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 WebsitePlumbagin, exhibits cytotoxicity in rodent models of carcinogenesis and carcinoma; has antifungal, antiviral, and antibacterial action.
More Information Supplier PageThe activity of Pluripotin (SC-1) is mediated by the combined inhibition of RasGAP and ERK1 with Kd values of 98 and 212 nM, respectively.
More Information Supplier PageThe activity of Pluripotin (SC-1) is mediated by the combined inhibition of RasGAP and ERK1 with Kd values of 98 and 212 nM, respectively.
More Information Supplier PageThe activity of Pluripotin (SC-1) is mediated by the combined inhibition of RasGAP and ERK1 with Kd values of 98 and 212 nM, respectively.
More Information Supplier PageThe activity of Pluripotin (SC-1) is mediated by the combined inhibition of RasGAP and ERK1 with Kd values of 98 and 212 nM, respectively.
More Information Supplier Pagestearoyl-CoA desaturase 1 (SCD1) inhibitor. Used to selectively eliminate undifferentiated human pluripotent stem cells (hPSCs) from culture; induces ER stress, attenuates protein synthesis and induces apoptosis in hPSCs. Prevents teratoma formation in immunocompromised mice.
More Information Supplier Pagestearoyl-CoA desaturase 1 (SCD1) inhibitor. Used to selectively eliminate undifferentiated human pluripotent stem cells (hPSCs) from culture; induces ER stress, attenuates protein synthesis and induces apoptosis in hPSCs. Prevents teratoma formation in immunocompromised mice.
More Information Supplier Pagestearoyl-CoA desaturase 1 (SCD1) inhibitor. Used to selectively eliminate undifferentiated human pluripotent stem cells (hPSCs) from culture; induces ER stress, attenuates protein synthesis and induces apoptosis in hPSCs. Prevents teratoma formation in immunocompromised mice.
More Information Supplier Pagestearoyl-CoA desaturase 1 (SCD1) inhibitor. Used to selectively eliminate undifferentiated human pluripotent stem cells (hPSCs) from culture; induces ER stress, attenuates protein synthesis and induces apoptosis in hPSCs. Prevents teratoma formation in immunocompromised mice.
More Information Supplier Pagestearoyl-CoA desaturase 1 (SCD1) inhibitor. Used to selectively eliminate undifferentiated human pluripotent stem cells (hPSCs) from culture; induces ER stress, attenuates protein synthesis and induces apoptosis in hPSCs. Prevents teratoma formation in immunocompromised mice.
More Information Supplier PagePLX4032 (Vemurafenib) also known as RG7204, Vemurafenib, R7204; RO5185426. PLX4032 is a B-raf inhibitor with an IC50 of 44 nM.
More Information Supplier PagePLX4032 (Vemurafenib) also known as RG7204, Vemurafenib, R7204; RO5185426. PLX4032 is a B-raf inhibitor with an IC50 of 44 nM.
More Information Supplier PagePLX4032 (Vemurafenib) also known as RG7204, Vemurafenib, R7204; RO5185426. PLX4032 is a B-raf inhibitor with an IC50 of 44 nM.
More Information Supplier PagePLX4032 (Vemurafenib) also known as RG7204, Vemurafenib, R7204; RO5185426. PLX4032 is a B-raf inhibitor with an IC50 of 44 nM.
More Information Supplier PagePLX4032 (Vemurafenib) also known as RG7204, Vemurafenib, R7204; RO5185426. PLX4032 is a B-raf inhibitor with an IC50 of 44 nM.
More Information Supplier PagePLX647 is a highly specific dual FMS/KIT kinase inhibitor with IC50 of 28/16 nM respectively.
More Information Supplier PagePLX647 is a highly specific dual FMS/KIT kinase inhibitor with IC50 of 28/16 nM respectively.
More Information Supplier PagePLX647 is a highly specific dual FMS/KIT kinase inhibitor with IC50 of 28/16 nM respectively.
More Information Supplier PagePMPA is a potent inhibitor of the neuropeptidase N-acetylated ??-linked acidic dipeptidase (NAALADase), which is a membrane-bound peptidase that hydrolyses N-acetyl-L-aspartate-L-glutamate (NAAG), a major brain peptide.
More Information Supplier PagePMPA is a potent inhibitor of the neuropeptidase N-acetylated ??-linked acidic dipeptidase (NAALADase), which is a membrane-bound peptidase that hydrolyses N-acetyl-L-aspartate-L-glutamate (NAAG), a major brain peptide.
More Information Supplier PagePMPA is a potent inhibitor of the neuropeptidase N-acetylated ??-linked acidic dipeptidase (NAALADase), which is a membrane-bound peptidase that hydrolyses N-acetyl-L-aspartate-L-glutamate (NAAG), a major brain peptide.
More Information Supplier PagePneumocandin B0 is the major analogue of a family of lipopeptides isolated from several species of several different genera, notably Cryptosporiopsis, Glarea and Pezicula. Pneumocandin B0 is a potent antifungal and acts by inhibition of the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi.
More Information Supplier PagePneumocandin B0 is the major analogue of a family of lipopeptides isolated from several species of several different genera, notably Cryptosporiopsis, Glarea and Pezicula. Pneumocandin B0 is a potent antifungal and acts by inhibition of the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi.
More Information Supplier PagePneumocandin B0 is the major analogue of a family of lipopeptides isolated from several species of several different genera, notably Cryptosporiopsis, Glarea and Pezicula. Pneumocandin B0 is a potent antifungal and acts by inhibition of the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi.
More Information Supplier PagePneumocandin B0 is the major analogue of a family of lipopeptides isolated from several species of several different genera, notably Cryptosporiopsis, Glarea and Pezicula. Pneumocandin B0 is a potent antifungal and acts by inhibition of the synthesis of ??-(1,3)-D-glucan, an essential component of the cell wall of susceptible fungi.
More Information Supplier PagePNU 282987 (PNU-282,987)is a drug that acts as a potent and selective agonist for the ??7 subtype of neural nicotinic acetylcholine receptors.
More Information Supplier PagePNU 282987 (PNU-282,987)is a drug that acts as a potent and selective agonist for the ??7 subtype of neural nicotinic acetylcholine receptors.
More Information Supplier PagePNU 282987 (PNU-282,987)is a drug that acts as a potent and selective agonist for the ??7 subtype of neural nicotinic acetylcholine receptors.
More Information Supplier PagePNU 282987 (PNU-282,987)is a drug that acts as a potent and selective agonist for the ??7 subtype of neural nicotinic acetylcholine receptors.
More Information Supplier PagePNU-120596 is a positive allosteric modulator of ??7 neuronal nicotinic acetylcholine receptors.
More Information Supplier PagePNU-120596 is a positive allosteric modulator of ??7 neuronal nicotinic acetylcholine receptors.
More Information Supplier PagePNU-120596 is a positive allosteric modulator of ??7 neuronal nicotinic acetylcholine receptors.
More Information Supplier PagePNU-120596 is a positive allosteric modulator of ??7 neuronal nicotinic acetylcholine receptors.
More Information Supplier PagePNU-120596 is a positive allosteric modulator of ??7 neuronal nicotinic acetylcholine receptors.
More Information Supplier PagePodophyllotoxin is a potent inhibitor of microtubule assembly that binds at the colchicine site of tubulin.
More Information Supplier PagePodophyllotoxin is a potent inhibitor of microtubule assembly that binds at the colchicine site of tubulin.
More Information Supplier PagePodophyllotoxin is a potent inhibitor of microtubule assembly that binds at the colchicine site of tubulin.
More Information Supplier PagePodophyllotoxin is a potent inhibitor of microtubule assembly that binds at the colchicine site of tubulin.
More Information Supplier PagePoliumoside, has been isolated from the aerial parts of Teucrium belion.
More Information Supplier PagePoliumoside, has been isolated from the aerial parts of Teucrium belion.
More Information Supplier PagePoliumoside, has been isolated from the aerial parts of Teucrium belion.
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