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| Catalog | name | Description | price |
|---|---|---|---|
| R-R-3601 | Pronethalol CAS No.54-80-8 | Pronethalol ((±)-Pronethalo)/CAS No.54-80-8 is a non-selective β-adrenergic antagonist. Pronethalol is a potent inhibitor of Sox2 expression. Pronethalol protects against and to reverse Digitalis-induced ventricular arrhythmias and limits the cerebral arteriovenous malformation (AVMs). | price> |
| R-C-1902 | Monastrol CAS:329689-23-8 | Monastrol((±)-Monastrol)is a cell-permeable small molecule inhibitor of kinesin-5(KIF11)which is essential for maintaining separation of the half-spindles. | price> |
| R-C-2262 | LY3405105 CAS:2326428-25-3 | LY3405105 is an orally active CDK7 inhibitor with an IC50 of 92.8nM.LY3405105 shows potential antineoplastic activity. | price> |
| R-R-3602 | Metoprolol succinate CAS No.98418-47-4 | Metoprolol succinate/CAS No.98418-47-4 is an orally active, selective β1-adrenoceptor antagonist. Metoprolol succinate shows anti-inflammation, antitumor and anti-angiogenic properties. | price> |
| R-C-1903 | TC-G-1008 (GPR39-C3) CAS:1621175-65-2 | TC-G-1008 is a GPR39(zinc receptor)agonist(EC50 values are 0.4 and 0.8nM for rat and human receptors respectively). | price> |
| R-C-2263 | BSJ-4-116 CAS:2519823-34-6 | BSJ-4-116 is a highly potent and selective CDK12 degrader(PROTAC)with an IC50 of 6 nM.BSJ-4-116 downregulates DDR genes through a premature termination of transcription,primarily through increasing poly(adenylation).BSJ-4-116 exhibits potent antiproliferative effects,alone and in combination with the poly(ADP-ribose)polymerase inhibitor Olaparib(HY-10162). | price> |
| R-R-3603 | Guanabenz hydrochloride CAS No.23113-43-1 | Guanabenz hydrochloride/CAS No.23113-43-1 is an orally active α-2-adrenoceptor agonist. Guanabenz hydrochloride has antihypertensive effect and antiparasitic activity. Guanabenz hydrochloride interferes ER stress-signalling and has protective effects in cardiac myocytes. Guanabenz hydrochloride also is used for the research of high blood pressure. | price> |
| R-C-1904 | M2I-1 CAS:312271-03-7 | M2I-1 is an inhibitor of Mad2(mitotic arrest deficient 2)targeting the binding of Mad2 to Cdc20,an essential protein-protein interaction(PPI)within the SAC(spindle assembly checkpoint). | price> |
| R-C-2264 | CC-671 CAS:1618658-88-0 | CC-671 is a dual TTK protein kinase/CDC2-like kinase(CLK2)inhibitor with IC50s of 0.005 and 0.006μM for TTK and CLK2,respectively. | price> |
| R-R-3604 | BI-167107 CAS No.1202235-68-4 | BI-167107/CAS No.1202235-68-4 is a high affinity, full agonist that binds to the β2 adrenergic receptor (β2AR) with a dissociation constant Kd of 84 pM. | price> |
| R-C-1905 | BAG956 CAS:853910-02-8 | BAG 956,also known as NVP-BAG956,is a dual PDK1 and class I PI 3-kinase inhibitor.BAG 956 has been shown to inhibit cellular AKT phosphorylation at Thr308.BAG 956 also blocks cell proliferation and causes arrest in the G1 phase of the cell cycle.BAG 956 has been shown to slow tumor progression in mouse xenograft models. | price> |
| R-R-3605 | Reboxetine mesylate CAS No.98769-84-7 | Reboxetine mesylate (FCE20124 mesylate)/CAS No.98769-84-7 is a potent, selective, and specific noradrenaline reuptake inhibitor (NARI) for the research of depression. Reboxetine mesylate inhibits the uptake of norepinephrine, with a Ki of 8 nM. | price> |
| R-C-1906 | KO-947 CAS:1695533-89-1 | KO-947 is a potent and selective inhibitor of ERK1/2 kinases.KO-947 blocks ERK signaling and proliferation of tumor cells exhibiting dysregulation of MAPK pathway signaling at low nanomolar concentrations. | price> |
| R-R-3606 | Idazoxan hydrochloride CAS No.79944-56-2 | Idazoxan hydrochloride (RX 781094 hydrochloride)/CAS No.79944-56-2 is an α2-adrenoceptor antagonist and is also a imidazoline receptors (IRs) antagonist competitively antagonized the centrally induced hypotensive effect of imidazoline-like agents (IMs). | price> |
| R-C-1907 | ARN-3236 CAS:1613710-01-2 | ARN-3236 is potent,orally active and selective SIK2 inhibitor.ARN-3236 inhibited the growth of 10 ovarian cancer cell lines at an IC50 of 0.8 to 2.6μmol/L. | price> |
| R-R-3607 | Vibegron CAS No.1190389-15-1 | Vibegron (MK-4618)/CAS No.1190389-15-1 is a potent, highly selective and orally active β3-adrenoceptor agonist (EC50=1.1 nM). Vibegron can be used for severe urgency urinary incontinence related to overactive bladder. | price> |
| R-C-1908 | SAR-20347 CAS:1450881-55-6 | SAR-20347 is a potent inhibitor of TYK2,JAK1,JAK2 and JAK3 with IC50 of 0.6 nM,23nM,26nM and 41nM,respectively.SAR-20347 inhibits TYK2- and JAK1-mediated IL-12 and IFN-α signaling. | price> |
| R-R-3608 | DL-Norepinephrine hydrochloride CAS No.55-27-6 | DL-Norepinephrine hydrochloride/CAS No.55-27-6 is a synthetic phenylethylamine that mimics the sympathomimetic actions of the endogenous norepinephrine.DL-Norepinephrine hydrochloride is a neurotransmitter targets α1 and β1 adrenoceptors, has an increasing effect on subendocardial oxygen tension. | price> |
| R-C-1909 | AD 80 CAS:1384071-99-1 | AD80,a multikinase inhibitor,shows strong activity against human RET(c-RET),BRAF,S6K,and SRC but were much less active than either AD57 or AD58 against mTOR.The IC50 value for RET is 4nM. | price> |
| R-R-3609 | Indacaterol maleate CAS No.753498-25-8 | Indacaterol maleate (QAB149)/CAS No.753498-25-8 is an orally active ultra-long-acting β2 adrenergic receptor (ADRB2) agonist. Indacaterol maleate inhibits NF-κB activity in a β-arrestin2-dependent manner, preventing further lung damage and improving lung function in COPD (chronic obstructive pulmonary disorder). Indacaterol maleate can also be used in cardiovascular disease research. | price> |

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