cys-tat

Cys-TAT(47-57) (Cys-[HIV-Tat (47-57)]) is an arginine-rich cell-penetrating peptide derived from the HIV-1 transactivating protein, corresponding to the protein transduction domain of the TAT protein.

Cys-TAT(47-57) acetate is derived from the HIV-1 transactivating protein. Cys-TAT(47-57) acetate is an arginine rich peptide that can penetrate cells.

Cys-TAT-HA2 is a conjugate of Cys and TAT-HA2. It acts as a transduction compound capable of delivering proteins, such as cardiac troponin C (Cardiac troponin C), into the cytoplasm of living cells. Cys-TAT-HA2 is applicable for real-time tracking studies of exogenous proteins.

L-Cystathionine (Cystathionine, L-) is a key nonprotein amino acid related to metabolic conditions of sulfur-containing amino acids. L-Cystathionine can be used in studies about cardiovascular protection.

2,3-Diaminopropionic acid hydrochloride (3-Amino-L-alanine hydrochloride) is a competitive cystathionase(CTH) inhibitor.

DL-Propargylglycine HCl (DL-Propargyl Glycine HCl) is a potent irreversible inhibitor of cystathionine γ-cleaving enzyme and can be used in the study of heart failure.

D,L-Cystathionine dihydrochloride is an intermediate in the synthesis of cysteine, which acts from the isotype of cysteine-β-synthase (CBS) produced by leucine and serine. Derived from cysteine. DL-cysteine contains a cysteine (βC-S) carbon-sulfur bond.

Cystatin Bagonist 1 is an orally active inhibitor of MMP-2/9. It suppresses U87 and T98G cells with IC50 values of 3.95 μM and 3.43 μM, respectively. Cystatin Bagonist 1 induces S-phase cell cycle arrest in MG cells and inhibits their angiogenesis, migration, and invasion. Additionally, it hinders tumor growth in U87 MG xenograft models. This compound is applicable for research in malignant glioma (MG).

Cystathionine-γ-lyase-IN-1 (SHIP-2a) is a selective inhibitor of cystathionine γ-lyase (CSE) enzyme (IC50= 6.3 μM).

Cystathionine β-lyase is a pyridoxal 5′-phosphate (PLP)-dependent enzyme that cleaves the Cβ-Sγ bond of cystathionine to convert L-cysteine into L-homocysteine. Cystathionine β-lyase is involved in the de novo synthesis of methionine in microorganisms and plants and plays an important role in bacterial virulence.

L-Cystathionine (Standard) is a reference standard for research and analysis in studies involving L-Cystathionine. L-Cystathionine (Cystathionine, L-) is a key nonprotein amino acid related to metabolic conditions of sulfur-containing amino acids. L-Cystathionine can be used in studies about cardiovascular protection.

D,L-Cystathionine-[D4] (Standard) is a reference standard of D,L-Cystathionine-[D4] intended for quantitative analysis, quality control, and related biochemical research applications.

L-Selenocystathionine is a nucleoside metabolite.

L-Cystathionine dihydrochloride is a non-protein sulfur-containing compound that plays a critical role in the metabolism of sulfur-containing amino acids (amino acids). It helps prevent homocysteine-induced, mitochondria-dependent apoptosis (apoptosis) in human umbilical vein endothelial cells (HUVECs) and is important in cardiovascular protection.

Cystathionine γ-lyase is a biocatalyst and a key enzyme in new biocatalyst technology. Enzyme engineering focuses on improving enzymatic reaction kinetics, substrate selectivity, and activity under harsh conditions (e.g., low or high pH). By introducing stimulus responsiveness through modifications, dynamic control of activity also becomes possible.

Cystatin C is an endogenous cysteine protease inhibitor belonging to the type 2 cystatin superfamily. The human Cystatin-C protein is encoded by the CST3 gene, is widely expressed, and maintains moderate levels. It serves as a crucial intrinsic marker of kidney function.

DL-Cystathionine dihydrochloride is a mixture of four stereoisomers of cystathionine and isopropylthionine, serving as an intermediate in the biosynthesis of the amino acid cysteine.

(Cys47)-HIV-1 tat Protein (47-57) possesses membrane translocation functionality and can serve as a surface derivatization agent for magnetic pharmaceuticals, enhancing their uptake into specific target cells.

Cys(Npys)-TAT (47-57), a peptide fragment corresponding to the transduction domain of the TAT peptide, contains an activated cysteine residue C and can electrostatically interact with plasmid DNA. Notably, TAT is a small nuclear transcriptional activator protein encoded by HIV-1 [1].

TAT (47-57) GGG-Cys(Npys) is a cell-penetrating peptide (CPP) with potential applications in intracellular drug delivery research [1].

Cys(Npys)-TAT (47-57), FAM-labeled, is a Cys(Npys)-activated cell-penetrating peptide (CPP) with a FAM label.