What is Fursultiamine Hydrochloride used for?

What is Fursultiamine Hydrochloride used for?

Fursultiamine is a member of pyrimidines. Compound used for therapy of thiamine deficiency. It has also been suggested for several non-deficiency disorders but has not yet proven useful. Fursultiamine is a vitamin B1 derivative.

Is thiamine hydrochloride the same as vitamin B1?

Thiamine is vitamin B1. Therefore, Thiamine mononitrate and thiamine hydrochloride are derivatives of vitamin B1. They have different molar masses and other physical properties depending on their chemical structures.

What is Lipothiamine?

Ecological Formulas / Cardiovascular Research – Lipothiamine, 60 tablets Lipothiamine is a scientifically designed food supplement and represents the biologically-active form of vitamin B1.

What is the chemical name of vitamin B1?

2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethanolThiamine / IUPAC ID

What is Sulbutiamine used for?

Sulbutiamine is used for weakness, fatigue, to enhance athletic performance, and many other conditions, but there is no good scientific evidence to support these uses. In December 2019, the U.S. Food and Drug Administration added sulbutiamine to the Dietary Supplement Ingredient Advisory List.

What is another name for thiamine hydrochloride?

Thiamine hydrochloride

PubChem CID 6202
Structure Find Similar Structures
Chemical Safety Laboratory Chemical Safety Summary (LCSS) Datasheet
Molecular Formula HC12H17ON4SCl2 or C12H18Cl2N4OS
Synonyms THIAMINE HYDROCHLORIDE 67-03-8 Thiamine HCL Vitamin B1 hydrochloride Aneurine hydrochloride More…

Is thiamine hydrochloride toxic?

May be harmful by inhalation, ingestion, or skin absorption. May cause skin or respiratory system irritation.

What is Lipothiamine good for?

Lipothiamine is a formula composed of Vitamin B1(thiamine), essential for neural function and carbohydrate metabolism. Severe thiamin deficiency results in Beriberi, a nerve and heart disease. Less severe deficiency nonspecific signs include malaise, weight loss, irritability and confusion.

Why do we give thiamine to alcoholics?

Thiamine supplementation reduces the risk of developing Wernicke syndrome, Korsakoff syndrome, and beriberi. Physicians working with patients with alcohol use disorders should have a high index of suspicion for Wernicke syndrome, particularly if the patient shows evidence of ophthalmoplegia, ataxia, or confusion.

What is the chemical name of vitamin b9?

(2S)-2-[(4-{[(2-amino-4-hydroxypteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioic acidFolate / IUPAC ID

When should I take sulbutiamine?

Sulbutiamine comes as a tablet and should be taken by mouth. It is taken with food. The tablets should be taken with sufficient quantity of water and should not be crushed, chewed or broken to avoid the release of the medicine at a time.

What is the brand name for fursultiamine?

Fursultiamine. AHFS / Drugs.com Fursultiamine ( INN; chemical name thiamine tetrahydrofurfuryl disulfide or TTFD; brand names Adventan, Alinamin-F, Benlipoid, Bevitol Lipophil, Judolor, Lipothiamine) is a medication and vitamin used to treat thiamine deficiency.

What is ferfursultiamine?

Fursultiamine is a member of pyrimidines. Compound used for therapy of thiamine deficiency. It has also been suggested for several non-deficiency disorders but has not yet proven useful. Fursultiamine is a vitamin B1 derivative.

Is fursultiamine a hepcidin antagonist?

Fursultiamine is used clinically for the treatment of vitamin B1 deficiency. High throughput screening identified fursultiamine as a hepcidin antagonist [152]. This thiamine derivate was shown to bind FPN and inhibit hepcidin-mediated degradation in vitro [152].

What is ferfursultiamine (TFTD)?

Fursultiamine ( INN; chemical name thiamine tetrahydrofurfuryl disulfide or TTFD; brand names Adventan, Alinamin-F, Benlipoid, Bevitol Lipophil, Judolor, Lipothiamine) is a medication and vitamin used to treat thiamine deficiency. Chemically, it is a disulfide derivative of thiamine and is similar in structure to allithiamine.

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