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Neurological Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN1441175 Fluphenazine dihydrochloride 146-56-5

    Fluphenazine dihydrochloride is a phenothiazine-class D1DR and D2DR inhibitor. It also inhibits Histamine H1 Receptor.

  • YN321598 Pilocarpine nitrate 148-72-1

    Pilocarpine nitrate is a selective M3-type muscarinic acetylcholine receptor (M3 muscarinic receptor) agonist.

  • YN481928 Butacaine 149-16-6

    Butacaine is a reversiblenerve conductionblocker. Butacaine acts on the nervous system and nerve fibers, can cause both sensory and motor paralysis.

  • YN321657 Serotonin hydrochloride 153-98-0

    Serotonin HCl is a monoamine neurotransmitter and Endogenous 5-HT receptor agonist.

  • YN484342 2-Phenylethylamine hydrochlor... 156-28-5

    2-Phenylethanamine hydrochloride is believed to function as a neuromodulator or neurotransmitter.

  • YN250158 6-Diazo-5-oxo-L-nor-Leucine 157-03-9

    L-6-Diazo-5-oxonorleucine (L-6-Diazo-5-oxonorleucine) is aglutaminasesantagonist with a Ki of 6μM. L-6-Diazo-5-oxonorleucine exhibits analgesic, antibacterial, antiviral and anticancer properties. L-6-Diazo-5-oxonorleucine dis...

  • YN374078 Norharmane 244-63-3

    Norharmane (Norharman), isolated from coffee, is a potent and selectivemonoamine oxidase A(MAO-A) inhibitor with a Ki of 3.34μM.

  • YN360752 Carbamazepine 298-46-4

    Carbamazepine (Carbatrol) is a sodium channel blocker with IC50 of 131 μM in rat brain synaptosomes.

  • YN321517 Arecoline hydrobromide 300-08-3

    Arecoline is a muscarinic acetylcholine receptor agonist.

  • YN370770 3-O-Methyldopa 300-48-1

    3-O-Methyldopa (3-Methoxy-L-tyrosine) is a metabolite of L-DOPA which is formed by catechol-O-methyltransferase (COMT). 3-O-Methyldopa competitively inhibits the pharmacodynamics of l-DOPA and dopamine.

  • YN370103 Hypotaurine 300-84-5

    Hypotaurine (2-aminoethanesulfinic acid), an intermediate in taurine biosynthesis from cysteine in astrocytes, is an endogenous inhibitory amino acid of theglycine receptor.

  • YN330521 Coenzyme Q10 303-98-0

    Coenzyme Q10 is an essential cofactor of the electron transport chain and a potent antioxidant agent.

  • YN481968 Etamivan 304-84-7

    Etamivan (Ethamivan), an orally active respiratory stimulant, is mainly used in the research of barbiturate overdose and chronic obstructive pulmonary disease.

  • YN380190 Iproniazid phosphate 305-33-9

    Iproniazid (Marsilid, Iprazid) phosphate is a non-selective, irreversible monoamine oxidase (MAO) inhibitor (MAOI) that is used as an antidepressive agent.

  • YN360798 Doxapram 309-29-5

    Doxapram is a central respiratory stimulant with a brief duration of action.

  • YN480633 ELN484228 312-63-0

    ELN484228 is a blocker ofα-synucleinwhich is a key protein in Parkinson’s disease.

  • YN321609 Pimethixene 314-03-4

    Pimethixene is antihistamine and antiserotonergic compound, acts as an antimigraine agent. Pimethixene is a highly potent antagonist of 5-HT1A, 5-HT2A, 5-HT2B, 5-HT2C, histamine H1, dopamine D2 and D4.4as well as muscari...

  • YN321537 Propranolol hydrochloride 318-98-9

    Propranolol HCl is a competitive non-selective beta-adrenergic receptors inhibitor with IC50 of 12 nM.

  • YN482348 D-Isoleucine 319-78-8

    D-Isoleucine ((R)-Isoleucine), an isoleucine stereoisomer, is a selective activator of Asc-1 antiporter, which enhances long-term potentiation at the hippocampal CA1-CA3 via release of endogenous D-serine.

  • YN374399 D-Leucine 328-38-1

    D-Leucine is a more potent anti-seizure agent than L-leucine. D-leucine potently terminates seizures even after the onset of seizure activity. D-leucine, but not L-leucine, reduces long-term potentiation but had no effect on basal syn...

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