imino$37600$ - definition. What is imino$37600$
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%ما هو (من)٪ 1 - تعريف

CARBOXYLIC ACIDS THAT CONTAIN A C=NH GROUP
Imino acids

Iminosugar         
  • The chemical structure of [[1-deoxynojirimycin]], an example of a simple iminosugar.
Wikipedia talk:Articles for creation/Iminosugars; Iminosugars; Imino sugars
An iminosugar, also known as an iminosaccharide, is any analog of a sugar where a nitrogen atom has replaced the oxygen atom in the ring of the structure.
Imine         
  • Hexafluoroacetone imine is an unusual primary ketimine that is readily isolable.<ref name=OS/>
  • Imine synthesis from a primary amine and a carbonyl compound.
  •  Steps in pyridoxal phosphate-mediated reactions of [[alanine]] and [[cysteine]], illustrating one biological role for aldimines.
ANY CHEMICAL COMPOUND HAVING THE STRUCTURE RN=CR′R″, THUS ANALOGUE OF ALDEHYDE OR KETONE IN WHICH AN OXYGEN ATOM IS REPLACED BY SUBSTITUTED OR UNSUBSTITUTED NITROGEN ATOM
Aldimine; Imino; Imines; Ketimine; Acyl imidate; Aldimines; Ketimines; Imino group
In organic chemistry, an imine ( or ) is a functional group or organic compound containing a carbon–nitrogen double bond (). The nitrogen atom can be attached to a hydrogen or an organic group (R).
imine         
  • Hexafluoroacetone imine is an unusual primary ketimine that is readily isolable.<ref name=OS/>
  • Imine synthesis from a primary amine and a carbonyl compound.
  •  Steps in pyridoxal phosphate-mediated reactions of [[alanine]] and [[cysteine]], illustrating one biological role for aldimines.
ANY CHEMICAL COMPOUND HAVING THE STRUCTURE RN=CR′R″, THUS ANALOGUE OF ALDEHYDE OR KETONE IN WHICH AN OXYGEN ATOM IS REPLACED BY SUBSTITUTED OR UNSUBSTITUTED NITROGEN ATOM
Aldimine; Imino; Imines; Ketimine; Acyl imidate; Aldimines; Ketimines; Imino group
['?mi:n]
¦ noun Chemistry an organic compound containing the group ?C=NH or ?C=NR (where R is an alkyl group).
Origin
C19: from amine, on the pattern of the pair amide, imide.

ويكيبيديا

Imino acid

In organic chemistry, an imino acid is any molecule that contains both imine (>C=NH) and carboxyl (-C(=O)-OH) functional groups.

Imino acids are structurally related to amino acids, which have amino group instead of imine—a difference of single vs double-bond between nitrogen and carbon. The simplest example is dehydroglycine.

D-Amino acid oxidase is an enzyme that is able to convert amino acids into imino acids. Also the direct biosynthetic precursor to the amino acid proline is the imino acid (S)-Δ1-pyrroline-5-carboxylate (P5C).