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 WebsiteUNC1215 is a potent, selective antagonist of L3MBTL3 with cellular activity.
More Information Supplier PageUNC1215 is a potent, selective antagonist of L3MBTL3 with cellular activity.
More Information Supplier PageUNC1215 is a potent, selective antagonist of L3MBTL3 with cellular activity.
More Information Supplier PageUNC1215 is a potent, selective antagonist of L3MBTL3 with cellular activity.
More Information Supplier PageUNC569 is a novel small-molecule MER inhibitor with efficacy against acute lymphoblastic leukemia in vitro and in vivo. UNC569 is the first small-molecule Mer inhibitor. UNC569 inhibited Mer activation and downstream signaling through ERK1/2 and AKT.
More Information Supplier PageUNC569 is a novel small-molecule MER inhibitor with efficacy against acute lymphoblastic leukemia in vitro and in vivo. UNC569 is the first small-molecule Mer inhibitor. UNC569 inhibited Mer activation and downstream signaling through ERK1/2 and AKT.
More Information Supplier PageUNC569 is a novel small-molecule MER inhibitor with efficacy against acute lymphoblastic leukemia in vitro and in vivo. UNC569 is the first small-molecule Mer inhibitor. UNC569 inhibited Mer activation and downstream signaling through ERK1/2 and AKT.
More Information Supplier PageUPF 1069 is a selective poly(ADP-ribose) polymerase (PARP) 2 inhibitor (IC50 values are 0.3 and 8.0 ??M for PARP-2 and PARP-1 respectively).
More Information Supplier PageUPF 1069 is a selective poly(ADP-ribose) polymerase (PARP) 2 inhibitor (IC50 values are 0.3 and 8.0 ??M for PARP-2 and PARP-1 respectively).
More Information Supplier PageUPF 1069 is a selective poly(ADP-ribose) polymerase (PARP) 2 inhibitor (IC50 values are 0.3 and 8.0 ??M for PARP-2 and PARP-1 respectively).
More Information Supplier PageUPF 1069 is a selective poly(ADP-ribose) polymerase (PARP) 2 inhibitor (IC50 values are 0.3 and 8.0 ??M for PARP-2 and PARP-1 respectively).
More Information Supplier PageUPF 1069 is a selective poly(ADP-ribose) polymerase (PARP) 2 inhibitor (IC50 values are 0.3 and 8.0 ??M for PARP-2 and PARP-1 respectively).
More Information Supplier PageUR-144 is a potent synthetic cannabinoid (CB) which preferentially binds the peripheral CB2 receptor (Ki = 1.8 nM) over the central CB1 receptor (Ki = 150 nM).
More Information Supplier PageUR-144 is a potent synthetic cannabinoid (CB) which preferentially binds the peripheral CB2 receptor (Ki = 1.8 nM) over the central CB1 receptor (Ki = 150 nM).
More Information Supplier PageUR-144 is a potent synthetic cannabinoid (CB) which preferentially binds the peripheral CB2 receptor (Ki = 1.8 nM) over the central CB1 receptor (Ki = 150 nM).
More Information Supplier PageUR-144 is a potent synthetic cannabinoid (CB) which preferentially binds the peripheral CB2 receptor (Ki = 1.8 nM) over the central CB1 receptor (Ki = 150 nM).
More Information Supplier PageUramustine is a chemotherapy drug which belongs to the class of alkylating agents.
More Information Supplier PageUramustine is a chemotherapy drug which belongs to the class of alkylating agents.
More Information Supplier PageUramustine is a chemotherapy drug which belongs to the class of alkylating agents.
More Information Supplier PageUrapidil hydrochloride is an ??1-adrenoceptor antagonist, 5-HT1A serotonin receptor partial agonist and anti-hypertensive.
More Information Supplier PageUrapidil hydrochloride is an ??1-adrenoceptor antagonist, 5-HT1A serotonin receptor partial agonist and anti-hypertensive.
More Information Supplier PageUrapidil hydrochloride is an ??1-adrenoceptor antagonist, 5-HT1A serotonin receptor partial agonist and anti-hypertensive.
More Information Supplier PageURB597 is a relatively selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH).
More Information Supplier PageURB597 is a relatively selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH).
More Information Supplier PageURB597 is a relatively selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH).
More Information Supplier PageURB597 is a relatively selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH).
More Information Supplier PageURB597 is a relatively selective inhibitor of the enzyme fatty acid amide hydrolase (FAAH).
More Information Supplier PageURB754 was originally reported to be a potent, noncompetitive inhibitor of monoacylglycerol lipase.
More Information Supplier PageURB754 was originally reported to be a potent, noncompetitive inhibitor of monoacylglycerol lipase.
More Information Supplier PageURB754 was originally reported to be a potent, noncompetitive inhibitor of monoacylglycerol lipase.
More Information Supplier PageURMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) inhibitor with IC50 of 19 nM, 42 nM, 14 nM, and 150 nM, for MLK1, MLK2, MLK3, and DLK, respectively.
More Information Supplier PageURMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) inhibitor with IC50 of 19 nM, 42 nM, 14 nM, and 150 nM, for MLK1, MLK2, MLK3, and DLK, respectively.
More Information Supplier PageURMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) inhibitor with IC50 of 19 nM, 42 nM, 14 nM, and 150 nM, for MLK1, MLK2, MLK3, and DLK, respectively.
More Information Supplier PageURMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) inhibitor with IC50 of 19 nM, 42 nM, 14 nM, and 150 nM, for MLK1, MLK2, MLK3, and DLK, respectively.
More Information Supplier PageUrsodeoxycholic acid (UDCS) is a cell protectant used extensively to mitigate hepatic and biliary diseases.
More Information Supplier PageUrsolic acid(Malol) is a pentacyclic triterpene acid, used in cosmetics, that is also capable of inhibiting various types of cancer cells by inhibiting the STAT3 activation pathway and human fibrosarcoma cells by reducing the expression of matrix metalloproteinase-9 by acting through the glucocorticoid receptor.
More Information Supplier PageUrsolic acid(Malol) is a pentacyclic triterpene acid, used in cosmetics, that is also capable of inhibiting various types of cancer cells by inhibiting the STAT3 activation pathway and human fibrosarcoma cells by reducing the expression of matrix metalloproteinase-9 by acting through the glucocorticoid receptor.
More Information Supplier PageUrsolic acid(Malol) is a pentacyclic triterpene acid, used in cosmetics, that is also capable of inhibiting various types of cancer cells by inhibiting the STAT3 activation pathway and human fibrosarcoma cells by reducing the expression of matrix metalloproteinase-9 by acting through the glucocorticoid receptor.
More Information Supplier PageVaccarin, a flavonoid glycoside, is considered one of the major active constituents of Vaccaria segetalis.
More Information Supplier PageVaccarin, a flavonoid glycoside, is considered one of the major active constituents of Vaccaria segetalis.
More Information Supplier PageVaccarin, a flavonoid glycoside, is considered one of the major active constituents of Vaccaria segetalis.
More Information Supplier PageVAL-083 is a bi-functional alkylating agent; inhibit U251 and SF188 cell growth in monolayer better than TMZ and caused apoptosis.
More Information Supplier PageVAL-083 is a bi-functional alkylating agent; inhibit U251 and SF188 cell growth in monolayer better than TMZ and caused apoptosis.
More Information Supplier PageVAL-083 is a bi-functional alkylating agent; inhibit U251 and SF188 cell growth in monolayer better than TMZ and caused apoptosis.
More Information Supplier PageValacyclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B.
More Information Supplier PageValacyclovir is an antiviral drug used in the management of herpes simplex, herpes zoster, and herpes B.
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