amf

PBE-AMF is a prodrug that activates H2O2 and exhibits anticancer activity. It impedes tumor proliferation by inhibiting DNA synthesis, reducing ATP levels, inducing cell death (apoptosis), and blocking the cell cycle. PBE-AMF effectively and selectively inhibits the proliferation of MDA-MB-231 cells (IC50=6.4 μM) while sparing non-cancerous MCF-10A cells.

PBA-AMF is activated by H2O2, releasing formamide (AMF). This compound selectively inhibits the proliferation of breast cancer cells without affecting non-cancerous cells. It works by inhibiting DNA synthesis, reducing ATP levels, inducing apoptosis (Apoptosis), and arresting the cell cycle, thereby suppressing tumor growth. PBA-AMF is useful in studies of tumors and other diseases associated with elevated levels of H2O2.

Amfenac Sodium Hydrate is a non-steroidal analgesic anti-inflammatory drug with acetic acid moiety.

Azidamfenicol inhibits ribosomal peptidyltransferase with a Ki of 22 µM. Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.

Oxamflatin (Metacept-3) is a selective histone deacetylase (HDAC) inhibitor characterized by high potency (IC50 = 15.7 nM) and the presence of an alkyne group capable of undergoing azide-alkyne cycloaddition reactions (CuAAc).

Amfenac promotes apoptosis in ARPE-19 cell culture.

Amfenac is a nonsteroidal anti-inflammatory drug. Amfenac also has acetic acid moiety.

Amfepentorex fumarate was marketed as an appetite suppressant.

Amfepentorex was marketed in France during the 1970s as an appetite suppressant.

Brolamfetamine, also known as Dimethoxybromoamphetamine (DOB) and bromo-DMA, is a substituted amphetamine and psychedelic compound belonging to the phenethylamine class.

Amfonelic Acid is a dopamine uptake blocker.

Isamfazone is utilized in the chemical and pharmacological studies on substituted pyridazones, the discovery of novel anti-inflammatory agents by aligning screening.

BAMF is a chemical reagent used in the chemical modification of proteins, mainly in the acetylation process.

Metamfazone is a biochemical.

Cipamfylline is a xanthine, a theophylline analogue, and is a potent and selective inhibitor of phosphodiesterase type 4 (PDE-4). Cipamfylline was tested in patients with a diagnosis of atopic dermatitis and in two human models of acute and chronic irritant contact dermatitis. The outcome of the study revealed that cipamfylline was more effective than vehicle in treating atopic dermatitis, but less effective than a group II steroid, hydrocortisone-17-butyrate both in the treatment of atopic dermatitis and irritant contact dermatitis. The absorption of cipamfylline and the subsequent systemic exposure might be the reason why further clinical studies with higher doses of cipamfylline have not been published.

Amflutizole used for the treatment of gout, and is a Xanthine oxidase inhibitor

GaMF1.39 is an antimycobacterial compound that targets the F-ATP synthase subunit γ, exhibiting enhanced anti-tuberculosis activity when used in combination with ETC inhibitors [1].

Diamfenetide is used in sheep and cattle for the treatment of liver fluxobacteria infections.

M-COPA is a golgi disruptor which inhibits cell surface expression of MET protein and the ADP-ribosylation factor 1 (Arf1) activation. M-COPA also inhibits angiogenesis through suppression of both VEGFR1 2 and nuclear factor-kappaB (NF-kappaB) signaling pathways.

2-Hydroxy arachidic acid methyl ester, a hydroxylated fatty acid methyl ester identified in sediment samples from the Harney River and in petroleum ether extracts of I. eriocarpa, serves as a volatile flavoring compound in anhydrous milk fat (AMF). Its presence is diminished upon treatment with lipases lipozyme-435 and TL-IM in a time-dependent fashion. [Matreya, LLC. Catalog No. 1710]