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Thiolutin

Catalog No. T3450 Name Sigma Aldrich
CAS Number 87-11-6 Website http://www.sigmaaldrich.com
M. F. C9H10N2O2S2 Telephone 1-800-521-8956
M. W. 242.3179 Fax
Purity ≥95% (HPLC) Email
Storage Chembase ID: 154387

SYNONYMS

IUPAC name
N-{4-methyl-5-oxo-4H,5H-[1,2]dithiolo[4,3-b]pyrrol-6-yl}propanamide
IUPAC Traditional name
aureothricin
Synonyms
N-(4,5-Dihydro-4-methyl-5-oxo-1,2-dithiolo[4,3-B]Pyrrol-6-yl)
Aureothricin
Farcinicin
Propiopyvothine

DATABASE IDS

MDL Number MFCD07370147
CAS Number 87-11-6

PROPERTIES

Biological Source from Streptomyces luteosporeus
Empirical Formula (Hill Notation) C8H8N2O2S2
Purity ≥95% (HPLC)
Shipped in wet ice
Solubility DMSO: soluble5 mg/mL
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H300
European Hazard Symbols Highly toxic Highly toxic (T+)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS Precautionary statements P264-P301 + P310
RID/ADR UN 2811 6.1/PG 2
Risk Statements 28
RTECS JP1355000
Safety Statements 45
Storage Temperature -20°C
Hazard Class 6.1
UN Number 2811
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Sulfur-containing antibiotic, which is a potent inhibitor of bacterial and yeast RNA polymerases. It was found to inhibit in vitro RNA synthesis directed by all three yeast RNA polymerases (I, II, and III). Thiolutin is also an inhibitor of mannan and glucan formation in Saccharomyces cerevisiae and used for the analysis of mRNA stability. Studies have shown that thiolutin inhibits adhesion of human umbilical vein endothelial cells (HUVECs) to vitronectin and thus suppresses tumor cell-induced angiogenesis in vivo.
Description (简体中文)
Biochem/physiol Actions
Sulfur-containing antibiotic, which is a potent inhibitor of bacterial and yeast RNA polymerases. It was found to inhibit in vitro RNA synthesis directed by all three yeast RNA polymerases (I, II, and III). Thiolutin is also an inhibitor of mannan and glucan formation in Saccharomyces cerevisiae and used for the analysis of mRNA stability. Studies have shown that thiolutin inhibits adhesion of human umbilical vein endothelial cells (HUVECs) to vitronectin and thus suppresses tumor cell-induced angiogenesis in vivo.

REFERENCES