CAS 538-28-3

Benzylisothiourea hydrochloride

Description:

Benzylisothiourea hydrochloride is a chemical compound characterized by its isothiourea functional group, which features a sulfur atom bonded to a nitrogen atom and a carbon atom. It appears as a white to off-white crystalline powder and is soluble in water and alcohol, making it suitable for various applications in biochemical research. This compound is known for its role as a potent inhibitor of nitric oxide synthase and has been utilized in studies related to cardiovascular and neurobiological research. Additionally, benzylisothiourea hydrochloride exhibits properties that can influence cellular signaling pathways, particularly in the context of cancer research. Its hydrochloride form enhances its stability and solubility, facilitating its use in laboratory settings. As with many chemical substances, proper handling and safety precautions are essential, as it may pose health risks if ingested or improperly managed. Overall, benzylisothiourea hydrochloride serves as a valuable tool in scientific investigations, particularly in the fields of pharmacology and biochemistry.

Formula: C₈H₁₀N₂S·ClH

InChI: InChI=1S/C8H10N2S.ClH/c9-8(10)11-6-7-4-2-1-3-5-7;/h1-5H,6H2,(H3,9,10);1H

InChI key: InChIKey=WJAASTDRAAMYNK-UHFFFAOYSA-N

SMILES: C(SC(=N)N)C1=CC=CC=C1.Cl

Synonyms:

• (Benzylsulfanyl)(imino)methanaminium chloride
• (Benzylsulfanyl)methanimidamide hydrochloride
• 2-Benzyl-2-Thiopseudourea Hydrochloride
• 208-688-6
• Benzituron
• Benzyl Carbamimidothioate Hydrochloride (1:1)
• Benzyl carbamimidothioate hydrochloride
• Benzyl thiopseudourea hydrochloride
• Benzylisothiourea hydrochloride
• Benzylisothiouronium chloride
• Benzylisothiuronium chloride
• Carbamimidothioic Acid Phenylmethyl Ester Monohydrochloride
• Carbamimidothioic Acid, Phenylmethyl Ester, Hydrochloride (1:1)
• Pseudourea, 2-benzyl-2-thio-, hydrochloride
• Pseudourea, 2-benzyl-2-thio-, monohydrochloride
• Pseudourea, 2-thio-2-benzyl-, hydrochloride
• S-Benzylisothiourea hydrochloride
• S-Benzylisothiouronium chloride
• S-Benzylisothiouronium hydrochloride
• S-Benzylisothiuronium chloride
• S-Benzylthioformamidine hydrochloride
• S-Benzylthiopseudourea hydrochloride
• S-Benzylthiourea hydrochloride
• S-Benzylthiouronium chloride
• S-Benzylthiuronium chloride

S-Benzylisothiourea Hydrochloride

CAS: 538-28-3

Formula: C₈H₁₀N₂S·HCl

Purity: >99.0%(T)

Color and Shape: White powder to crystal

Molecular weight: 202.70

Ref: 3B-B0442

S-Benzylisothiourea hydrochloride

CAS: 538-28-3

Formula: C₈H₁₁ClN₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 202.7043

Ref: IN-DA0038O8

Benzyl carbamimidothioate hydrochloride

CAS: 538-28-3

Benzyl carbamimidothioate hydrochloride

Purity: 98%

Molecular weight: 202.70g/mol

Ref: 54-OR79350

2-Benzyl-2-thiopseudourea Hydrochloride

Controlled Product

CAS: 538-28-3

Formula: C₈H₁₀N₂S·HCl

Color and Shape: Neat

Molecular weight: 202.7

Ref: TR-B315165

S-Benzylisothiourea hydrochloride

CAS: 538-28-3

S-Benzylisothiourea hydrochloride (SBIT) is a potent inhibitor of the influenza virus by binding to the polymerase domain of the virus’s RNA-dependent RNA polymerase. SBIT inhibits viral transcription and replication, as well as viral assembly, release, and infectivity. SBIT has been shown to inhibit avian influenza A/H5N1 in cell culture and in mice models with no observable adverse effects. The mechanism of action for this drug is not yet understood but may be related to its ability to inhibit the kinase domain of avian influenza NS1 protein which is involved in regulating inflammatory responses.

Formula: C₈H₁₀N₂S·HCl

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 202.71 g/mol

Ref: 3D-FB71164

S-Benzylisothiourea hydrochloride

CAS: 538-28-3

Formula: C₈H₁₁ClN₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 202.7

Ref: 10-F099378