AdooQ BioScience is a supplier of biochemicals located in Irvine, CA since 2006. In the past five years, we have been a renowned name engaged in manufacturing and supplying small molecule inhibitors including kinase inhibitors on kinds of signal pathway, such as PI3K, AKT, HDAC, MARP etc.
Company WebsiteBenazepril hydrochloride is a non-peptide angiotensin-converting enzyme (ACE) inhibitor. Reduces blood pressure and myocardial hypertrophy in spontaneous hypertensive rats.
More Information Supplier PageBendamustine Hydrochloride is a small molecule bifunctional DNA alkylating agent, combining a nitrogen mustard functionality with a purine-analog structure. The dense DNA-damaging functionality of Bendamustine differentiates it from other compounds used as antiproliferative agents, and these functionalities are thought to promote cell death through a variety of different pathways including apoptosis and mitotic catastrophe.
More Information Supplier PageBendamustine Hydrochloride is a small molecule bifunctional DNA alkylating agent, combining a nitrogen mustard functionality with a purine-analog structure. The dense DNA-damaging functionality of Bendamustine differentiates it from other compounds used as antiproliferative agents, and these functionalities are thought to promote cell death through a variety of different pathways including apoptosis and mitotic catastrophe.
More Information Supplier PageBendamustine Hydrochloride is a small molecule bifunctional DNA alkylating agent, combining a nitrogen mustard functionality with a purine-analog structure. The dense DNA-damaging functionality of Bendamustine differentiates it from other compounds used as antiproliferative agents, and these functionalities are thought to promote cell death through a variety of different pathways including apoptosis and mitotic catastrophe.
More Information Supplier PageBendamustine Hydrochloride is a small molecule bifunctional DNA alkylating agent, combining a nitrogen mustard functionality with a purine-analog structure. The dense DNA-damaging functionality of Bendamustine differentiates it from other compounds used as antiproliferative agents, and these functionalities are thought to promote cell death through a variety of different pathways including apoptosis and mitotic catastrophe.
More Information Supplier PageBenfotiamine is a synthetic S-acyl derivative of thiamine (vitamin B1), an antioxidant dietary supplement.
More Information Supplier PageBenidipine hydrochloride is a long-acting T-type calcium channel blocker, on blood pressure and renal function in hypertensive patients with diabetes mellitus.
More Information Supplier PageBenidipine hydrochloride is a long-acting T-type calcium channel blocker, on blood pressure and renal function in hypertensive patients with diabetes mellitus.
More Information Supplier PageBenserazid hydrochloride is an inhibitor of L-aromatic amino acid decarboxylase.
More Information Supplier PageBenserazid hydrochloride is an inhibitor of L-aromatic amino acid decarboxylase.
More Information Supplier PageBenserazid hydrochloride is an inhibitor of L-aromatic amino acid decarboxylase.
More Information Supplier PageBenserazid hydrochloride is an inhibitor of L-aromatic amino acid decarboxylase.
More Information Supplier PageBenserazid hydrochloride is an inhibitor of L-aromatic amino acid decarboxylase.
More Information Supplier PageBenzamide is the amide derivative of benzoic acid and an inhibitor of poly(ADP-ribose) polymerase-1 (PARP-1).
More Information Supplier PageBenzamide is the amide derivative of benzoic acid and an inhibitor of poly(ADP-ribose) polymerase-1 (PARP-1).
More Information Supplier PageBenzamide is the amide derivative of benzoic acid and an inhibitor of poly(ADP-ribose) polymerase-1 (PARP-1).
More Information Supplier PageBenzoylpaeoniflorin is a monoterpene glycosides in Radix Paeoniae Alba.
More Information Supplier PageBenzoylpaeoniflorin is a monoterpene glycosides in Radix Paeoniae Alba.
More Information Supplier PageBenzoylpaeoniflorin is a monoterpene glycosides in Radix Paeoniae Alba.
More Information Supplier PageBepotastine is a non-sedating, selective antagonist of the histamine 1 (H1) receptor.
More Information Supplier PageBepotastine is a non-sedating, selective antagonist of the histamine 1 (H1) receptor.
More Information Supplier PageBepotastine is a non-sedating, selective antagonist of the histamine 1 (H1) receptor.
More Information Supplier PageBepotastine is a non-sedating, selective antagonist of the histamine 1 (H1) receptor.
More Information Supplier PageBepotastine Beslilate (Bepreve) is a histamine H1 receptor anatagonist.
More Information Supplier PageBepotastine Beslilate (Bepreve) is a histamine H1 receptor anatagonist.
More Information Supplier PageBepotastine Beslilate (Bepreve) is a histamine H1 receptor anatagonist.
More Information Supplier PageBepotastine Beslilate (Bepreve) is a histamine H1 receptor anatagonist.
More Information Supplier PageBepotastine Beslilate (Bepreve) is a histamine H1 receptor anatagonist.
More Information Supplier PageBerberine hydrochloride is a conventional component in Chinese medicine, and is characterized by a diversity of pharmacological effects.
More Information Supplier PageBerberine hydrochloride was novelly found that it has various beneficial effects on the cardiovascular system and significant anti-inflammatory activities. Berberine can effectively reduce intracellular superoxide levels in LPS-stimulated macrophages. Such a restoration of cellular redox by berberine is mediated by its selective inhibition of gp91phox expression and enhancement of SOD activity.
More Information Supplier PageBerberine hydrochloride was novelly found that it has various beneficial effects on the cardiovascular system and significant anti-inflammatory activities. Berberine can effectively reduce intracellular superoxide levels in LPS-stimulated macrophages. Such a restoration of cellular redox by berberine is mediated by its selective inhibition of gp91phox expression and enhancement of SOD activity.
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