Results 161 to 170 of about 12,701 (222)

Safety and efficacy of a feed additive consisting of a tincture derived from the leaves or aerial parts of <i>Thymus serpyllum</i> L. (wild thyme tincture) for use in all animal species (FEFANA asbl). [PDF]

open access: yesEFSA J
EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP)   +23 more
europepmc   +1 more source

Decoupling thermal stability and insulation in dielectric polymers via donor-acceptor rearrangement. [PDF]

open access: yesNat Commun
Wan Y   +8 more
europepmc   +1 more source

Safety and efficacy of a feed additive consisting of a tincture derived from the leaves of <i>Salvia officinalis</i> L. (sage tincture) for use in all animal species (FEFANA asbl). [PDF]

open access: yesEFSA J
EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP)   +23 more
europepmc   +1 more source

Assessment of the structure-activity relationship of analogs of the <i>Naegleria fowleri</i> enolase inhibitor HEX. [PDF]

open access: yesRSC Med Chem
Kwain S   +10 more
europepmc   +1 more source

Flavouring Group Evaluation 80, Revision 2 (FGE.80Rev2): Consideration of alicyclic, alicyclic-fused and aromatic-fused ring lactones evaluated by the JECFA (61st and 82nd meetings) structurally related to an aromatic lactone evaluated in FGE.27. [PDF]

open access: yesEFSA J
EFSA Panel on Food Additives and Flavourings (FAF)   +27 more
europepmc   +1 more source
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Configuration of Alicyclic Amino-Alcohols

Nature, 1949
WE have extended our investigations1 on the acyl migration reaction N6666666 O to acyl derivatives of diastereoisomeric alicyclic amino-alcohols2, such as 2-amino-cyclohexanol3, with the view of establishing the relative steric positions4 (that is, configuration) of hydroxyl and acylamido groups.
G, FODOR, J, KISS
exaly   +3 more sources

Alicyclic Analogue of Mescaline

Nature, 1968
WE wish to describe the preliminary pharmacology of a mescaline analogue, 2-(3,4,5-trimethoxyphenyl)-cyclopropylamine (TMT, II). This compound was selected for synthesis as a potential long-acting psychotomimetic which would be useful for studying the mode of action of mescaline-like compounds.
G C, Walters, P D, Cooper
openaire   +2 more sources

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