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THIOLUTIN

THIOLUTIN Structure
CAS No.
87-11-6
Chemical Name:
THIOLUTIN
Synonyms
T-00098;NSC 3927;THIOLUTIN;Acetopyrrothin;Thiolutin ,80%;acetopyrrothine;THIOLUTIN USP/EP/BP;THIOLUTIN (ACETOPYRROTHIN);Thiolutin, from Streptomyces;Thiolutin NSC 3927
CBNumber:
CB3435551
Molecular Formula:
C8H8N2O2S2
Molecular Weight:
228.29
MOL File:
87-11-6.mol
Modify Date:
2023/6/8 9:01:59

THIOLUTIN Properties

Melting point 273-276℃
Boiling point 200°C (rough estimate)
Density 1.4614 (rough estimate)
refractive index 1.5690 (estimate)
storage temp. −20°C
solubility DMSO: 5 mg/mL
form Yellow crystalline solid.
pka 10.54±0.20(Predicted)
color Brilliant-yellow needles from 1-butanol
Stability Stable for 3 years as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
EPA Substance Registry System Thiolutin (87-11-6)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H300
Precautionary statements  P264-P270-P301+P310-P405-P501
Hazard Codes  T+,T
Risk Statements  28
Safety Statements  45
RIDADR  UN 2811 6.1/PG 2
WGK Germany  3
RTECS  JP1355000
HS Code  29419090
Toxicity LD50 in mice (mg/kg): 25 s.c.; 25 orally (Seneca)
NFPA 704
0
4 0

THIOLUTIN price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) T3450 Thiolutin from Streptomyces luteosporeus, ≥95% (HPLC) 87-11-6 1MG ₹39900.95 2022-06-14 Buy
Product number Packaging Price Buy
T3450 1MG ₹39900.95 Buy

THIOLUTIN Chemical Properties,Uses,Production

Description

Thiolutin is a natural dithiol that reversibly inhibits bacterial and yeast RNA polymerases (IC50 = 3 μg/ml). Because of this, it can be used for the analysis of mRNA stability. Thiolutin also inhibits endothelial cell adhesion (IC50 < 1 μM) and S180 tumor-induced angiogenesis in mice by inhibiting Hsp27 interactions with cytoskeletal elements.

Chemical Properties

Yellow solid

Uses

Thiolutin is an antibiotic isolated from several strains of Streptomyces albus. Thiolutin is a natural dithiol that reversibly inhibits bacterial and yeast RNA polymerases.

Biological Activity

Antibiotic; inhibits bacterial RNA polymerase. Inhibits adhesion of HUVEC cells to vitronectin (IC 50 = 0.83 mM) and subsequently reduces paxillin levels. Suppresses tumor cell-induced angiogenesis.

Safety Profile

Poison by ingestion andsubcutaneous routes. When heated to decomposition itemits very toxic fumes of NOx and SOx.

THIOLUTIN Preparation Products And Raw materials

Raw materials

Preparation Products

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acetopyrrothine 6-acetamido-4-methyl-2-dithiolo(4.3-b)pyrrol-5(4h)-one 6-acetamido-4-methyl-1,2-dithiolo(4,3-b)pyrrol-5(4h)-one 6-(acetylamino)-4-methyl-1,2-dithiolo(4,3-b)pyrrol-5(4h)-one N-(4-methyl-5-oxodithiolo[4,3-b]pyrrol-6-yl)acetamide N-(4-methyl-5-oxo-[1,2]dithiolo[4,3-b]pyrrol-6-yl)ethanamide T-00098 4-Methyl-6-(acetylamino)-4,5-dihydro-1,2-dithiolo[4,3-b]pyrrole-5-one 4-Methyl-6-(acetylamino)-1,2-dithiolo[4,3-b]pyrrole-5(4H)-one Thiolutin from Streptomyces luteosporeus Aureothricin, Farcinicin, Propiopyvothine 6-acetamido-4-methyl-1,2-dithiolo[4,3-b]pyrrol-5-one Thiolutin NSC 3927 NSC 3927 Acetopyrrothin Thiolutin ,80% N-(5-keto-4-methyl-dithiolo[4,3-b]pyrrol-6-yl)acetamide N-acetylpyrrothine, Farcinicine, Acetopyrrothine N-(4-Methyl-5-oxo-4,5-dihydro-[1,2]dithiolo[4,3-b]pyrrol-6-yl)acetaMide 3-acetamido-5-methylpyrrolin-4-one(4,3-d)-1,2-dithiole N-(4,5-DIHYDRO-4-METHYL-5-OXO-1,2-DITHIOLO[4,3-B]PYRROL-6-YL)ACETAMIDE THIOLUTIN THIOLUTIN USP/EP/BP Thiolutin, from Streptomyces Acetamide, N-(4,5-dihydro-4-methyl-5-oxo-1,2-dithiolo[4,3-b]pyrrol-6-yl)- THIOLUTIN (ACETOPYRROTHIN) 87-11-6 1987-11-6 C8H8N2S2O2 Antibiotics A to Z Antibiotics Antibiotics T-Z BioChemical pharmacetical Antibiotics Sulfur & Selenium Compounds Pharmaceuticals Intermediates & Fine Chemicals Heterocycles antibiotic