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Ethionamide

Ethionamide Structure
CAS No.
536-33-4
Chemical Name:
Ethionamide
Synonyms
Thioamide;Trecator;Amidazine;Atina;1314th;Aetina;Aetiva;Ethina;Etimid;th1314
CBNumber:
CB1292374
Molecular Formula:
C8H10N2S
Molecular Weight:
166.24
MOL File:
536-33-4.mol
Modify Date:
2024/7/2 8:55:00

Ethionamide Properties

Melting point 164 °C
Boiling point 167 °C / 1mmHg
Density 1.1332 (rough estimate)
refractive index 1.5500 (estimate)
Flash point >110°(230°F)
storage temp. 2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka pKa 4.37(H2O t=25.0 I=0.025) (Uncertain)
color Yellow
Water Solubility Soluble in DMSO. Sparingly soluble in water
Merck 14,3737
BCS Class 3/1
InChIKey AEOCXXJPGCBFJA-UHFFFAOYSA-N
CAS DataBase Reference 536-33-4(CAS DataBase Reference)
IARC 3 (Vol. 13, Sup 7) 1987
NIST Chemistry Reference Ethionamide(536-33-4)
EPA Substance Registry System Ethionamide (536-33-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Warning
Hazard statements  H302-H361
Precautionary statements  P280-P301+P312+P330
Hazard Codes  Xn
Risk Statements  22-63
Safety Statements  36/37
WGK Germany  3
RTECS  NS0350000
HS Code  29333990
Toxicity LD50 oral in rat: 1320mg/kg
NFPA 704
0
1 0

Ethionamide price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) E6005 Ethionamide 536-33-4 5G ₹11517.8 2022-06-14 Buy
Sigma-Aldrich(India) E6005 Ethionamide 536-33-4 25G ₹36155.5 2022-06-14 Buy
Sigma-Aldrich(India) E6005 Ethionamide 536-33-4 100G ₹86708.25 2022-06-14 Buy
TCI Chemicals (India) E0695 Ethionamide 536-33-4 5G ₹7200 2022-05-26 Buy
TCI Chemicals (India) E0695 Ethionamide 536-33-4 25G ₹7800 2022-05-26 Buy
Product number Packaging Price Buy
E6005 5G ₹11517.8 Buy
E6005 25G ₹36155.5 Buy
E6005 100G ₹86708.25 Buy
E0695 5G ₹7200 Buy
E0695 25G ₹7800 Buy

Ethionamide Chemical Properties,Uses,Production

Description

Ethionamide is an antimycobacterial compound that is active against M. tuberculosis (MICs = 0.3-1.25 μg/ml). It is activated via oxidation by flavin monooxygenase and inhibits the InhA enzyme involved in mycolic acid biosynthesis. Formulations containing ethionamide have been used in the second-line treatment of multi-drug resistant tuberculosis.

Chemical Properties

Yellow Solid

Uses

Ethionamide is used in antimicrobials and in potency assay of test compounds on M. tuberculosis.

Indications

Ethionamide (Trecator) is a derivative of isonicotinic acid and is chemically related to isoniazid. It is a secondary agent used in combination when primary agents are ineffective or contraindicated; it is a bacteriostatic antituberculosis agent. Its exact mechanism of action is unknown but is believed to involve inhibition of oxygen-dependent mycolic acid synthesis. It is thought that mutations in the region of the (inhA) gene that are involved in mycolic acid synthesis can cause both isoniazid and ethionamide resistance.

Definition

ChEBI: A thiocarboxamide that is pyridine-4-carbothioamide substituted by an ethyl group at position 2. A prodrug that undergoes metabolic activation by conversion to the corresponding S-oxide.

General Description

Yellow crystals or canary yellow powder with a faint to moderate sulfide odor.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

A thiocarbamate/amine. Thiocarbamates slowly decompose in aqueous solution to form carbon disulfide and methylamine or other amines. Such decompositions are accelerated by acids. Flammable gases are generated by the combination of thiocarbamates and dithiocarbamates with aldehydes, nitrides, and hydrides. Thiocarbamates and dithiocarbamates are incompatible with acids, peroxides, and acid halides.

Fire Hazard

Flash point data for Ethinamide are not available. Ethinamide is probably combustible.

Mechanism of action

Evidence has been presented suggesting that the mechanism of action of ethionamide is similar to that of INH. Similar to INH, ethionamide is considered to be a pro-drug, which is converted via oxidation by catalase-peroxidase to an active acylating agent, ethionamide sulfoxide, which in turn inactivates the inhA enoyl reductase enzyme. In the case of ethionamide, it has been proposed that the ethionamide sulfoxide acylates Cys-243 in inhA protein.

Pharmacology

Ethionamide is well absorbed following oral administration. It is rapidly and widely distributed to all body tissues and fluids, including the cerebrospinal fluid. Metabolism of ethionamide is extensive, and several dihydropyridine metabolites are produced. Less than 1% of the drug is eliminated in the urine unchanged. GI disturbances, including nausea, vomiting, and intense gastric irritation, are frequent. In addition, ethionamide may cause a wide range of neurological side effects, such as confusion, peripheral neuropathy, psychosis, and seizures. Neurological effects can be minimized by pyridoxine supplementation. Other rare side effects include gynecomastia, impotence, postural hypotension, and menorrhagia.

Clinical Use

2-Ethylthioisonicotinamide (Trecator SC) occurs as a yellowcrystalline material that is sparingly soluble in water. Thisnicotinamide has weak bacteriostatic activity in vitro but, becauseof its lipid solubility, is effective in vivo. In contrast tothe isoniazid series, 2-substitution enhances activity in thethioisonicotinamide series.
Ethionamide is rapidly and completely absorbed followingoral administration. It is widely distributed throughoutthe body and extensively metabolized to predominantly inactiveforms that are excreted in the urine. Less than 1% ofthe parent drug appears in the urine.Ethionamide is considered a secondary drug for the treatmentof tuberculosis. It is used in the treatment of isoniazidresistanttuberculosis or when the patient is intolerant toisoniazid and other drugs. Because of its low potency, thehighest tolerated dose of ethionamide is usually recommended.Gastrointestinal intolerance is the most commonside effect associated with its use. Visual disturbances andhepatotoxicity have also been reported.

Metabolism

Ethionamide is orally active but is not well tolerated in a single large dose (>500 mg). The GI irritation can be reduced by administration with meals. Additional side effects may include central nervous system (CNS) effects, hepatitis, and hypersensitivities. Less than 1% of the drug is excreted in the free form, with the remainder of the drug appearing as one of six metabolites. Among the metabolites are ethionamide sulfoxide, 2-ethylisonicotinamide, and the N-methylated- 6-oxodihydropyridines.

Purification Methods

It crystallises from EtOH as lemon yellow needles. The hydrochloride crystallises from EtOH (+ few drops of HCl) as orange yellow needles with m 212-214o. [Kutscherowa et al. J Gen Chem USSR (English transl) 29 915 1959, Beilstein 22 III/IV 737.] It causes peripheral and occular neuropathy and is carcinogenic and teratogenic.

Ethionamide Preparation Products And Raw materials

Global( 287)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Dikora Bulk Drug Pvt. Ltd. +91-7588687403 +91-7588687403 Maharashtra, India 26 58 Inquiry
Alfa Omega Pharma +91-8050045945 +91-9972665399 Maharashtra, India 126 58 Inquiry
Bioxera Pharma Pvt. Ltd. +91-2261842739 +91-2266862739 Maharashtra, India 20 58 Inquiry
Nakshatra Chemicals 09819631316 Mumbai, India 162 58 Inquiry
Eastern Chemicals (Mumbai) Pvt. Ltd +91 22 6736 5900 - 98 Mumbai, India 37 58 Inquiry
Innovative Synthetic Molecules +91 40-24111684 Hyderabad, India 527 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
Alfa-Omega Pharma 08080929094 Karnataka, India 73 58 Inquiry
Simson Pharma +91-22 40068689 Mumbai, India 25 58 Inquiry
Ruskin Chemipharm 09820476680 Mumbai, India 22 58 Inquiry

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