Imidazopyridines
Sigma Aldrich Fine Chemicals Biosciences 2-AAPA hydrate 95 HPLC5MG
2-Acetylamino-3-[4-(2-acetylamino-2-carboxy-ethylsulfanylthiocarbonylamino)phenylthiocarbamoylsulfanyl]propionic acid (2-AAPA) can block reductase systems thereby modulating peroxiredoxin oxidation and mitochondrial function in A172 glioblastoma cells.
AdipoGen Stevioside hydrate
Chemical. CAS 57817-89-7 anhydrous. Formula C38H60O18 . xH2O. MW 804.9 anhydrous basis. Isolated from Stevia rebaudiana. Noncaloric natural sweetener, 300 times more potent than sucrose. Antidiabetic. Antihyperglycaemic and antihypoglycaemic. Potentiates insulin secretion. Enhances acetyl-CoA carboxylase ACC gene expression. Increases insulin sensitivity. Antihypertensive. Ca2 influx inhibitor. Anticancer compound. Chemopreventive. Anti-inflammatory. IKKbeta, NF-kappaB and MAPK signaling inhibitor. Induces TNF-alpha, IL-1beta and nitric oxide release. Immunomodulator. Increasees phagocytic activity, haemagglutination antibody titre, delayed type hypersensitivity. Increased proliferation in LPS and Con A stimulated B and T cells. Peripheral µ-opioid receptors activator. Important for regulation of glucose homeostasis. Anti-atherosclerotic. Review.
Medchemexpress LLC Odoroside A | 12738-19-1 | 10 MG
Odoroside A is an active ingredient extracted from the leaves of Nerium oleander Linn. It exhibits anti-cancer activity by inducing apoptosis and cell cycle arrest through the ROS/p53 signaling pathway, leading to tumor cell death.
- Active ingredient extracted from Nerium oleander Linn
- Exhibits anti-cancer activity
- Induces apoptosis and cell cycle arrest
- Works via the ROS/p53 signaling pathway
- Leads to tumor cell death
- High purity of 99.73%
- Molecular weight: 518.68
- Molecular formula: C₃₀H₄₆O₇
- Appearance: White to off-white solid
- Soluble in DMSO
- Targeted pathway: Apoptosis
- For research use only
Medchemexpress LLC Cxcr7 antagonist-1 | 1613021-99-0 | 99.9% | 390.41 | 50 MG
CXCR7 antagonist-1 is a CXCR7 antagonist that inhibits the binding of the SDF-1 chemokine (also known as the CXCL12 chemokine) or I-TAC (also known as CXCL11) to the chemokine receptor CXCR7. It is useful in preventing tumor cell proliferation, tumor formation, inflammatory diseases, and many other diseases.
- Inhibits binding of SDF-1 (CXCL12) or I-TAC (CXCL11) to the chemokine receptor CXCR7.
- Useful in preventing tumor cell proliferation and formation.
- Applied in inflammatory diseases.
- Restores CXCL11 or RSV infection-induced β2-adrenergic receptor (β2AR) downregulation in infant airway smooth muscle cells.
- Inhibits airway smooth muscle relaxation induced by RSV-infection in BALB/c mouse models.
![eMolecules 429690-42-6 | Ethyl 3-bromoimidazo[1,2-a]pyridine-5-carboxylate | MFCD10566747 | 250mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502137970.JPG-250.jpg)
eMolecules 429690-42-6 | Ethyl 3-bromoimidazo[1,2-a]pyridine-5-carboxylate | MFCD10566747 | 250mg
Ambeed | 1-(1H-Benzo[d]imidazol-2-yl)ethanone | 1g | 552701489 | A307673 | 939-70-8 | MFCD00159994 | 160.176 | C9H8N2O
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