fe²⁺

N14G-Fe, the Fe3+ chelated form of N14G, can identify Mycobacterium tuberculosis in sputum samples from tuberculosis patients, exhibiting exceptional fluorescence properties. Additionally, N14G-Fe effectively traverses the cell wall and the inner membrane region where IrtAB is located.

Fe-TMPyP binds to the prion protein PrP and inhibits misfolding. Fe-TMPyP is also a peroxynitrite decomposition catalyst.

Notoginsenoside Fe (Ginsenoside Mb) is a natural compound found in Panax japlcus var.

FE-200041 is a peripheral efficacious kappa opioid agonist.

FE-999011 is a dipeptidyl peptidase IV inhibitor.

Notoginsenoside Fe (Standard) is a reference standard for research and analysis in studies involving Notoginsenoside Fe. Notoginsenoside Fe (Ginsenoside Mb) is a natural compound found in Panax japlcus var.

Fe(III)(TDCPP) chloride is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.

Elesclomol (STA-4783) is an oxidative stress inducer and a highly lipophilic copper ion carrier. Elesclomol induces apoptosis in tumor cells and is used in copper death related studies. Elesclomol also inhibits FDX1-mediated Fe-S cluster biosynthesis.

Olamkicept (FE-301) is a soluble gp130-Fc-fusion protein that selectively inhibits interleukin 6 (IL-6) trans-signaling by binding to the soluble IL-6 receptor/IL-6 complex.

Metronidazole (Metronidazol) is a synthetic nitroimidazole derivative with antiprotozoal and antibacterial activities.

BFMO (biogenic Fe-Mn oxides) (N,N'-Difurfuryloxamide) could eliminate or decrease Fe(II), Mn(II), and As(III&V) species simultaneously. Moreover, BFMO (biogenic Fe-Mn oxides) can be used for As removal from water containing high concentrations of Fe(II) and Mn(II).

Degarelix is a peptide and selective GnRH (human gonadotropin-releasing hormone) receptor antagonist that treats prostate cancer by lowering testosterone levels in the body.

Deferasirox (Fe3+ chelate) is an orally available iron chelator with potential anticancer activity, inhibits the anti-apoptotic activity of MCL-1, and can be used to study iron overload.

Fe (III) Etioporphyrin I chloride, a porphyrin compound, is widely used as a component in thin-film electronic devices. Additionally, Etioporphyrin I is employed in studies concerning crystal growth rates.

Merotocin is a potent and highly selective peptidic agonist of the oxytocin receptor.

Selepressin, an analog of vasopressin, is a potent, selective vasopressin V1a receptor agonist.

FE-999024 is a selective tissue kalkinase-like inhibitor that significantly inhibits plasma kalkinase-like activity in the pancreas.

Fe-Cap folic is an encapsulated dosage for use as an iron supplement in pregnancy.

Iron Dextran (Fero Gradumet) is an iron supplement, used in the study of iron deficiency anemia.

L-Mimosine (Leucenol) is an antineoplastic alanine-substituted pyridine derivative isolated from Leucena glauca and acts as an iron chelator.

Barusiban is an oxytocin receptor antagonist.

RK-52 is a synthetic inhibitor of rhodesain, characterized by an impressive ksecond value (ksecond = 67000 × 103 M−1 min−1) and by a picomolar affinity toward the trypanosomal protease (Ki = 38 pM).

Nordimaprit is effective agonist in the inhibition of lymphocyte activation.

GR-127935 is a potent and selective 5-HT1B/1D receptor antagonist.