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 WebsiteVGX-1027 is a potent nitric oxide-donating immunomodulatory compound.
More Information Supplier PageVGX-1027 is a potent nitric oxide-donating immunomodulatory compound.
More Information Supplier PageVialinin A is a terphenyl compound originally isolated from the fungi T. terrestris and T. vialis.
More Information Supplier PageVialinin A is a terphenyl compound originally isolated from the fungi T. terrestris and T. vialis.
More Information Supplier PageVialinin A is a terphenyl compound originally isolated from the fungi T. terrestris and T. vialis.
More Information Supplier PageVicriviroc Malate is a second generation orally active CCR5 antagonist, which is also a potent inhibitor of HIV-1 entry into target cells, with a mean IC50 =0.46 nM and IC50 =1~10 nM to HIV isolates (n=52).
More Information Supplier PageVicriviroc Malate is a second generation orally active CCR5 antagonist, which is also a potent inhibitor of HIV-1 entry into target cells, with a mean IC50 =0.46 nM and IC50 =1~10 nM to HIV isolates (n=52).
More Information Supplier PageVicriviroc Malate is a second generation orally active CCR5 antagonist, which is also a potent inhibitor of HIV-1 entry into target cells, with a mean IC50 =0.46 nM and IC50 =1~10 nM to HIV isolates (n=52).
More Information Supplier PageVicriviroc Malate is a second generation orally active CCR5 antagonist, which is also a potent inhibitor of HIV-1 entry into target cells, with a mean IC50 =0.46 nM and IC50 =1~10 nM to HIV isolates (n=52).
More Information Supplier PageVicriviroc maleate is a CCR5 antagonist with IC50 of 0.91 nM in clinical development for the treatment of HIV-1.
More Information Supplier PageVicriviroc maleate is a CCR5 antagonist with IC50 of 0.91 nM in clinical development for the treatment of HIV-1.
More Information Supplier PageVicriviroc maleate is a CCR5 antagonist with IC50 of 0.91 nM in clinical development for the treatment of HIV-1.
More Information Supplier PageVigabatrin is an antiepileptic drug that inhibits the breakdown of gamma-aminobutyric acid (GABA) by acting as a suicide inhibitor of GABA transaminase (GABA-T).
More Information Supplier PageVigabatrin is a structural analog of the inhibitory neurotransmitter ??-aminobutyric acid (GABA) that irreversibly inhibits the catabolism of GABA by GABA transaminase.
More Information Supplier PageVigabatrin is an antiepileptic drug that inhibits the breakdown of gamma-aminobutyric acid (GABA) by acting as a suicide inhibitor of GABA transaminase (GABA-T).
More Information Supplier PageVigabatrin is a structural analog of the inhibitory neurotransmitter ??-aminobutyric acid (GABA) that irreversibly inhibits the catabolism of GABA by GABA transaminase.
More Information Supplier PageVigabatrin is an antiepileptic drug that inhibits the breakdown of gamma-aminobutyric acid (GABA) by acting as a suicide inhibitor of GABA transaminase (GABA-T).
More Information Supplier PageVigabatrin is a structural analog of the inhibitory neurotransmitter ??-aminobutyric acid (GABA) that irreversibly inhibits the catabolism of GABA by GABA transaminase.
More Information Supplier PageVilazodone acts as a serotonin reuptake inhibitor (IC50 = 0.5 nM) and 5-HT1A receptor partial agonist (IC50 = 0.2 nM; IA = ~60-70%).
More Information Supplier PageVilazodone acts as a serotonin reuptake inhibitor (IC50 = 0.5 nM) and 5-HT1A receptor partial agonist (IC50 = 0.2 nM; IA = ~60-70%).
More Information Supplier PageVilazodone acts as a serotonin reuptake inhibitor (IC50 = 0.5 nM) and 5-HT1A receptor partial agonist (IC50 = 0.2 nM; IA = ~60-70%).
More Information Supplier PageVilazodone acts as a serotonin reuptake inhibitor (IC50 = 0.5 nM) and 5-HT1A receptor partial agonist (IC50 = 0.2 nM; IA = ~60-70%).
More Information Supplier PageVincristine is an inhibitor of polymerization of microtubules by binding to tubulin with IC50 of 32 ??M.
More Information Supplier PageVincristine is an inhibitor of polymerization of microtubules by binding to tubulin with IC50 of 32 ??M.
More Information Supplier PageVincristine is an inhibitor of polymerization of microtubules by binding to tubulin with IC50 of 32 ??M.
More Information Supplier PageVincristine is an inhibitor of polymerization of microtubules by binding to tubulin with IC50 of 32 ??M.
More Information Supplier PageVincristine is a mitotic inhibitor, and is used in cancer chemotherapy.
More Information Supplier PageVincristine is a mitotic inhibitor, and is used in cancer chemotherapy.
More Information Supplier PageVincristine is a mitotic inhibitor, and is used in cancer chemotherapy.
More Information Supplier PageVincristine is a mitotic inhibitor, and is used in cancer chemotherapy.
More Information Supplier PageVincristine is a mitotic inhibitor, and is used in cancer chemotherapy.
More Information Supplier PageVinflunine Tartrate is a tartrate salt of vinflunine that destabilizes microtubules with an IC50 of 18.8 nM and interferes with the dynamics of microtubules during cell division.
More Information Supplier PageVinflunine Tartrate is a tartrate salt of vinflunine that destabilizes microtubules with an IC50 of 18.8 nM and interferes with the dynamics of microtubules during cell division.
More Information Supplier PageVinflunine Tartrate is a tartrate salt of vinflunine that destabilizes microtubules with an IC50 of 18.8 nM and interferes with the dynamics of microtubules during cell division.
More Information Supplier PageVinflunine Tartrate is a tartrate salt of vinflunine that destabilizes microtubules with an IC50 of 18.8 nM and interferes with the dynamics of microtubules during cell division.
More Information Supplier PageVinflunine Tartrate is a tartrate salt of vinflunine that destabilizes microtubules with an IC50 of 18.8 nM and interferes with the dynamics of microtubules during cell division.
More Information Supplier PageVinorelbine is the first 5??NOR semi-synthetic vinca alkaloid. It is obtained by semi-synthesis from alkaloids extracted from the rosy periwinkle, Catharanthus roseus.
More Information Supplier PageVinorelbine is the first 5??NOR semi-synthetic vinca alkaloid. It is obtained by semi-synthesis from alkaloids extracted from the rosy periwinkle, Catharanthus roseus.
More Information Supplier PageVinorelbine is the first 5??NOR semi-synthetic vinca alkaloid. It is obtained by semi-synthesis from alkaloids extracted from the rosy periwinkle, Catharanthus roseus.
More Information Supplier PageVinorelbine is the first 5??NOR semi-synthetic vinca alkaloid. It is obtained by semi-synthesis from alkaloids extracted from the rosy periwinkle, Catharanthus roseus.
More Information Supplier PageVinorelbine Tartrate is a semi-synthetic vinca alkaloid, and inhibits mitosis through interaction with tubulin.
More Information Supplier PageVinorelbine Tartrate is a semi-synthetic vinca alkaloid, and inhibits mitosis through interaction with tubulin.
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