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Cyclopentamine acts as a releasing agent of the catecholamine neurotransmitters norepinephrine (noradrenaline), epinephrine (adrenaline), and dopamine. [1] Its effects on norepinephrine and epinephrine mediate its decongestant effects, while its effects on all three neurotransmitters are responsible for its stimulant properties.
2-Cyclopentenones can be synthesized in a number of ways. One of the routes involves elimination of α-bromo-cyclopentanone using lithium carbonate [2] and Claisen condensation-decarboxylation-isomerization cascades of unsaturated diesters as shown below. [3] Industrial synthesis of cyclopentenone
Cyclopentanone is common precursor to fragrances, especially those related to jasmine and jasmone. Examples include 2-pentyl- and 2-heptylcyclopentanone. [4] It is a versatile synthetic intermediate, being a precursor to cyclopentobarbital. [5] Cyclopentobarbital, a drug made from cyclopentanone
as a large single dose (usually intravenously) BP, Ph.Br. Pharmacopoeia Britannica: British Pharmacopoeia BS blood sugar BSA body surface area b.t. bedtime mistaken for "b.i.d", meaning twice daily bucc. bucca: buccal (inside cheek) cap., caps. capsula: capsule cap. capiat: let him take (let the patient take) c.m. cras mane: tomorrow morning c.m.s.
Cyclopentenone prostaglandins are a subset of prostaglandins (PGs) or prostanoids (see Eicosanoid §§ Classic eicosanoids and Nonclassic eicosanoids) that has 15-deoxy-Δ12,14-prostaglandin J2 (15-d-Δ12,14-PGJ2), Δ12-PGJ2, and PGJ2 as its most prominent members but also including PGA2, PGA1, and, while not classified as such, other PGs. 15-d-Δ12,14-PGJ2, Δ12-PGJ2, and PGJ2 share a common ...
Modified-release dosage and its variants are mechanisms used in tablets (pills) and capsules to dissolve a drug over time in order to be released more slowly and steadily into the bloodstream, while having the advantage of being taken at less frequent intervals than immediate-release (IR) formulations of the same drug.
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