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Inflammation/Immunology

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN372909 Dichlorisone acetate 79-61-8

    Dichlorisone acetate is a synthetic glucocorticoid corticosteroid used as an anti-inflammatory agent.

  • YN482516 DL-Threonine 80-68-2

    DL-Threonine, an essential amino acid, has the potential to treat hypostatic leg ulceration.

  • YN251965 Saccharin 81-07-2

    Saccharin is an artificial sweetener with effectively no food energy.

  • YN372911 D-Panthenol 81-13-0

    Dexpanthenol is an alcoholic analogue of D-pantothenic acid and cholinergic agent.

  • YN372949 Taurocholic acid 81-24-3

    Taurocholic acid (N-Choloyltaurine) is a bile acid involved in the emulsification of fats.

  • YN321438 Methylprednisolone 83-43-2

    Methylprednisolone is a synthetic glucocorticoid receptor agonist, used to achieve prompt suppression of inflammation.

  • YN373064 Beta-Sitosterol (purity>80%) 83-46-5

    Beta-Sitosterol (purity>80%) includes β-sitosterol (≥80%), stigmasterol, campesterol and brassicasterol mainly. Beta-Sitosterol is a plant sterol. Beta-Sitosterol (purity>98%) interfere with multiple cell signaling pathways, inclu...

  • YN373051 Stigmasterol 83-48-7

    Stigmasterol is a plant sterol which has been focused on the cholesterol-lowering activity and is valued as an anti-stiffness factor in the therapy of rheumatic diseases.

  • YN373177 Phytic acid 83-86-3

    Phytic acid is the principal storage form of phosphorus in many plant tissues, especially bran and seeds. It can act as a cofactor in DNA repair by nonhomologous end-joining.

  • YN482768 Skimmianine 83-95-4

    Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with analgesic, antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer...

  • YN330523 Rutaecarpine 84-26-4

    Rutaecarpine is an indolopyridoquinazolinone alkaloid isolated from Evodia rutaecarpa and related herbs a new class of COX-2 inhibitor.

  • YN251733 Lapachol 84-79-7

    Lapachol is a naphthoquinone that was first isolated fromTabebuia avellanedae(Bignoniaceae). Lapachol shows anti-abscess, anti-ulcer, antileishmanial, anticarcinomic, antiedemic, anti-inflammatory, antimalarial, antiseptic, antitumor, a...

  • YN480896 Alimemazine 84-96-8

    Alimemazine is a phenothiazine derivative that is generally used as an antipruritic agent and also ahemagglutinin(HA)-receptorantagonist.Alimemazine (Trimeprazine) is also acts as a partial agonist against the histamine H1 receptor ...

  • YN482065 Phenanthrene 85-01-8

    Phenanthrene is a polycyclic aromatic hydrocarbon (PAH) and has been frequently used as an indicator for monitoring PAH contaminated matrices. Phenanthrene induces oxidative stress and inflammation.

  • YN251291 Amodiaquine 86-42-0

    Amodiaquine is a synthetic aminoquinoline that acts by binding to the protozoal or parasitic DNA and preventing DNA and RNA production and subsequent protein synthesis. It is used for the therapy of malaria.

  • YN330709 2,5-Di-tert-butylhydroquinone 88-58-4

    BHQ is a potent and selective inhibitor of the sarco-endoplasmic reticulum Ca2+-ATPase (SERCA).

  • YN360052 Quinolinic acid 89-00-9

    Quinolinic acid is an endogenous N-methyl-D-aspartate (NMDA) receptoragonist synthesized from L-tryptophan via the kynurenine pathway and thereby has the potential of mediating N-methyl-D-aspartate neuronal damage and dysfunct...

  • YN372252 5-Aminosalicylic Acid 89-57-6

    Mesalamine is a specific inhibitor of TNFα-induced IKK activity, used to treat inflammatory bowel disease.

  • YN360955 Pulegone 89-82-7

    Pulegone has cytotoxicity followed by regenerative cell proliferation is the MOA for Pulegone-induced urothelial tumors in female rats. Pulegone induces a verapamil-sensitive psychostimulant effect that appears to independ on the open...

  • YN251721 Thymol 89-83-8

    Thymol, a naturally occurring monocyclic phenolic compound derived from Thymus vulgaris (Lamiaceae), has been reported to exhibit anti-inflammatory property in vivo and vitro.

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