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Neurological Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN360043 U93631 152273-12-6

    U93631 is a GABAA receptor lig and of novel chemical structure with IC50 of 100nM, and has been shown to induce a rapid, time-dependent decay of GABA-induced whole-cell Cl-currents in recombinant GABAA receptors.

  • YN380285 Amyloid β-Protein 10-20 152286-31-2

    Amyloid β-Protein (10-20) is a fragment of Amyloid-β peptide, maybe used in the research of neurological disease.

  • YN320722 7-Desmethyl-agomelatine 152302-45-9

    7-Desmethyl-agomelatine is a metabolite of Agomelatine. Agomelatineis a potent agonist at melatonin receptors (MT1 and MT2), and also is an antagonist of 5-HT2C.

  • YN320181 Alniditan 152317-89-0

    Alniditan is a potent5-HT1B/1Dreceptorsagonist, with IC50 of 1.7 and 1.3nM in HEK 293 cells,and pKivalue of 8.96 and 9.40 for 5-HT1B/1Dreceptors, respectively.

  • YN320635 Nalfurafine 152657-84-6

    Nalfurafine (TRK-820) is a potent selective and orally active G protein-biasedkappa opioid receptor (KOR)-agonist with high translational potential. Nalfurafine (TRK-820) enhances the therapeutic potential of MOR-targeting...

  • YN320636 Nalfurafine hydrochloride 152658-17-8

    Nalfurafine hydrochloride (TRK-820 hydrochloride) is a potent selective  and  orally active G protein-biasedkappa opioid receptor (KOR)-agonist with high translational potential. Nalfurafine hydrochloride (TRK-820 h...

  • YN1730120 U91356 152886-85-6

    U91356 is adopamine receptoragonist.

  • YN1730083 AB-MECA 152918-26-8

    AB-MECA is a high affinity A3 adenosine receptor agonist, has high affinity for recombinant A1 and A3 receptors.

  • YN360201 Lanicemine 153322-05-5

    Lanicemine (AZD6765) is a low-trappingNMDA channel blockerwith a binding (Ki) of 0.56-2.1 μM.

  • YN280154 Ginkgolide K 153355-70-5

    Ginkgolide K, isolated fromGinkgo biloba, induces protective autophagy through the AMPK/mTOR/ULK1 signaling pathway. Ginkgolide K possesses neuroprotective activity.

  • YN321310 Cevimeline hydrochloride hemi... 153504-70-2

    Cevimeline (AF 102B, SNI 2011, SNK 508) is a parasympathomimetic agent that act as an agonist at the muscarinic acetylcholine receptors M1 and M3.

  • YN321912 [D-Trp34]-Neuropeptide Y 153549-84-9

    [D-Trp34]-Neuropeptide Y is a potent and selectiveneuropeptide Y (NPY) Y5receptoragonist. [D-Trp34]-Neuropeptide Y is a significantly less potent agonist at the NPY Y1, Y2, Y4, and y6receptors. [D-Trp34]-Neuropepti...

  • YN361076 S16961 153874-14-7

    S16961 is anicotinic receptoragonist.

  • YN360097 RPR104632 154106-92-0

    RPR104632 is a specific antagonist of NMDA receptor, with potent neuroprotective properties.

  • YN320369 PD 144418 154130-99-1

    PD 144418 is a highly affinity, potent and selectivesigma 1 (σ1) receptorlig and (Kivalues of 0.08nM and 1377nM forσ1 and σ2 respectively). PD 144418 devoids of any significant affinity for other receptors, ion channels and...

  • YN360515 YM90K 154164-30-4

    YM90K is a potent and selectiveAMPA receptorantagonist with a Ki of 84nM. YM90K is less potent in inhibiting kainate (Kiof 2.2μM) and nMDA (Kiof 37μM) receptors. YM90K has neuroprotective actions.

  • YN360235 CX516 154235-83-3

    Ampalex (CX-516, Ampakine CX 516, BDP-12, SPD 420) is a positive allosteric modulator of AMPA receptor. Ampalex exhibits potential treatment for Alzheimer's disease, schizophrenia and mild cognitive impairment (MC...

  • YN321478 Almotriptan 154323-57-6

    Almotriptan is a 5-HT1B/1D-receptor agonist used to treat migraine. Almotriptan is a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) receptor agonist, used for the treatment of Migraine attacks in adults. Almotriptan showed low...

  • YN1730028 Istradefylline 155270-99-8

    Istradefylline is a selective adenosine A2A receptor (A2AR) antagonist with Ki of 2.2 nM. Phase 3.

  • YN1730118 KF21213 155271-17-3

    KF21213 is a highly selective lig and for mapping CNS adenosineA2Areceptors. KF21213 shows a high affinity for the adenosineA2Areceptors (Ki=3.0nM).

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