BOC Sciences
(+)-Cloprostenol isopropyl ester is a derivative of cloprostenol which has been found to be a FP receptor agonist as well as a luteolytic agent and could be used commonly as a veterinary drug for its effect in terminating pregnancy.
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(+)-Cloprostenol is a synthetic analog of prostaglandin F2α (PGF2α). It is an FP receptor agonist and a potent luteolytic agent in rats and hamsters.
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BOC Sciences
(+)-Cloprostenol sodium salt is the d-enantiomer of Cloprostenol, which is an aryl-oxymethyl analog of prostaglandin F2α. It has luteolytic effects and is used for the synchronization of estrus in cattle. It is also an FP receptor agonist.
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BOC Sciences
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(+)-Cytisine
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| Purity Not Available
BOC Sciences
(+)-delta-Cadinene
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| Purity Not Available
BOC Sciences
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BOC Sciences
(+)-Diethyl L-tartrate is a chiral resolution reagent to separate racemic compounds into different mirror isomers and is an important tool for the production of optically active drugs.
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(+)-Dihydro-α-cyperol is an intermediate in the synthesis of α-Eudesmol (E938595) which is an isomer of β-Eudesmol (E938600), a sesquiterpenoid known to induce neurite outgrowth. β-Eudesmol exhibits antiangiogenic activity.
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(+)-DIOP
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| >95%
BOC Sciences
(+)-DIOP is a chiral phosphine ligand for enantioselective synthesis with high yield and high enantioselective results.
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(+)-Donepezil is one of Donepezil isomers. Donepezil, a highly specific reversible acetylcholinesterase (AChE) inhibitor, is used to treat moderate to severe Alzheimer’s disease.
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(+)-Epibatidine dihydrochloride is a highly potent nicotinic agonist and (+)-Enantiomer of (±)-Epibatidine dihydrochloride.
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BOC Sciences
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(+)-Epinephrine (-)-Bitartrate is an enantiomer of Epinephrine. Epinephrine is an endogenous catcholamine with combined α-and β-agonist activity and its principal sympathomimetic hormone is produced by the adrenal medulla.
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BOC Sciences
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(+)-Epoxylinolein is a coumarin isolated from Hesperethusa crenulata. Epoxy Suberosin has anti-Leishmania activity.
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Igmesine is a selective σ1 receptor ligand (KD = 19.1 nM), with nearly no activity at σ2 receptors (IC50 > 1000 nM). It was developed by Pfizer. Igmesine inhibits the NMDA-induced increase in cGMP in a concentration-dependent manner and IC50 value is approximately 100 nM. Igmesine can weekly inhibit brain 5-HT uptake in vitro. It […]
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BOC Sciences