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 WebsiteDesacetyl asperulosidic acid, extracted from Morinda officinalis How. dried root.
More Information Supplier PageDesacetyl asperulosidic acid, extracted from Morinda officinalis How. dried root.
More Information Supplier PageDesacetyl asperulosidic acid, extracted from Morinda officinalis How. dried root.
More Information Supplier PageDesacetylnimbin is a new limonoid from Arisaema decipiens, a traditional antitumor herb.
More Information Supplier PageDesacetylnimbin is a new limonoid from Arisaema decipiens, a traditional antitumor herb.
More Information Supplier PageDesacetylnimbin is a new limonoid from Arisaema decipiens, a traditional antitumor herb.
More Information Supplier PageDesmethyldoxepin is the primary metabolite of doxepin, produced by metabolism at the liver. Doxepin is a tricyclic antidepressant.
More Information Supplier PageDesmethyldoxepin is the primary metabolite of doxepin, produced by metabolism at the liver. Doxepin is a tricyclic antidepressant.
More Information Supplier PageDesmopressin is a synthetic vasopressin analog that acts as an agonist at V1B and V2 receptors (EC50 values are 11.4 and 23.9 nM and Ki values are 5.84 and 65.9 nM respectively).
More Information Supplier PageDesmopressin is a synthetic vasopressin analog that acts as an agonist at V1B and V2 receptors (EC50 values are 11.4 and 23.9 nM and Ki values are 5.84 and 65.9 nM respectively).
More Information Supplier PageDesmopressin is a synthetic vasopressin analog that acts as an agonist at V1B and V2 receptors (EC50 values are 11.4 and 23.9 nM and Ki values are 5.84 and 65.9 nM respectively).
More Information Supplier PageDesmopressin is a synthetic vasopressin analog that acts as an agonist at V1B and V2 receptors (EC50 values are 11.4 and 23.9 nM and Ki values are 5.84 and 65.9 nM respectively).
More Information Supplier PageDesmopressinDDAVP) acetate is the synthetic analogue of the antidiuretic hormone arginine vasopressin.
More Information Supplier PageDesmopressinDDAVP) acetate is the synthetic analogue of the antidiuretic hormone arginine vasopressin.
More Information Supplier PageDesmopressinDDAVP) acetate is the synthetic analogue of the antidiuretic hormone arginine vasopressin.
More Information Supplier PageDesonide is the generic name of a low-potency topical corticosteroid .
More Information Supplier PageDesonide is the generic name of a low-potency topical corticosteroid .
More Information Supplier PageDesonide is the generic name of a low-potency topical corticosteroid .
More Information Supplier PageDesonide is the generic name of a low-potency topical corticosteroid .
More Information Supplier PageDesonide is the generic name of a low-potency topical corticosteroid .
More Information Supplier PageDesvenlafaxine succinate hydrate is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI).
More Information Supplier PageDesvenlafaxine succinate hydrate is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI).
More Information Supplier PageDesvenlafaxine succinate hydrate is an antidepressant of the serotonin-norepinephrine reuptake inhibitor (SNRI).
More Information Supplier PageDetomidine is a sedative with analgesic properties. ??2-adrenergic agonists produce dose-dependent sedative and analgesic effects, mediatated by activation of ??2 catecholamine receptors, thus inducing a negative feedback response, reducing production of excitatory neurotransmitters.
More Information Supplier PageDetomidine is a sedative with analgesic properties. ??2-adrenergic agonists produce dose-dependent sedative and analgesic effects, mediatated by activation of ??2 catecholamine receptors, thus inducing a negative feedback response, reducing production of excitatory neurotransmitters.
More Information Supplier PageDetomidine is a sedative with analgesic properties. ??2-adrenergic agonists produce dose-dependent sedative and analgesic effects, mediatated by activation of ??2 catecholamine receptors, thus inducing a negative feedback response, reducing production of excitatory neurotransmitters.
More Information Supplier PageDetomidine is a sedative with analgesic properties. ??2-adrenergic agonists produce dose-dependent sedative and analgesic effects, mediatated by activation of ??2 catecholamine receptors, thus inducing a negative feedback response, reducing production of excitatory neurotransmitters.
More Information Supplier PageDetomidine is a sedative with analgesic properties. ??2-adrenergic agonists produce dose-dependent sedative and analgesic effects, mediatated by activation of ??2 catecholamine receptors, thus inducing a negative feedback response, reducing production of excitatory neurotransmitters.
More Information Supplier PageDexamethasone is a potent synthetic member of the glucocorticoid class of steroid drugs. It acts as an anti-inflammatory and immunosuppressant. Its potency is about 20-30 times that of the naturally occurring hormone hydrocortisone and 4-5 times of prednisone.
More Information Supplier PageDexamethasone is a potent synthetic member of the glucocorticoid class of steroid drugs. It acts as an anti-inflammatory and immunosuppressant. Its potency is about 20-30 times that of the naturally occurring hormone hydrocortisone and 4-5 times of prednisone.
More Information Supplier PageDexamethasone is a potent synthetic member of the glucocorticoid class of steroid drugs. It acts as an anti-inflammatory and immunosuppressant. Its potency is about 20-30 times that of the naturally occurring hormone hydrocortisone and 4-5 times of prednisone.
More Information Supplier PageDexmedetomidine hydrochloride is the active isomer of medetomide which acts a potent, highly selective ??2-AR (??2-adrenoceptor) agonist.
More Information Supplier PageDexmedetomidine hydrochloride is the active isomer of medetomide which acts a potent, highly selective ??2-AR (??2-adrenoceptor) agonist.
More Information Supplier PageDexmedetomidine hydrochloride is the active isomer of medetomide which acts a potent, highly selective ??2-AR (??2-adrenoceptor) agonist.
More Information Supplier PageDexmedetomidine hydrochloride is the active isomer of medetomide which acts a potent, highly selective ??2-AR (??2-adrenoceptor) agonist.
More Information Supplier PageDexpramipexole dihydrochloride is a neuroprotective agent and weak non-ergoline dopamine agonist.
More Information Supplier PageDexpramipexole dihydrochloride is a neuroprotective agent and weak non-ergoline dopamine agonist.
More Information Supplier PageDexpramipexole dihydrochloride is a neuroprotective agent and weak non-ergoline dopamine agonist.
More Information Supplier PageDexrazoxane hydrochloride is a cardioprotective agent. As a derivative of EDTA, dexrazoxane chelates iron, but the precise mechanism by which it protects the heart is not known. This agent is used to protect the heart against the cardiotoxic side effects of anthracyclines, such as doxorubicin.
More Information Supplier PageDexrazoxane hydrochloride is a cardioprotective agent. As a derivative of EDTA, dexrazoxane chelates iron, but the precise mechanism by which it protects the heart is not known. This agent is used to protect the heart against the cardiotoxic side effects of anthracyclines, such as doxorubicin.
More Information Supplier PageDexrazoxane hydrochloride is a cardioprotective agent. As a derivative of EDTA, dexrazoxane chelates iron, but the precise mechanism by which it protects the heart is not known. This agent is used to protect the heart against the cardiotoxic side effects of anthracyclines, such as doxorubicin.
More Information Supplier PageDexrazoxane hydrochloride is a cardioprotective agent. As a derivative of EDTA, dexrazoxane chelates iron, but the precise mechanism by which it protects the heart is not known. This agent is used to protect the heart against the cardiotoxic side effects of anthracyclines, such as doxorubicin.
More Information Supplier PageDexrazoxane hydrochloride is a cardioprotective agent. As a derivative of EDTA, dexrazoxane chelates iron, but the precise mechanism by which it protects the heart is not known. This agent is used to protect the heart against the cardiotoxic side effects of anthracyclines, such as doxorubicin.
More Information Supplier PageDGAT-1 inhibitor 2 is an effective inhibitor of DGAT-1;antiobesity agents.
More Information Supplier PageDGAT-1 inhibitor 2 is an effective inhibitor of DGAT-1;antiobesity agents.
More Information Supplier PageDGAT-1 inhibitor 2 is an effective inhibitor of DGAT-1;antiobesity agents.
More Information Supplier PageDiacetylkorseveriline is an antiarrhythmic (classes i and iv)? belonging to a novel structural class. effective against arrhythmia caused by aconitine? cacl2? electric stimulation of the ventricles or ligature of the aorta, recommended dose for one cycle of experiment on mice: 3.0-30.0 mg/kg? intravenously.
More Information Supplier PageDiacetylkorseveriline is an antiarrhythmic (classes i and iv)? belonging to a novel structural class. effective against arrhythmia caused by aconitine? cacl2? electric stimulation of the ventricles or ligature of the aorta, recommended dose for one cycle of experiment on mice: 3.0-30.0 mg/kg? intravenously.
More Information Supplier PageDiacetylkorseveriline is an antiarrhythmic (classes i and iv)? belonging to a novel structural class. effective against arrhythmia caused by aconitine? cacl2? electric stimulation of the ventricles or ligature of the aorta, recommended dose for one cycle of experiment on mice: 3.0-30.0 mg/kg? intravenously.
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