fp

FP0429 is an agonist of mGlu4.

Notoginsenoside FP2 is a natural product isolated from the fruit pedicels of Panax notoginseng and can be used in studies about the treatment of cardiovascular diseases.

Latanoprost acid is a selective agonist of prostanoid receptors and inhibits RANKL-induced osteoclastogenesis and function through the inhibition of c-fos/NFATc1 pathway. Latanoprost acid can be used in studies about lowering pressure inside the eyes.

Sulfentrazone (FP-846) is purified form of sulfentrazone which acts as a protoporphyrinogen oxidase inhibitor.It is a phenyl triazolinone herbicide

L 888607 is an effective and selective CRTH2 agonist (Ki: 0.8 nM).

GJN75561 is a VMAT2 imaging agent.

Bimatoprost acid (17-phenyl trinor PGF2α) is a metabolically stable analog of PGF2α and has a potential antagonistic activity for the FP receptor. It has a relative potency of 756% compared to PGF2α for binding to the FP receptor on ovine luteal cells.

Linvemastat (Compound FC-4) is an orally active MMP-12 inhibitor with an IC50 of less than 10 nM and demonstrates high selectivity over MMP-1, -2, -3, -7, -9, -10, and -14. It significantly reduces lung fibrosis in a mouse model of bleomycin-induced unilateral pulmonary fibrosis and effectively alleviates kidney damage, interstitial inflammation, or fibrosis in a unilateral ureteral obstruction renal fibrosis model. Linvemastat is suitable for research into inflammatory diseases such as idiopathic pulmonary fibrosis (IPF), inflammatory bowel disease (IBD), and asthma.

Latanoprost (Xalatan) is a prostaglandin F2alpha analogue and a prostanoid selective FP receptor agonist with an ocular hypertensive effect.

Bexmarilimab (FP-1305) is a highly potent, humanized anti-CLEVER-1 IgG4 antibody with an IC50 value of 4.51 nM, promoting immune conversion of tumor-associated macrophage phenotype M2 to M1, and can be used to study cancer.

Aderamastat (FP-025) is an orally active matrix metalloproteinase 12 (MMP-12) inhibitor used for research in allergic asthma, COPD, and pulmonary fibrosis.

FP-18 disodium is a TLR-4 agonist and acts as a vaccine adjuvant.

FP-20 sodium is a selective TLR4 agonist and serves as a vaccine adjuvant. It induces MAPK and NLRP3-dependent inflammasome activation. In experiments with mouse OVA antigen vaccination, FP-20 sodium showed no toxicity and facilitated IgG production.

Acetyl-6-formylpterin (Ac-6-FP) serves as a hapten that forms a covalent bond with MR1 via the Lys43 residue, which leads to the upregulation of the protein. This compound is employed in research related to inflammation [1].

FP-21399, an HIV fusion inhibitor, is used potentially for the treatment of HIV infection.

FP-biotin is a potent organophosphorus toxicant ideal for identifying novel biomarkers of organophosphorus exposure. It measures FAAH, ABHD6, and MAG-lipase activity specifically in plasma studies, thanks to the efficient purification of biotinylated peptides through binding to immobilized avidin beads.

FP20Rha is a potent TLR4 agonist that enhances the efficacy of vaccines against Pseudomonas aeruginosa.

α-Rhamnosyl FP20 sodium functions as a TLR-4 agonist and serves as a vaccine adjuvant.

α-Galactosyl FP20 sodium acts as a TLR-4 agonist and functions as a vaccine adjuvant.

α-Glucosyl FP20 sodium is a TLR-4 agonist and serves as a vaccine adjuvant.

Notoginsenoside FP1 (Standard) is a reference standard for research and analysis in studies involving Notoginsenoside FP1. Notoginsenoside FP1 is a natural product that can be used in related research in the field of life sciences. Its product number is TN8463.

Notoginsenoside FP2 (Standard) is a reference standard for research and analysis in studies involving Notoginsenoside FP2. Notoginsenoside FP2 is a natural product isolated from the fruit pedicels of Panax notoginseng and can be used in studies about the treatment of cardiovascular diseases.

Notoginsenoside FP1 is a natural product that can be used in related research in the field of life sciences. Its product number is TN8463.

CP7-FP13-2 is a polypeptide with properties that counteract virulence factors and exhibit antimicrobial activity. It effectively inhibits the formation of Staphylococcus aureus biofilms and demonstrates significant antibacterial efficacy in mice.