of flowering plant in the dogwood family Cornaceae. Despite its name, it is native to China and Korea as well as Japan. It is not to be confused with C. mas, which is also known as the Cornelian cherry. It is not closely related to the true cherries of the genus Prunus.
Alvocidib is a flavonoid alkaloid CDK9 kinase inhibitor under clinical development by Tolero Pharmaceuticals for the treatment of acute myeloid leukemia. It has been studied also for the treatment of arthritis and atherosclerotic plaque formation. The target of alvocidib is the positive transcription elongation factor P-TEFb. Treatment of cells with alvocidib leads to inhibition of P-TEFb and the loss of mRNA production.
Tetrandrine, a bis-benzylisoquinoline alkaloid, is a calcium channel blocker. It is isolated from the plant Stephania tetrandra, and other Chinese and Japanese herbs.
Aucubin is an iridoid glycoside. Iridoids are commonly found in plants and function as defensive compounds. Iridoids decrease the growth rates of many generalist herbivores.
Verbascoside is a caffeoyl phenylethanoid glycoside in which the phenylpropanoid caffeic acid and the phenylethanoid hydroxytyrosol form an ester and an ether bond respectively, to the rhamnose part of a disaccharide, namely β-(3′,4′-dihydroxyphenyl)ethyl-O-α-L-rhamnopyranosyl(1→3)-β-D-(4-O-caffeoyl)-glucopyranoside.
c-Met inhibitors are a class of small molecules that inhibit the enzymatic activity of the c-Met tyrosine kinase, the receptor of hepatocyte growth factor/scatter factor (HGF/SF). These inhibitors may have therapeutic application in the treatment of various types of cancers.
A flavonoid alkaloid also known as a flavoalkaloid is a type of natural product produced by plants that contains both a flavonoid core structure and a nitrogen containing substituent so that the substance is also classified as an alkaloid. The most common flavonoid alkaloids contain a nitrogen heterocycle such as a pyridine or piperidine which is covalently bonded to the A-ring of a chromone. One flavonoid alkaloid, lilaline, was isolated from Lilium candidum in 1987. The synthesis of flavonoid alkaloids has been achieved
Harpagoside is a natural product found in the plant Harpagophytum procumbens, also known as devil's claw. It is the active chemical constituent responsible for the medicinal properties of the plant, which have been used for centuries by the Khoisan people of southern Africa to treat diverse health disorders, including fever, diabetes, hypertension, and various blood related diseases.
Dysoxylum gotadhora is a tree in the family Meliaceae. It is native to Bhutan, India, Laos, Nepal, Thailand, and Vietnam. The name Dysoxylum ficiforme (Wight) Gamble in India and Sri Lanka is categorized as the same plant as is D. binectariferum.
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