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 WebsiteNimorazole is a nitroimidazole anti-infective. It is also being investigated for the treatment of head and neck cancer.
More Information Supplier PageNimorazole is a nitroimidazole anti-infective. It is also being investigated for the treatment of head and neck cancer.
More Information Supplier PageNimorazole is a nitroimidazole anti-infective. It is also being investigated for the treatment of head and neck cancer.
More Information Supplier PageNimorazole is a nitroimidazole anti-infective. It is also being investigated for the treatment of head and neck cancer.
More Information Supplier Pagenipradilol is an alpha(1),beta-blocker with a nitric oxide donative action
More Information Supplier Pagenipradilol is an alpha(1),beta-blocker with a nitric oxide donative action
More Information Supplier Pagenipradilol is an alpha(1),beta-blocker with a nitric oxide donative action
More Information Supplier Pagenipradilol is an alpha(1),beta-blocker with a nitric oxide donative action
More Information Supplier PageNiranthin is a lignan isolated from the aerial parts of the plant Phyllanthus amarus, exhibits a wide spectrum of pharmacological activities.
More Information Supplier PageNiranthin is a lignan isolated from the aerial parts of the plant Phyllanthus amarus, exhibits a wide spectrum of pharmacological activities.
More Information Supplier PageNiranthin is a lignan isolated from the aerial parts of the plant Phyllanthus amarus, exhibits a wide spectrum of pharmacological activities.
More Information Supplier PageNiranthin is a lignan isolated from the aerial parts of the plant Phyllanthus amarus, exhibits a wide spectrum of pharmacological activities.
More Information Supplier PageNisoxetine hydrochloride is a selective and potent inhibitor of norepinephrine transporter with little or no affinity for a range of other neurotransmitter receptors. Nisoxetine hydrochloride is an inhibitor of SLC6A2.
More Information Supplier PageNisoxetine hydrochloride is a selective and potent inhibitor of norepinephrine transporter with little or no affinity for a range of other neurotransmitter receptors. Nisoxetine hydrochloride is an inhibitor of SLC6A2.
More Information Supplier PageNisoxetine hydrochloride is a selective and potent inhibitor of norepinephrine transporter with little or no affinity for a range of other neurotransmitter receptors. Nisoxetine hydrochloride is an inhibitor of SLC6A2.
More Information Supplier PageNitidine chloride, a natural benzophenanthridine alkaloid, has been shown to inhibit cancer growth via induction of cell apoptosis and suppression of cancer angiogenesis.
More Information Supplier PageNitidine chloride, a natural benzophenanthridine alkaloid, has been shown to inhibit cancer growth via induction of cell apoptosis and suppression of cancer angiogenesis.
More Information Supplier PageNitidine chloride, a natural benzophenanthridine alkaloid, has been shown to inhibit cancer growth via induction of cell apoptosis and suppression of cancer angiogenesis.
More Information Supplier PageNitrisinone is a competitive inhibitor that reversibly inhibits 4-Hydroxyphenylpyruvate oxidase (dioxygenase).
More Information Supplier PageNitrisinone is a competitive inhibitor that reversibly inhibits 4-Hydroxyphenylpyruvate oxidase (dioxygenase).
More Information Supplier PageNitrisinone is a competitive inhibitor that reversibly inhibits 4-Hydroxyphenylpyruvate oxidase (dioxygenase).
More Information Supplier PageNitrisinone is a competitive inhibitor that reversibly inhibits 4-Hydroxyphenylpyruvate oxidase (dioxygenase).
More Information Supplier PageNitrarine 2HCl is a hypotensive? spasmolytic? coronary dilator? sedative in experimental arrhythmias. in experimental arrhythmias in the cat? caused by calcium chloride? Aconitine and electric cardiac stimulation? Nitrarine dihydrochloride presents a hypotensive? spasmolytic? coronary dilating and sedative action. Its antiarrhythmic properties are due to its stabilizating effects on the membrane and its coronary dilating action. […]
More Information Supplier PageNitrarine 2HCl is a hypotensive? spasmolytic? coronary dilator? sedative in experimental arrhythmias. in experimental arrhythmias in the cat? caused by calcium chloride? Aconitine and electric cardiac stimulation? Nitrarine dihydrochloride presents a hypotensive? spasmolytic? coronary dilating and sedative action. Its antiarrhythmic properties are due to its stabilizating effects on the membrane and its coronary dilating action. […]
More Information Supplier PageNitrarine 2HCl is a hypotensive? spasmolytic? coronary dilator? sedative in experimental arrhythmias. in experimental arrhythmias in the cat? caused by calcium chloride? Aconitine and electric cardiac stimulation? Nitrarine dihydrochloride presents a hypotensive? spasmolytic? coronary dilating and sedative action. Its antiarrhythmic properties are due to its stabilizating effects on the membrane and its coronary dilating action. […]
More Information Supplier PageNivocasan is a novel caspase-inhibitor has demonstrated hepatoprotective activity in fibrosis/apoptosis animal models.
More Information Supplier PageNivocasan is a novel caspase-inhibitor has demonstrated hepatoprotective activity in fibrosis/apoptosis animal models.
More Information Supplier PageNivocasan is a novel caspase-inhibitor has demonstrated hepatoprotective activity in fibrosis/apoptosis animal models.
More Information Supplier PageNK314 is a novel synthetic benzo[c]phenanthridine alkaloid that shows strong antitumor activity. It inhibited topoisomerase II activity and stabilized topoisomerase II-DNA cleavable complexes.
More Information Supplier PageNK314 is a novel synthetic benzo[c]phenanthridine alkaloid that shows strong antitumor activity. It inhibited topoisomerase II activity and stabilized topoisomerase II-DNA cleavable complexes.
More Information Supplier PageNK314 is a novel synthetic benzo[c]phenanthridine alkaloid that shows strong antitumor activity. It inhibited topoisomerase II activity and stabilized topoisomerase II-DNA cleavable complexes.
More Information Supplier PageNKP608 is a non-peptidic derivative of 4-aminopiperidine which acts as a selective, specific and potent antagonist at the neurokinin-1 (NK-1) receptor both in vitro(IC50=2.6 nM) and in vivo.
More Information Supplier PageNKP608 is a non-peptidic derivative of 4-aminopiperidine which acts as a selective, specific and potent antagonist at the neurokinin-1 (NK-1) receptor both in vitro(IC50=2.6 nM) and in vivo.
More Information Supplier PageNKP608 is a non-peptidic derivative of 4-aminopiperidine which acts as a selective, specific and potent antagonist at the neurokinin-1 (NK-1) receptor both in vitro(IC50=2.6 nM) and in vivo.
More Information Supplier PageNKY 80 is an inhibitor of adenylyl cyclase (AC). Exhibits greater affinity for AC5 over AC3 and AC2 (IC50 values are 8.3 ??M, 132 ??M and 1.7 mM respectively).
More Information Supplier PageNKY 80 is an inhibitor of adenylyl cyclase (AC). Exhibits greater affinity for AC5 over AC3 and AC2 (IC50 values are 8.3 ??M, 132 ??M and 1.7 mM respectively).
More Information Supplier PageNKY 80 is an inhibitor of adenylyl cyclase (AC). Exhibits greater affinity for AC5 over AC3 and AC2 (IC50 values are 8.3 ??M, 132 ??M and 1.7 mM respectively).
More Information Supplier PageNKY 80 is an inhibitor of adenylyl cyclase (AC). Exhibits greater affinity for AC5 over AC3 and AC2 (IC50 values are 8.3 ??M, 132 ??M and 1.7 mM respectively).
More Information Supplier PageNLG919 is an orally available inhibitor of indoleamine 2,3-dioxygenase 1 (IDO1), with potential immunomodulating and antineoplastic activities.
More Information Supplier PageNLG919 is an orally available inhibitor of indoleamine 2,3-dioxygenase 1 (IDO1), with potential immunomodulating and antineoplastic activities.
More Information Supplier PageNLG919 is an orally available inhibitor of indoleamine 2,3-dioxygenase 1 (IDO1), with potential immunomodulating and antineoplastic activities.
More Information Supplier PageNLG919 is an orally available inhibitor of indoleamine 2,3-dioxygenase 1 (IDO1), with potential immunomodulating and antineoplastic activities.
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