structure of 2-[(2-Amino-4-methyl-1,3-thiazol-5-yl)sulfanyl]acetamide

2-[(2-Amino-4-methyl-1,3-thiazol-5-yl)sulfanyl]acetamide

CAS No.: 1000933-46-9
M. Wt: 203.3
M. Fa: C6H9N3OS2
InChI Key: DYDYXSPFKLYGRR-UHFFFAOYSA-N

Names and Identifiers of 1000933-46-9

CAS Number

1000933-46-9

MDL Number

MFCD09935034

IUPAC Name

2-[(2-amino-4-methyl-1,3-thiazol-5-yl)sulfanyl]acetamide

InChI

InChI=1S/C6H9N3OS2/c1-3-5(11-2-4(7)10)12-6(8)9-3/h2H2,1H3,(H2,7,10)(H2,8,9)

InChIKey

DYDYXSPFKLYGRR-UHFFFAOYSA-N

Canonical SMILES

CC1=C(SC(=N1)N)SCC(=O)N

UNSPSC Code

12352100

Physical and chemical properties of 1000933-46-9

H Bond Acceptors

3

H Bond Donors

2

LogP

-0.227347272

Molecular Formula

C6H9N3OS2

Molecular Weight

203.3

Safety Information of 1000933-46-9

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000933-46-9

The potential applications of 2-[(2-Amino-4-methyl-1,3-thiazol-5-yl)sulfanyl]acetamide are broad and may include:

  • Pharmaceutical Development: As a lead compound in drug discovery for infectious diseases or cancer treatment.
  • Agricultural Chemicals: Potential use as a fungicide or pesticide due to its antimicrobial properties.
  • Biochemical Research: Utilized in studies investigating enzyme inhibition or receptor interaction.

Interaction Studies of 1000933-46-9

Interaction studies are crucial for understanding how 2-[(2-Amino-4-methyl-1,3-thiazol-5-yl)sulfanyl]acetamide interacts with biological systems. These studies may focus on:

  • Protein Binding Affinity: Assessing how well the compound binds to target proteins or enzymes.
  • Mechanism of Action: Investigating how the compound exerts its biological effects at the molecular level.

These studies are essential for determining the therapeutic potential and safety profile of the compound.

Biological Activity of 1000933-46-9

Research indicates that 2-[(2-Amino-4-methyl-1,3-thiazol-5-yl)sulfanyl]acetamide exhibits various biological activities. Compounds containing thiazole rings are often investigated for their antimicrobial, antifungal, and anticancer properties. Preliminary studies suggest that this specific compound may have potential as:

  • Antimicrobial Agent: It may inhibit the growth of certain bacteria and fungi.
  • Anticancer Activity: Some derivatives of thiazole compounds have shown promise in cancer cell line studies.

Further investigation is required to fully elucidate its biological profile.