Basic information Safety Supplier Related

GLIOVIRIN

Basic information Safety Supplier Related

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
Product Categories:
  • Antibiotic
Mol File:
83912-90-7.mol
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GLIOVIRIN Chemical Properties

storage temp. 
Store at -20°C
solubility 
DMSO: soluble,Ethanol: soluble,Methanol: soluble
form 
A solid
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Safety Information

HS Code 
2941900000
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GLIOVIRIN Usage And Synthesis

Description

Gliovirin 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).

GLIOVIRINSupplier

BOC Sciences
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Shanghai EFE Biological Technology Co., Ltd.
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021-65675885 18964387627
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ChemeGen(Shanghai) Biotechnology Co.,Ltd.
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18818260767
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Zhejiang Huida Biotech Co., LTD
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TCI (Shanghai) Chemical Trading Co., Ltd.
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021-021-61109150
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