Adooq Bioscience

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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.

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SB 743921 50mg 50mg  | Purity Not Available

Adooq Bioscience

SB 743921, a second generation KSP inhibitor, is a highly potent and active therapeutic in preclinical models of cancer.

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SB 743921 5mg 5mg  | Purity Not Available

Adooq Bioscience

SB 743921, a second generation KSP inhibitor, is a highly potent and active therapeutic in preclinical models of cancer.

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SB-222200 100mg 100mg  | Purity Not Available

Adooq Bioscience

SB 222200 is a selective, reversible and competitive antagonist of human NK-3 receptor(Ki=4.4 nM) that effectively crosses the blood-brain barrier.

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SB-222200 10mg 10mg  | Purity Not Available

Adooq Bioscience

SB 222200 is a selective, reversible and competitive antagonist of human NK-3 receptor(Ki=4.4 nM) that effectively crosses the blood-brain barrier.

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SB-222200 50mg 50mg  | Purity Not Available

Adooq Bioscience

SB 222200 is a selective, reversible and competitive antagonist of human NK-3 receptor(Ki=4.4 nM) that effectively crosses the blood-brain barrier.

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SB-242235 10mg 10mg  | Purity Not Available

Adooq Bioscience

SB-242235 is a potent and selective p38 MAP kinase inhibitor that may be an effective therapy for cytokine-mediated diseases such as autoimmune or inflammatory diseases.

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SB-242235 25mg 25mg  | Purity Not Available

Adooq Bioscience

SB-242235 is a potent and selective p38 MAP kinase inhibitor that may be an effective therapy for cytokine-mediated diseases such as autoimmune or inflammatory diseases.

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SB-242235 5mg 5mg  | Purity Not Available

Adooq Bioscience

SB-242235 is a potent and selective p38 MAP kinase inhibitor that may be an effective therapy for cytokine-mediated diseases such as autoimmune or inflammatory diseases.

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SB-277011 10mg 10mg  | Purity Not Available

Adooq Bioscience

SB-277011 is a drug which acts as a potent and selective dopamine D3 receptor antagonist which is around 80-100x selective for D3 over D2 and lacks any partial agonist activity.

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SB-277011 25mg 25mg  | Purity Not Available

Adooq Bioscience

SB-277011 is a drug which acts as a potent and selective dopamine D3 receptor antagonist which is around 80-100x selective for D3 over D2 and lacks any partial agonist activity.

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SB-277011 50mg 50mg  | Purity Not Available

Adooq Bioscience

SB-277011 is a drug which acts as a potent and selective dopamine D3 receptor antagonist which is around 80-100x selective for D3 over D2 and lacks any partial agonist activity.

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SB-277011 5mg 5mg  | Purity Not Available

Adooq Bioscience

SB-277011 is a drug which acts as a potent and selective dopamine D3 receptor antagonist which is around 80-100x selective for D3 over D2 and lacks any partial agonist activity.

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SB-3CT 10mg 10mg  | Purity Not Available

Adooq Bioscience

SB-3CT is an effective and selective gelatinase inhibitor with Ki of 13.9 nM and 600 nM for MMP-2 and MMP-9.

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SB-3CT 25mg 25mg  | Purity Not Available

Adooq Bioscience

SB-3CT is an effective and selective gelatinase inhibitor with Ki of 13.9 nM and 600 nM for MMP-2 and MMP-9.

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SB-3CT 5mg 5mg  | Purity Not Available

Adooq Bioscience

SB-3CT is an effective and selective gelatinase inhibitor with Ki of 13.9 nM and 600 nM for MMP-2 and MMP-9.

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SB-408124 100mg 100mg  | Purity Not Available

Adooq Bioscience

SB-408124 is a selective non-peptide orexin OX1 receptor antagonist (Kb values are 21.7 and 1405 nM for human OX1 and OX2 receptors respectively). Blocks orexin-A induced grooming following oral administration in vivo.

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SB-408124 10mg 10mg  | Purity Not Available

Adooq Bioscience

SB-408124 is a selective non-peptide orexin OX1 receptor antagonist (Kb values are 21.7 and 1405 nM for human OX1 and OX2 receptors respectively). Blocks orexin-A induced grooming following oral administration in vivo.

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SB-408124 10mM * 1mL in DMSO 10mM * 1mL in DMSO  | Purity Not Available

Adooq Bioscience

SB-408124 is a selective non-peptide orexin OX1 receptor antagonist (Kb values are 21.7 and 1405 nM for human OX1 and OX2 receptors respectively). Blocks orexin-A induced grooming following oral administration in vivo.

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SB-408124 25mg 25mg  | Purity Not Available

Adooq Bioscience

SB-408124 is a selective non-peptide orexin OX1 receptor antagonist (Kb values are 21.7 and 1405 nM for human OX1 and OX2 receptors respectively). Blocks orexin-A induced grooming following oral administration in vivo.

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SB-408124 50mg 50mg  | Purity Not Available

Adooq Bioscience

SB-408124 is a selective non-peptide orexin OX1 receptor antagonist (Kb values are 21.7 and 1405 nM for human OX1 and OX2 receptors respectively). Blocks orexin-A induced grooming following oral administration in vivo.

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SB-408124 Hydrochloride 100mg 100mg  | Purity Not Available

Adooq Bioscience

SB408124 Hcl is a non-peptide antagonist for OX1 receptor with Ki of 57 nM and 27 nM in both whole cell and membrane, respectively; exhibits 50-fold selectivity over OX2 receptor.

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SB-408124 Hydrochloride 250mg 250mg  | Purity Not Available

Adooq Bioscience

SB408124 Hcl is a non-peptide antagonist for OX1 receptor with Ki of 57 nM and 27 nM in both whole cell and membrane, respectively; exhibits 50-fold selectivity over OX2 receptor.

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SB-505124 100mg 100mg  | Purity Not Available

Adooq Bioscience

SB-505124 is a selective inhibitor of transforming growth factor-?? type I receptor (ALK5), ALK4 and ALK7 (IC50 values are 47 and 129 nM for ALK5 and ALK4 respectively).

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SB-505124 10mM * 1mL in DMSO 10mM * 1mL in DMSO  | Purity Not Available

Adooq Bioscience

SB-505124 is a selective inhibitor of transforming growth factor-?? type I receptor (ALK5), ALK4 and ALK7 (IC50 values are 47 and 129 nM for ALK5 and ALK4 respectively).

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SB-505124 25mg 25mg  | Purity Not Available

Adooq Bioscience

SB-505124 is a selective inhibitor of transforming growth factor-?? type I receptor (ALK5), ALK4 and ALK7 (IC50 values are 47 and 129 nM for ALK5 and ALK4 respectively).

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SB-505124 50mg 50mg  | Purity Not Available

Adooq Bioscience

SB-505124 is a selective inhibitor of transforming growth factor-?? type I receptor (ALK5), ALK4 and ALK7 (IC50 values are 47 and 129 nM for ALK5 and ALK4 respectively).

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SB-505124 5mg 5mg  | Purity Not Available

Adooq Bioscience

SB-505124 is a selective inhibitor of transforming growth factor-?? type I receptor (ALK5), ALK4 and ALK7 (IC50 values are 47 and 129 nM for ALK5 and ALK4 respectively).

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SB-674042 10mg 10mg  | Purity Not Available

Adooq Bioscience

SB-674042 is a potent and selective non-peptide orexin OX1 receptor antagonist (Kd = 3.76 nM); exhibits 100-fold selectivity for OX1 over OX2 receptors.

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SB-674042 50mg 50mg  | Purity Not Available

Adooq Bioscience

SB-674042 is a potent and selective non-peptide orexin OX1 receptor antagonist (Kd = 3.76 nM); exhibits 100-fold selectivity for OX1 over OX2 receptors.

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SB-674042 5mg 5mg  | Purity Not Available

Adooq Bioscience

SB-674042 is a potent and selective non-peptide orexin OX1 receptor antagonist (Kd = 3.76 nM); exhibits 100-fold selectivity for OX1 over OX2 receptors.

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SB-742457 10mg 10mg  | Purity Not Available

Adooq Bioscience

SB-742457 is a selective 5-HT6 receptor antagonist with cognition, memory, and learning-enhancing effects.

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SB-742457 25mg 25mg  | Purity Not Available

Adooq Bioscience

SB-742457 is a selective 5-HT6 receptor antagonist with cognition, memory, and learning-enhancing effects.

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SB-742457 5mg 5mg  | Purity Not Available

Adooq Bioscience

SB-742457 is a selective 5-HT6 receptor antagonist with cognition, memory, and learning-enhancing effects.

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SB225002 10mg 10mg  | Purity Not Available

Adooq Bioscience

SB225002 is a potent, and selective CXCR2 antagonist with IC50 of 22 nM for inhibiting interleukin IL-8 binding to CXCR2, > 150-fold selectivity over the other 7-TMRs tested.

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SB225002 10mM * 1mL in DMSO 10mM * 1mL in DMSO  | Purity Not Available

Adooq Bioscience

SB225002 is a potent, and selective CXCR2 antagonist with IC50 of 22 nM for inhibiting interleukin IL-8 binding to CXCR2, > 150-fold selectivity over the other 7-TMRs tested.

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