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Metabolic Disease

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN370023 E 64c 76684-89-4

    Loxistatin Acid (E-64C), a derivative of E-64, is an irreversible and membrane-permeant cysteine protease inhibitor.

  • YN321471 Famotidine 76824-35-6

    Famotidine is a histamine H2–receptor antagonist with IC50 of 0.6 mM, commonly used to treat heartburn, GERD, ulcers, and other digestive conditions.

  • YN373490 Speract 76901-59-2

    Speract, a sea urchin egg peptide that regulates sperm motility, also stimulates sperm mitochondrial metabolism.

  • YN370156 Thyroxine sulfate 77074-49-8

    Thyroxine sulfate is a thyroid hormone metabolite.

  • YN484007 β-Casomorphin (1-6), bovine 77434-43-6

    β-Casomorphin (1-6), bovine is a opioid-like bioactive peptide of β-Casomorphin.

  • YN321937 Adrenocorticotropic Hormone ... 77465-10-2

    Adrenocorticotropic Hormone (ACTH) (1-39), rat is a potentmelanocortin 2 (MC2) receptoragonist.

  • YN481696 Glycolic acid oxidase inhibit... 77529-42-1

    Glycolic acid oxidase inhibitor 1 is aglycolate oxidaseinhibitor, extracted from patent EP0021228A1, in Table IV.

  • YN360533 Picoprazole 78090-11-6

    Picoprazole is a specific inhibitor ofH+/K+-ATPasewith IC50 of 3.1±0.4μM.

  • YN372509 Trequinsin hydrochloride 78416-81-6

    Trequinsin hydrochloride (HL 725) is an extremely potent inhibitor of platelet CAMPphosphodiesterase (PDE), with an IC50 of 0.25nM. Trequinsin hydrochloride (HL 725) is an extremely potent inhibitor of the aggregation of h...

  • YN482685 Plantagoside 78708-33-5

    Plantagoside, a flavanone glucoside isolated from the seeds of Plantago asiatica, is a specific and non-competitive alpha-mannosidase inhibitor with IC50 of 5 μM.

  • YN470013 Calcifediol-D6 78782-98-6

    Calcifediol-D6 is the deuterated form of Calcifediol(25-hydroxy Vitamin D3), which is a prehormone that is produced in the liver by hydroxylation of vitamin D3 (cholecalciferol) by the enzyme cholecalciferol 25-hydroxylase This met...

  • YN470040 Calcitriol D6 78782-99-7

    Calcitriol D6 is the deuterated form of Calcitriol(1,25-Dihydroxyvitamin D3; Rocaltrol ), which is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (V...

  • YN480590 3β-Ursodeoxycholic acid 78919-26-3

    3β-Ursodeoxycholic acid (Isoursodeoxycholic acid) is a bile acid. 3β-Ursodeoxycholic acid (Isoursodeoxycholic acid) shows good tolerance and well intestinal absorption by oral adminstation. 3β-Ursodeoxycholic acid (Isoursodeoxych...

  • YN320490 VU0119498 79183-37-2

    VU0119498 is a pan GqmAChR M1, M3, M5positive allosteric modulator (PAM), with EC50s of 6.04, 6.38, and 4.08 µM, respectively. VU0119498 has antidiabetic activity .

  • YN372957 Fluazifop-P-butyl 79241-46-6

    Fluazifop-P-butyl, a graminicide from arylophenoxypropionate group, is aacetyl-CoA carboxylase (ACCase)inhibitor.

  • YN321508 Azelastine hydrochloride 79307-93-0

    Azelastine HCl is a potent, second-generation, selective, histamine receptor antagonist, used in the treatment of rhinitis.

  • YN483115 Eleutheroside D 79484-75-6

    Eleutheroside D is an active lignan isolated from the root ofEleutherococcus senticosus, has anti-inflammatory and hypoglycemic activities. Eleutheroside D is an optical isomer of Eleutheroside E (HY-N0272).

  • YN370581 (±)8-HETE 79495-84-4

    (±)8-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid (HY-109590). The biological activity of (±)8-HETE is likely to resemble that of its constituent enantiomers (8(R)-...

  • YN290476 L-165041 79558-09-1

    L-165041 is a cell permeablePPARδagonist, with Kis of 6nM and appr 730nM for PPARδ and PPARγ, respectively, and induces adipocyte differentiation in NIH-PPARδ cells.

  • YN322035 Midaglizole hydrochloride 79689-25-1

    Midaglizole hydrochloride (DG5128) is a preferentialα2-adrenoceptorantagonist. Midaglizole hydrochloride (DG5128) exhibits 7.4 times higher affinity (pKi=6.28) toward α2-adrenoceptor than α1-adrenoceptor.

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