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 WebsiteCabazitaxel is a semi-synthetic derivative of a natural taxoid. Cabazitaxel in combination with prednisone is a treatment option for hormone-refractory prostate cancer following docetaxel-based treatment
More Information Supplier PageCabazitaxel is a semi-synthetic derivative of a natural taxoid. Cabazitaxel in combination with prednisone is a treatment option for hormone-refractory prostate cancer following docetaxel-based treatment
More Information Supplier PageCabazitaxel is a semi-synthetic derivative of a natural taxoid. Cabazitaxel in combination with prednisone is a treatment option for hormone-refractory prostate cancer following docetaxel-based treatment
More Information Supplier PageCabergoline, a lysergic acid amide derivative, is a potent dopamine D2 receptor agonist.
More Information Supplier PageCabergoline, a lysergic acid amide derivative, is a potent dopamine D2 receptor agonist.
More Information Supplier PageCabergoline, a lysergic acid amide derivative, is a potent dopamine D2 receptor agonist.
More Information Supplier PageCabergoline, a lysergic acid amide derivative, is a potent dopamine D2 receptor agonist.
More Information Supplier PageCaCCinh-A01 inhibits CaCC currents in human bronchial and intestinal cells. Also inhibits TMEM16A channels (IC50 = 2.1 ??M, in TMEM16A-expressing FRT cells).
More Information Supplier PageCaCCinh-A01 inhibits CaCC currents in human bronchial and intestinal cells. Also inhibits TMEM16A channels (IC50 = 2.1 ??M, in TMEM16A-expressing FRT cells).
More Information Supplier PageCaCCinh-A01 inhibits CaCC currents in human bronchial and intestinal cells. Also inhibits TMEM16A channels (IC50 = 2.1 ??M, in TMEM16A-expressing FRT cells).
More Information Supplier PageCadherin Peptide, avian, is a class of type-1 transmembrane proteins.
More Information Supplier PageCadherin Peptide, avian, is a class of type-1 transmembrane proteins.
More Information Supplier PageCadherin Peptide, avian, is a class of type-1 transmembrane proteins.
More Information Supplier PageCaffeic acid is an organic compound that is classified as hydroxycinnamic acid.
More Information Supplier PageCaffeic acid is an organic compound that is classified as hydroxycinnamic acid.
More Information Supplier PageCaffeic acid phenethyl ester is a potent and specific inhibitor of NF-??B activation
More Information Supplier PageCaffeic acid phenethyl ester is a potent and specific inhibitor of NF-??B activation
More Information Supplier PageCaffeic acid phenethyl ester is a potent and specific inhibitor of NF-??B activation
More Information Supplier PageCaftaric acid is a non-flavanoid that impacts the color of white wine.
More Information Supplier PageCaftaric acid is a non-flavanoid that impacts the color of white wine.
More Information Supplier PageCaftaric acid is a non-flavanoid that impacts the color of white wine.
More Information Supplier PageCaftaric acid is a non-flavanoid that impacts the color of white wine.
More Information Supplier PageCAL-101 is an isoform-selective inhibitor of PI3K that induces apoptosis of chronic lymphocytic leukemia (CLL) cells.
More Information Supplier PageCAL-101 is an isoform-selective inhibitor of PI3K that induces apoptosis of chronic lymphocytic leukemia (CLL) cells.
More Information Supplier PageCAL-101 is an isoform-selective inhibitor of PI3K that induces apoptosis of chronic lymphocytic leukemia (CLL) cells.
More Information Supplier PageCAL-101 is an isoform-selective inhibitor of PI3K that induces apoptosis of chronic lymphocytic leukemia (CLL) cells.
More Information Supplier PageCAL-101 is an isoform-selective inhibitor of PI3K that induces apoptosis of chronic lymphocytic leukemia (CLL) cells.
More Information Supplier PageCAL-130 is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported that combined inhibition of PI3K??/?? as therapy for T cell acute lymphoblastic leukemia (T-ALL).
More Information Supplier PageCAL-130 is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported that combined inhibition of PI3K??/?? as therapy for T cell acute lymphoblastic leukemia (T-ALL).
More Information Supplier PageCAL-130 is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported that combined inhibition of PI3K??/?? as therapy for T cell acute lymphoblastic leukemia (T-ALL).
More Information Supplier PageCAL-130 Hydrochloride is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported that combined inhibition of PI3K??/?? as therapy for T cell acute lymphoblastic leukemia (T-ALL).
More Information Supplier PageCAL-130 Hydrochloride is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported that combined inhibition of PI3K??/?? as therapy for T cell acute lymphoblastic leukemia (T-ALL).
More Information Supplier PageCAL-130 Hydrochloride is a novel phosphoinositide 3-kinase (PI3K) inhibitor. It is reported that combined inhibition of PI3K??/?? as therapy for T cell acute lymphoblastic leukemia (T-ALL).
More Information Supplier PageCalcifediol is a major circulating metabolite of vitamin D3 and acts as a competitive inhibitor with an apparent Ki of 3.9 ??M. It also suppresses PTH secretion and mRNA (ED50=2 nM)
More Information Supplier PageCalcifediol is a major circulating metabolite of vitamin D3 and acts as a competitive inhibitor with an apparent Ki of 3.9 ??M. It also suppresses PTH secretion and mRNA (ED50=2 nM)
More Information Supplier PageCalcifediol is a major circulating metabolite of vitamin D3 and acts as a competitive inhibitor with an apparent Ki of 3.9 ??M. It also suppresses PTH secretion and mRNA (ED50=2 nM)
More Information Supplier PageCalcifediol is a major circulating metabolite of vitamin D3 and acts as a competitive inhibitor with an apparent Ki of 3.9 ??M. It also suppresses PTH secretion and mRNA (ED50=2 nM)
More Information Supplier PageCalcifediol is a major circulating metabolite of vitamin D3 and acts as a competitive inhibitor with an apparent Ki of 3.9 ??M. It also suppresses PTH secretion and mRNA (ED50=2 nM)
More Information Supplier PageCalcifediol monohydrate(25-hydroxy Vitamin D3) is a prehormone that is produced in the liver by hydroxylation of vitamin D3 (cholecalciferol) by the enzyme cholecalciferol 25-hydroxylase.
More Information Supplier PageCalcifediol monohydrate(25-hydroxy Vitamin D3) is a prehormone that is produced in the liver by hydroxylation of vitamin D3 (cholecalciferol) by the enzyme cholecalciferol 25-hydroxylase.
More Information Supplier PageCalcifediol monohydrate(25-hydroxy Vitamin D3) is a prehormone that is produced in the liver by hydroxylation of vitamin D3 (cholecalciferol) by the enzyme cholecalciferol 25-hydroxylase.
More Information Supplier PageCalcineurin inhibitory peptide is a selective inhibitor of Ca2+-calmodulin-dependent protein phosphatase (calcineurin) (IC50 ~ 10 ??M). Does not inhibit PP1, PP2A or CaM kinase II (IC50 > 100 mM).
More Information Supplier PageCalcineurin inhibitory peptide is a selective inhibitor of Ca2+-calmodulin-dependent protein phosphatase (calcineurin) (IC50 ~ 10 ??M). Does not inhibit PP1, PP2A or CaM kinase II (IC50 > 100 mM).
More Information Supplier PageCalcipotriol hydrate is the hydrate form of vitamin D3 that displays minimal effects on calcium homeostasis.
More Information Supplier PageCalcipotriol hydrate is the hydrate form of vitamin D3 that displays minimal effects on calcium homeostasis.
More Information Supplier PageCalcipotriol hydrate is the hydrate form of vitamin D3 that displays minimal effects on calcium homeostasis.
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