3,4-Diamino-2-hydroxypyridine is an organic compound characterized by its pyridine ring, which is substituted with two amino groups and one hydroxyl group. This compound typically appears as a solid and is soluble in water due to the presence of the hydroxyl group, which can form hydrogen bonds. The amino groups contribute to its basicity and potential reactivity, making it a versatile intermediate in organic synthesis. It is often used in the preparation of various pharmaceuticals and agrochemicals. The presence of both amino and hydroxyl groups allows for a range of chemical reactions, including acylation and alkylation. Additionally, 3,4-Diamino-2-hydroxypyridine can exhibit biological activity, which may include antimicrobial or antitumor properties, although specific biological effects can vary based on structural modifications and the context of use. Safety data should be consulted for handling and potential hazards associated with this compound, as with any chemical substance.

3,4-Diamino-2-hydroxypyridine

3,4-Diamino-2-hydroxypyridine (3,4-DAHP) is a novel ns3 protease inhibitor that has been shown to inhibit the activity of this enzyme in cancer cells. 3,4-DAHP binds to the active site of ns3 protease and inhibits its ability to cleave proteins. This inhibition leads to decreased cell proliferation and an increase in apoptosis. 3,4-DAHP is also effective against a range of cancer cell lines with different levels of ns3 protease expression. This compound has shown anticancer activity against several types of cancer cells including breast and prostate cancers. 3,4-DAHP also has inhibitory effects on other enzymes such as alkoxycarbonyl reductases and nitros reductases.

CAS 33631-02-6: 3,4-Diamino-2-hydroxypyridine

3,4-Diamino-2-hydroxypyridine

Ref: IN-DA00C70J

3,4-Diamino-2-hydroxypyridine

Ref: 3D-FD153007

3,4-Diamino-1H-pyridin-2-one

Ref: 54-OR15984

3,4-Diaminopyridin-2-ol

Ref: 10-F239386