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 WebsiteLithospermoside, extracted from Lithospermum ery-throrhizon Sieb. et Zucc. dried roots.
More Information Supplier PageLLY-507 is a cell-active, small molecule inhibitor of SMYD2 with IC50 of= 15 nM.
More Information Supplier PageLLY-507 is a cell-active, small molecule inhibitor of SMYD2 with IC50 of= 15 nM.
More Information Supplier PageLLY-507 is a cell-active, small molecule inhibitor of SMYD2 with IC50 of= 15 nM.
More Information Supplier PageLM22A-4 is a potent tropomyosin-related kinase B (TrkB) agonist (IC50 = 47 nM).
More Information Supplier PageLM22A-4 is a potent tropomyosin-related kinase B (TrkB) agonist (IC50 = 47 nM).
More Information Supplier PageLM22A-4 is a potent tropomyosin-related kinase B (TrkB) agonist (IC50 = 47 nM).
More Information Supplier PageLMK-235 is a selective histone deacetylase (HDAC) 4 and HDAC5 inhibitor.
More Information Supplier PageLMK-235 is a selective histone deacetylase (HDAC) 4 and HDAC5 inhibitor.
More Information Supplier PageLMK-235 is a selective histone deacetylase (HDAC) 4 and HDAC5 inhibitor.
More Information Supplier PageA nucleoside analog used in the treatment of viral infections (including those caused by human immunodeficiency virus, cytomegalovirus, and herpes virus).
More Information Supplier PageA nucleoside analog used in the treatment of viral infections (including those caused by human immunodeficiency virus, cytomegalovirus, and herpes virus).
More Information Supplier PageA nucleoside analog used in the treatment of viral infections (including those caused by human immunodeficiency virus, cytomegalovirus, and herpes virus).
More Information Supplier PageA nucleoside analog used in the treatment of viral infections (including those caused by human immunodeficiency virus, cytomegalovirus, and herpes virus).
More Information Supplier PageLoganic acid, extracted from Gentiana macrophylla Pall root and rhizome.
More Information Supplier PageLoganic acid, extracted from Gentiana macrophylla Pall root and rhizome.
More Information Supplier PageLoganic acid, extracted from Gentiana macrophylla Pall root and rhizome.
More Information Supplier PageLomeguatrib is a potent inhibitor of O6-alkylguanine-DNA-alkyltransferase.
More Information Supplier PageLomeguatrib is a potent inhibitor of O6-alkylguanine-DNA-alkyltransferase.
More Information Supplier PageLomeguatrib is a potent inhibitor of O6-alkylguanine-DNA-alkyltransferase.
More Information Supplier PageLomeguatrib is a potent inhibitor of O6-alkylguanine-DNA-alkyltransferase.
More Information Supplier PageLomitapide is a potent microsomal triglyceride transfer protein (MTP) inhibitor.
More Information Supplier PageLomitapide is a potent microsomal triglyceride transfer protein (MTP) inhibitor.
More Information Supplier PageLomitapide is a potent microsomal triglyceride transfer protein (MTP) inhibitor.
More Information Supplier PageLomitapide is a potent microsomal triglyceride transfer protein (MTP) inhibitor.
More Information Supplier PageLomustine is an alkylating nitrosourea compound that possesses antitumor activity similar to Carmustine causing DNA interstrand cross-linking.
More Information Supplier PageLomustine is an alkylating nitrosourea compound that possesses antitumor activity similar to Carmustine causing DNA interstrand cross-linking.
More Information Supplier PageLomustine is an alkylating nitrosourea compound that possesses antitumor activity similar to Carmustine causing DNA interstrand cross-linking.
More Information Supplier PageLomustine is an alkylating nitrosourea compound that possesses antitumor activity similar to Carmustine causing DNA interstrand cross-linking.
More Information Supplier PageLomustine is an alkylating nitrosourea compound that possesses antitumor activity similar to Carmustine causing DNA interstrand cross-linking.
More Information Supplier PageLonafarnib (SCH 66336) is a selectively FPTase inhibitor for H-ras, K-ras-4B and N-ras with IC50 of 1.9 nM, 5.2 nM and 2.8 nM, respectively.
More Information Supplier PageLonafarnib (SCH 66336) is a selectively FPTase inhibitor for H-ras, K-ras-4B and N-ras with IC50 of 1.9 nM, 5.2 nM and 2.8 nM, respectively.
More Information Supplier PageLonafarnib (SCH 66336) is a selectively FPTase inhibitor for H-ras, K-ras-4B and N-ras with IC50 of 1.9 nM, 5.2 nM and 2.8 nM, respectively.
More Information Supplier PageLonafarnib (SCH 66336) is a selectively FPTase inhibitor for H-ras, K-ras-4B and N-ras with IC50 of 1.9 nM, 5.2 nM and 2.8 nM, respectively.
More Information Supplier PageLonafarnib (SCH 66336) is a selectively FPTase inhibitor for H-ras, K-ras-4B and N-ras with IC50 of 1.9 nM, 5.2 nM and 2.8 nM, respectively.
More Information Supplier PageLonaprisan is an orally bioavailable pentafluoroethyl derivative of a mifepristone-related steroid with antiprogestagenic activity.
More Information Supplier PageLonaprisan is an orally bioavailable pentafluoroethyl derivative of a mifepristone-related steroid with antiprogestagenic activity.
More Information Supplier PageLonaprisan is an orally bioavailable pentafluoroethyl derivative of a mifepristone-related steroid with antiprogestagenic activity.
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