LEVORIN A2

LEVORIN A2 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:Candicidin D;LIA 0704;LIA-0704;LIA0704;Levorin A2;Candicidin D1
CAS:39372-30-0
Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Products Intro: Product Name:Candicidin D
CAS:39372-30-0
Remarks:Reach out to us for more information about custom solutions.
LEVORIN A2 Basic information
Product Name:LEVORIN A2
Synonyms:Candicidin D1
CAS:39372-30-0
MF:C59H84N2O18
MW:1109.31
EINECS:
Product Categories:
Mol File:39372-30-0.mol
LEVORIN A2 Structure
LEVORIN A2 Chemical Properties
Boiling point 1273.3±65.0 °C(Predicted)
density 1.30±0.1 g/cm3(Predicted)
pka3.95±0.70(Predicted)
Safety Information
MSDS Information
LEVORIN A2 Usage And Synthesis
UsesCandicidin D (CndD) is an antibiotic, which exhibits antifungal activity through interaction with steroids in cell membranes. Candicidin D inhibits S. cerevisiae, Candida albicans and other Candida spp. with MIC of 0.25-1 μg/mL in RPMI-1640 medium.
DefinitionChEBI: 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, -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 fr m a strain of Streptomyces griseus.
References[1] Borzyszkowska-Bukowska J, et al., Quest for the Molecular Basis of Improved Selective Toxicity of All-Trans Isomers of Aromatic Heptaene Macrolide Antifungal Antibiotics. Int J Mol Sci. 2021 Sep 18;22(18):10108. DOI:10.3390/ijms221810108
LEVORIN A2 Preparation Products And Raw materials
Tag:LEVORIN A2(39372-30-0) Related Product Information
Ethyl 3-oxodecanoate ACETOACETIC ACID N-HEPTYL ESTER Isobutyl acetoacetate ACETOACETIC ACID SEC-BUTYL ESTER ACETOACETIC ACID HEXYL ESTER METHYL 3-OXOTETRADECANOATE ACETOACETIC ACID N-OCTYL ESTER methyl 3-oxooctadecanoate ETHYL STEAROYLACETATE methyl 3-oxododecanoate 4-aminohexanoylphenone ETHYL 7-OXOUNDECANOATE 7-Oxooctadecanoic Acid Methyl Ester 22-TRICOSENOIC ACID ETHYL 3-OXOTETRADECANOATE NONADECANEDIOIC ACID LEVORIN A2 methyl 3-oxohexadecanoate

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