(-ìmino)

  • 61quinone diimine — ˈdīəˌmēn noun Etymology: diimine from di + imine 1. : a colorless crystalline compound HN . C6H4 . NH regarded as derived from quinone (sense 1a) by replacement of both oxygen atoms by imino groups but made by oxidation of para phenylenediamine… …

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  • 62GTPase — GTPases (singular GTPase) are a large family of hydrolase enzymes that can bind and hydrolyze guanosine triphosphate (GTP). The GTP binding and hydrolysis takes place in the highly conserved G domain common to all GTPases. They help GTP binding… …

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  • 63Tricyclic antidepressant — Tricyclic antidepressants (abbreviation TCAs) are a class of antidepressant drugs first used in the 1950s. They are named after the drugs molecular structure, which contains three rings of atoms (compare tetracyclic antidepressant). Example… …

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  • 64Proline — For other uses, see Proline (disambiguation). Proline …

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  • 65Polyamine — [ thumb|spermine] The polyamines are organic compounds having two or more primary amino groups such as putrescine, cadaverine, spermidine, and spermine that are growth factors in both eucaryotic and procaryotic cells. Cyclen is the main… …

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  • 66Hydroxyproline — Chembox new ImageFile = Hydroxyproline structure.svg ImageSize = IUPACName = (2S,4R) 4 hydroxypyrrolidine 2 carboxylic acid OtherNames = Section1 = Chembox Identifiers CASNo = 51 35 4 PubChem = 825 SMILES = OC1CNC(C1)C(O)=O MeSHName =… …

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  • 67Pinner reaction — The Pinner reaction (after Adolf Pinner) is an organic reaction of a nitrile with an alcohol under acid catalysis for instance hydrochloric acid. The product formed is the hydrochloric acid salt of an imino ester or an alkyl imidate, which… …

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  • 68Tetrodotoxin — Chembox new ImageFile=Tetrodotoxin 2D skeletal.png ImageSize= ImageFile2=Tetrodotoxin 3D balls.png IUPACName=Octahydro 12 (hydroxymethyl) 2 imino 5,9:7,10a dimethano 10aH [1,3] dioxocino [6,5 d] pyrimidine 4,7,10,11,12 pentol… …

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  • 69IUPAC nomenclature of organic chemistry — The IUPAC nomenclature of organic chemistry is a systematic method of naming organic chemical compounds as recommended[1] by the International Union of Pure and Applied Chemistry (IUPAC). Ideally, every possible organic compound should have a… …

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  • 70Schiff base — or substituted phenyl, can be called an anil . [GoldBookRef|title=anils|file=A00357] Schiff bases can be synthesized from an aromatic amine and a carbonyl compound by nucleophilic addition forming a hemiaminal, followed by a dehydration to… …

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