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GLIOVIRIN

Product Name
GLIOVIRIN
CAS No.
83912-90-7
Chemical 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;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)-;(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
CBNumber
CB8261524
Molecular Formula
C20H20N2O8S2
Formula Weight
480.51
MOL File
83912-90-7.mol
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GLIOVIRIN Property

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

HS Code 
2941900000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P271Use only outdoors or in a well-ventilated area.

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N-Bromosuccinimide Price

Cayman Chemical
Product number
28583
Product name
Gliovirin
Packaging
1mg
Price
$499
Updated
2024/03/01
American Custom Chemicals Corporation
Product number
API0019200
Product name
GLIOVIRIN
Purity
95.00%
Packaging
5MG
Price
$502.56
Updated
2021/12/16
Apolloscientific
Product number
BIBR1047
Product name
Gliovirin
Packaging
1mg
Price
$522
Updated
2021/12/16
AK Scientific
Product number
4611ED
Product name
Gliovirin
Packaging
1mg
Price
$700
Updated
2021/12/16
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GLIOVIRIN Chemical Properties,Usage,Production

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).

GLIOVIRIN Preparation Products And Raw materials

Raw materials

Preparation Products

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GLIOVIRIN Suppliers

BOC Sciences
Tel
1-631-485-4226; 16314854226
Email
info@bocsci.com
Country
United States
ProdList
14059
Advantage
65

83912-90-7, GLIOVIRINRelated Search:


  • 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)-
  • 83912-90-7
  • C20H20N2O8S2
  • Antibiotic