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 WebsiteAnacetrapib (MK-0859) is a CETP inhibitor being developed to treat hypercholesterolemia (elevated cholesterol levels) and prevent cardiovascular disease.
More Information Supplier PageAnacetrapib (MK-0859) is a CETP inhibitor being developed to treat hypercholesterolemia (elevated cholesterol levels) and prevent cardiovascular disease.
More Information Supplier PageAnacetrapib (MK-0859) is a CETP inhibitor being developed to treat hypercholesterolemia (elevated cholesterol levels) and prevent cardiovascular disease.
More Information Supplier PageAnacetrapib (MK-0859) is a CETP inhibitor being developed to treat hypercholesterolemia (elevated cholesterol levels) and prevent cardiovascular disease.
More Information Supplier PageAnagliptin is a pharmaceutical drug for the treatment of type 2 diabetes mellitus.
More Information Supplier PageAnagliptin is a pharmaceutical drug for the treatment of type 2 diabetes mellitus.
More Information Supplier PageAnagliptin is a pharmaceutical drug for the treatment of type 2 diabetes mellitus.
More Information Supplier PageAnamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin fumarate is a synthetic orally active ghrelin receptor agonist which is under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin fumarate is a synthetic orally active ghrelin receptor agonist which is under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin fumarate is a synthetic orally active ghrelin receptor agonist which is under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnamorelin is currently under development for the management of non-small lung cancer associated cachexia/anorexia.
More Information Supplier PageAnastrozole binds reversibly to the aromatase enzyme through competitive inhibition, inhibits the conversion of androgens to estrogens in peripheral tissues (outside the CNS), and a few CNS sites in various regions within the brain. The severity of breast cancer is increased by estrogen, as sex hormones cause hyperplasia, and differentiation at estrogen receptor sites. Anastrozole […]
More Information Supplier PageAnastrozole binds reversibly to the aromatase enzyme through competitive inhibition, inhibits the conversion of androgens to estrogens in peripheral tissues (outside the CNS), and a few CNS sites in various regions within the brain. The severity of breast cancer is increased by estrogen, as sex hormones cause hyperplasia, and differentiation at estrogen receptor sites. Anastrozole […]
More Information Supplier PageAnastrozole binds reversibly to the aromatase enzyme through competitive inhibition, inhibits the conversion of androgens to estrogens in peripheral tissues (outside the CNS), and a few CNS sites in various regions within the brain. The severity of breast cancer is increased by estrogen, as sex hormones cause hyperplasia, and differentiation at estrogen receptor sites. Anastrozole […]
More Information Supplier PageAnastrozole binds reversibly to the aromatase enzyme through competitive inhibition, inhibits the conversion of androgens to estrogens in peripheral tissues (outside the CNS), and a few CNS sites in various regions within the brain. The severity of breast cancer is increased by estrogen, as sex hormones cause hyperplasia, and differentiation at estrogen receptor sites. Anastrozole […]
More Information Supplier PageAnastrozole binds reversibly to the aromatase enzyme through competitive inhibition, inhibits the conversion of androgens to estrogens in peripheral tissues (outside the CNS), and a few CNS sites in various regions within the brain. The severity of breast cancer is increased by estrogen, as sex hormones cause hyperplasia, and differentiation at estrogen receptor sites. Anastrozole […]
More Information Supplier PageAndarine (GTX-007) is an investigational selective androgen receptor modulator (SARM).
More Information Supplier PageAndarine (GTX-007) is an investigational selective androgen receptor modulator (SARM).
More Information Supplier PageAndarine (GTX-007) is an investigational selective androgen receptor modulator (SARM).
More Information Supplier PageAndarine (GTX-007) is an investigational selective androgen receptor modulator (SARM).
More Information Supplier PageAndarine (GTX-007) is an investigational selective androgen receptor modulator (SARM).
More Information Supplier PageAndrographolide is an interesting pharmacophore with anticancer and immunomodulatory activities and hence has the potential for being developed as a cancer therapeutic agent.
More Information Supplier PageAndrographolide is an interesting pharmacophore with anticancer and immunomodulatory activities and hence has the potential for being developed as a cancer therapeutic agent.
More Information Supplier PageAndrographolide is an interesting pharmacophore with anticancer and immunomodulatory activities and hence has the potential for being developed as a cancer therapeutic agent.
More Information Supplier PageAndrographolide is an interesting pharmacophore with anticancer and immunomodulatory activities and hence has the potential for being developed as a cancer therapeutic agent.
More Information Supplier PageAnemarsaponin B, extracted from rhizoma anemarrhenae root barks and barks.
More Information Supplier PageAnemarsaponin B, extracted from rhizoma anemarrhenae root barks and barks.
More Information Supplier PageAnemarsaponin B, extracted from rhizoma anemarrhenae root barks and barks.
More Information Supplier PageAnemarsaponin E was extracted from rhizoma anemarrhenae root barks and barks.
More Information Supplier PageAnemarsaponin E was extracted from rhizoma anemarrhenae root barks and barks.
More Information Supplier PageAnemarsaponin E was extracted from rhizoma anemarrhenae root barks and barks.
More Information Supplier PageAnemoside A3 isolated from Pulsatilla chinensis modulates synaptic connectivity in circuits central to memory enhancement.
More Information Supplier PageAnemoside A3 isolated from Pulsatilla chinensis modulates synaptic connectivity in circuits central to memory enhancement.
More Information Supplier PageAnemoside A3 isolated from Pulsatilla chinensis modulates synaptic connectivity in circuits central to memory enhancement.
More Information Supplier PageAnethol is an organic compound that is widely used as a flavoring substance.
More Information Supplier PageAngelicin is a furanocoumarin typically isolated from the seeds of P. corylifolia. It has also been shown to prevent tacrine-induced cytotoxicity in human liver-derived HepG2 cells (EC50 = 47 ug/ml) and vascular relaxation in phenylephrine-precontracted rat aorta.
More Information Supplier PageAngelicin is a furanocoumarin typically isolated from the seeds of P. corylifolia. It has also been shown to prevent tacrine-induced cytotoxicity in human liver-derived HepG2 cells (EC50 = 47 ug/ml) and vascular relaxation in phenylephrine-precontracted rat aorta.
More Information Supplier PageAngelicin is a furanocoumarin typically isolated from the seeds of P. corylifolia. It has also been shown to prevent tacrine-induced cytotoxicity in human liver-derived HepG2 cells (EC50 = 47 ug/ml) and vascular relaxation in phenylephrine-precontracted rat aorta.
More Information Supplier PageAngiotensin (1-7) is an endogenous peptide fragment that can be produced from Ang I or Ang II via endo- or carboxy-peptidases respectively.
More Information Supplier PageAngiotensin (1-7) is an endogenous peptide fragment that can be produced from Ang I or Ang II via endo- or carboxy-peptidases respectively.
More Information Supplier PageAngiotensin (1-7) is an endogenous peptide fragment that can be produced from Ang I or Ang II via endo- or carboxy-peptidases respectively.
More Information Supplier PageAngiotensin 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 (1-5) is a peptide that contains the amino acids 1-5 and is converted from Angiotensin I/II.
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