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Candicidin

Product Name
Candicidin
CAS No.
1403-17-4
Chemical Name
Candicidin
Synonyms
candimon;NSC94219;CARBOPRST;candeptin;Levorinum;NSC 94219;NSC-94219;candicidin;Canitracin;candizidin
CBNumber
CB6501392
Molecular Formula
C21H36O5
Formula Weight
368.51
MOL File
1403-17-4.mol
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Candicidin Property

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)
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Safety

Toxicity
LD50 i.p. in mice: 14 mg/kg (Vining)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
26708
Product name
Levorin Complex
Packaging
1mg
Price
$335
Updated
2024/03/01
Cayman Chemical
Product number
26708
Product name
Levorin Complex
Packaging
5mg
Price
$1169
Updated
2024/03/01
AK Scientific
Product number
V1816
Product name
Candicidin
Packaging
5mg
Price
$1400
Updated
2021/12/16
AK Scientific
Product number
V1816
Product name
Candicidin
Packaging
1mg
Price
$471
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
68510
Product name
Candicidin
Packaging
10mg
Price
$610
Updated
2021/12/16
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Candicidin Chemical Properties,Usage,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

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Candicidin Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6005
Advantage
61
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9815
Advantage
79
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9806
Advantage
58
Lynnchem
Tel
86-(0)29-85992781 17792393971
Email
info@lynnchem.com
Country
China
ProdList
4587
Advantage
58
Novachemistry
Tel
44-20819178-90 02081917890
Fax
(0)2080432064
Email
info@novachemistry.com
Country
United Kingdom
ProdList
4381
Advantage
58
Shanghai Hongye Biotechnology Co. Ltd
Tel
400-9205774
Email
sales@glpbio.cn
Country
China
ProdList
6777
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com
Country
China
ProdList
57412
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
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View Lastest Price from Candicidin manufacturers

Dideu Industries Group Limited
Product
Candicidin
Price
US $1.10/g
Min. Order
1g
Purity
99.9%
Supply Ability
100 Tons Min
Release date
2021-06-22