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 Websiteinhibits p53 binding to mitochondria by reducing its affinity for antiapoptotic proteins Bcl-2 and Bcl-XL.
More Information Supplier Pageinhibits p53 binding to mitochondria by reducing its affinity for antiapoptotic proteins Bcl-2 and Bcl-XL.
More Information Supplier Pageinhibits p53 binding to mitochondria by reducing its affinity for antiapoptotic proteins Bcl-2 and Bcl-XL.
More Information Supplier Pageinhibits p53 binding to mitochondria by reducing its affinity for antiapoptotic proteins Bcl-2 and Bcl-XL.
More Information Supplier Pageinhibits p53 binding to mitochondria by reducing its affinity for antiapoptotic proteins Bcl-2 and Bcl-XL.
More Information Supplier PagePIK-293 is a PI3-K inhibitor. PIK-293 inhibits the p110??, p110??, p110??. PIK-293 is the parent compound of PIK-294.
More Information Supplier PagePIK-293 is a PI3-K inhibitor. PIK-293 inhibits the p110??, p110??, p110??. PIK-293 is the parent compound of PIK-294.
More Information Supplier PagePIK-293 is a PI3-K inhibitor. PIK-293 inhibits the p110??, p110??, p110??. PIK-293 is the parent compound of PIK-294.
More Information Supplier PagePIK-293 is a PI3-K inhibitor. PIK-293 inhibits the p110??, p110??, p110??. PIK-293 is the parent compound of PIK-294.
More Information Supplier PagePIK-293 is a PI3-K inhibitor. PIK-293 inhibits the p110??, p110??, p110??. PIK-293 is the parent compound of PIK-294.
More Information Supplier PagePIK-294 is a PI3 Kinase inhibitor that is 20- to 60-fold more potent than the parent compound, PIK-293. It is one of the most potent p110??-selective inhibitors that has been reported.
More Information Supplier PagePIK-294 is a PI3 Kinase inhibitor that is 20- to 60-fold more potent than the parent compound, PIK-293. It is one of the most potent p110??-selective inhibitors that has been reported.
More Information Supplier PagePIK-294 is a PI3 Kinase inhibitor that is 20- to 60-fold more potent than the parent compound, PIK-293. It is one of the most potent p110??-selective inhibitors that has been reported.
More Information Supplier PagePIK-294 is a PI3 Kinase inhibitor that is 20- to 60-fold more potent than the parent compound, PIK-293. It is one of the most potent p110??-selective inhibitors that has been reported.
More Information Supplier PagePIK-294 is a PI3 Kinase inhibitor that is 20- to 60-fold more potent than the parent compound, PIK-293. It is one of the most potent p110??-selective inhibitors that has been reported.
More Information Supplier PagePIK-75 is an imidazopyridine that selectively inhibits p110?? with an IC50 value of 5.8 nM.2 It inhibits p110?? and p110?? considerably less effectively with IC50 values of 0.076 ??M and 1.3 ??M, respectively.
More Information Supplier PagePIK-75 is an imidazopyridine that selectively inhibits p110?? with an IC50 value of 5.8 nM.2 It inhibits p110?? and p110?? considerably less effectively with IC50 values of 0.076 ??M and 1.3 ??M, respectively.
More Information Supplier PagePIK-75 is an imidazopyridine that selectively inhibits p110?? with an IC50 value of 5.8 nM.2 It inhibits p110?? and p110?? considerably less effectively with IC50 values of 0.076 ??M and 1.3 ??M, respectively.
More Information Supplier PagePIK-75 is an imidazopyridine that selectively inhibits p110?? with an IC50 value of 5.8 nM.2 It inhibits p110?? and p110?? considerably less effectively with IC50 values of 0.076 ??M and 1.3 ??M, respectively.
More Information Supplier PagePIK-90 is a synthetic phosphoinositide 3-kinase (PI3K) inhibitor with IC50 values (nM) of 11, 350, 18, and 58 for p110 ??, ??, ?? and ?? isoforms, low mTOR activity.
More Information Supplier PagePIK-90 is a synthetic phosphoinositide 3-kinase (PI3K) inhibitor with IC50 values (nM) of 11, 350, 18, and 58 for p110 ??, ??, ?? and ?? isoforms, low mTOR activity.
More Information Supplier PagePIK-90 is a synthetic phosphoinositide 3-kinase (PI3K) inhibitor with IC50 values (nM) of 11, 350, 18, and 58 for p110 ??, ??, ?? and ?? isoforms, low mTOR activity.
More Information Supplier PagePIK-90 is a synthetic phosphoinositide 3-kinase (PI3K) inhibitor with IC50 values (nM) of 11, 350, 18, and 58 for p110 ??, ??, ?? and ?? isoforms, low mTOR activity.
More Information Supplier PagePIK 93 selectively inhibits the type III PI 4-kinase enzyme, and small interfering RNA-mediated down-regulation of the individual PI 4-kinase enzymes.
More Information Supplier PagePIK 93 selectively inhibits the type III PI 4-kinase enzyme, and small interfering RNA-mediated down-regulation of the individual PI 4-kinase enzymes.
More Information Supplier PagePIK 93 selectively inhibits the type III PI 4-kinase enzyme, and small interfering RNA-mediated down-regulation of the individual PI 4-kinase enzymes.
More Information Supplier PagePIK 93 selectively inhibits the type III PI 4-kinase enzyme, and small interfering RNA-mediated down-regulation of the individual PI 4-kinase enzymes.
More Information Supplier PagePIK 93 selectively inhibits the type III PI 4-kinase enzyme, and small interfering RNA-mediated down-regulation of the individual PI 4-kinase enzymes.
More Information Supplier PagePimecrolimus is a natural ascomycin macrolactam that binds to macrophilin-12 (FKBP-12) and inhibits calcineurin as well as prolyl isomerase (rotamase).
More Information Supplier PagePimecrolimus is a natural ascomycin macrolactam that binds to macrophilin-12 (FKBP-12) and inhibits calcineurin as well as prolyl isomerase (rotamase).
More Information Supplier PagePimecrolimus is a natural ascomycin macrolactam that binds to macrophilin-12 (FKBP-12) and inhibits calcineurin as well as prolyl isomerase (rotamase).
More Information Supplier PagePimecrolimus is a natural ascomycin macrolactam that binds to macrophilin-12 (FKBP-12) and inhibits calcineurin as well as prolyl isomerase (rotamase).
More Information Supplier PagePimobendan (Vetmedin) is a calcium sensitizer with positive inotropic and vasodilator effects. It is also a selective inhibitor of phosphodiesterase III (PDE3).
More Information Supplier PagePimobendan (Vetmedin) is a calcium sensitizer with positive inotropic and vasodilator effects. It is also a selective inhibitor of phosphodiesterase III (PDE3).
More Information Supplier PagePimobendan (Vetmedin) is a calcium sensitizer with positive inotropic and vasodilator effects. It is also a selective inhibitor of phosphodiesterase III (PDE3).
More Information Supplier PagePimobendan (Vetmedin) is a calcium sensitizer with positive inotropic and vasodilator effects. It is also a selective inhibitor of phosphodiesterase III (PDE3).
More Information Supplier PagePimobendan (Vetmedin) is a calcium sensitizer with positive inotropic and vasodilator effects. It is also a selective inhibitor of phosphodiesterase III (PDE3).
More Information Supplier PagePinaverium Bromide is a spasmolytic agent with low incidence of anticholinergic effects. Pinaverium Bromide is also an antispasmodic.
More Information Supplier PagePinaverium Bromide is a spasmolytic agent with low incidence of anticholinergic effects. Pinaverium Bromide is also an antispasmodic.
More Information Supplier PagePinaverium Bromide is a spasmolytic agent with low incidence of anticholinergic effects. Pinaverium Bromide is also an antispasmodic.
More Information Supplier PagePinaverium Bromide is a spasmolytic agent with low incidence of anticholinergic effects. Pinaverium Bromide is also an antispasmodic.
More Information Supplier PagePindolol is a nonselective beta blocker with partial beta-adrenergic receptor agonist activity.
More Information Supplier PagePindolol is a nonselective beta blocker with partial beta-adrenergic receptor agonist activity.
More Information Supplier PagePindolol is a nonselective beta blocker with partial beta-adrenergic receptor agonist activity.
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