Welcome to ULS!
Welcome to ULS!
> Products > Research Areas > Neurological Disease
Products
Neurological Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN482810 Sibiricose A5 107912-97-0

    Sibiricose A5 displays antidepressant-like action, it may prevent or relieve depression. Sibiricose A5 is a lactate dehydrogenase inhibitor. Sibiricose A5 can protect PC12 cells damage induced by P. tenuifolia. Sibiricose A5...

  • YN320261 SKF-83566 hydrobromide 108179-91-5

    SKF-83566 hydrobromide is a potent, blood-brain permeable and orally activeD1-like dopamine receptor (D1DR)antagonist and a weaker competitive antagonist at the vascular 5-HT2receptor (Ki=11nM). SKF-83566 is a competitive...

  • YN322090 Benzamide Derivative 1 108226-05-7

    Benzamide Derivative 1 is a benzamide derivative from patent EP0213775A1, compound 18. Benzamide Derivative 1 may be useful in treatment of gastrointestinal disorders.

  • YN330144 RCGD423 108237-91-8

    RCGD-423 is a modulator of gp130 signalling that regulates cartilage growth and differentiation.

  • YN361029 Syntide 2 108334-68-5

    Syntide 2, aCa2+- and calmodulin (CaM)-dependent protein kinase II (CaMKII)substrate peptide, selectively inhibits the gibberellin (GA) response, leaving constitutive and abscisic acid-regulated events unaffected.

  • YN380293 β-Amyloid (1-28) 109770-29-8

    β-Amyloid (1-28) is a β-Amyloid protein fragment involved in metal binding. Beta-amyloid is a peptide that forms amyloid plaques in the brains of Alzheimer's disease (AD) patients.

  • YN360153 Zaldaride maleate 109826-27-9

    Zaldaride maleate (CGS-9343B) is a potent, orally active and selective inhibitor ofcalmodulin. Zaldaride maleate (CGS-9343B) inhibits CaM (calmodulin)-stimulated cAMP phosphodiesterase activity, with an IC50 of 3.3nM. Z...

  • YN321380 Granisetron 109889-09-0

    Granisetron is a serotonin receptor (5HT-3 selective) antagonist that is used as an antiemetic and antinauseant for cancer chemotherapy.

  • YN370871 ALLM 110115-07-6

    ALLM (Calpain inhibitor II) is a potent inhibitor ofcalpain and cathepsinproteases. ALLM inhibits neuronal cell death and improves chronic neurological function after spinal cord injury (SCI).

  • YN360523 Selfotel 110347-85-8

    Selfotel (CGS 19755) is a selective and competitive antagonist at N-methyl-D-aspartate(NMDA)-preferring receptor. CGS 19755 inhibits the binding of [3H]-3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid tonMDA-type rece...

  • YN380178 Paroxetine hydrochloride hemi... 110429-35-1

    Paroxetine hydrochloride hemihydrate is a potent selectiveserotonin-reuptakeinhibitor, commonly prescribed as an antidepressant and has GRK2 inhibitory ability with IC50 of 14 μM.

  • YN361028 Myomodulin 110570-93-9

    Myomodulin is a neuropeptide present in molluscs, insects, and gastropods.

  • YN321834 [Sar9,Met(O2)11]-Substance... 110880-55-2

    [Sar9,Met(O2)11]-Substance P is atachykinin NK1receptorselective agonist.

  • YN360980 Annonacin 111035-65-5

    Annonacin is anAcetogenin and promotes cytotoxicity via a pathway inhibiting the mitochondrial complex. Annonacin is the active agent found in Graviola leaf extract to act as an inhibitor ofsodium/potassium (NKA) and sarcoplasmic re...

  • YN320105 Naltrindole hydrochloride 111469-81-9

    Naltrindole hydrochloride is a highly potent and selective non-peptideδ opioidreceptor antagonist with a Ki of 0.02nM.

  • YN320882 Quetiapine 111974-69-7

    Quetiapine is an atypical antipsychotic used for the treatment of schizophrenia, bipolar disorder, and major depressive disorder.

  • YN321373 Quetiapine hemifumarate 111974-72-2

    Quetiapine Fumarate is an atypical antipsychotic used in the treatment of schizophrenia, bipolar I mania, bipolar II depression, bipolar I depression and shows affinity for various neurotransmitter receptors including serotonin, dopam...

  • YN380305 β-Amyloid (18-28) 112163-49-2

    β-Amyloid (18-28) is a peptide fragment of β-Amyloid.

  • YN480635 Soluflazine 112415-83-5

    Soluflazine is anucleoside transportinhibitor with anticonvulsant action. Soluflazine can be used as an antiepileptic agent.

  • YN321378 Tandospirone citrate 112457-95-1

    T and ospirone citrate is a potent and selective 5-HT1A receptor partial agonist (Ki = 27nM) that displays selectivity over SR-2, SR-1C, α1, α2, D1 and D2 receptors (Ki values ranging from 1300-41000nM).

    Contact

    TELL : +86-020-82000279

    Email: sales@ubiochem.com

    Add:Room 519, Block F, Guangzhou International Business Incubator, No.3 Lanyue Road, Science Town, Huangpu District, Guangzhou, China.

ULS products are chemical reagents for Research Use Only!Copyright © 2020-2021 ULS. All Rights Reserved.备案号:粤ICP备2021013238号-2
2.460189s