(+) coclaurine

(+)-Coclaurine is a natural product.

(S)-Coclaurine (Coclaurine) is an antagonist of nAChR isolated from Sarcopetalum harveyanum.

(±)-Coclaurine, a natural product sourced from Roemeria refracta, demonstrates antioxidative activity and impacts cardiovascular health [1] [2] [3].

(-)-Coclaurine hydrochloride is an antagonist of nAChRs isolated from Sarcopetalum harveyanum.

(S)-Coclaurine-N-methyltransferase (EC 2.1.1.140) specifically recognizes the (S)-isomer of coclaurine and can also accept norcoclaurine as a substrate.

(+)-Coclaurine hydrochloride, also known as (+)-(R)-Coclaurine, is a benzyltetrahydroisoquinoline alkaloid extracted from multiple plant species. This compound exhibits anti-aging properties, as reported in sources [1] [2].

Higenamine hydrochloride (norcoclaurine HCl) has been demonstrated to be a β2 adrenoreceptor agonist. Adrenergic receptors, or adrenoceptors, belong to the class of G protein–coupled receptors, and are the most prominent receptors in the adipose membrane, besides also being expressed in skeletal muscle tissue.

N-Methyl-3'-hydroxycoclaurine (3'-Hydroxy-N-methylcoclaurine) hydrochloride is an impurity of Coclaurine.

N-Methylcoclaurine (±) acts as a selective antagonist at the α2-adrenoceptor [1].

N-Methylcoclaurine shows binding affinities for the ĸ opioid receptor with the equilibrium dissociation constant (Ki) value of 0.9 ± 0.1 uM. N-methylcoclaurine also shows promising butyrylcholinesterase inhibition activities, with the IC50 value of 1

N-Methyldehydrococlaurine is a natural product that can be used as a reference standard.

(S)-Norcoclaurine synthase (EC 3.5.99.14) catalyzes the formation of a six-membered ring by creating a bond between the C-6 of 3,4-dihydroxyphenyl in dopamine and the C-1 of an imine aldehyde. Additionally, (S)-Norcoclaurine synthase facilitates the reaction of 4-(2-aminoethyl)phen-1,2-diol with (3,4-dihydroxyphenyl)acetaldehyde to produce (S)-norcoclaurine.