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 WebsiteMicrocystin-LR is a potent protein phosphatase inhibitor with IC50 of 0.04 nM for PP2A, >40-fold selectivity over PP1.
More Information Supplier PageMicrocystin-LR is a potent protein phosphatase inhibitor with IC50 of 0.04 nM for PP2A, >40-fold selectivity over PP1.
More Information Supplier PageMIF antagonist is an inhibitor of the dopachrome tautomerase activity of MIF in vitro (IC50 = 7 M) and in cells (IC50 = 25 M).
More Information Supplier PageMIF antagonist is an inhibitor of the dopachrome tautomerase activity of MIF in vitro (IC50 = 7 M) and in cells (IC50 = 25 M).
More Information Supplier PageMIF antagonist is an inhibitor of the dopachrome tautomerase activity of MIF in vitro (IC50 = 7 M) and in cells (IC50 = 25 M).
More Information Supplier PageMifamurtide is a liposomal formulation containing a muramyl dipeptide (MDP) analogue with potential immunomodulatory and antineoplastic activities
More Information Supplier PageMifamurtide is a liposomal formulation containing a muramyl dipeptide (MDP) analogue with potential immunomodulatory and antineoplastic activities
More Information Supplier PageMifamurtide is a liposomal formulation containing a muramyl dipeptide (MDP) analogue with potential immunomodulatory and antineoplastic activities
More Information Supplier PageMifamurtide is a liposomal formulation containing a muramyl dipeptide (MDP) analogue with potential immunomodulatory and antineoplastic activities
More Information Supplier PageMifepristone, an antioxidant and glucocorticoid receptor antagonist, demonstrates the ability to suppress activation of NF??B, a nuclear transcription factor that affects the expression of various adhesion molecules and several inflammatory genes.
More Information Supplier PageMifepristone, an antioxidant and glucocorticoid receptor antagonist, demonstrates the ability to suppress activation of NF??B, a nuclear transcription factor that affects the expression of various adhesion molecules and several inflammatory genes.
More Information Supplier PageMifepristone, an antioxidant and glucocorticoid receptor antagonist, demonstrates the ability to suppress activation of NF??B, a nuclear transcription factor that affects the expression of various adhesion molecules and several inflammatory genes.
More Information Supplier PageMifepristone, an antioxidant and glucocorticoid receptor antagonist, demonstrates the ability to suppress activation of NF??B, a nuclear transcription factor that affects the expression of various adhesion molecules and several inflammatory genes.
More Information Supplier PageMifepristone, an antioxidant and glucocorticoid receptor antagonist, demonstrates the ability to suppress activation of NF??B, a nuclear transcription factor that affects the expression of various adhesion molecules and several inflammatory genes.
More Information Supplier PageMiglitol inhibits glycoside hydrolase enzymes called alpha-glucosidases. It is primarily used in diabetes mellitus type 2 for establishing greater glycemic control by preventing the digestion of carbohydrates (such as disaccharides, oligosaccharides, and polysaccharides) into monosaccharides which can be absorbed by the body.
More Information Supplier PageMiglitol inhibits glycoside hydrolase enzymes called alpha-glucosidases. It is primarily used in diabetes mellitus type 2 for establishing greater glycemic control by preventing the digestion of carbohydrates (such as disaccharides, oligosaccharides, and polysaccharides) into monosaccharides which can be absorbed by the body.
More Information Supplier PageMiglitol inhibits glycoside hydrolase enzymes called alpha-glucosidases. It is primarily used in diabetes mellitus type 2 for establishing greater glycemic control by preventing the digestion of carbohydrates (such as disaccharides, oligosaccharides, and polysaccharides) into monosaccharides which can be absorbed by the body.
More Information Supplier PageMiglustat hydrochloride is an orally active ??-glucosidase I and II and ceramide-specific glycosyltransferase inhibitor.
More Information Supplier PageMiglustat hydrochloride is an orally active ??-glucosidase I and II and ceramide-specific glycosyltransferase inhibitor.
More Information Supplier PageMiglustat hydrochloride is an orally active ??-glucosidase I and II and ceramide-specific glycosyltransferase inhibitor.
More Information Supplier PageMiglustat hydrochloride is an orally active ??-glucosidase I and II and ceramide-specific glycosyltransferase inhibitor.
More Information Supplier PageMilrinone(Primacor) is a a potent and selective phosphodiesterase 3 inhibitor with an IC50 of 0.42 ??M for the inhibition of FIII PDE
More Information Supplier PageMilrinone(Primacor) is a a potent and selective phosphodiesterase 3 inhibitor with an IC50 of 0.42 ??M for the inhibition of FIII PDE
More Information Supplier PageMilrinone(Primacor) is a a potent and selective phosphodiesterase 3 inhibitor with an IC50 of 0.42 ??M for the inhibition of FIII PDE
More Information Supplier PageMilrinone(Primacor) is a a potent and selective phosphodiesterase 3 inhibitor with an IC50 of 0.42 ??M for the inhibition of FIII PDE
More Information Supplier PageMilrinone(Primacor) is a a potent and selective phosphodiesterase 3 inhibitor with an IC50 of 0.42 ??M for the inhibition of FIII PDE
More Information Supplier PageMiltefosine is an inhibitor of CTP:phosphocholine cytidylyl transferase and has antimetastatic properties.
More Information Supplier PageMiltefosine is an inhibitor of CTP:phosphocholine cytidylyl transferase and has antimetastatic properties.
More Information Supplier PageMiltefosine is an inhibitor of CTP:phosphocholine cytidylyl transferase and has antimetastatic properties.
More Information Supplier PageMinoxidil (U-10858) is a selective ATP dependent K+ (Kir6) channel activator.
More Information Supplier PageMinoxidil (U-10858) is a selective ATP dependent K+ (Kir6) channel activator.
More Information Supplier PageMinoxidil (U-10858) is a selective ATP dependent K+ (Kir6) channel activator.
More Information Supplier PageMinoxidil (U-10858) is a selective ATP dependent K+ (Kir6) channel activator.
More Information Supplier PageMIRA-1 restores wild-type conformation, function and DNA binding activity to mutant p53. Induces p53 transcriptional transactivation of p21, MDM2 and PUMA.
More Information Supplier PageMIRA-1 restores wild-type conformation, function and DNA binding activity to mutant p53. Induces p53 transcriptional transactivation of p21, MDM2 and PUMA.
More Information Supplier PageMirabegron is a potent bladder relaxant and reagent for diabetes remedy.
More Information Supplier PageMirabegron is a potent bladder relaxant and reagent for diabetes remedy.
More Information Supplier PageMirabegron is a potent bladder relaxant and reagent for diabetes remedy.
More Information Supplier PageMirabegron is a potent bladder relaxant and reagent for diabetes remedy.
More Information Supplier PageMirabegron is a potent bladder relaxant and reagent for diabetes remedy.
More Information Supplier PageMiriplatin hydrate is a lipophilic platinum complex containing myristates as leaving groups, and can be easily suspended in ethyl esters of iodized fatty acids obtained from poppy seed oil.
More Information Supplier PageMiriplatin hydrate is a lipophilic platinum complex containing myristates as leaving groups, and can be easily suspended in ethyl esters of iodized fatty acids obtained from poppy seed oil.
More Information Supplier PageMiriplatin hydrate is a lipophilic platinum complex containing myristates as leaving groups, and can be easily suspended in ethyl esters of iodized fatty acids obtained from poppy seed oil.
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