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Neurological Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN380058 Pirimicarb 23103-98-2

    Pirimicarb is a fast-acting selective carbamate insecticide on a wide range of crops including cereals, sugar beet, potatoes, fruits and vegetables. Pirimicarb is anAChEinhibitor and an acaricide.

  • YN310159 Nicotinamide riboside chlorid... 23111-00-4

    Nicotinamide Riboside Chloride (NIAGEN) is the chloride salt form of nicotinamide riboside(NR).NR is a new form pyridine-nucleoside of vitamin B3 that functions as a precursor to nicotinamide adenine dinucleotide(NAD)

  • YN373080 Paeoniflorin 23180-57-6

    Paeoniflorin is a herbal constituent extracted from the root of Paeonia albiflora Pall.

  • YN360387 Ifenprodil tartrate 23210-58-4

    Ifenprodil is an atypical noncompetitive antagonist at the NMDA receptor, it interacts with high affinity at a homogeneous population of NMDA receptors in neonatal rat forebrain with IC50 of 0.3 μM.

  • YN1730014 Levophacetoperane hydrochlori... 23257-56-9

    Levophacetoperane inhibits in vitro in a competitive manner,norepinephrinuptake and dopamineuptake.

  • YN450139 Nefopam hydrochloride 23327-57-3

    Nefopam HCl is a centrally-acting but non-opioid analgesic drug by blocking voltage-gated sodium channel and inhibition of serotonin, dopamine and noradrenaline reuptake.

  • YN322106 2-Palmitoylglycerol 23470-00-0

    2-Palmitoylglycerol (2-Palm-Gl), an congener of 2-arachidonoylglycerol (2-AG), is a modestcannabinoid receptor CB1agonist. 2-Palmitoylglycerol also may be an endogenous lig and for GPR119.

  • YN380111 Hoechst 34580 23555-00-2

    Hoechst 34580 (HOE 34580) is a cell-permeable blue fluorescent dye to stain DNA and nuclei. Hoechst 34580 is also a good candidate for treating the Alzheimer's disease by inhibiting amyloid beta (Aβ) formation with IC50 ...

  • YN481182 Droxidopa 23651-95-8

    Droxidopa is a psychoactive drug and acts as a prodrug to the neurotransmitters norepinephrine (noradrenaline) and epinephrine (adrenaline).

  • YN1730101 Levosulpiride 23672-07-3

    Levosulpiride is a selective antagonist for D2 dopamine receptors used as an antipsychotic and prokinetic agent.

  • YN1730089 Sultopride hydrochloride 23694-17-9

    Sultopride hydrochloride (LIN-1418 hydrochloride) is a selective antagonist ofdopamine D2 receptor.

  • YN482435 Nardosinone 23720-80-1

    Nardosinone has inhibitory effect on Ang II-induced hypertrophy in H9c2 cells, might be mediated by targeting PI3K/Akt and MEK/ERK signaling pathways. Nardosinone could protect against the neuronal injury exposed to OG...

  • YN372879 Ambroxol hydrochloride 23828-92-4

    AmbroxolHCl is a potent inhibitor of the neuronal Na+ channels, inhibits TTX-resistant Na+ currents with IC50 of 35.2 μM and 22.5 μM for tonic and phasic block, inhibits TTX-sensitive Na+ currents with IC50 of 100 μM. ...

  • YN481825 Articaine hydrochloride 23964-57-0

    Articaine is a dental local anesthetic which contains an additional ester group that is metabolized by estearases in blood and tissue.

  • YN321760 Meranzin 23971-42-8

    Meranzin is an absorbed bioactive compound from the Traditional Chinese Medicine (TCM) Chaihu-Shugan-San (CSS). Meranzin, isolated from leaves ofMurraya exoticaL., regulates the shared alpha 2-adrenoceptor and involves th...

  • YN360096 Ethyl dirazepate 23980-14-5

    Ethyl dirazepate is a drug which is abenzodiazepinederivative. It has anxiolytic and hypnotic and possibly other characteristic benzodiazepine properties.

  • YN360077 QX-314 bromide 24003-58-5

    QX-314 bromide is a membrane-impermeable permanently chargedsodium channelblocker.

  • YN482426 Farrerol 24211-30-1

    Farrerol, an important bioactive constituent of rhododendron, exhibits broad activities such as anti-oxidative and anti-inflammatory effects.

  • YN321408 Mianserin 24219-97-4

    Mianserin is a H1 receptor inverse agonist and is a psychoactive agent of the tetracyclic antidepressant.

  • YN361027 Apamin 24345-16-2

    Apamin (Apamine) is an 18 amino acid peptide neurotoxin found in apitoxin (bee venom), is known as a specifically selective blocker ofCa2+-activatedK+(SK) channels and exhibits anti-inflammatory and anti-fibrotic activity.

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