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 WebsiteExherin is a small, cyclic pentapeptide vascular-targeting agent with potential antineoplastic and antiangiogenic activities.
More Information Supplier PageExherin is a small, cyclic pentapeptide vascular-targeting agent with potential antineoplastic and antiangiogenic activities.
More Information Supplier PageEzatiostat is a liposomal small-molecule glutathione analog inhibitor of glutathione S-transferase (GST) P1-1 with hematopoiesis-stimulating activity.
More Information Supplier PageEzatiostat is a liposomal small-molecule glutathione analog inhibitor of glutathione S-transferase (GST) P1-1 with hematopoiesis-stimulating activity.
More Information Supplier PageEzatiostat is a liposomal small-molecule glutathione analog inhibitor of glutathione S-transferase (GST) P1-1 with hematopoiesis-stimulating activity.
More Information Supplier PageEzetimibe is a compound that lowers cholesterol. It acts by decreasing cholesterol absorption in the intestine. Ezetimibe localises at the brush border of the small intestine, where ezetimibe inhibits the absorption of cholesterol from the intestine.
More Information Supplier PageEzetimibe is a compound that lowers cholesterol. It acts by decreasing cholesterol absorption in the intestine. Ezetimibe localises at the brush border of the small intestine, where ezetimibe inhibits the absorption of cholesterol from the intestine.
More Information Supplier PageEzetimibe is a compound that lowers cholesterol. It acts by decreasing cholesterol absorption in the intestine. Ezetimibe localises at the brush border of the small intestine, where ezetimibe inhibits the absorption of cholesterol from the intestine.
More Information Supplier PageFABP4 Inhibitor is a cell-permeable biphenylazolo-oxyacetate that acts as a potent and selective inhibitor of adipocyte Fatty-Acid-Binding Protein (aFABP/aP2) by targeting its fatty acid-binding pocket (Ki = < 2 nM in a competitive binding assay using 1,8-ANS), while exhibiting much lower affinity for muscle and epidermal FABP's (Ki = 250 nM and 350 nM, respectively).
More Information Supplier PageFABP4 Inhibitor is a cell-permeable biphenylazolo-oxyacetate that acts as a potent and selective inhibitor of adipocyte Fatty-Acid-Binding Protein (aFABP/aP2) by targeting its fatty acid-binding pocket (Ki = < 2 nM in a competitive binding assay using 1,8-ANS), while exhibiting much lower affinity for muscle and epidermal FABP's (Ki = 250 nM and 350 nM, respectively).
More Information Supplier PageFABP4 Inhibitor is a cell-permeable biphenylazolo-oxyacetate that acts as a potent and selective inhibitor of adipocyte Fatty-Acid-Binding Protein (aFABP/aP2) by targeting its fatty acid-binding pocket (Ki = < 2 nM in a competitive binding assay using 1,8-ANS), while exhibiting much lower affinity for muscle and epidermal FABP's (Ki = 250 nM and 350 nM, respectively).
More Information Supplier PageFABP4 Inhibitor is a cell-permeable biphenylazolo-oxyacetate that acts as a potent and selective inhibitor of adipocyte Fatty-Acid-Binding Protein (aFABP/aP2) by targeting its fatty acid-binding pocket (Ki = < 2 nM in a competitive binding assay using 1,8-ANS), while exhibiting much lower affinity for muscle and epidermal FABP's (Ki = 250 nM and 350 nM, respectively).
More Information Supplier PageFadrozole is a nonsteroidal aromatase inhibitor exhibiting a very potent and selective inhibitory effect of the aromatase enzyme system in vivo and estrogen biosynthesis in vivo.
More Information Supplier PageFadrozole is a nonsteroidal aromatase inhibitor exhibiting a very potent and selective inhibitory effect of the aromatase enzyme system in vivo and estrogen biosynthesis in vivo.
More Information Supplier PageFadrozole is a nonsteroidal aromatase inhibitor exhibiting a very potent and selective inhibitory effect of the aromatase enzyme system in vivo and estrogen biosynthesis in vivo.
More Information Supplier PageFadrozole is a nonsteroidal aromatase inhibitor exhibiting a very potent and selective inhibitory effect of the aromatase enzyme system in vivo and estrogen biosynthesis in vivo.
More Information Supplier PageD-Fagomine is an iminosugar originally isolated from seeds of buckwheat (Fagopyrum sculentum Moench)
More Information Supplier PageD-Fagomine is an iminosugar originally isolated from seeds of buckwheat (Fagopyrum sculentum Moench)
More Information Supplier PageD-Fagomine is an iminosugar originally isolated from seeds of buckwheat (Fagopyrum sculentum Moench)
More Information Supplier PageD-Fagomine is an iminosugar originally isolated from seeds of buckwheat (Fagopyrum sculentum Moench)
More Information Supplier PageFangchinoline is an isolate of Stephania tetrandra that has anticancer activity.
More Information Supplier PageFangchinoline is an isolate of Stephania tetrandra that has anticancer activity.
More Information Supplier PageFangchinoline is an isolate of Stephania tetrandra that has anticancer activity.
More Information Supplier PageFarampator has been investigated for its effect on AMPA receptors and researched for potential use in the treatment of schizophrenia and Alzheimer’s Disease. It was found to improve short-term memory, but impaired episodic memory.
More Information Supplier PageFarampator has been investigated for its effect on AMPA receptors and researched for potential use in the treatment of schizophrenia and Alzheimer’s Disease. It was found to improve short-term memory, but impaired episodic memory.
More Information Supplier PageFarampator has been investigated for its effect on AMPA receptors and researched for potential use in the treatment of schizophrenia and Alzheimer’s Disease. It was found to improve short-term memory, but impaired episodic memory.
More Information Supplier PageFargesin, a component of Flos Magnoliae, stimulates glucose uptake in L6 myotubes.
More Information Supplier PageFargesin, a component of Flos Magnoliae, stimulates glucose uptake in L6 myotubes.
More Information Supplier PageFargesin, a component of Flos Magnoliae, stimulates glucose uptake in L6 myotubes.
More Information Supplier PageFas C- Terminal Tripeptide is a tri-peptide with the sequence AC-SER-LEU-VAL-OH.
More Information Supplier PageFas C- Terminal Tripeptide is a tri-peptide with the sequence AC-SER-LEU-VAL-OH.
More Information Supplier PageFas C- Terminal Tripeptide is a tri-peptide with the sequence AC-SER-LEU-VAL-OH.
More Information Supplier PageFasudil HCl is a cyclic nucleotide-dependent protein kinase inhibitor and Rho-associated kinase inhibitor (IC50 = 10.7 ??M).
More Information Supplier PageFasudil HCl is a cyclic nucleotide-dependent protein kinase inhibitor and Rho-associated kinase inhibitor (IC50 = 10.7 ??M).
More Information Supplier PageFebuxostat is a non-purine inhibitor of xanthine oxidase (Ki = 1.2 nM).
More Information Supplier PageFebuxostat is a non-purine inhibitor of xanthine oxidase (Ki = 1.2 nM).
More Information Supplier PageFebuxostat is a non-purine inhibitor of xanthine oxidase (Ki = 1.2 nM).
More Information Supplier PageFebuxostat is a non-purine inhibitor of xanthine oxidase (Ki = 1.2 nM).
More Information Supplier PageFebuxostat is a non-purine inhibitor of xanthine oxidase (Ki = 1.2 nM).
More Information Supplier PageFelbamate is an antagonist at the NMDA-associated glycine binding site.
More Information Supplier PageFelbamate is an antagonist at the NMDA-associated glycine binding site.
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