Results 141 to 150 of about 10,911 (198)

Discovery of a plant-like tridomain bifunctional <i>syn</i>-abieta-7,13-diene synthase in <i>Streptomyces</i>.

Org Biomol Chem
McCadden CA, Łomowska-Keehner DP, Qu T, Nafie J, Alsup TA, Rudolf JD.   +5 more
europepmc   +1 more source

Talaroacids A-D and Talaromarane A, Diterpenoids with Anti-Inflammatory Activities from Mangrove Endophytic Fungus Talaromyces sp. JNQQJ-4. [PDF]

Int J Mol Sci
Wang G, Wu J, Li Z, Chen T, Liu Y, Wang B, Chen Y, She Z.   +7 more
europepmc   +1 more source

Grewiifopenes A-K, bioactive clerodane diterpenoids from Casearia grewiifolia Vent. [PDF]

Nat Prod Bioprospect
Pailee P, Batsomboon P, Yaosanit W, Thananthaisong T, Mahidol C, Ploypradith P, Reuk-Ngam N, Khlaychan P, Techasakul S, Ruchirawat S, Prachyawarakorn V.   +10 more
europepmc   +1 more source

Advances in the Structures, Pharmacological Activities, and Biosynthesis of Plant Diterpenoids. [PDF]

J Microbiol Biotechnol
Li L, Fu J, Liu N.
europepmc   +1 more source

Novel Diterpenoids From Salvia rosmarinus Reveal a Compound With Antiproliferative and Antioxidant Activities. [PDF]

Arch Pharm (Weinheim)
Pérez-Juanchi D, Bustos-Brito C, Ramírez-Apan MT, Nieto-Camacho A, Quijano L, Esquivel B.   +5 more
europepmc   +1 more source

Between scents and sterols: Cyclization of labdane-related diterpenes as model systems for enzymatic control of carbocation cascades. [PDF]

J Biol Chem
Peters RJ.
europepmc   +1 more source

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Clerodane diterpenes of Croton hovarum

Phytochemistry, 1997
Abstract A clerodane- and a nor-clerodane-type furano-diterpene were obtained from the methanolic extract of the leaves of Croton hovarum . Structural determinations which were made from spectroscopic data led to 3,12-dioxo-15,16-epoxy-cleroda-13(16), 14-dien-9-al and 3α,4β-dihydroxy-15,16-epoxy-19-nor-12-oxo-cleroda-5(10), 13 13(16),14-triene ...
Hans C. Krebs, Harisolo Ramiarantsoa
openaire   +2 more sources

Stereochemistry of -clerodane diterpenes

Tetrahedron, 1986
Abstract To piscicidal solidagolactones [IV, V, VII and VIII (1~4, cis -clerodane diterpenes)] isolated from Solidago altissima , a non-steroidal conformation was assigned on the basis of chemical and physicocheaical evidence. 13C NMR chemical shifts of methyl groups proved useful for determining stereochemistry of the A/B ring ...
Shunichi Manabe, Chikao Nishino
openaire   +1 more source

Clerodane diterpenes of croton ururucana

Phytochemistry, 1998
Abstract Sonderianin and two novel furoclerodane diterpenes with a trans A\B ring junction were obtained from the barks of Croton ururucana . Their structures were elucidated by detailed NMR investigation, and the relative configurations established by NOE experiments. 13 C NMR values for the carbonyls of sonderianin were corrected.
Marize T.Lopes P Peres, Moacir G Pizzolatti, Rosendo A Yunes, Franco Delle Monache   +3 more
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