[go: up one dir, main page]

El–Dakhakhny et al., 1962 - Google Patents

THE STEROID CONSTITUENTS OF PRUNUS MAHALEB L. FRUIT KERNELS II1

El–Dakhakhny et al., 1962

Document ID
6725386139843744432
Author
El–Dakhakhny M
Fayez M
Publication year
Publication venue
Planta Medica

External Links

Snippet

Summary β–sitosterol was isolated from the nonsaponifiable matter of Prunus mahaleb L. kernel oil. It was also found in the defatted meal as β–sitosteryl–D–glucoside. β–sitosteryl acetate, bezoate and 3, 5–dinitrobenzoate were prepared from the free β–sitosterol and from …
Continue reading at www.thieme-connect.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J71/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
    • C07J71/0036Nitrogen-containing hetero ring
    • C07J71/0042Nitrogen only
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J71/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
    • C07J71/0005Oxygen-containing hetero ring
    • C07J71/001Oxiranes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K36/00Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18Magnoliophyta (angiosperms)
    • A61K36/185Magnoliopsida (dicotyledons)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/20Carbocyclic rings
    • C07H15/24Condensed ring systems having three or more rings
    • C07H15/256Polyterpene radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J9/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J17/00Normal steroids containing carbon, hydrogen, halogen or oxygen, having an oxygen-containing hetero ring not condensed with the cyclopenta(a)hydrophenanthrene skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J13/00Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J63/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J75/00Processes for the preparation of steroids in general
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H17/00Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
    • C07H17/04Heterocyclic radicals containing only oxygen as ring hetero atoms
    • C07H17/06Benzopyran radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J7/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms

Similar Documents

Publication Publication Date Title
Chen et al. Trinorcucurbitane and cucurbitane triterpenoids from the roots of Momordica charantia
Tsai et al. Constituents and bioactive principles of Polygonum chinensis
Kupchan et al. Tumor inhibitors. LVI. Cucurbitacins O, P, and Q, the cytotoxic principles of Brandegea bigelovii
Sim et al. Constituents of brucea sumatrana. I. Brusatol
DE2801186C2 (en)
Lavie et al. Constituents of Citrullus colocynthis (L.) Schrad.
CN106632577B (en) A kind of Ursane triterpenoid saponin and its preparation process in masson pine branch
Kenfack et al. A new flavonol glycoside from Tristemma hirtum (Melastomataceae)
Tupkari et al. Phytochemical study of Solanum xanthocarpum
Abu-Mustafa et al. Constituents of local plants—IV.: Ficus carica L., F. sycomorus L. and F. salicifolia L. leaves
Akhtar et al. Extraction, isolation and structural characterization of two triterpenoid glycosides from the fruits of Ficus bengalensis
Patnaik et al. Isolation of triterpenoid glycoside from bark of Terminalia arjuna using chromatographic technique and investigation of pharmacological behavior upon muscle tissues
Kupchan et al. Tumor inhibitors. XLIV. Isolation and characterization of hellebrigenin 3-acetate and hellebrigenin 3, 5-diacetate, Bufadienolide tumor inhibitors from Bersama abyssinica
El–Dakhakhny et al. THE STEROID CONSTITUENTS OF PRUNUS MAHALEB L. FRUIT KERNELS II1
Pettit et al. Steroids and related natural products—xxvii. Salvia apiana
Gopal et al. Chemical constituents of Salmalia malabarica Schott and Endl. flowers
Ghorbani et al. Phytochemical Reinvestigation of Xysmalobium undulatum Roots (Uzara) 1
CN104761445A (en) Method for extracting chemical components from root of mongolian medicine Cymbaria dahurica
Kind et al. Steroids of the Virginia snakeroot, Aristolochia serpentaria
Ali et al. New Naphthyl Substituted Phytosterol and Lanostane Type-triterpenic Esters from the Stem Bark of Ficus religiosa L.
Bongmo et al. Secondary Metabolites from Anthonotha cladantha (Harms) J. Léonard
Djerassi et al. Terpenoids. XXVIII. 1 The Triterpene Composition of the Genus Myrtillocactus2
Fayez et al. Constituents of Local Plants. V.
Issidorides et al. Selenium dioxide oxidation of methyl Δ3-cholenate
Takeda et al. Studies on the steroidal components of domestic plants—XLVI: constituents of hosta species (3) 1 Δ25 (27)-sapogenins