The chemical substance known as "4-Amino-1-[[(carbamoylamino)acetyl]methylamino]-1,4-dideoxy-3-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-β-L-lyxo-heptopyranosyl)-6-O-methyl-L-chiro-inositol," with the CAS number 62874-51-5, is a complex organic compound characterized by its intricate structure, which includes multiple functional groups such as amino, carbamoyl, and methyl groups. This compound features a dideoxy sugar moiety and is linked to a chiro-inositol derivative, indicating potential biological activity, particularly in the context of glycosylation and cellular signaling pathways. Its structural complexity suggests that it may exhibit specific interactions with biological macromolecules, potentially influencing metabolic processes. The presence of amino and carbamoyl groups implies that it may participate in various biochemical reactions, including those related to amino acid metabolism. Due to its unique structure, this compound may have applications in medicinal chemistry or as a biochemical probe, although specific biological activities and therapeutic potentials would require further investigation through empirical studies.

4-Amino-1-[[(carbamoylamino)acetyl]methylamino]-1,4-dideoxy-3-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-β-L-lyxo-heptopyranosyl)-6-O-methyl-L-chiro-inositol

62874-51-5: The chemical substance known as "4-Amino-1-[[(carbamoylamino)acetyl]methylamino]-1,4-dideoxy-3-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-β-L-lyxo-heptopyranosyl)-6-O-methyl-L-chiro-inositol," with the CAS number 62874-51-5, is a complex organic compound characterized by its intricate structure, which includes multiple functional groups such as amino, carbamoyl, and methyl groups. This compound features a dideoxy sugar moiety and is linked to a chiro-inositol derivative, indicating potential biological activity, particularly in the context of glycosylation and cellular signaling pathways. Its structural complexity suggests that it may exhibit specific interactions with biological macromolecules, potentially influencing metabolic processes. The presence of amino and carbamoyl groups implies that it may participate in various biochemical reactions, including those related to amino acid metabolism. Due to its unique structure, this compound may have applications in medicinal chemistry or as a biochemical probe, although specific biological activities and therapeutic potentials would require further investigation through empirical studies.

<p>Fortimicin C is a bioactive chemical.</p>

CAS 62874-51-5

4-Amino-1-[[(carbamoylamino)acetyl]methylamino]-1,4-dideoxy-3-O-(2,6-diamino-2,3,4,6,7-pentadeoxy-β-L-lyxo-heptopyranosyl)-6-O-methyl-L-chiro-inositol

Fortimicin C

Ref: TM-T31855