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 WebsiteMelanocyte stimulating hormone release inhibiting factor is an endogenous peptide fragment derived from cleavage of the hormone oxytocin, but having generally different actions in the body(1).
More Information Supplier PageMelanocyte stimulating hormone release inhibiting factor is an endogenous peptide fragment derived from cleavage of the hormone oxytocin, but having generally different actions in the body(1).
More Information Supplier PageMelanocyte stimulating hormone release inhibiting factor is an endogenous peptide fragment derived from cleavage of the hormone oxytocin, but having generally different actions in the body(1).
More Information Supplier PageMelanotan II is a high affinity melanocortin receptor agonist (Ki values are 0.67, 6.6, 34 and 46 nM for MC1, MC4, MC3 and MC5 receptors respectively).
More Information Supplier PageMelanotan II is a high affinity melanocortin receptor agonist (Ki values are 0.67, 6.6, 34 and 46 nM for MC1, MC4, MC3 and MC5 receptors respectively).
More Information Supplier PageMelanotan II is a high affinity melanocortin receptor agonist (Ki values are 0.67, 6.6, 34 and 46 nM for MC1, MC4, MC3 and MC5 receptors respectively).
More Information Supplier PageMelanotan II is a high affinity melanocortin receptor agonist (Ki values are 0.67, 6.6, 34 and 46 nM for MC1, MC4, MC3 and MC5 receptors respectively).
More Information Supplier PageMelatonin is a endogenous hormone that acts as an agonist at melatonin receptors MT1 and MT2.
More Information Supplier PageMelatonin is a endogenous hormone that acts as an agonist at melatonin receptors MT1 and MT2.
More Information Supplier PageMelatonin is a endogenous hormone that acts as an agonist at melatonin receptors MT1 and MT2.
More Information Supplier PageMelatonin is a endogenous hormone that acts as an agonist at melatonin receptors MT1 and MT2.
More Information Supplier PageMelittin is a Na+/K+ ATPase inhibitor. It inhibits Gs and stimulates Gi activity. It inhibits protein kinase C and cAMP-dependent protein kinases.
More Information Supplier PageMelittin is a Na+/K+ ATPase inhibitor. It inhibits Gs and stimulates Gi activity. It inhibits protein kinase C and cAMP-dependent protein kinases.
More Information Supplier PageMelphalan is a cytotoxic drug used to treat multiple myeloma. Phenylamine derivative of mechorethamine.
More Information Supplier PageMelphalan is a cytotoxic drug used to treat multiple myeloma. Phenylamine derivative of mechorethamine.
More Information Supplier PageMelphalan is a cytotoxic drug used to treat multiple myeloma. Phenylamine derivative of mechorethamine.
More Information Supplier PageMemantine hydrochloride is an antagonist at the NMDA receptor, binding to the ion channel site. it was used in the treatment of Parkinsonism.
More Information Supplier PageMemantine hydrochloride is an antagonist at the NMDA receptor, binding to the ion channel site. it was used in the treatment of Parkinsonism.
More Information Supplier PageMemantine hydrochloride is an antagonist at the NMDA receptor, binding to the ion channel site. it was used in the treatment of Parkinsonism.
More Information Supplier PageMemantine hydrochloride is an antagonist at the NMDA receptor, binding to the ion channel site. it was used in the treatment of Parkinsonism.
More Information Supplier PageMeprednisone is a glucocorticoid and a methylated derivative of prednisone
More Information Supplier PageMeprednisone is a glucocorticoid and a methylated derivative of prednisone
More Information Supplier PageMeprednisone is a glucocorticoid and a methylated derivative of prednisone
More Information Supplier PageMeprednisone is a glucocorticoid and a methylated derivative of prednisone
More Information Supplier PageMeprednisone is a glucocorticoid and a methylated derivative of prednisone
More Information Supplier PageMercaptopurine has been shown to interfere with DNA and RNA synthesis and cause inhibition of de novo purine syntehsis.
More Information Supplier PageMercaptopurine has been shown to interfere with DNA and RNA synthesis and cause inhibition of de novo purine syntehsis.
More Information Supplier PageMercaptopurine has been shown to interfere with DNA and RNA synthesis and cause inhibition of de novo purine syntehsis.
More Information Supplier PageMercaptopurine has been shown to interfere with DNA and RNA synthesis and cause inhibition of de novo purine syntehsis.
More Information Supplier PageMercaptopurine has been shown to interfere with DNA and RNA synthesis and cause inhibition of de novo purine syntehsis.
More Information Supplier PageMeropenem is a ??-lactam antibiotic of the carbapenem subclass that has been shown to inhibit penicillinase-negative, -positive and methicillin-susceptible staphylococci.
More Information Supplier PageMeropenem is a ??-lactam antibiotic of the carbapenem subclass that has been shown to inhibit penicillinase-negative, -positive and methicillin-susceptible staphylococci.
More Information Supplier PageMeropenem is a ??-lactam antibiotic of the carbapenem subclass that has been shown to inhibit penicillinase-negative, -positive and methicillin-susceptible staphylococci.
More Information Supplier PageMeropenem is a ??-lactam antibiotic of the carbapenem subclass that has been shown to inhibit penicillinase-negative, -positive and methicillin-susceptible staphylococci.
More Information Supplier PageMeropenem is a ??-lactam antibiotic of the carbapenem subclass that has been shown to inhibit penicillinase-negative, -positive and methicillin-susceptible staphylococci.
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