proline

Oleoyl proline ammonium is a novel n-acyl amine compound that is a food additive that enhances the flavor of fruit drinks.

N-Boc-cis-4-hydroxy-L-proline methyl ester serves as a non-cleavable linker in antibody-drug conjugate (ADC) synthesis and functions as an alkyl chain-based PROTAC linker for PROTAC construction [2].

Ipragliflozin is a highly potent and selective SGLT2 inhibitor with an IC50 of 2.8 nM; little and NO potency for SGLT1/3/4/5/6.

L-Proline 4-methoxy-β-naphthylamide hydrochloride (H-Pro-4MβNA hydrochloride) is a chemical compound used in the preparation of Fap-activated anti-tumor compounds.

1-(Anilinocarbonyl)proline is a compound utilized for identifying dual-action probes within a cell model of Huntington's disease.

N-Cbz-hydroxy-L-proline 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.

L-Proline-CoA (L-Proline-coenzyme A) is a derivative of Coenzyme A.

L-Proline (proline) is a nonessential amino acid in humans. It is an essential component of collagen and is important for proper functioning of joints and tendons. It also helps maintain and strengthen heart muscles.

cis-L-Hydroxyproline inhibits the synthesis and extracellular deposition of collagen. The growth inhibition of pancreatic cancer cells induced by the Hyp isomer could be due to endoplasmatic reticulum stress.

Collagen proline hydroxylase inhibitor-1 exhibits antifibroproliferative activity.

Collagen proline hydroxylase inhibitor is an inhibitor collagen proline hydroxylase and useful for antifibrotic proliferative agents.

Carbobenzoxyproline (Carbobenzoxy-S-proline) is a prolidase inhibitor.

L-Hydroxyproline (L-Hydroxyprolin) is one of the hydroxyproline (Hyp) isomers. L-Hydroxyproline is a useful chiral building block in the production of many pharmaceuticals.

Fmoc-L-Proline (Fmoc-Pro-OH) is a proline derivative.

DL-Proline is a DL mixture of proline with multiple biological activities, capable of inhibiting EGFR and sodium-dependent proline transporters, and is commonly used in solid-phase or liquid-phase peptide synthesis.

N-Acetyl-L-proline is a chemically defined derivative of the amino acid L-proline that is widely applied across pharmaceutical formulation development, cosmetic science, and advanced biochemical research due to its distinctive cyclic structure, where it is deliberately employed to improve peptide stability, optimize solubility profiles, enhance membrane permeability, and support drug delivery strategies including experimental evaluation of blood–brain barrier transport while also serving as a robust building block for peptide synthesis, enzyme characterization studies such as angiotensin-converting enzyme investigations, and nutrition-focused cognitive enhancement research.

Hygric acid (N-Methyl-L-proline) is a proline analogue found in citrus juices and bergamot juice.

H-D-cis-Hyp-OH (D-allo-Hydroxyproline) belongs to the class of organic compounds known as proline and derivatives. Proline and derivatives are compounds containing proline or a derivative thereof resulting from a reaction of proline at the amino group or the carboxyl group, or from the replacement of any hydrogen of glycine by a heteroatom.

(R)-pyrrolidine-2-carboxylic acid (D-Proline) is an isomer of the naturally occurring amino acid L-Proline. D-amino acids, including D-Proline, are found in relatively high abundance in human plasma and saliva, potentially originating from bacterial sources or endogenous production via amino acid racemase activity.

Prolyl-4-hydroxylase Inhibitor 11, a novel proline 4-hydroxylase inhibitor, shows protective effects against oxidative stress and Cu(II) toxicity in Chlorella vulgaris.

NVP-TAE 226 (TAE226) is a potent FAK inhibitor (IC50: 5.5 nM), exhibiting even greater efficacy against Pyk2 (IC50: 3.5 nM), and is 10- to 100-fold less effective against IGF-1R, InsR, c-Met, and ALK.

Prothioconazole (Proline 480 SC Fungicide) is a chiral triazole fungicide in plant pathogen control.

PF-562271 hydrochloride (PF-562271 HCl) is a potent, ATP-competitive, reversible inhibitor of FAK with IC50 of 1.5 nM in cell-free assays, ~10-fold less potent for Pyk2 than FAK and >100-fold selectivity against other protein kinases, except for some CDKs.

PF-431396 is a dual PYK2/FAK inhibitor (IC50: 11/2 nM).