Candicidin

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Structural formula
Structural formula of candicidin
General
Surname Candicidin
Molecular formula C 59 H 84 N 2 O 18
Brief description

white solid

External identifiers / databases
CAS number
  • 1403-17-4 (mixture)
  • 39372-30-0 (Candicidin D)
EC number 215-763-7
ECHA InfoCard 100.014.330
DrugBank DB01152
Wikidata Q61653285
Drug information
ATC code

G01 AA04

properties
Molar mass 1109.32 g mol −1
Physical state

firmly

Melting point

150 ° C (decomposition)

solubility
  • almost insoluble in water and most organic solvents
  • soluble in DMSO, DMF and ethyl acetate
safety instructions
Please note the exemption from the labeling requirement for drugs, medical devices, cosmetics, food and animal feed
GHS hazard labeling
no classification available
Toxicological data

14 mg kg −1 ( LD 50mouse , ip )

As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Candicidin is a four-component antibiotic. The main component, Candicidin D, is a chemical compound from the group of macrolides and heptaenes . Candicidin was first described by Lechevalier in 1953 and named after its action against Candida fungi.

Occurrence

Candicidin occurs naturally in Streptomyces griseus and other Streptomycetes .

properties

Candicidin is a white solid that is insoluble in water.

use

Candicidin is used as a fungicide against Candida albicans . It is not absorbed systemically and causes few toxic phenomena. Its effectiveness is still being investigated.

Individual evidence

  1. ^ A b c d e f G. WA Milne: Gardner's Commercially Important Chemicals Definitions, Trade Names, and Properties . John Wiley & Sons, 2005, ISBN 0-471-73661-9 , pp. 111 ( limited preview in Google Book search).
  2. ^ S. Huneck, Joachim Thiem: RÖMPP Lexikon Naturstoffe, 1st edition, 1997 . Georg Thieme Verlag, 2014, ISBN 3-13-179291-4 , p. 107 ( limited preview in Google Book search).
  3. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  4. Patrizia Diana, Girolamo Cirrincione: Biosynthesis of Heterocycles From Isolation to Gene Cluster . John Wiley & Sons, 2015, ISBN 978-1-118-02867-4 , pp. 706 ( limited preview in Google Book search).
  5. a b TOKU-E: Candicidin - PRODUCT DATA SHEET ( Memento from April 8, 2014 in the Internet Archive ), accessed on September 5, 2015.
  6. ^ Josef Kimmig: Therapy of skin and sexually transmitted diseases . Springer-Verlag, 2013, ISBN 978-3-642-94850-3 , pp. 1263 ( limited preview in Google Book search).
  7. FH Meyers, E. Jawetz, A. Goldfien: Textbook of Pharmacology For students of medicine of all study stages and for doctors . Springer-Verlag, 2013, ISBN 978-3-642-66183-9 , p. 616 ( limited preview in Google Book search).