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Neurological Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN480742 Homobaldrinal 67910-07-0

    Homobaldrinal is adecomposition productof Valepotriate (HY-N0718). Homobaldrinal exhibits genotoxic activity in the Salmonella/microsome test.

  • YN321941 Substance P(1-7) 68060-49-1

    Substance P(1-7) is a fragment of the neuropeptide, substance P (SP). Substance P(1-7) gives depressor and bradycardic effects when applied to the nucleus tractus solitarius.

  • YN360176 (2S)-6-Prenylnaringenin 68236-13-5

    (2S)-6-Prenylnaringenin is the most efficient compound in forebrain. (2S)-6-Prenylnaringenin acts as aGABAApositive allosteric modulator at α+β- binding interface.

  • YN481604 (R)-Oxiracetam 68252-28-8

    (R)-Oxiracetam is the (R)-enantiomer of the nootropic drug oxiracetam. Oxiracetam (ISF 2522) is a nootropic drug of the racetam family and stimulant.

  • YN360739 Zonisamide 68291-97-4

    Zonisamide is a voltage-dependent sodium channel and T-type calcium channel blocker, used as an antiepileptic drug.

  • YN360740 Zonisamide sodium 68291-98-5

    Zonisamide sodium (AD 810 sodium; CI 912 sodium) is an inhibitor of zinc enzymecarbonic anhydrase (CA), with Kis of 35.2nM and 20.6nM for human mitochondrial isozyme hCA II and hCA V, respectively. Zonisamide sodium ha...

  • YN484265 Verilopam 68318-20-7

    Verilopam is a potent analgesic.

  • YN481586 Pramiracetam 68497-62-1

    Pramiracetam is a more potent nootropic drug derived from piracetam.

  • YN360534 Vigabatrin 68506-86-5

    Vigabatrin (γ-Vinyl-GABA), a inhibitory neurotransmitter GABA vinyl-derivative, is an orally active and irreversible GABA transaminaseinhibitor. Vigabatrin is an antiepileptic agent, which acts by increasing GABA level...

  • YN360055 Isoguvacine hydrochloride 68547-97-7

    Isoguvacine hydrochloride is a GABA receptor agonist.

  • YN350223 (Rac)-Hesperetin 69097-99-0

    (Rac)-Hesperetin is the racemate of Hesperetin. Hesperetin is a natural flavanone, and acts as a potent and broad-spectrum inhibitor against humanUGTactivity. Hesperetin induces apoptosis via p38 MAPK activation.

  • YN270574 Gomisin N 69176-52-9

    Gomisin N, isolated from Schis and ra chinensis, produces beneficial sedative and hypnotic bioactivity. Gomisin N has the potential for use in the treatment of allergy. Gomisin N is an anti-cancer drug c and idate capable of inhibi...

  • YN360610 (R)-Baclofen 69308-37-8

    (R)-baclofen is a derivative of gamma-aminobutyric acid primarily used to treat spasticity.

  • YN483940 ACTH (34-39) 69454-10-0

    ACTH (34-39) is an adrenocorticotropic hormone fragment.

  • YN360202 Pivagabine 69542-93-4

    Pivagabine (CXB 722) is a hydrophobic 4-aminobutyric acid derivative with neuromodulatory activity. Pivagabine penetrates the blood-brain barrier in rats. Pivagabine antagonizes the effects of foot shock on both GABAA receptor f...

  • YN361092 GI-530159 69563-88-8

    GI-530159 is a selective, mechanosensitive opener ofTREK1 (K2P2.1) and TREK2 (K2P10.1) channels, with an EC50 of 0.76μM for TREK1. GI-530159 displays selectivity for TREK1/2 over TRAAK, TASK3 and other...

  • YN480257 18:0 LYSO-PE 69747-55-3

    18:0 LYSO-PE is an agent that can induce [Ca2+]iincrease.

  • YN330189 Pelubiprofen 69956-77-0

    Pelubiprofen, an orally active and non-steroidal anti-inflammatory drug, is a member of the 2-arylpropionic acid family and has relatively selective effects onCOX-2activity. Pelubiprofen inhibits COX activity and the transform...

  • YN1730067 ABT-724 70006-24-5

    ABT-724 is a potent and highly selectivedopamine D4receptoragonist with an EC50 of 12.4nM forhuman dopamine D4receptor. ABT-724 is a potent partial agonist at therat D4(EC50of 14.3nM) and theferret D4receptor(EC50of 23...

  • YN380265 Obtusin 70588-05-5

    Obtusin, isolated fromCassia obtusifoliaLinn seed, is a highly selective and competitivehuman monoamine oxidase-A (hMAO-A)inhibitor with an IC50 of 11.12μM and a Ki of 6.15μM. Obtusin plays a preventive role in neurodege...

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