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Neurological Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN481377 PKR-IN-C16 608512-97-6

    PKR-IN-C16 (imoxin, C16, Imidazolo-oxindole PKR inhibitor C16) is a specific inhibitor of RNA-dependent protein kinase (PKR, Protein Kinase R, EIF2AK2). PKR-IN-C16 prevents apoptosis and IL...

  • YN320915 Tasimelteon 609799-22-6

    Tasimelteon is a melatonin MT1 and MT2 receptor agonist.

  • YN420186 AZD1080 612487-72-6

    AZD1080 is a selective, orally active, brain permeable GSK3 inhibitor, inhibits human GSK3α and GSK3β with Ki of 6.9 nM and 31 nM, respectively, shows >14-fold selectivity against CDK2, CDK5, CDK1 and Erk2.

  • YN320503 CB1 antagonist 2 614726-85-1

    CB1 antagonist 2 is caimabinoid 1 (CB1) antagonist extracted from patent WO2016184310A1, compound 3, inhibits CB1 in vivo with an IC50 of 25.5nM.

  • YN483737 Argireline 616204-22-9

    Argireline (Acetyl hexapeptide-3) is a non-toxic, skin-permeable, antiwrinkle peptide. Argireline significantly inhibits Ca2+dependent neurotransmitter release (acetylcholine) at the neuromuscular junction. Argireline has antiwrinkle ...

  • YN370499 AZD5904 618913-30-7

    AZD5904 is a potent and irreversible inhibitor of humanMyeloperoxidase(MPO) with an IC50 of 140nM and has similar potency in mouse and rat.

  • YN483188 Bacopaside V 620592-16-7

    Bacopaside V is a bioactive triterpenoid glycoside ofBacopa monniera, a herb having confirmed nervine tonic activity.

  • YN321086 Tradipitant 622370-35-8

    Tradipitant (VLY-686) is aneurokinin-1(NK-1) antagonist.

  • YN1730087 PD-168077 maleate 630117-19-0

    PD-168077 maleate is a selective dopamineD4receptor agonist, with aKiof 9nM.

  • YN380307 β-Amyloid (33-40) 634204-57-2

    β-Amyloid (33-40) is a peptide consisting of amino acid of 33 to 40 of beta amyloid protein.

  • YN320892 TBPB 634616-95-8

    TBPB is an allosteric M1 mAChR agonist(EC50=289nM) that regulates amyloid processing and produces antipsychotic-like

  • YN480638 AER-271 634913-39-6

    AER-271, a phosphonate prodrug derivative of AER-270, is anaquaporin-4(AQP4) inhibitor for the research of acute ischemic stroke.

  • YN321288 LY404039 635318-11-5

    LY404039 is a potent agonist of recombinant human mGlu2/mGlu3 receptors with Ki of 149 nM/92 nM, shows >100-fold selectivity over ionotropic glutamate receptors, glutamate transporters, and other receptors. Phase 3.

  • YN320277 Pomaglumetad methionil hydroc... 635318-26-2

    Pomaglumetad methionil hydrochloride (LY2140023 hydrochloride) is an orally active, methionine prodrug of the selective mGlu2/3 receptor agonist LY404039. Pomaglumetad methionil hydrochloride has the potential for schizophrenia resea...

  • YN320887 Pomaglumetad methionil anhydr... 635318-55-7

    Pomaglumetad methionil anhydrous (LY2140023) is an orally active, methionine prodrug of the selective mGlu2/3 receptor agonist LY404039. LY2140023 has the potential for schizophrenia research.

  • YN321251 F-15599 635323-95-4

    F-15599 is a highly selective G-protein biased5-HT1A receptoragonist, with Kiof 3.4nM.

  • YN360168 Salfaprodil free base 640290-67-1

    Salfaprodil free base (Neu2000) is an NR2B-selective and uncompetitive antagonist ofN-methyl-D-aspartate (NMDA), and a free radical scavenger. Salfaprodil free base has excellent neuroprotection againstnMDA- and free ra...

  • YN481017 Jedi2 651005-90-2

    Jedi2 is aPiezo1channel activator, but no specific Piezo2 activators. Jedi2 binds to the mouse Piezo1 proteins with a Kdof 2770  μM.

  • YN360166 AMG 517 659730-32-2

    AMG 517 is a potent and selective TRPV1 antagonist, and antagonizes capsaicin, proton, and heat activation of TRPV1 with IC50 of 0.76 nM, 0.62 nM and 1.3 nM, respectively.

  • YN321140 Levalbuterol tartrate 661464-94-4

    Levalbuterol HCl is a relatively selective beta2-adrenergic receptor agonist used for the treatment of asthma.

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