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Candicidin

CAS No.
1403-17-4
Chemical Name:
Candicidin
Synonyms
candimon;NSC94219;CARBOPRST;candeptin;Levorinum;NSC 94219;NSC-94219;Canitracin;candizidin;candicidin
CBNumber:
CB6501392
Molecular Formula:
C21H36O5
Molecular Weight:
368.51
MDL Number:
MOL File:
1403-17-4.mol
Last updated:2023-05-21 10:59:17

Candicidin Properties

Boiling point 878.79°C (rough estimate)
Density 1.1100 (rough estimate)
refractive index 1.6200 (estimate)
storage temp. Store at -20°C
solubility DMSO:4.9(Max Conc. mg/mL);10.08(Max Conc. mM)
Ethanol:12.5(Max Conc. mg/mL);25.72(Max Conc. mM)
form A solid
Water Solubility 13.47g/L(21 ºC)
FDA 21 CFR 310.545
EWG's Food Scores 1
FDA UNII 48N2IYJ202
ATC code G01AA04

SAFETY

Risk and Safety Statements

Toxicity LD50 i.p. in mice: 14 mg/kg (Vining)

Candicidin price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 26708 Levorin Complex 1403-17-4 1mg $335 2024-03-01 Buy
Cayman Chemical 26708 Levorin Complex 1403-17-4 5mg $1169 2024-03-01 Buy
AK Scientific V1816 Candicidin 1403-17-4 5mg $1400 2021-12-16 Buy
AK Scientific V1816 Candicidin 1403-17-4 1mg $471 2021-12-16 Buy
Medical Isotopes, Inc. 68510 Candicidin 1403-17-4 10mg $610 2021-12-16 Buy
Product number Packaging Price Buy
26708 1mg $335 Buy
26708 5mg $1169 Buy
V1816 5mg $1400 Buy
V1816 1mg $471 Buy
68510 10mg $610 Buy

Candicidin Chemical Properties,Uses,Production

Originator

Candeptin,Schmidt,US,1964

Uses

Candicidin is a macrocyclic heptaene antifungal complex produced by Streptomyces griseus and isolated by Lechevalier and colleagues in 1953. The candicidin complex comprises analogues A, B, C and D, with candicidin D as the major component. Candicidin is active against fungi, in particular Candida albicans, and is used clinically to treat vaginal candidiasis. Like all polyene antifungal metabolites, candicidin acts by binding to ergosterol and disrupting the fungal membrane.

Definition

ChEBI: Candicidin D is a 38-membered ring lactone containing seven (E)-double bonds between positions 22 and 35 and substituted by hydroxy groups at positions 9, 11, 13, 17 and 19, oxo groups at positions 3, 7 and 15, a carboxy group at position 18, a 3-amino-3,6-dideoxymannopyranosyloxy group at position 21, a methyl group at position 36 and a 7-(4-aminophenyl)-5-hydroxy-4-methyl-7-oxoheptan-2-yl group at position 37. It is the major component of candicidin, a mixture of antifungal heptaene macrolides obtained from a strain of Streptomyces griseus. It has a role as a bacterial metabolite and an antifungal drug. It is a macrolide antibiotic and a polyene antibiotic.

Manufacturing Process

Hubert Lechevalier et al were the first to describe "Candicidin, a New Antifungal Antibiotic," in Mycologia XLV, No. 2, 155-171, March-April 1953. They produced candicidin by growing a culture of the organism streptomyces griseus No. 3570 on a yeast-glucose medium, isolating a "crude candicidin" from the resulting broth and purifying it. An improved extraction and purification method is described in US Patent 2,872,373 and is shown in the flow diagram below.
Another extraction and separation process is described in US Patent 2,992,162.

brand name

Vanobid (Sanofi Aventis).

Therapeutic Function

Topical antifungal

Candicidin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 40)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9320 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29220 58
BOC Sciences
+16314854226 inquiry@bocsci.com United States 19743 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 52927 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
Chembest Research Laboratories Limited 021-20908456 sales@BioChemBest.com China 6011 61
LGM Pharma 1-(800)-881-8210 inquiries@lgmpharma.com United States 2127 70
Sinopharm Chemical Reagent Co,Ltd. 86-21-63210123 sj_scrc@sinopharm.com China 9823 79
Lynnchem 86-(0)29-85992781 17792393971 info@lynnchem.com China 4587 58

View Lastest Price from Candicidin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Candicidin USP/EP/BP pictures 2021-06-23 Candicidin USP/EP/BP
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
candeptin candicidin candimon candizidin CANDICIDIN (200 MG) Candicidine CARBOPRST Canitracin Candicidin complex Levorin Complex Candicidin USP/EP/BP Candicidin DISCONTINUED Levorinum NSC 94219 NSC94219 NSC-94219 1403-17-4