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 WebsiteIMD 0354 is an inhibitor of I??B kinase-?? (IKK??) that blocks NF-??B nuclear translocation.
More Information Supplier PageIMD 0354 is an inhibitor of I??B kinase-?? (IKK??) that blocks NF-??B nuclear translocation.
More Information Supplier PageIMD 0354 is an inhibitor of I??B kinase-?? (IKK??) that blocks NF-??B nuclear translocation.
More Information Supplier PageIMD 0354 is an inhibitor of I??B kinase-?? (IKK??) that blocks NF-??B nuclear translocation.
More Information Supplier PageImidafenacin is a potent and selective inhibitor of M3 receptors with Kb of 0.317 nM; less potent for M2 receptors(IC50=4.13 nM).
More Information Supplier PageImidafenacin is a potent and selective inhibitor of M3 receptors with Kb of 0.317 nM; less potent for M2 receptors(IC50=4.13 nM).
More Information Supplier PageImidapril (Tanatril) is an inhibitor of angiotensin converting enzyme (ACE).
More Information Supplier PageImidapril (Tanatril) is an inhibitor of angiotensin converting enzyme (ACE).
More Information Supplier PageImidapril (Tanatril) is an inhibitor of angiotensin converting enzyme (ACE).
More Information Supplier PageImidapril (Tanatril) is an inhibitor of angiotensin converting enzyme (ACE).
More Information Supplier PageImidapril (Tanatril) is an inhibitor of angiotensin converting enzyme (ACE).
More Information Supplier PageImipenem is an intravenous ??-lactam antibiotic discovered by Merck scientists Burton Christensen, William Leanza, and Kenneth Wildonger in 1980.
More Information Supplier PageImipenem is an intravenous ??-lactam antibiotic discovered by Merck scientists Burton Christensen, William Leanza, and Kenneth Wildonger in 1980.
More Information Supplier PageImipenem is an intravenous ??-lactam antibiotic discovered by Merck scientists Burton Christensen, William Leanza, and Kenneth Wildonger in 1980.
More Information Supplier PageImipramine Hydrochloride is a tricyclic antidepressant. Inhibits the serotonin and norepinephrine transporters but has little effect on the dopamine transporter.
More Information Supplier PageImipramine Hydrochloride is a tricyclic antidepressant. Inhibits the serotonin and norepinephrine transporters but has little effect on the dopamine transporter.
More Information Supplier PageImipramine Hydrochloride is a tricyclic antidepressant. Inhibits the serotonin and norepinephrine transporters but has little effect on the dopamine transporter.
More Information Supplier PageImipramine Hydrochloride is a tricyclic antidepressant. Inhibits the serotonin and norepinephrine transporters but has little effect on the dopamine transporter.
More Information Supplier PageImiquimod (Aldara) is a a heterocyclic imidazoquinoline amide that acts as an immune response modifier.
More Information Supplier PageImiquimod (Aldara) is a a heterocyclic imidazoquinoline amide that acts as an immune response modifier.
More Information Supplier PageImmethridine hydrobromide is a strong and highly selective histamine H3 receptor agonist (pEC50 = 9.74) that displays 300-fold selectivity over the H4 receptor (pKi values are 9.07 and 6.61 respectively).
More Information Supplier PageImmethridine hydrobromide is a strong and highly selective histamine H3 receptor agonist (pEC50 = 9.74) that displays 300-fold selectivity over the H4 receptor (pKi values are 9.07 and 6.61 respectively).
More Information Supplier PageImmethridine hydrobromide is a strong and highly selective histamine H3 receptor agonist (pEC50 = 9.74) that displays 300-fold selectivity over the H4 receptor (pKi values are 9.07 and 6.61 respectively).
More Information Supplier PageImperatorin is a furocoumarin present in citrus fruits, which is used in HIV-1 research.
More Information Supplier PageImperatorin is a furocoumarin present in citrus fruits, which is used in HIV-1 research.
More Information Supplier PageImperatorin is a furocoumarin present in citrus fruits, which is used in HIV-1 research.
More Information Supplier PageImpurity B of Calcitriol, Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
More Information Supplier PageImpurity B of Calcitriol, Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
More Information Supplier PageImpurity C of Alfacalcidol. Alfacalcidol is a non-selective VDR activator medication.
More Information Supplier PageImpurity C of Alfacalcidol. Alfacalcidol is a non-selective VDR activator medication.
More Information Supplier PageImpurity C of Calcitriol, Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
More Information Supplier PageImpurity C of Calcitriol, Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
More Information Supplier PageImpurity of Calcipotriol, Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
More Information Supplier PageImpurity of Calcipotriol, Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
More Information Supplier PageImpurity of Calcipotriol, Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
More Information Supplier PageInauhzin is a potent SIRT inhibitor, which effectively reactivates p53 by inhibiting SIRT1 activity, promotes p53-dependent apoptosis of human cancer cells without causing apparently genotoxic stress.
More Information Supplier PageInauhzin is a potent SIRT inhibitor, which effectively reactivates p53 by inhibiting SIRT1 activity, promotes p53-dependent apoptosis of human cancer cells without causing apparently genotoxic stress.
More Information Supplier PageInauhzin is a potent SIRT inhibitor, which effectively reactivates p53 by inhibiting SIRT1 activity, promotes p53-dependent apoptosis of human cancer cells without causing apparently genotoxic stress.
More Information Supplier PageInauhzin is a potent SIRT inhibitor, which effectively reactivates p53 by inhibiting SIRT1 activity, promotes p53-dependent apoptosis of human cancer cells without causing apparently genotoxic stress.
More Information Supplier PageINCA-6 is a potent and selective inhibitor of calcineurin-NFAT (Nuclear Factor of Activated T cells) signaling.
More Information Supplier PageINCA-6 is a potent and selective inhibitor of calcineurin-NFAT (Nuclear Factor of Activated T cells) signaling.
More Information Supplier PageINCB 3284 dimesylate is a potent, selective hCCR2 antagonist that exhibits potenct antagonism against monocyte chemoattractant molecule binding to hCCR2 and chemotaxis activity.
More Information Supplier PageINCB 3284 dimesylate is a potent, selective hCCR2 antagonist that exhibits potenct antagonism against monocyte chemoattractant molecule binding to hCCR2 and chemotaxis activity.
More Information Supplier PageINCB 3284 dimesylate is a potent, selective hCCR2 antagonist that exhibits potenct antagonism against monocyte chemoattractant molecule binding to hCCR2 and chemotaxis activity.
More Information Supplier PageINCB 3284 dimesylate is a potent, selective hCCR2 antagonist that exhibits potenct antagonism against monocyte chemoattractant molecule binding to hCCR2 and chemotaxis activity.
More Information Supplier PageINCB018424 is a potent and selective inhibitor of Janus-associated kinase (JAK) 1 and 2, with IC50 to be 2.7, 4.5 and 332 nM for JAK1, JAK2 and JAK3 respectively;
More Information Supplier PageINCB018424 is a potent and selective inhibitor of Janus-associated kinase (JAK) 1 and 2, with IC50 to be 2.7, 4.5 and 332 nM for JAK1, JAK2 and JAK3 respectively;
More Information Supplier PageINCB018424 is a potent and selective inhibitor of Janus-associated kinase (JAK) 1 and 2, with IC50 to be 2.7, 4.5 and 332 nM for JAK1, JAK2 and JAK3 respectively;
More Information Supplier PageINCB018424 is a potent and selective inhibitor of Janus-associated kinase (JAK) 1 and 2, with IC50 to be 2.7, 4.5 and 332 nM for JAK1, JAK2 and JAK3 respectively;
More Information Supplier PageINCB018424 is a potent and selective inhibitor of Janus-associated kinase (JAK) 1 and 2, with IC50 to be 2.7, 4.5 and 332 nM for JAK1, JAK2 and JAK3 respectively;
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