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 WebsiteAbacavir is a nucleoside analog reverse transcriptase inhibitor (NRTI); guanosine analog used to treat HIV and AIDS.
More Information Supplier PageAbacavir is a nucleoside analog reverse transcriptase inhibitor (NRTI); guanosine analog used to treat HIV and AIDS.
More Information Supplier PageAbacavir is a nucleoside analog reverse transcriptase inhibitor (NRTI); guanosine analog used to treat HIV and AIDS.
More Information Supplier PageAbacavir is a nucleoside analog reverse transcriptase inhibitor (NRTI); guanosine analog used to treat HIV and AIDS.
More Information Supplier PageAbacavir sulfate is a nucleoside analog reverse transcriptase inhibitor (NRTI); guanosine analog used to treat HIV and AIDS.
More Information Supplier PageAbacavir sulfate is a nucleoside analog reverse transcriptase inhibitor (NRTI); guanosine analog used to treat HIV and AIDS.
More Information Supplier PageAbacavir sulfate is a nucleoside analog reverse transcriptase inhibitor (NRTI); guanosine analog used to treat HIV and AIDS.
More Information Supplier PageAbacavir sulfate is a nucleoside analog reverse transcriptase inhibitor (NRTI); guanosine analog used to treat HIV and AIDS.
More Information Supplier PageAbarelix acetate is a synthetic peptide gonadotropin releasing hormone receptor (GnRH) antagonist
More Information Supplier PageAbarelix acetate is a synthetic peptide gonadotropin releasing hormone receptor (GnRH) antagonist
More Information Supplier PageAbarelix acetate is a synthetic peptide gonadotropin releasing hormone receptor (GnRH) antagonist
More Information Supplier PageAbarelix acetate is a synthetic peptide gonadotropin releasing hormone receptor (GnRH) antagonist
More Information Supplier PageABC294640 is an orally available, aryladamantane compound and selective inhibitor of sphingosine kinase-2 (SK2) with potential antineoplastic activity.
More Information Supplier PageABC294640 is an orally available, aryladamantane compound and selective inhibitor of sphingosine kinase-2 (SK2) with potential antineoplastic activity.
More Information Supplier PageABC294640 is an orally available, aryladamantane compound and selective inhibitor of sphingosine kinase-2 (SK2) with potential antineoplastic activity.
More Information Supplier PageAbiraterone (CB-7598) inhibits 17 ??-hydroxylase/C17,20 lyase (CYP17A1), an enzyme which is expressed in testicular, adrenal, and prostatic tumor tissues.
More Information Supplier PageAbiraterone (CB-7598) inhibits 17 ??-hydroxylase/C17,20 lyase (CYP17A1), an enzyme which is expressed in testicular, adrenal, and prostatic tumor tissues.
More Information Supplier PageAbiraterone (CB-7598) inhibits 17 ??-hydroxylase/C17,20 lyase (CYP17A1), an enzyme which is expressed in testicular, adrenal, and prostatic tumor tissues.
More Information Supplier PageAbiraterone (CB-7598) inhibits 17 ??-hydroxylase/C17,20 lyase (CYP17A1), an enzyme which is expressed in testicular, adrenal, and prostatic tumor tissues.
More Information Supplier PageAbiraterone acetate (CB7630) is an orally active acetate ester of the steroidal compound Abiraterone with antiandrogen activity. Abiraterone inhibits 17 ??-hydroxylase/C17,20 lyase (CYP17A1).
More Information Supplier PageAbiraterone acetate (CB7630) is an orally active acetate ester of the steroidal compound Abiraterone with antiandrogen activity. Abiraterone inhibits 17 ??-hydroxylase/C17,20 lyase (CYP17A1).
More Information Supplier PageAbiraterone acetate (CB7630) is an orally active acetate ester of the steroidal compound Abiraterone with antiandrogen activity. Abiraterone inhibits 17 ??-hydroxylase/C17,20 lyase (CYP17A1).
More Information Supplier PageAbiraterone acetate (CB7630) is an orally active acetate ester of the steroidal compound Abiraterone with antiandrogen activity. Abiraterone inhibits 17 ??-hydroxylase/C17,20 lyase (CYP17A1).
More Information Supplier PageAbscisic Acid is a plant hormone, which is involved in many plant developmental processes, modulates ion homeostasis and metabolism.
More Information Supplier PageAbscisic Acid is a plant hormone, which is involved in many plant developmental processes, modulates ion homeostasis and metabolism.
More Information Supplier PageAbscisic Acid is a plant hormone, which is involved in many plant developmental processes, modulates ion homeostasis and metabolism.
More Information Supplier PageAbscisic Acid is a plant hormone, which is involved in many plant developmental processes, modulates ion homeostasis and metabolism.
More Information Supplier PageABT (1-Aminobenzotriazole )is a suicide substrate for (CYP)cytochrome P-450 and chloroperoxidase.
More Information Supplier PageABT (1-Aminobenzotriazole )is a suicide substrate for (CYP)cytochrome P-450 and chloroperoxidase.
More Information Supplier PageABT (1-Aminobenzotriazole )is a suicide substrate for (CYP)cytochrome P-450 and chloroperoxidase.
More Information Supplier PageABT 492 was more potent against quinolone-susceptible and -resistant gram-positive organisms, had activity similar to that of ciprofloxacin against certain members of the family Enterobacteriaceae, and had comparable activity against quinolone-susceptible, nonfermentative, gram-negative organisms. in vitro:
More Information Supplier PageABT 492 was more potent against quinolone-susceptible and -resistant gram-positive organisms, had activity similar to that of ciprofloxacin against certain members of the family Enterobacteriaceae, and had comparable activity against quinolone-susceptible, nonfermentative, gram-negative organisms. in vitro:
More Information Supplier PageABT 492 was more potent against quinolone-susceptible and -resistant gram-positive organisms, had activity similar to that of ciprofloxacin against certain members of the family Enterobacteriaceae, and had comparable activity against quinolone-susceptible, nonfermentative, gram-negative organisms. in vitro:
More Information Supplier PageABT (1-Aminobenzotriazole )is a suicide substrate for (CYP)cytochrome P-450 and chloroperoxidase.
More Information Supplier PageABT-046 is a potent, selective, and orally bioavailable Diacylglycerol acyltransferase 1 (DGAT-1 ) inhibitor (IC50= 8 nM).
More Information Supplier PageABT-046 is a potent, selective, and orally bioavailable Diacylglycerol acyltransferase 1 (DGAT-1 ) inhibitor (IC50= 8 nM).
More Information Supplier PageABT-046 is a potent, selective, and orally bioavailable Diacylglycerol acyltransferase 1 (DGAT-1 ) inhibitor (IC50= 8 nM).
More Information Supplier PageABT-199 is a so-called BH3-mimetic drug, which is designed to block the function of the protein Bcl 2.
More Information Supplier PageABT-199 is a so-called BH3-mimetic drug, which is designed to block the function of the protein Bcl 2.
More Information Supplier PageABT-199 is a so-called BH3-mimetic drug, which is designed to block the function of the protein Bcl 2.
More Information Supplier PageABT-199 is a so-called BH3-mimetic drug, which is designed to block the function of the protein Bcl 2.
More Information Supplier PageABT-199 is a so-called BH3-mimetic drug, which is designed to block the function of the protein Bcl 2.
More Information Supplier PageABT-263 (Navitoclax) is a potent orally bioavailable SMI that is structurally related to ABT-737. ABT-263 disrupts Bcl-2 – Bcl-XL interactions with pro-apoptotic proteins .
More Information Supplier PageABT-263 (Navitoclax) is a potent orally bioavailable SMI that is structurally related to ABT-737. ABT-263 disrupts Bcl-2 – Bcl-XL interactions with pro-apoptotic proteins .
More Information Supplier PageABT-263 (Navitoclax) is a potent orally bioavailable SMI that is structurally related to ABT-737. ABT-263 disrupts Bcl-2 – Bcl-XL interactions with pro-apoptotic proteins .
More Information Supplier PageABT-263 (Navitoclax) is a potent orally bioavailable SMI that is structurally related to ABT-737. ABT-263 disrupts Bcl-2 – Bcl-XL interactions with pro-apoptotic proteins .
More Information Supplier PageABT-263 (Navitoclax) is a potent orally bioavailable SMI that is structurally related to ABT-737. ABT-263 disrupts Bcl-2 – Bcl-XL interactions with pro-apoptotic proteins .
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