Life Science

An intermediate for the synthesis of glucosylceramide synthase inhibitors such as 1-dNM, a glucose analog that potently inhibits &alpha-glucosidase I and II.

An intermediate for the synthesis of glucosylceramide synthase inhibitors such as 1-dNM, a glucose analog that potently inhibits &alpha-glucosidase I and II.

An intermediate for the synthesis of glucosylceramide synthase inhibitors such as 1-dNM, a glucose analog that potently inhibits &alpha-glucosidase I and II.

A biotinylated form of DEPMPO, which is used to spin trap reactive O-, N-, S-, and C-centered radicals offers monitored biodistribution in cells, tissues and organs when used with an avidin-conjugated reporter binds free radicals on proteins,

A biotinylated form of DEPMPO, which is used to spin trap reactive O-, N-, S-, and C-centered radicals offers monitored biodistribution in cells, tissues and organs when used with an avidin-conjugated reporter binds free radicals on proteins,

A biotinylated form of DEPMPO, which is used to spin trap reactive O-, N-, S-, and C-centered radicals offers monitored biodistribution in cells, tissues and organs when used with an avidin-conjugated reporter binds free radicals on proteins,

A biotinylated form of DEPMPO, which is used to spin trap reactive O-, N-, S-, and C-centered radicals offers monitored biodistribution in cells, tissues and organs when used with an avidin-conjugated reporter binds free radicals on proteins,

Anabasine is an alkaloid originally found in species of Nicotiana it is a structural isomer of nicotine. Anabasine inhibits aromatase and nicotinic acetylcholine receptors (nAChRs) and may produce a depolarizing neuromuscular junction (NMJ) block.

Anabasine is an alkaloid originally found in species of Nicotiana it is a structural isomer of nicotine. Anabasine inhibits aromatase and nicotinic acetylcholine receptors (nAChRs) and may produce a depolarizing neuromuscular junction (NMJ) block.

Angiotensin peptides exhibit pressor (vasoconstrictive) activity through binding of the angiotensin II type 1 (AT1) receptor, increasing blood pressure and volume. Angiotensin I (AT I) is a cleavage product of angiotensin and serves no primary

Angiotensin peptides exhibit pressor (vasoconstrictive) activity through binding of the angiotensin II type 1 (AT1) receptor, increasing blood pressure and volume. Angiotensin I (AT I) is a cleavage product of angiotensin and serves no primary

Angiotensin peptides exhibit pressor (vasoconstrictive) activity through binding of the angiotensin II type 1 (AT1) receptor, increasing blood pressure and volume. Angiotensin I (AT I) is a cleavage product of angiotensin and serves no primary