enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Pyrrole - Wikipedia

    en.wikipedia.org/wiki/Pyrrole

    Pyrrole is a heterocyclic, aromatic, organic compound, a five-membered ring with the formula C 4 H 4 NH. [3] It is a colorless volatile liquid that darkens readily upon exposure to air. Substituted derivatives are also called pyrroles, e.g., N -methylpyrrole, C 4 H 4 NCH 3 .

  3. Structural scheduling of synthetic cannabinoids - Wikipedia

    en.wikipedia.org/wiki/Structural_scheduling_of...

    Naphthoylpyrroles: Any compound containing a 3-(1-naphthoyl)pyrrole structure with substitution at the nitrogen atom of the pyrrole ring by an alkyl, haloalkyl, alkenyl, cycloalkylmethyl, cycloalkylethyl, 1-(N-methyl-2-piperidinyl)methyl, or 2-(4-morpholinyl)ethyl group whether or not further substituted in the pyrrole ring to any extent and ...

  4. Heterocyclic compound - Wikipedia

    en.wikipedia.org/wiki/Heterocyclic_compound

    A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). [1] Heterocyclic organic chemistry is the branch of organic chemistry dealing with the synthesis, properties, and applications of organic heterocycles .

  5. Pyrrolidine - Wikipedia

    en.wikipedia.org/wiki/Pyrrolidine

    It is found in many drugs such as procyclidine and bepridil. It also forms the basis for the racetam compounds (e.g. piracetam, aniracetam). The amino acids proline and hydroxyproline are, in a structural sense, derivatives of pyrrolidine. Nicotine contains an N-methylpyrrolidine ring linked to a pyridine ring.

  6. Tryptamine - Wikipedia

    en.wikipedia.org/wiki/Tryptamine

    Tryptamine is an indolamine metabolite of the essential amino acid tryptophan. [9] [10] The chemical structure is defined by an indole—a fused benzene and pyrrole ring, and a 2-aminoethyl group at the second carbon (third aromatic atom, with the first one being the heterocyclic nitrogen). [9]

  7. Pyrrolizidine alkaloid - Wikipedia

    en.wikipedia.org/wiki/Pyrrolizidine_alkaloid

    A second detoxifying pathway is the formation of the N-oxide [26] [27] In the liver and lungs of certain mammal species enzymes called monooxygenase can prevent aromatization of the double 5-ring and in turn prevent the formation of the pyrrole-protein adduct. [20]

  8. Pentabromopseudilin - Wikipedia

    en.wikipedia.org/wiki/Pentabromopseudilin

    This was indeed proven when isotopically labeled 4-HBA was observed to be incorporated into the phenol ring of PBP at >80%. [10] Despite this groundbreaking study, no 13 C incorporation was observed in the pyrrole ring of PBP. In 2004, a follow-up study described the PBP pyrrole ring as derived from L-proline. [11]

  9. Thiophene - Wikipedia

    en.wikipedia.org/wiki/Thiophene

    Thiophene is a heterocyclic compound with the formula C 4 H 4 S. Consisting of a planar five-membered ring, it is aromatic as indicated by its extensive substitution reactions. It is a colorless liquid with a benzene-like odor. In most of its reactions, it resembles benzene.