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Neurological Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN1730004 CGP 25454A 104391-26-6

    CGP 25454A is a novel and selective presynaptic dopamine autoreceptor antagonist. In vitro: CGP 25454A increase the field-stimulated [3H]- and [14C]-overflow from rat striatal slices preloaded with [3H]dopamine and [14C]...

  • YN480019 Ipenoxazone 104454-71-9

    Ipenoxazone is a potent and centrally acting muscle relaxant.

  • YN480771 EC23 104561-41-3

    EC23 (AGN 190205) is a stable synthetic retinoid analogue and induces neuronal differentiation.

  • YN1730075 Pramipexole dihydrochloride 104632-25-9

    Pramipexole dihydrochloride is a dopamine agonist of the non-ergoline class indicated for treating Parkinson's disease (PD) and restless legs syndrome (RLS) with Ki values of 3.9 nM, 2.2 nM, 0.5 nM and 5.1 nM for D2S receptor,...

  • YN1730095 Pramipexole 104632-26-0

    Pramipexole is a partial/full D2S, D2L, D3, D4 receptor agonist with a Ki of 3.9, 2.2, 0.5 and 5.1 nM for D2S, D2L, D3, D4 receptor, respectively.

  • YN1730076 Dexpramipexole dihydrochlorid... 104632-27-1

    Dexpramipexole dihydrochloride ((R)-Pramipexole dihydrochloride) is a neuroprotective agent and weak non-ergoline dopamine agonist.

  • YN1730077 Dexpramipexole 104632-28-2

    Dexpramipexole(KNS-760704), also known as R-(+)-Pramipexole, is a neuroprotective agent and weak non-ergoline dopamine Dexpramipexole has been found to have neuroprotective effects and is being investigated for treatment of amyot...

  • YN480626 Eslicarbazepine 104746-04-5

    Eslicarbazepine is an oral anticonvulsant indicated for the adjunctive treatment of partial seizures.

  • YN360225 NF023 hexasodium 104869-31-0

    NF023 hexasodium is a selective and competitiveP2X1receptorantagonist, with IC50 values of 0.21μM, 28.9μM, > 50μM and > 100μM for human P2X1, P2X3, P2X2, and P2X4-mediated responses respectively.

  • YN380248 Aloeresin D 105317-67-7

    Aloeresin D is a chromone glycoside isolated fromAloe vera, inhibits β-Secretase (BACE1) activity, with an IC50 of 39μM.

  • YN380098 RS 8359 105365-76-2

    RS 8359 is a selective and reversibleMAO-Ainhibitor, with antidepressant activity.

  • YN361098 Linopirdine 105431-72-9

    Linopirdine (DuP 996) is an orally active, selectiveM-type K+current (IM; Kv7; KCNQ Channels)inhibitor with an IC50 of 2.4μM. Linopirdine is aTRPV1agonist. Linopirdine, a putative cognition enhancing drug, increases a...

  • YN321372 Tropisetron Hydrochloride 105826-92-4

    Tropisetron HCl is a potent and selective 5-HT3 receptor antagonist and α7-nicotinic receptor agonist, used to treat nausea and vomiting following chemotherapy.

  • YN360641 Radafaxine hydrochloride 106083-71-0

    Radafaxine hydrochloride (GW-353162A) is aDAT (dopamine transporter) and NET(norepinephrine transporter)transporters inhibitor, and nAChR family modulator. Radafaxine hydrochloride (GW-353162A) is a potent metabolite of b...

  • YN321800 Senktide 106128-89-6

    Senktide is a tachykininNK3receptoragonist.

  • YN321553 Tamsulosin 106133-20-4

    Tamsulosin is a selective α1 receptor antagonist that has preferential selectivity for the α1A receptor in the prostate versus the α1B receptor in the blood vessels.

  • YN320563 Thioperamide 106243-16-7

    Thioperamide (MR-12842) is a potent, orally available, brain penetrant and selectiveH3 receptorantagonist with a Ki of 4.3nM for inhibition of [3H]histamine release. Thioperamide inhibits [3H]histamine synthesis with a Ki of 31n...

  • YN320410 Risperidone 106266-06-2

    Risperidone is a mutil-targeted antagonist for dopamine, serotonin, adrenergic and histamine receptors, used to treat schizophrenia and bipolar disorder.

  • YN481748 Rufinamide 106308-44-5

    Rufinamide is a voltage-gated sodium channel blocker, used an anticonvulsant medication.

  • YN361022 ω-Conotoxin GVIA 106375-28-4

    ω-Conotoxin GVIA is an inhibitor of the N-typeCa2+channel.

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