Thiazoles

Organic heterocyclic compounds that consist of an azole with both sulfur and nitrogen atoms; includes compounds that are derived from thiazoles.

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4,036 – 4,050 of 6,894 results

4,036

Aobchem 1-(5-Chloro-2-benzofuranyl)ethanone | ≥95% | CAS 1646-32-8 | C10H7ClO2 | 500mg

1-(5-Chloro-2-benzofuranyl)ethanone | ≥95% | CAS 1646-32-8 | C10H7ClO2 | 500mg

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4,037

Aobchem 2-Chloro-1-(2-naphthalenyl)ethanone | ≥95% | CAS 50846-93-0 | C12H9ClO | 500mg

2-Chloro-1-(2-naphthalenyl)ethanone | ≥95% | CAS 50846-93-0 | C12H9ClO | 500mg

Pricing & Availability

4,038

Aobchem 2-Chloro-1-(2-naphthalenyl)ethanone | ≥95% | CAS 50846-93-0 | C12H9ClO | 1g

2-Chloro-1-(2-naphthalenyl)ethanone | ≥95% | CAS 50846-93-0 | C12H9ClO | 1g

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4,039

Aobchem 1-(4 5-Dimethyl-2-thiazolyl)-2 2-dimethyl-1-propanone | ≥95% | CAS 1534816-83-5 | C10H15NOS | 1g

1-(4 5-Dimethyl-2-thiazolyl)-2 2-dimethyl-1-propanone | ≥95% | CAS 1534816-83-5 | C10H15NOS | 1g

Pricing & Availability

4,040

Medchemexpress LLC KL-11743 | 1369452-53-8 | 99.4% | C30H30N6O3 | 50 MG

KL-11743 is a potent, orally active, and glucose-competitive inhibitor of class I glucose transporters (GLUT1, GLUT2, GLUT3, and GLUT4). It blocks glucose metabolism and can synergize with electron transport inhibitors to induce cell death. Additionally, KL-11743 induces the formation of disulfide bonds in actin cytoskeletal proteins, leading to cellular disulfidptosis.

Potent, orally active, and glucose-competitive inhibitor of class I glucose transporters
Blocks glucose metabolism and synergizes with electron transport inhibitors to induce cell death
Induces cellular disulfidptosis
Inhibits the growth of various cancer cell lines in vitro
Effective in decreasing tumor growth in animal models