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 Website4-Methylumbelliferone is a selective inhibitor of Hyaluronan (HA) synthesis which is thought to function as an inhibitor via the depletion of UDP-glucuronic acid, the common substrate for HA synthesis.
More Information Supplier Page4-Methylumbelliferone is a selective inhibitor of Hyaluronan (HA) synthesis which is thought to function as an inhibitor via the depletion of UDP-glucuronic acid, the common substrate for HA synthesis.
More Information Supplier Page4-O-Caffeoylquinic acid, also known as cryptochlorogenic acid, is an isomer of chlorogenic acid and possesses antioxidant properties.
More Information Supplier Page4-O-Caffeoylquinic acid, also known as cryptochlorogenic acid, is an isomer of chlorogenic acid and possesses antioxidant properties.
More Information Supplier Page4-O-Caffeoylquinic acid, also known as cryptochlorogenic acid, is an isomer of chlorogenic acid and possesses antioxidant properties.
More Information Supplier Page4E1RCat is a dual inhibitor of eIF4E:eIF4G and eIF4E:4E-BP1 interaction.
More Information Supplier Page4E1RCat is a dual inhibitor of eIF4E:eIF4G and eIF4E:4E-BP1 interaction.
More Information Supplier Page4E1RCat is a dual inhibitor of eIF4E:eIF4G and eIF4E:4E-BP1 interaction.
More Information Supplier Page4E1RCat is a dual inhibitor of eIF4E:eIF4G and eIF4E:4E-BP1 interaction.
More Information Supplier Page4EGI-1 is a competitive eIF4E/eIF4G interaction inhibitor by binding to eIF4E with KD of 25 ??M.
More Information Supplier Page4EGI-1 is a competitive eIF4E/eIF4G interaction inhibitor by binding to eIF4E with KD of 25 ??M.
More Information Supplier Page4EGI-1 is a competitive eIF4E/eIF4G interaction inhibitor by binding to eIF4E with KD of 25 ??M.
More Information Supplier Page4EGI-1 is a competitive eIF4E/eIF4G interaction inhibitor by binding to eIF4E with KD of 25 ??M.
More Information Supplier Page4SC-202 is an orally bioavailable benzamide and inhibitor of human class I histone deacetylases (HDACs) isoenzymes 1, 2 and 3, with potential antineoplastic activity.
More Information Supplier Page4SC-202 is an orally bioavailable benzamide and inhibitor of human class I histone deacetylases (HDACs) isoenzymes 1, 2 and 3, with potential antineoplastic activity.
More Information Supplier Page4SC-202 is an orally bioavailable benzamide and inhibitor of human class I histone deacetylases (HDACs) isoenzymes 1, 2 and 3, with potential antineoplastic activity.
More Information Supplier Page4SC-202 is an orally bioavailable benzamide and inhibitor of human class I histone deacetylases (HDACs) isoenzymes 1, 2 and 3, with potential antineoplastic activity.
More Information Supplier Page4??8C is a potent and selective IRE1 Rnase inhibitor with IC50 of 76 nM.
More Information Supplier Page4??8C is a potent and selective IRE1 Rnase inhibitor with IC50 of 76 nM.
More Information Supplier Page4??8C is a potent and selective IRE1 Rnase inhibitor with IC50 of 76 nM.
More Information Supplier Page4??8C is a potent and selective IRE1 Rnase inhibitor with IC50 of 76 nM.
More Information Supplier Page5-Aminolevulinic acid hydrochloride is a naturally occurring amino acid; precursor of tetrapyrroles in the biosynthesis of chlorophyll and heme.
More Information Supplier Page5-Aminolevulinic acid hydrochloride is a naturally occurring amino acid; precursor of tetrapyrroles in the biosynthesis of chlorophyll and heme.
More Information Supplier Page5-Aminolevulinic acid hydrochloride is a naturally occurring amino acid; precursor of tetrapyrroles in the biosynthesis of chlorophyll and heme.
More Information Supplier Page5-BrdU is a synthetic thymidine analog; incorporated into DNA during replication. Used in assays for cell proliferation.
More Information Supplier Page5-BrdU is a synthetic thymidine analog; incorporated into DNA during replication. Used in assays for cell proliferation.
More Information Supplier Page5-BrdU is a synthetic thymidine analog; incorporated into DNA during replication. Used in assays for cell proliferation.
More Information Supplier Page5-BrdU is a synthetic thymidine analog; incorporated into DNA during replication. Used in assays for cell proliferation.
More Information Supplier Page5-hydroxymethyl tolterodine is a metabolite of Tolterodine, a muscarinic receptor antagonist used in the treatment of urinary incontinence.
More Information Supplier Page5-hydroxymethyl tolterodine is a metabolite of Tolterodine, a muscarinic receptor antagonist used in the treatment of urinary incontinence.
More Information Supplier Page5-hydroxymethyl tolterodine is a metabolite of Tolterodine, a muscarinic receptor antagonist used in the treatment of urinary incontinence.
More Information Supplier Page5-hydroxymethyl tolterodine is a metabolite of Tolterodine, a muscarinic receptor antagonist used in the treatment of urinary incontinence.
More Information Supplier Page5-hydroxymethyl tolterodine is a metabolite of Tolterodine, a muscarinic receptor antagonist used in the treatment of urinary incontinence.
More Information Supplier Page5-Hydroxytryptophan (5-HTP) is a naturally occurring amino acid and chemical precursor as well as a metabolic intermediate in the biosynthesis of the neurotransmitters serotonin and melatonin from tryptophan.
More Information Supplier Page5-Hydroxytryptophan (5-HTP) is a naturally occurring amino acid and chemical precursor as well as a metabolic intermediate in the biosynthesis of the neurotransmitters serotonin and melatonin from tryptophan.
More Information Supplier Page5-Hydroxytryptophan (5-HTP) is a naturally occurring amino acid and chemical precursor as well as a metabolic intermediate in the biosynthesis of the neurotransmitters serotonin and melatonin from tryptophan.
More Information Supplier Page5-Hydroxytryptophan (5-HTP) is a naturally occurring amino acid and chemical precursor as well as a metabolic intermediate in the biosynthesis of the neurotransmitters serotonin and melatonin from tryptophan.
More Information Supplier Page5-Iodo-A-85380 2HCl is a highly potent and subtype-selective agonist for the a4b2 and a6b2 nicotinic acetylcholine receptors.
More Information Supplier Page5-Iodo-A-85380 2HCl is a highly potent and subtype-selective agonist for the a4b2 and a6b2 nicotinic acetylcholine receptors.
More Information Supplier Page5-Iodo-A-85380 2HCl is a highly potent and subtype-selective agonist for the a4b2 and a6b2 nicotinic acetylcholine receptors.
More Information Supplier Page5-Iodotubercidin (Itu) is an adenosine derivative that initiates glycogen synthesis in hepatocytes by causing inactivation of phosphorylase ?? and activation of glycogen synthase ?? (maximal effects with ~20 ?M Itu).
More Information Supplier Page5-Iodotubercidin (Itu) is an adenosine derivative that initiates glycogen synthesis in hepatocytes by causing inactivation of phosphorylase ?? and activation of glycogen synthase ?? (maximal effects with ~20 ?M Itu).
More Information Supplier Page5-o-methylvisammioside has analgesic, antipyretic, anti-inflammatory and anti-platelet aggregation effect.
More Information Supplier Page5-o-methylvisammioside has analgesic, antipyretic, anti-inflammatory and anti-platelet aggregation effect.
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