cycloheximide (Q412895)

English Wikipedia

chemical structure

Cycloheximide.svg
1,170 × 960; 17 KB

0 references

mass

281.163 dalton

1 reference

cycloheximide (English)

4-[(2R)-2-[(1R,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione

19 October 2016

stereoisomer of

2 references

based on heuristic

inferred from InChIKey

1 reference

4-[(2R)-2-[(1S,3R,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₅H₂₃NO₄

1 reference

cycloheximide (English)

19 October 2016

canonical SMILES

CC1CC(C(=O)C(C1)C(CC2CC(=O)NC(=O)C2)O)C

1 reference

cycloheximide (English)

19 October 2016

isomeric SMILES

C[C@H]1C[C@@H](C(=O)[C@@H](C1)[C@@H](CC2CC(=O)NC(=O)C2)O)C

1 reference

cycloheximide (English)

World Health Organisation international non-proprietary name

19 October 2016

cicloheximide (English)

1 reference

cycloheximide (English)

19 October 2016

found in taxon

Streptomyces pulveraceus

1 reference

Epiderstatin, a new inhibitor of the mitogenic activity induced by epidermal growth factor. I. Taxonomy, fermentation, isolation and characterization.

Streptomyces griseus

10 references

The Structure of Actidione, An Antibiotic From Streptomyces griseus

The Structure of Actidione, An Antibiotic From Streptomyces griseus

Cycloheximide and actiphenol production in Streptomyces sp. YIM56141 governed by single biosynthetic machinery featuring an acyltransferase-less type I polyketide synthase

Exploitation of potential bioactive compounds from two soil derived actinomycetes, Streptomyces sp. strain 196 and RI.24

New antifungal cycloheximide epimers produced by Streptomyces sp. YG7

Cycloheximide production by Streptomyces griseus: alleviation of end-product inhibition by dialysis-extraction fermentation

Actidione, an antibiotic from Streptomyces griseus

The Production, Assay, and Antibiotic Activity of Actidione, an Antiobiotic from Streptomyces griseus

The production, assay, and antibiotic activity of actidione, an antibiotic from Streptomyces griseus.

Cycloheximide production by Streptomyces griseus: control mechanisms of cycloheximide biosynthesis

Streptomyces

2 references

Yeast glycogen synthase kinase-3beta pathway inhibitors from an organic extract of Streptomyces sp.

Oridamycins A and B, Anti-Saprolegnia parasiticaIndolosesquiterpenes Isolated fromStreptomycessp. KS84

Sporormiella similis

1 reference

Preussilides A-F, Bicyclic Polyketides from the Endophytic Fungus Preussia similis with Antiproliferative Activity.

Setosphaeria

1 reference

Spiro-Phthalides and Isocoumarins Isolated from the Marine-Sponge-Derived Fungus Setosphaeria sp. SCSIO41009

1 reference

1 reference

protein synthesis inhibitor

English Wikipedia

subject has role

1 reference

Medical Subject Headings

15 March 2018

1 reference

Medical Subject Headings

MeSH descriptor ID

D003513

15 March 2018

glutarimide antibiotic

0 references

developmental toxicant

start time

1 January 1989

1 reference

California Proposition 65 list of chemicals

https://oehha.ca.gov/chemicals/cycloheximide

24 February 2020

reference URL

Commons category

Cycloheximide

0 references

Identifiers

InChI

InChI=1S/C15H23NO4/c1-8-3-9(2)15(20)11(4-8)12(17)5-10-6-13(18)16-14(19)7-10/h8-12,17H,3-7H2,1-2H3,(H,16,18,19)/t8-,9-,11-,12+/m0/s1

1 reference

cycloheximide (English)

19 October 2016

2 references

cycloheximide (English)

19 October 2016

ChEBI release 2020-09-01

CAS Registry Number

66-81-9

2 references

Global Substance Registration System

UNII

98600C0908

https://commonchemistry.cas.org/detail?cas_rn=66-81-9

cycloheximide (English)

19 October 2016

6 April 2021

1 reference

Cycloheximide (English)

19 October 2016

2 references

cycloheximide (English)

19 October 2016

Reaxys registry number

88868

1 reference

cycloheximide (English)

19 October 2016

ChEBI ID

27641

mapping relation type

2 references

cycloheximide (English)

19 October 2016

International Chemical Identifier

InChI

InChI=1S/C15H23NO4/c1-8-3-9(2)15(20)11(4-8)12(17)5-10-6-13(18)16-14(19)7-10/h8-12,17H,3-7H2,1-2H3,(H,16,18,19)/t8-,9-,11-,12+/m0/s1

1 reference

CYCLOHEXIMIDE (English)

19 October 2016

2 references

inferred from InChIKey

splash10-0002-0290000000-dd29fc30efb15bc92f1d

1 reference

MassBank accession ID

MSBNK-Fiocruz-FIO00835

0 references

MSBNK-Fiocruz-FIO00836

0 references

MSBNK-Fiocruz-FIO00837

0 references

MSBNK-Fiocruz-FIO00838

0 references

MSBNK-Fiocruz-FIO00839

0 references

MSBNK-UPAO-UPA00019

0 references

SPLASH

0 references

0 references

0 references

MA4375000

1 reference

Spanish Wikipedia

ZVG number

510136

1 reference

Hazardous Substances Data Bank

1 reference

28 October 2019

CYCLOHEXIMIDE (English)

10 May 2021

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

0 references

1 reference

Global Substance Registration System

UNII

98600C0908

cycloheximide (English)

ECHA Substance Infocard ID

19 October 2016

100.000.578

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.000.578

27 December 2018

PesticideInfo chemical ID

Cicloheximide (English)

quotation

CAS no.: 66-81-9 (English)

PRI2364

0 references

Guide to Pharmacology Ligand ID

5433

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

5433

reason for deprecated rank

cycloheximide (English)

19 October 2016

Cycloheximide

0 references

0 references

cannot be confirmed by other sources

1 reference

Global Substance Registration System

cycloheximide (English)

19 October 2016

2 references

UNII

98600C0908

cycloheximide (English)

19 October 2016

0 references

1 reference

California Proposition 65 list of chemicals

cycloheximide (English)

19 October 2016

0 references

1 reference

https://oehha.ca.gov/chemicals/cycloheximide

12 December 2019

reference URL

1 reference

28 October 2013

Gran Enciclopèdia Catalana ID

cicloheximida

0 references

Gran Enciclopèdia Catalana ID (former scheme)

0267840

0 references

HCIS ID

1114

0 references

Microsoft Academic ID

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

5GAK (English)