Barros et al., 2011 - Google Patents
Amyrin esters induce cell death by apoptosis in HL-60 leukemia cellsBarros et al., 2011
View PDF- Document ID
- 9344472787409517425
- Author
- Barros F
- Bandeira P
- Lima D
- Meira A
- de Farias S
- Albuquerque M
- dos Santos H
- Lemos T
- de Morais M
- Costa-Lotufo L
- do Ó Pessoa C
- Publication year
- Publication venue
- Bioorganic & medicinal chemistry
External Links
Snippet
Four derivatives of an α, β-amyrin mixture were synthesized by acylation with appropriate anhydrides. The structures of the compounds were confirmed by means of IR and 1H and 13C NMR. The compounds were screened for cytotoxic activity using four human tumor cell …
- 206010059512 Apoptosis 0 title abstract description 15
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/75—Rutaceae (Rue family)
- A61K36/758—Zanthoxylum, e.g. pricklyash
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/06—Peri-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/24—Apocynaceae (Dogbane family), e.g. plumeria or periwinkle
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. cannabinols, methantheline
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J63/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
- C07J63/008—Expansion of ring D by one atom, e.g. D homo steroids
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Barros et al. | Amyrin esters induce cell death by apoptosis in HL-60 leukemia cells | |
Liu et al. | Antioxidant triterpenoids from the stems of Momordica charantia | |
Begum et al. | Carandinol: First isohopane triterpene from the leaves of Carissa carandas L. and its cytotoxicity against cancer cell lines | |
Rodríguez-Hernández et al. | Hederagenin as a triterpene template for the development of new antitumor compounds | |
Reyes et al. | Activity of lupane triterpenoids from Maytenus species as inhibitors of nitric oxide and prostaglandin E2 | |
Csuk et al. | Tormentic acid derivatives: Synthesis and apoptotic activity | |
Pagning et al. | New triterpene and new flavone glucoside from Rhynchospora corymbosa (Cyperaceae) with their antimicrobial, tyrosinase and butyrylcholinesterase inhibitory activities | |
Viau et al. | The natural triterpene 3β, 6β, 16β-trihydroxy-lup-20 (29)-ene obtained from the flowers of Combretum leprosum induces apoptosis in MCF-7 breast cancer cells | |
Efdi et al. | Sentulic acid: a cytotoxic ring A-seco triterpenoid from Sandoricum koetjape Merr | |
Momtaz et al. | Growth inhibition and induction of apoptosis in human cancerous HeLa cells by Maytenus procumbens | |
Logrado et al. | Synthesis and cytotoxicity screening of substituted isobenzofuranones designed from anacardic acids | |
Hueso-Falcón et al. | Synthesis and induction of apoptosis signaling pathway of ent-kaurane derivatives | |
Spindola et al. | Furanoditerpenes from Pterodon pubescens Benth with selective in vitro anticancer activity for prostate cell line | |
Lin et al. | Xanthine oxidase inhibitory lanostanoids from Ganoderma tsugae | |
Saleem et al. | New bioactive natural products from Launaea nudicaulis | |
Choudhary et al. | Chlorinated and diepoxy withanolides from Withania somnifera and their cytotoxic effects against human lung cancer cell line | |
Sridhar et al. | Flavonoids, triterpenoids and a lignan from Vitex altissima | |
Adfa et al. | Antileukemic activity of lignans and phenylpropanoids of Cinnamomum parthenoxylon | |
Hung et al. | Cassaine diterpene alkaloids from Erythrophleum fordii and their anti-angiogenic effect | |
Lenta et al. | Anti-plasmodial and cholinesterase inhibiting activities of some constituents of Psorospermum glaberrimum | |
Zhang et al. | Cyclooxygenase-2 enzyme inhibitory triterpenoids from Picrorhiza kurroa seeds | |
Popović et al. | Sesquiterpene lactones from the extracts of two Balkan endemic Laserpitium species and their cytotoxic activity | |
Yang et al. | Five new C17/C15 sesquiterpene lactone dimers from Carpesium abrotanoides | |
Kiplimo et al. | Ring A-seco limonoids and flavonoids from the Kenyan Vepris uguenensis Engl. and their antioxidant activity | |
Pattnaik et al. | Synthesis of ring-C modified oleanolic acid derivatives and their cytotoxic evaluation |