17
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T2150 | Guanfacine hydrochloride | Tenex,Intuniv,Guanfacine | Adrenergic Receptor |
Guanfacine hydrochloride (Intuniv) is a centrally acting antihypertensive agent with specificity towards ADRENERGIC ALPHA-2 RECEPTORS. | |||
T11894 | Lusaperidone | R107474 | Adrenergic Receptor |
Lusaperidone (R107474) is a potent α2-adrenergic receptor antagonist, a potential radioligand for the α (2)-adrenergic receptor, with inhibitory effects on α2A and α2C, with Ki values of 0.13 and 0.15 nM, respectively. | |||
T6522 | Guanabenz Acetate | Wy8678 acetate,BR-750,Wytensin | Adrenergic Receptor |
Guanabenz Acetate (Wytensin) is a specific agonist of adrenergic receptor. The pEC50 for α2a-adrenergic receptor, α2b-adrenergic receptor and α2c-adrenergic receptor is 8.25, 7.01 and ~5, respectively. | |||
T13804 | OPC-28326 | Adrenergic Receptor | |
OPC-28326 is a specific an α2-adrenergic receptor antagonist and acts as a peripheral vasodilator. OPC-28326 inhibits α2A-, α2B- and α2C-adrenoceptors with Ki of 2040, 285, and 55 nM, respectively. | |||
T3360 | ZK 756326 | ZK756326 2HCl | CCR |
ZK 756326 is a selective, non-peptide CCR8 chemokine receptor agonist (IC50: 1.8 μM, in human; 2.6 μM, in mouse). Displays no activity at CCR4/5 and CXCR3/4 and shows higher 28-fold selectivity over 26 other GPCRs (less ... | |||
T12343 | Benzquinamide | BZQ,P2647,Benzoquinamide | Adrenergic Receptor |
Benzquinamide (P2647), an antiemetic agent with anticancer activity, inhibits p-glycoprotein-mediated drug efflux and potentiates the cytotoxicity of anticancer drugs in multidrug-resistant cells.The Ki values of Benzqui... | |||
T31602 | Ecopipam | Sch-39166,UNII-0X748O646K,Sch 39166 | Dopamine Receptor |
Ecopipam (UNII-0X748O646K) is a potent, selective and orally active antagonist of dopamine D1/D5 receptor, with Kis of 1.2 nM and 2.0 nM, respectively. Ecopipam shows more than 40-flod selectivity over D2, D4, 5-HT, and ... | |||
T1735 | Lurasidone hydrochloride | Lurasidone HCl,SM-13496 (Hydrochloride),SM-13496 | Dopamine Receptor , 5-HT Receptor , Norepinephrine |
Lurasidone hydrochloride (Lurasidone HCl) is a thiazole derivative and atypical antipsychotic agent that functions as a dopamine D2 receptor antagonist; serotonin 5-HT2 receptor antagonist, serotonin 5-HT7 receptor antag... | |||
T26690 | AVN-101 | 5-HT Receptor , Adrenergic Receptor , Histamine Receptor | |
AVN-101 is a potent 5-HT7 receptor antagonist. | |||
T22824 | Guanfacine | Others | |
Guanfacine is a selective agonist of the α2A receptor. | |||
T60548 | Guanoxabenz hydrochloride | ||
Guanoxabenz (Hydroxyguanabenz) hydrochloride is an agonist of α2 adrenergic receptor. It has a Ki of 4000 nM and the fully activated form 40 nM for an α2A adrenoceptor[1][2][3]. | |||
T10264 | AGN 192836 | Others | |
AGN 192836 is a potent and selective α2 adrenergic agonist (EC50s: 8.7, 41 and 6.6 nM for α2A, α2B and α2C receptor). | |||
T3278 | Piribedil | EU-4200,Trivastan,ET-495,Trivastal | Dopamine Receptor , Histone Methyltransferase , Adrenergic Receptor |
Piribedil (Trivastan) is a dopamine D2 agonist, used in the treatment of Parkinson's disease. | |||
T35591 | Guanfacine-13C,15N3 | Guanfacine-13C,15N3 | |
Guanfacine-13C,15N3is intended for us as an internal standard for the quantification of guanfacine by GC- or LC-MS. Guanfacine is an α2-adrenergic receptor (α2-AR) agonist with Kivalues of 93, 1,380, and 3,890 nM for α2A... | |||
T83956 | CELT-133 | ||
CELT-133 is a selective fluorescent antagonist for the hα1A adrenergic receptor, demonstrating complete selectivity towards α1A over α2A receptors, with a Ki of 5 nM and 15% displacement at 1 μM in radioligand binding as... | |||
T21446 | Rotigotine Hydrochloride | Rotigotine (Hydrochloride),N 0923,N-0924,Rotigotine HCl,N-0923 | Dopamine Receptor , 5-HT Receptor , Adrenergic Receptor |
Rotigotine Hydrochloride (N-0924), a dopamine receptor agonist prefering for D3 receptors over D1 and D2, has effective activity of anti-Parkinsonian. Racemic rotigotine hydrochloride is about 50 times as potent as quinp... | |||
T11286 | Fiduxosin | A 185980.1,ABT 980 | Adrenergic Receptor |
Fiduxosin is a selective and potent α1-adrenoceptor antagonist with inhibitory effects on α1a-adrenoceptor, α1b-adrenoceptor and α1d-adrenoceptor, with Ki values of 0.160 nM, 24.9 nM and 0.920 nM, respectively. Fiduxosin... |