α-Campholenic aldehyde can be used as an intermediate in the synthesis of sandalwood fragrances.

α-Carboline-[15N2] is an isotopically labelled analogue of α-Carboline, a compound useful in organic synthesis.

α-Carboline-[15N2] N-Oxide is an isotope labelled compound of α-Carboline N-Oxide, a compound useful in organic synthesis. Intermediate in the preparation of labelled α-Carboline derivatives.

α-Cedrene is a sesquiterpene constituent of cedarwood oils. α-Cedrene has anti-leukemic, antimicrobial and anti-obesity activities.

α-CGRP (human) is an endogenous calcitonin gene-related peptide receptor (CGRP) agonist.

α-Chlorocinnamaldehyde (CAS# 18365-42-9 ) is a useful research chemical.

α-Chlorocyclohexanecarbonyl Chloride is a versatile compound used in various synthetic preparations. It is used as a reactant in the synthesis of Thiophenes.

α-Chloroethyl Phenyl Sulfoxide is an intermediate in synthesizing 3-Deoxy-3-acetylabiraterone-3-ene (D232060), which is an impurity of Abiraterone (A108490), a steroidal cytochrome P 450 17α-hydroxylase-17,20-lyase inhibitor (CYP17), is currently undergoing phase II clinical trials as a potential drug for the treatment of androgen-dependent prostate cancer.

α-Chloromethyl-4-nitrobenzenemethanol is a reagent used in the synthesis of monocyclic nitroimidazole analogs of econazole which have antitubercular activity.

α-Chlorophenylacetic acid (CAS# 4755-72-0) is a useful research chemical.

α-Chlorophenylacetyl chloride (CAS# 2912-62-1) is a reagent used for dehydrohalogenation of ketones.

α-Cholesterol-[2,2,3,4,4,6-d6] is the labelled analogue of α-Cholesterol, which is a stereoisomer of Cholesterol. Cholesterol is the principal sterol of the higher animals. Cholesterol was found in all body tissues, especially in the brain, spinal cord, and in animal fats or oils. Cholesterol is the main constituent of gallstones.

α-Clofarabine is a second generation purine nucleoside analog; antimetabolite that inhibits DNA synthesis and resists deamination by adenosine deaminase. Antineoplastic.

α-Conidendrin isolated from the barks of Tsuga dumosa.

α-Conotoxin AuIB is a selective antagonist of α3β4 nicotinic acetylcholine receptors. It shows > 100-fold selectivity over other receptor subunit combinations.

α-Conotoxin EI is a selective antagonist of neuromuscular nicotinic receptors α1β1γδ. It shows selectivity for α/δ sites over α/γ sites in Torpedo.

α-conotoxin GI (alpha-conotoxin GI) is a conopeptide that has been isolated from the venom of the cone snail Conus geographus. α-conotoxin GI is a competitive antagonist of the muscle-type nicotinic acetylcholine receptors (nAChR) such as α-conotoxin MI or d-Turbocurarine.

α-Conotoxin ImI is a nicotinic acetylcholine receptor ligand isolated from the snail Conus imperialis. It shows selectivity for homomeric α7 and α9 receptors with IC50 values of 220 and 1800 nM respectively, but shows no effect on α2β2, α2β4, α3β2, α3β3, α4β2 and α4β4 subunit combinations. It mainly acts as an antagonist in central nervous […]

α-Conotoxin MII is a nicotinic acetylcholine receptor antagonist. It is highly potent, selective and competitive for α3β2 subunit. Its IC50 value is 0.5-3.5 nM at α3β2 expressed in Xenopus oocytes. It also potently prevents β3-containing neuronal nicotinic receptors.

α-Conotoxin PIA is a nicotinic acetylcholine receptor antagonist. It is selective for α6-containing nicotinic receptors. It can discriminate between the closely related α6 and α3 subunits. It was sold under license for Cognetix for research purposes only.

α-Conotoxin PnIA is a nicotinic acetylcholine receptor antagonist. It is selective for α3β2 nAChR receptors with IC50 value of 9.56 nM. It was sold under license for Cognetix for research purposes only.

α-conotoxin MI (alpha-conotoxin MI) is a conotoxin that has been isolated from the venom of the cone snail Conus magus. α-conotoxin MI is a competitive antagonist of the muscle-type nicotinic acetylcholine receptors (nAChR) such as α-conotoxin GI or d-Turbocurarine.

α-Cyano-2,4-difluorocinnamic Acid was investigated as a matrix along with several peptides as analytes for UV-MALDI mass spectrometry.

CHC is a monocarboxylic acid transport (MCT) inhibitor, displaying antitumoral and antiangiogenic activity in gliomas in vivo. It decreases glycolytic metabolism, migration and invasion in U251 cells, enhances the effect of temozolomide.

α-Cyano-4-hydroxycinnamic acid-[d7], is the labelled analogue of α-Cyano-4-hydroxycinnamic acid. CHCA is a monocarboxylic acid transport (MCT) inhibitor, displaying antitumoral and antiangiogenic activity in gliomas in vivo. It decreases glycolytic metabolism, migration and invasion in U251 cells, enhances the effect of temozolomide.

α-Cyano-β-methyl-β-ethoxyacrylonitrile-[13C2] is an isotopically labelled analogue of (1-Ethoxyethylidene)malononitrile. (1-Ethoxyethylidene)malononitrile was used in the synthesis of benzyl 5-amino-4-cyano-3-methyl-1H pyrazole-1-carboxylate and 2-amino-6-mercaptopyridine-3,5-dicarbonitrile derivatives.

α-Cyclodextrin is a 6 member dextrin ring used as an encapsulation agent for bioactive compounds and pharmaceuticals.