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

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN360292 Hyperforin dicyclohexylammoni... 238074-03-8

    Hyperforin dicyclohexylammonium salt (Hyperforin DCHA) is atransient receptor canonical 6 (TRPC6)channels activator. Hyperforin dicyclohexylammonium salt modulates Ca2+levels by activating Ca2+-conducting non-selective canonica...

  • YN482815 Sibiricose A6 241125-75-7

    Sibiricose A6 is an oligosaccharide ester isolated fromPolygalae Radixwith potent antioxidant activity.

  • YN360023 N-type calcium channel blocke... 241499-17-2

    N-type calcium channel blocker-1 is an orally active analgesic agent which shows high affinity to functionally block N-type calcium channelswith an IC50 of 0.7μM in the IMR32 assay.

  • YN321337 Solifenacin 242478-37-1

    Solifenacin is a novel muscarinic receptor antagonist with pKis of 7.6, 6.9 and 8.0 for M1, M2 and M3 receptors, respectively.

  • YN321318 Solifenacin Succinate 242478-38-2

    Solifenacin succinate is a urinary antispasmodic of the antimuscarinic class.

  • YN320713 JTC-801 244218-51-7

    JTC-801 is a selective opioid receptor-like1 (ORL1) receptor antagonist with IC50 of 94 nM, weakly inhibits receptors δ, κ, and μ.

  • YN321886 FSLLRY-NH2 245329-02-6

    FSLLRY-NH2 is aprotease-activated receptor 2 (PAR2)inhibitor.

  • YN380276 Rubrofusarin triglucoside 245724-07-6

    Rubrofusarin triglucoside is a glycoside compound isolated fromCassia obtusifolia Linnseeds. Rubrofusarin triglucoside inhibitshuman monoamine oxidase A (hMAO-A)with an IC50 of 85.5μM.

  • YN360010 Varenicline 249296-44-4

    Varenicline is highly selective and blocks more potently to α4β2 receptors than to other common nicotinic receptors (>500-fold α3β4, >3,500-fold α7, >20,000-fold α1βγδ), or to non-nicotinic receptors and transporters (>2,000-fold)...

  • YN320389 SB-334867 249889-64-3

    SB-334867 (SB 334867A) is an excellent,selective and blood–brain barrier permeableorexin-1 (OX1) receptorantagonist, shows selectivity overOX2(pKb=7.4), 100-fold over 5-HT2B, 5-HT2Cwith pKi values. of 5.4 and 5.3, resp...

  • YN300075 Dynamin inhibitory peptide 251634-21-6

    Dynamin inhibitory peptide competitively blocks binding ofdynaminto amphiphysin, thus preventing endocytosis. Dynamin inhibitory peptide blocks the dopamine D3 effect on GABAA receptors.

  • YN300079 DynaMin inhibitory peptide, ... 251634-22-7

    DynaMin inhibitory peptide, myristoylated is aDynaMininhibitor to interfere with the binding of amphiphysin with dynamin. DynaMin inhibitory peptide, myristoylated is a membrane-permeant form of the peptide that prevents endocytosis.

  • YN483494 Hydroxy-Epsilon-Sanshool 252193-26-3

    Hydroxy-Epsilon-Sanshool is an alkylamide isolated fromZanthoxylum bungeanum. Hydroxy-Epsilon-Sanshool produces key tingling and numbing chemosensates, and its content is important in determinant the pungency intensity ofZanthox...

  • YN322010 T 82 252264-92-9

    T 82 is a potent5-HT3antagonist and acetylcholinesterase (AChE)inhibitor, used for treatment of Alzheimer's Disease.

  • YN360102 TPA 023 252977-51-8

    TPA 023 is aGABAA α2/α3subtype-selective agonist, with Kiof 0.19-0.41nM.

  • YN250099 Emricasan 254750-02-2

    Emricasan is a potent irreversible pan-caspase inhibitor.

  • YN322098 SEW​2871 256414-75-2

    SEW2871 is a highly selective, orally activeS1P1agonist with an EC50 of 13.8nM. SEW2871 activates ERK, Akt, and Rac signaling pathways and induces S1P1 internalization and recycling. SEW2871 reduces lymphocyte num...

  • YN480270 Secoisolariciresinol diglucos... 257930-74-8

    Secoisolariciresinol diglucoside ((S,S)-SDG), the main lignan in wholegrain flaxseed, known for its beneficial effects including anti-inflammatory, antioxidant, anti-mutagenic, anti-microbial, anti-obesity, hypolipidemic, and neuro...

  • YN480010 Enecadin 259525-01-4

    Enecadin is a neuroprotective agent extracted from patent US 8623823 B2.

  • YN360276 TRPM8 antagonist 2 259674-19-6

    TRPM8 antagonist 2 is a potent and selectiveTRPM8antagonist, with an IC50 of 0.2nM, used in the research of neuropathic pain syndromes.

    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
3.971082s