Dopamine | C8H11NO2 | CID 681 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Dopamine (DA, a contraction of 3,4-dihydroxyphenethylamine) is a neuromodulatory molecule that plays several important roles in cells. It is an organic chemical of the catecholamine and phenethylamine families. Dopamine constitutes about 80% …

Molecular weight: 153.1784 IUPAC Standard InChI: InChI=1S/C8H11NO2/c9-4-3-6-1-2-7(10)8(11)5-6/h1-2,5,10-11H,3-4,9H2 Copy IUPAC Standard InChIKey: VYFYYTLLBUKUHU-UHFFFAOYSA-N Copy

2024年8月22日 · The molecular structure of dopamine consists of a catechol structure (a benzene ring with two adjacent hydroxyl groups) attached to an ethylamine side chain. This unique arrangement of atoms gives dopamine its characteristic properties and enables it to bind to specific receptors in the brain.

2024年8月22日 · Dopamine’s structure can be divided into three main components, each playing a specific role in its function and interactions within the brain. 1. Catechol Ring Structure: The catechol ring is the core of the dopamine molecule. It consists of a benzene ring with two adjacent hydroxyl groups.

The dopamine molecule contains a total of 22 bond(s). There are 11 non-H bond(s), 6 multiple bond(s), 2 rotatable bond(s), 6 aromatic bond(s), 1 six-membered ring(s), 1 primary amine(s) (aliphatic), and 2 aromatic hydroxyl(s). Images of the chemical structure of …

Dopamine (DA, a contraction of 3,4-dihydroxyphenethylamine) is a neuromodulatory molecule that plays several important roles in cells. It is an organic chemical of the catecholamine and phenethylamine families. Dop amine constitutes about 80% …

2024年5月11日 · Chemical Structure: Dopamine is a monoamine neurotransmitter with the chemical formula C8H11NO2. Structurally, it consists of a catechol ring (a benzene ring with two hydroxyl groups) attached to an aminoethyl side chain.

Dopamine is synthesized from the aromatic amino acid precursor tyrosine, which is converted to l-3,4-dihydroxyphenylalanine (L-DOPA) by the addition of a hydroxyl group in a reaction catalyzed by tyrosine hydroxylase, the rate-limiting enzyme in catecholamine synthesis.

2021年5月7日 · d1-Dopamine | C8H11NO2 | CID 18598659 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.