l homocysteine

L-Homocysteine is a biological thiol involved in various diseases and pathological conditions. It is a marker for atherosclerosis and can exacerbate intestinal inflammation in inflammatory bowel disease (IBD) by promoting the expression of 5-LOX and COX-2, making it suitable for inducing vascular endothelial inflammation models.

L-Homocysteine thiolactone hydrochloride is neurotoxic and can induce epilepsy and Alzheimer's disease.

L-Homocysteine-d4 is the deuterium-labeled variant of L-Homocysteine.

N-butyryl-L-Homocysteine thio-lactone, an analog of N-butyryl-L-homoserine lactone, is a small diffusible signaling molecule involved in quorum sensing for controlling gene expression and cellular metabolism. It induces violacein expression in C. violaceum mutants usually not able to produce acylhomoserine lactone (AHL), regulating genes like LuxIR family transcriptional regulators.

S-(D-Carboxybutyl)-L-homocysteine-CoA (S-(D-Carboxybutyl)-L-homocysteine-coenzyme A) is a derivative of coenzyme A.

S-Adenosyl-L-homocysteine-CoA (S-Adenosyl-L-homocysteine-coenzyme A) is a derivative of coenzyme A.

N-Palmitoyl homocysteine (PHC) ammonium is a pH-sensitive lipid that cleaves under endosomal pH conditions (pH 5.5).

3-deazaneplanocin A (DZNeP)HCl, an analog of adenosine, is a competitive inhibitor of S-adenosylhomocysteine hydrolase with Ki of 50 pM.

3-Deazaadenosine hydrochloride is an inhibitor of S-adenosylhomocysteine hydrolase (Ki: 3.9 µM). It has anti-inflammatory, anti-proliferative, and anti-HIV activity.

Adenosine Dialdehyde (Periodate-oxidized adenosine) is a purine nucleoside analogue. Adenosine Dialdehyde is a potent inhibitor of S-Adenosylhomocysteine hydrolase (SAHH) (Ki=3.3 nM). Adenosine Dialdehyde exhibits potent anti-tumor activity in vivo.

DL-Homocysteine thiolactone hydrochloride (DL-Homocysteinethiolactone hydrochloride) is a cysteine derivative that binds to and induces conformational changes in various plasma proteins, slowing coagulation and inducing oxidative stress. It decreases left ventricular systolic blood pressure and cardiac force and induces seizures in vivo.

S-Aristeromycinylhomocysteine is an inhibitor of adenosylmethionine decarboxylase.

3-Deazaadenosine (3-DAA) is a potent S-adenosylhomocysteine (SAH) hydrolase inhibitor. It inhibits methylation reactions by inducing intracellular SAH accumulation, exhibiting antiviral, anti-inflammatory, and immunomodulatory activities.

Aristeromycin (U 99468) is a broad-spectrum antiviral antibiotic that targets RNA viruses and is an inhibitor of S-adenosylhomocysteine hydrolase (AHCY).

S-N6-Methyladenosylhomocysteine (Chart 1-1) is a potent inhibitor of the histone methyltransferase DOT1L, with an IC50 of 0.29 μM. This compound plays a significant role in cancer research.

Palmitoyl homocysteine is a lipid nanocarrier.

S-Hydroxyethylhomocysteine is a bioactive chemical.

DL-Homocysteine (2-Amino-4-mercaptobutyric acid) is a potential marker for tumor cell growth. increased plasma homocysteine is a risk factor for coronary heart disease and carcinogenesis.

DL-Homocysteine-3,3,4,4-d4 is a deuterated compound of DL-Homocysteine (2-Amino-4-mercaptobutyric acid).DL-Homocysteine is a weak neurotoxin that affects canine uric acid production.

DL-Homocysteine (Standard) is a reference standard for research and analysis in studies involving DL-Homocysteine. DL-Homocysteine (2-Amino-4-mercaptobutyric acid) is a potential marker for tumor cell growth. increased plasma homocysteine is a risk factor for coronary heart disease and carcinogenesis.

SAH (SAH (S-Adenosylhomocysteine)) is an inhibitor for the METTL3-METTL14 heterodimer complex (METTL3-14, IC50: 0.9 μM).

N-acetyl-L-methionine is nutritionally and metabolically equivalent to L-methionine. Methionine is a dietary indispensable amino acid required for normal growth and development of humans, other mammals, and avian species. In addition to being a substrate

Vinthionine binds covalently to rat liver DNA, RNA, and protein in vivo, but not in vitro.

Homocystine is the double-bonded form of homocysteine, but it occurs only transiently before being converted to the harmless cystathionine via a vitamin B6-dependent enzyme. Increasing evidence supports a role for an elevation of homocysteine in schizophr