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 WebsiteCrotamiton is a drug that is used both as a scabicidal (for treating scabies) and as a general antipruritic (anti-itching drug).
More Information Supplier PageCRT0044876 is a potent and selective APE1 inhibitor with IC50 of ~3 ??M.
More Information Supplier PageCRT0044876 is a potent and selective APE1 inhibitor with IC50 of ~3 ??M.
More Information Supplier PageCRT0044876 is a potent and selective APE1 inhibitor with IC50 of ~3 ??M.
More Information Supplier PageCRT0044876 is a potent and selective APE1 inhibitor with IC50 of ~3 ??M.
More Information Supplier PageCryptotanshinone, a natural compound isolated from the roots of Salvia miltiorrhiza Bunge (Danshen), dramatically blocks STAT3 Tyr705 phosphorylation but not STAT3 Ser727 phosphorylation in DU145 cells, and significantly inhibits JAK2 phosphorylation with IC50 of ~5 ??M without affecting the phosphorylation of upstream kinases c-Src and EGFR.
More Information Supplier PageCryptotanshinone, a natural compound isolated from the roots of Salvia miltiorrhiza Bunge (Danshen), dramatically blocks STAT3 Tyr705 phosphorylation but not STAT3 Ser727 phosphorylation in DU145 cells, and significantly inhibits JAK2 phosphorylation with IC50 of ~5 ??M without affecting the phosphorylation of upstream kinases c-Src and EGFR.
More Information Supplier PageCryptotanshinone, a natural compound isolated from the roots of Salvia miltiorrhiza Bunge (Danshen), dramatically blocks STAT3 Tyr705 phosphorylation but not STAT3 Ser727 phosphorylation in DU145 cells, and significantly inhibits JAK2 phosphorylation with IC50 of ~5 ??M without affecting the phosphorylation of upstream kinases c-Src and EGFR.
More Information Supplier PageCrystal violet is a triarylmethane dye. The dye is used as a histological stain and in Gram??s method of classifying bacteria.
More Information Supplier PageCrystal violet is a triarylmethane dye. The dye is used as a histological stain and in Gram??s method of classifying bacteria.
More Information Supplier PageCrystal violet is a triarylmethane dye. The dye is used as a histological stain and in Gram??s method of classifying bacteria.
More Information Supplier PageCTEP is a highly potent, selective and orally bioavailable allosteric antagonist of mGlu5 receptor with an IC50 of 2.2 nM.
More Information Supplier PageCTEP is a highly potent, selective and orally bioavailable allosteric antagonist of mGlu5 receptor with an IC50 of 2.2 nM.
More Information Supplier PageCTEP is a highly potent, selective and orally bioavailable allosteric antagonist of mGlu5 receptor with an IC50 of 2.2 nM.
More Information Supplier PageCTEP is a highly potent, selective and orally bioavailable allosteric antagonist of mGlu5 receptor with an IC50 of 2.2 nM.
More Information Supplier PageCTS-1027 is a potent MMP inhibitor that protects Against TNF??- and ??-Fas-Induced liver Injury.
More Information Supplier PageCTS-1027 is a potent MMP inhibitor that protects Against TNF??- and ??-Fas-Induced liver Injury.
More Information Supplier PageCTS-1027 is a potent MMP inhibitor that protects Against TNF??- and ??-Fas-Induced liver Injury.
More Information Supplier PageCTS-1027 is a potent MMP inhibitor that protects Against TNF??- and ??-Fas-Induced liver Injury.
More Information Supplier PageCTX-0294885 is a novel broad-spectrum kinase inhibitor. CTx-0294885 exhibits inhibitory activity against a broad range of kinases in vitro.
More Information Supplier PageCTX-0294885 is a novel broad-spectrum kinase inhibitor. CTx-0294885 exhibits inhibitory activity against a broad range of kinases in vitro.
More Information Supplier PageCTX-0294885 is a novel broad-spectrum kinase inhibitor. CTx-0294885 exhibits inhibitory activity against a broad range of kinases in vitro.
More Information Supplier PageCucurbitacin B, a natural triterpenoid is well-known for its strong anticancer activity, and recent studies showed that the compound inhibits JAK/STAT3 pathway.
More Information Supplier PageCucurbitacin B, a natural triterpenoid is well-known for its strong anticancer activity, and recent studies showed that the compound inhibits JAK/STAT3 pathway.
More Information Supplier PageCucurbitacin B, a natural triterpenoid is well-known for its strong anticancer activity, and recent studies showed that the compound inhibits JAK/STAT3 pathway.
More Information Supplier PageCucurbitacin E is a biochemical compound from the family of Cucurbitacins.
More Information Supplier PageCucurbitacin E is a biochemical compound from the family of Cucurbitacins.
More Information Supplier PageCucurbitacin E is a biochemical compound from the family of Cucurbitacins.
More Information Supplier PageCucurbitacin I, Cucumis sativus L. has been found to suppress levels of phosphotyrosine Stat3 (signal transducer and activator of transcription 3) in v-Src-transformed NIH 3T3 cells.
More Information Supplier PageCucurbitacin I, Cucumis sativus L. has been found to suppress levels of phosphotyrosine Stat3 (signal transducer and activator of transcription 3) in v-Src-transformed NIH 3T3 cells.
More Information Supplier PageCucurbitacin I, Cucumis sativus L. has been found to suppress levels of phosphotyrosine Stat3 (signal transducer and activator of transcription 3) in v-Src-transformed NIH 3T3 cells.
More Information Supplier PageCUDC-101 is a novel compound which inhibits multiple targets, which is designed to inhibit HDAC, EGFR and Her2.
More Information Supplier PageCUDC-101 is a novel compound which inhibits multiple targets, which is designed to inhibit HDAC, EGFR and Her2.
More Information Supplier PageCUDC-101 is a novel compound which inhibits multiple targets, which is designed to inhibit HDAC, EGFR and Her2.
More Information Supplier PageCUDC-101 is a novel compound which inhibits multiple targets, which is designed to inhibit HDAC, EGFR and Her2.
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