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Cicloesimide

Structure via PubChem · Public domain (PubChem)

EntityQ412895· pop 19· linked from 65 articles

Cicloesimide

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Also known as FT 3422-2, naramycin A, NM-MCD 80, NSC 185, 3-((R)-2-((1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl)-2-hydroxyethyl)glutarimide, naramycin

farmaco

Chemical data

Formula
C15H23NO4
Molecular weight
281.35 g/mol
IUPAC name
4-[(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione
SMILES
C[C@H]1C[C@@H](C(=O)[C@@H](C1)[C@@H](CC2CC(=O)NC(=O)C2)O)C
InChIKey
YPHMISFOHDHNIV-FSZOTQKASA-N
XLogP
0.5
Polar surface area
83.5 Ų
H-bond donors
2
H-bond acceptors
4
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
281.163
Show 7 more facts
Commons category
Cycloheximide
chemical formula
C₁₅H₂₃NO₄
canonical SMILES
CC1CC(C(=O)C(C1)C(CC2CC(=O)NC(=O)C2)O)C
isomeric SMILES
C[C@H]1C[C@@H](C(=O)[C@@H](C1)[C@@H](CC2CC(=O)NC(=O)C2)O)C
World Health Organisation international non-proprietary name
cicloheximide
found in taxon
Setosphaeria
has characteristic
natural product
Sources (4)

via Wikidata · CC0

Article · Italiano

La cicloesimide è un composto chimico che inibisce la sintesi proteica in cellule eucariote bloccando l'attacco e l'uscita del tRNA dal ribosoma. Induce apoptosi in vari tipi cellulari. È prodotta dal batterio Streptomyces griseus.

Abstract from DBpedia / Wikipedia · CC BY-SA