The complete data for Arginine ( ) | ||||||||||||||||
General information Chemical formula : C 6 H 14 N 4 O 2 Molar mass : 174.2 g·mol−1 Systematic name : 2-amino-5-(diaminomethylidene amino)pentanoic acid Abbreviations : R, Arg Synonyms : 2-amino-5-guanidinopentanoic acid 2-amino-5-guanidinovaleric acid AIDS{-}121865 AIDS{-}159840 Argamine Arginin Argivene CHEBI:29016 CHEMBANK2983 Detoxargin Harg Levargin Minophagen A R-Gene | ||||||||||||||||
Database data | ||||||||||||||||
SMILES : NC(=N)NCCCC(N)C(=O)O InChI =1/C6H14N4O2/c7-4(5(11)12)2-1-3-10-6(8)9/h4H,1-3,7H2,(H,11,12)(H4,8,9,10)/f/h11H,8-9H2
| ||||||||||||||||
Physical properties | ||||||||||||||||
| ||||||||||||||||
Hazard properties | ||||||||||||||||
| ||||||||||||||||
Chemical properties | ||||||||||||||||
| ||||||||||||||||
Pharmacological properties |
Sodium cyanide is a poisonous compound with the formula NaCN. It is a white, water-soluble solid. Cyanide has a high affinity for metals, which leads to the high toxicity of this salt. Its main application, in gold mining, also exploits its high reactivity toward metals. It is a moderately strong base.
PubChem is a database of chemical molecules and their activities against biological assays. The system is maintained by the National Center for Biotechnology Information (NCBI), a component of the National Library of Medicine, which is part of the United States National Institutes of Health (NIH). PubChem can be accessed for free through a web user interface. Millions of compound structures and descriptive datasets can be freely downloaded via FTP. PubChem contains multiple substance descriptions and small molecules with fewer than 100 atoms and 1,000 bonds. More than 80 database vendors contribute to the growing PubChem database.
In enzymology, a NAD(P)+-protein-arginine ADP-ribosyltransferase (EC 2.4.2.31) is an enzyme that catalyzes the chemical reaction using nicotinamide adenine dinucleotide
Protein arginine N-methyltransferase 5 is an enzyme that in humans is encoded by the PRMT5 gene. PRMT5 symmetrically dimethylates H2AR3, H4R3, H3R2, and H3R8 in vivo, all of which are linked to a range of transcriptional regulatory events.