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L-Cysteine hydrochloride hydrate also known as L-Cysteine?HCl hydrate, is commonly used as a starting material in the synthesis of L-cysteine (alkylated, acidic, and alcoholic) derivatives. Uses: L-cysteine hydrochloride hydrate is used as a standard solution to determine the quantity of thiol groups attached on mucoadhesiveness. Additional or Alternative Names: L-Cysteine?HCl hydrate. Product Category: Amino Acids. CAS No. 345909-32-2. Molecular formula: HSCH2CH(NH2)CO2H·HCl·xH2O. Mole weight: 157.62 (anhydrous basis). Canonical SMILES: Cl[H].[H]O[H].N[C@@H](CS)C(O)=O. ECNumber: 200-157-7. Product ID: ACM345909322-1. Alfa Chemistry ISO 9001:2015 Certified. Categories: L-Cysteine hydrochloride monohydrate.
Cl-amidine is an inhibitor of irreversible protein pan-peptidylarginine deiminase (PAD) with IC50 values of 5.9 ± 0.3 μM, 0.8 ± 0.3 μM, 6.2 ± 1.0 μM for PAD4, PAD1 and PAD3, respectively. It irreversibly inactivates all four PAD subtypes by covalently modifying an active site cysteine that is important for its catalytic activity. Synonyms: N-[(1S)-1-(aminocarbonyl)-4-[(2-chloro-1-iminoethyl)amino]butyl]-benzamide monohydrochloride. Grades: ≥95%. CAS No. 1373232-26-8. Molecular formula: C14H19ClN4O2·HCl. Mole weight: 347.24.
D-Cysteine hydrochloride monohydrate
raw material for Tamiflu; Oseltamivir. CAS No. 32443-99-5. Product ID: 8-01661. Molecular formula: C4H10N4O4 HCl. Mole weight: 214.61. Source :
The lysine analog, thialysine, has been implicated in the mechanism for the inhibitory effect of the on human acute leukemia Jurkat T cells. When Jurkat T cells were treated with thialysine (0.32-2.5mM), apoptotic cell death along with several biochemical events such as mitochondrial cytochrome c release, caspase-9 activation, caspase-3 activation, degradation of poly (ADP-ribose) polymerase, and DNA fragmentation was induced in a dose- and time-dependent manner. However, these thialysine-induced apoptotic events were significantly abrogated by an ectopic expression of Bcl-xL, which is known to block mitochondrial cytochrome c release. Decylubiquinone, a mitochondrial permeability transition pore inhibitor, also suppressed thialysine-induced apoptotic events. Comparison of the thialysine-induced alterations in the cell cycle distribution between Jurkat T cells transfected with Bcl-xL gene (J/Bcl-xL) and Jurkat T cells transfected with vector (J/Neo) revealed that the apoptotic cells we Group: Biochemicals. Alternative Names: S-(2-Aminoethyl)-L-cysteine Monohydrochloride; NSC 186915;S-(2-Aminoethyl)-L-cysteine Hydrochloride;S-(2-Aminoethyl)-L-cysteine Monohydrochloride;S-( β-Aminoethyl)-L-cysteine Hydrochloride; Thialysine Hydrochloride. Grades: Highly Purified. CAS No. 4099-35-8. Pack Sizes: 1g, 5g. Molecular Formula: C5H12N2O2S·HCl, Molecular Weight: 200.7. US Biological Life Sciences.
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