For research use only. Not for therapeutic Use.
L-Alaninol , also known as 2-Aminopropanol, is an amino acid derivative that inhibits melanoma proliferation and increases cytrochrome C reductase and tau-glutamyl transpeptidase.
| Catalog Number | R059134 |
| CAS Number | 2749-11-3 |
| Synonyms | ((S)-2-Hydroxy-1-methylethyl)amine; (+)-2-Amino-1-propanol; (+)-2-Aminopropanol; (+)-Alaninol; (2S)-(+)-2-Aminopropan-1-ol; (2S)-2-Amino-1-propanol; (2S)-2-Aminopropan-1-ol; (S)-2-Amino-1-propanol; (S)-2-Aminopropanol; (S)-Alaninol; 2-(S)-Amino-propa |
| Molecular Formula | C3H9NO |
| Purity | ≥95% |
| Target | melanoma proliferation inhibitor |
| Storage | Store at +4C |
| IUPAC Name | (2S)-2-aminopropan-1-ol |
| InChI | InChI=1S/C3H9NO/c1-3(4)2-5/h3,5H,2,4H2,1H3/t3-/m0/s1 |
| InChIKey | BKMMTJMQCTUHRP-VKHMYHEASA-N |
| SMILES | CC(CO)N |
| Reference | </br>1:Stereostructural implication by the differential bond polarizability: ROA intensity study of chiral s 2-amino 1-propanol. Wu G, Wang P.Chirality. 2014 May;26(5):255-9. doi: 10.1002/chir.22300. Epub 2014 Mar 18. PMID: 24639243 </br>2:How coenzyme B12-dependent ethanolamine ammonia-lyase deals with both enantiomers of 2-amino-1-propanol as substrates: structure-based rationalization. Shibata N, Higuchi Y, Toraya T.Biochemistry. 2011 Feb 1;50(4):591-8. doi: 10.1021/bi101696h. Epub 2010 Dec 30. PMID: 21142024 </br>3:2-amino-1-propanol versus 1-amino-2-propanol: valence band and C 1s core-level photoelectron spectra. Catone D, Turchini S, Contini G, Zema N, Irrera S, Prosperi T, Stener M, Di Tommaso D, Decleva P.J Chem Phys. 2007 Oct 14;127(14):144312. PMID: 17935400 |
