1.0 2016-09-30 22:49:50 UTC 2020-04-22 15:09:21 UTC BMDB0002006 BMDB02006 2,3-Diaminopropionic acid Dpr L-2,3-Diaminopropanoate L-2,3-Diaminopropanoic acid L-2,3-Diaminopropionate L-2,3-Diaminopropionic acid 3-Amino-L-alanine (S)-2,3-Diaminopropanoate (S)-2,3-Diaminopropanoic acid 2,3-Diaminopropionate 2,3-Diaminopropanoic acid 2,3-Diaminopropionic acid, (D)-isomer 2,3-Diaminopropionic acid, (DL)-isomer 2,3-Diaminopropionic acid, (DL)-isomer, monohydrochloride 2,3-Diaminopropionic acid, (L)-isomer 2,3-Diaminopropionic acid, (L)-isomer, monohydrochloride 2-Amino-beta-alanine 3-Aminoalanine alpha,beta-Diaminopropionic acid beta-Aminoalanine (2S)-2,3-Diaminopropanoate (2S)-2,3-Diaminopropanoic acid 2,3-Diamino-propionate 2,3-Diaminopropionic acid C3H8N2O2 104.1078 104.05857751 (2S)-2,3-diaminopropanoic acid L-2,3-diaminopropionic acid 4033-39-0 NC[C@H](N)C(O)=O InChI=1S/C3H8N2O2/c4-1-2(5)3(6)7/h2H,1,4-5H2,(H,6,7)/t2-/m0/s1 PECYZEOJVXMISF-REOHCLBHSA-N belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues L-alpha-amino acids Amino acids Carbonyl compounds Carboxylic acids Hydrocarbon derivatives Monoalkylamines Monocarboxylic acids and derivatives Organic oxides Organopnictogen compounds Aliphatic acyclic compound Amine Amino acid Carbonyl group Carboxylic acid Hydrocarbon derivative L-alpha-amino acid Monocarboxylic acid or derivatives Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Primary aliphatic amine Primary amine Aliphatic acyclic compounds 3-aminoalanine Amino fatty acids L-alanine derivative non-proteinogenic L-alpha-amino acid Solid logp -3.88 ALOGPS logs 0.53 ALOGPS logp -4 ChemAxon pka_strongest_acidic 2.1 ChemAxon pka_strongest_basic 9.57 ChemAxon iupac (2S)-2,3-diaminopropanoic acid ChemAxon average_mass 104.1078 ChemAxon mono_mass 104.05857751 ChemAxon smiles NC[C@H](N)C(O)=O ChemAxon formula C3H8N2O2 ChemAxon inchi InChI=1S/C3H8N2O2/c4-1-2(5)3(6)7/h2H,1,4-5H2,(H,6,7)/t2-/m0/s1 ChemAxon inchikey PECYZEOJVXMISF-REOHCLBHSA-N ChemAxon polar_surface_area 89.34 ChemAxon refractivity 23.7 ChemAxon polarizability 9.88 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 4 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon number_of_rings 0 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::MsIr 1520 Specdb::MsIr 1521 Specdb::MsIr 1522 Specdb::NmrTwoD 1775 Specdb::CMs 11741 Specdb::CMs 38220 Specdb::CMs 153663 Specdb::MsMs 1944 Specdb::MsMs 1945 Specdb::MsMs 1946 Specdb::MsMs 291916 Specdb::MsMs 291917 Specdb::MsMs 291918 Specdb::MsMs 331951 Specdb::MsMs 331952 Specdb::MsMs 331953 Specdb::MsMs 2232182 Specdb::MsMs 2234351 Specdb::MsMs 2234573 Specdb::MsMs 2240718 Specdb::MsMs 2240954 Specdb::MsMs 2244956 Specdb::MsMs 2245174 Specdb::MsMs 2247069 Specdb::MsMs 2247216 Specdb::MsMs 2249180 Specdb::MsMs 2249216 Specdb::MsMs 2251150 Specdb::MsMs 2251246 Specdb::MsMs 2826544 Specdb::MsMs 2826545 Specdb::MsMs 2826546 Specdb::NmrOneD 1835 Specdb::NmrOneD 148680 Specdb::NmrOneD 148681 Specdb::NmrOneD 148682 Specdb::NmrOneD 148683 Specdb::NmrOneD 148684 Specdb::NmrOneD 148685 Specdb::NmrOneD 148686 Specdb::NmrOneD 148687 Specdb::NmrOneD 148688 Specdb::NmrOneD 148689 Specdb::NmrOneD 148690 Specdb::NmrOneD 148691 Specdb::NmrOneD 148692 Specdb::NmrOneD 148693 Specdb::NmrOneD 148694 Specdb::NmrOneD 148695 Specdb::NmrOneD 148696 Specdb::NmrOneD 148697 Specdb::NmrOneD 148698 Specdb::NmrOneD 148699 C03401 FDB022790 97328 87849 16303 2,3-Diaminopropionic_acid 6429