GLIOVIRIN

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Products Intro: Product Name:Gliovirin
CAS:83912-90-7
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Products Intro: Product Name:Gliovirin
CAS:83912-90-7
Purity:70% Package:1mg
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Products Intro: Product Name:Gliovirin
CAS:83912-90-7
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
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Products Intro: Product Name:Glioverin
CAS:83912-90-7
Purity:99% HPLC Package:10mg;100mg;1g;10g;100g
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Products Intro: Product Name:Gliovirin
CAS:83912-90-7
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GLIOVIRIN Basic information
Product Name:GLIOVIRIN
Synonyms:GLIOVIRIN;(1aS,12aS)-4,4aβ,8,9-Tetrahydro-4β-hydroxy-9β-(2-hydroxy-3,4-dimethoxyphenyl)-12H-8α,11aα-(iminomethano)-1aαH,7H-[1,2,4]dithiazepino[4,3-b]oxireno[e][1,2]benzoxazine-7,13-dione;(1AS-(1AALPHA,4BETA,4ABETA,8ALPHA,9BETA,11AALPHA,12AR*))-4,4A,8,9-TETRAHYDRO-4-HYDROXY-9-(2-HYDROXY-3,4-DIMETHOXYPHENYL)-12H-8,11-(IMINOMETHANO)-1AH,7H-(1,2,4)DITHIAZEPINO(4,3-B)OXIRENO(E)(1,2)BENZOXAZINE-7,13-DIONE;12H-8,11a-(Iminomethano)-1aH,7H-[1,2,4]dithiazepino[4,3-b]oxireno[e][1,2]benzoxazine-7,13-dione, 4,4a,8,9-tetrahydro-4-hydroxy-9-(2-hydroxy-3,4-dimethoxyphenyl)-, (1aS,4R,4aS,8S,9R,11aR,12aS)-
CAS:83912-90-7
MF:C20H20N2O8S2
MW:480.51
EINECS:
Product Categories:Antibiotic
Mol File:83912-90-7.mol
GLIOVIRIN Structure
GLIOVIRIN Chemical Properties
storage temp. Store at -20°C
solubility DMSO: soluble,Ethanol: soluble,Methanol: soluble
form A solid
Safety Information
HS Code 2941900000
MSDS Information
GLIOVIRIN Usage And Synthesis
DescriptionGliovirin is a fungal metabolite that has been found in T. harzianum and has fungicidal, antimicrobial and anti-inflammatory activities. It is active against the plant pathogenic fungus P. ultimum (MIC = 60 ng/ml) and the parasite T. brucei brucei (IC50 = 90 ng/ml), but has no effect on the plant pathogenic fungi R. solani, P. omnivorum, T. basicola, R. arrhizus, and V. dahliae or the bacteria B. thuringiensis, P. fluorescens, and X. malvacearum when used at concentrations up to 1,000 ng/ml. Gliovirin decreases phorbol 12-myristate 13-acetate (TPA)- and ionomycin-induced increased expression of COX-2 (IC50 = 1 μM) and protein levels of IL-2 in Jurkat cells (IC50 = 5.2 μM).
References[1] JAN RETHER. Inhibition of inducible tumor necrosis factor-alpha expression by the fungal epipolythiodiketopiperazine gliovirin.[J]. Biological Chemistry, 2007, 388 6: 627-637. DOI: 10.1515/bc.2007.066
[2] HOWELL C R, STIPANOVIC R. Gliovirin, a new antibiotic from Gliocladium virens, and its role in the biological control of Pythium ultimum[C]//57 1. 1983: 0. DOI: 10.1139/m83-053
[3] MASATO IWATSUKI. In vitro antitrypanosomal activity of 12 low-molecular-weight antibiotics and observations of structure/activity relationships[J]. Journal of Antibiotics, 2010, 63 10: 619-622. DOI: 10.1038/ja.2010.99
GLIOVIRIN Preparation Products And Raw materials
Tag:GLIOVIRIN(83912-90-7) Related Product Information
sec-Butyl disulfide CYCLO(-LEU-GLY) 2-(d-alpha-Methylphenethylamino)ethanethiol (S)-3-(2-HYDROXYETHYL)-2,5-DIKETOPIPERAZINE N-METHOXY-N-METHYL-3-PHENYL-PROPIONAMIDE GLIOVIRIN