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 WebsiteAngiotensin 1/2 (1-5) is a peptide that contains the amino acids 1-5 and is converted from Angiotensin I/II.
More Information Supplier PageAngiotensin 1/2 (1-6) is a peptide that contains the amino acids 1-6 and is converted from Angiotensin I/II peptide.
More Information Supplier PageAngiotensin 1/2 (1-6) is a peptide that contains the amino acids 1-6 and is converted from Angiotensin I/II peptide.
More Information Supplier PageAngiotensin 1/2 (1-6) is a peptide that contains the amino acids 1-6 and is converted from Angiotensin I/II peptide.
More Information Supplier PageAngiotensin 1/2 (1-9) is a peptide (ASP-ARG-VAL-TYR-ILE-HIS-PRO-PHE-HIS) containing the amino acids 1-9 that are converted from Angiotensin I/II peptide.
More Information Supplier PageAngiotensin 1/2 (1-9) is a peptide (ASP-ARG-VAL-TYR-ILE-HIS-PRO-PHE-HIS) containing the amino acids 1-9 that are converted from Angiotensin I/II peptide.
More Information Supplier PageAngiotensin 1/2 (1-9) is a peptide (ASP-ARG-VAL-TYR-ILE-HIS-PRO-PHE-HIS) containing the amino acids 1-9 that are converted from Angiotensin I/II peptide.
More Information Supplier PageAngiotensin 1/2 + A (2 – 8), potent endogenous vasoconstrictor peptide; derivative of angiotensin (Ang) II.
More Information Supplier PageAngiotensin 1/2 + A (2 – 8), potent endogenous vasoconstrictor peptide; derivative of angiotensin (Ang) II.
More Information Supplier PageAngiotensin 1/2 + A (2 – 8), potent endogenous vasoconstrictor peptide; derivative of angiotensin (Ang) II.
More Information Supplier PageAngiotensin II (Ang II) is an octapeptide hormone that plays a central role in cardiovascular homeostasis.
More Information Supplier PageAngiotensin II (Ang II) is an octapeptide hormone that plays a central role in cardiovascular homeostasis.
More Information Supplier PageAngiotensin II (Ang II) is an octapeptide hormone that plays a central role in cardiovascular homeostasis.
More Information Supplier PageAngiotensin III is a hexapeptide formed as a result of a cleavage at the N-terminus of Angiotensin II, a key factor in the Renin-Angiotensin-Aldosterone (RAAS) system by angiotensinases located in red blood cells and the vascular beds of most tissues.
More Information Supplier PageAngiotensin III is a hexapeptide formed as a result of a cleavage at the N-terminus of Angiotensin II, a key factor in the Renin-Angiotensin-Aldosterone (RAAS) system by angiotensinases located in red blood cells and the vascular beds of most tissues.
More Information Supplier PageAngiotensin III is a hexapeptide formed as a result of a cleavage at the N-terminus of Angiotensin II, a key factor in the Renin-Angiotensin-Aldosterone (RAAS) system by angiotensinases located in red blood cells and the vascular beds of most tissues.
More Information Supplier PageAnguizole is a small molecule inhibits HCV replication and alters NS4B’s subcellular distribution.
More Information Supplier PageAnguizole is a small molecule inhibits HCV replication and alters NS4B’s subcellular distribution.
More Information Supplier PageAnguizole is a small molecule inhibits HCV replication and alters NS4B’s subcellular distribution.
More Information Supplier PageAnguizole is a small molecule inhibits HCV replication and alters NS4B’s subcellular distribution.
More Information Supplier PageAnidulafungin is a semi-synthetic cyclic lipopeptide belonging to the echinocandin class that was reported in 1995 and commercially developed by Eli Lilly. Anidulafungin inhibits the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi and is extensively referenced in the literature with over 400 citations.
More Information Supplier PageAnidulafungin is a semi-synthetic cyclic lipopeptide belonging to the echinocandin class that was reported in 1995 and commercially developed by Eli Lilly. Anidulafungin inhibits the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi and is extensively referenced in the literature with over 400 citations.
More Information Supplier PageAnidulafungin is a semi-synthetic cyclic lipopeptide belonging to the echinocandin class that was reported in 1995 and commercially developed by Eli Lilly. Anidulafungin inhibits the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi and is extensively referenced in the literature with over 400 citations.
More Information Supplier PageAnidulafungin is a semi-synthetic cyclic lipopeptide belonging to the echinocandin class that was reported in 1995 and commercially developed by Eli Lilly. Anidulafungin inhibits the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi and is extensively referenced in the literature with over 400 citations.
More Information Supplier PageAniracetam is an ampakine and nootropic of the racetam chemical class purported to be considerably more potent than piracetam.
More Information Supplier PageAniracetam is an ampakine and nootropic of the racetam chemical class purported to be considerably more potent than piracetam.
More Information Supplier PageAniracetam is an ampakine and nootropic of the racetam chemical class purported to be considerably more potent than piracetam.
More Information Supplier PageAniracetam is an ampakine and nootropic of the racetam chemical class purported to be considerably more potent than piracetam.
More Information Supplier PageAnisole methoxybenzene is a colorless liquid with a smell reminiscent of anise seed, and in fact many of its derivatives are found in natural and artificial fragrances.
More Information Supplier PageAnisole methoxybenzene is a colorless liquid with a smell reminiscent of anise seed, and in fact many of its derivatives are found in natural and artificial fragrances.
More Information Supplier PageAnsamitocin P-3 is a maytansine analog which displays potent cytotoxicity against the human solid tumor cell lines A-549 and HT-29.
More Information Supplier PageAnsamitocin P-3 is a maytansine analog which displays potent cytotoxicity against the human solid tumor cell lines A-549 and HT-29.
More Information Supplier PageAnsamitocin P-3 is a maytansine analog which displays potent cytotoxicity against the human solid tumor cell lines A-549 and HT-29.
More Information Supplier PageAnsamitocin P-3 is a maytansine analog which displays potent cytotoxicity against the human solid tumor cell lines A-549 and HT-29.
More Information Supplier PageAnti-Inflammatory Peptide 1, belongs to the group of synthetic oligopeptides corresponding to a region of high amino-acid sequence similarity between uteroglobin and lipocortin I.
More Information Supplier PageAnti-Inflammatory Peptide 1, belongs to the group of synthetic oligopeptides corresponding to a region of high amino-acid sequence similarity between uteroglobin and lipocortin I.
More Information Supplier PageAnti-Inflammatory Peptide 1, belongs to the group of synthetic oligopeptides corresponding to a region of high amino-acid sequence similarity between uteroglobin and lipocortin I.
More Information Supplier PageANX-510 is a folate-based biomodulator with potential antineoplastic activity. 5,10-methylenetetrahydrofolate (MTHF) stabilizes the covalent binding of the fluorouracil metabolite 5-5-fluoro-2′-deoxyuridine-5′-O-monophosphate (FdUMP) to its target enzyme, thymidylate synthase, which results in inhibition of thymidylate synthase, depletion of thymidine triphosphate (TTP), a necessary constituent of DNA, and tumor cell death. Unlike leucovorin, MTHF, as the active form […]
More Information Supplier PageANX-510 is a folate-based biomodulator with potential antineoplastic activity. 5,10-methylenetetrahydrofolate (MTHF) stabilizes the covalent binding of the fluorouracil metabolite 5-5-fluoro-2′-deoxyuridine-5′-O-monophosphate (FdUMP) to its target enzyme, thymidylate synthase, which results in inhibition of thymidylate synthase, depletion of thymidine triphosphate (TTP), a necessary constituent of DNA, and tumor cell death. Unlike leucovorin, MTHF, as the active form […]
More Information Supplier PageANX-510 is a folate-based biomodulator with potential antineoplastic activity. 5,10-methylenetetrahydrofolate (MTHF) stabilizes the covalent binding of the fluorouracil metabolite 5-5-fluoro-2′-deoxyuridine-5′-O-monophosphate (FdUMP) to its target enzyme, thymidylate synthase, which results in inhibition of thymidylate synthase, depletion of thymidine triphosphate (TTP), a necessary constituent of DNA, and tumor cell death. Unlike leucovorin, MTHF, as the active form […]
More Information Supplier PageANX-510 is a folate-based biomodulator with potential antineoplastic activity. 5,10-methylenetetrahydrofolate (MTHF) stabilizes the covalent binding of the fluorouracil metabolite 5-5-fluoro-2′-deoxyuridine-5′-O-monophosphate (FdUMP) to its target enzyme, thymidylate synthase, which results in inhibition of thymidylate synthase, depletion of thymidine triphosphate (TTP), a necessary constituent of DNA, and tumor cell death. Unlike leucovorin, MTHF, as the active form […]
More Information Supplier PageAP1903 is a lipid-permeable tacrolimus analogue with homodimerizing activity. Dimerizer drug AP1903 homodimerizes an analogue of human protein FKBP12 (Fv) which contains a single acid substitution (Phe36Val) so that AP1903 binds to wild-type FKBP12 with 1000-fold lower affinity.
More Information Supplier PageAP1903 is a lipid-permeable tacrolimus analogue with homodimerizing activity. Dimerizer drug AP1903 homodimerizes an analogue of human protein FKBP12 (Fv) which contains a single acid substitution (Phe36Val) so that AP1903 binds to wild-type FKBP12 with 1000-fold lower affinity.
More Information Supplier PageAP1903 is a lipid-permeable tacrolimus analogue with homodimerizing activity. Dimerizer drug AP1903 homodimerizes an analogue of human protein FKBP12 (Fv) which contains a single acid substitution (Phe36Val) so that AP1903 binds to wild-type FKBP12 with 1000-fold lower affinity.
More Information Supplier PageAP24534 (Ponatinib) is a potent multi-kinase and pan-BCR-ABL inhibitor.
More Information Supplier PageAP24534 (Ponatinib) is a potent multi-kinase and pan-BCR-ABL inhibitor.
More Information Supplier PageAP24534 (Ponatinib) is a potent multi-kinase and pan-BCR-ABL inhibitor.
More Information Supplier PageAP24534 (Ponatinib) is a potent multi-kinase and pan-BCR-ABL inhibitor.
More Information Supplier PageAP24534 (Ponatinib) is a potent multi-kinase and pan-BCR-ABL inhibitor.
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