Mrv1652304202019302D 10 9 0 0 0 0 999 V2000 9984.3765 9984.8046 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 9984.3765 9983.9809 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 9985.0910 9983.5674 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9985.8065 9983.9809 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9985.0910 9982.7428 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9983.6623 9985.2170 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9982.9481 9984.8046 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9983.6623 9986.0417 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9985.0910 9985.2170 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9985.8065 9984.8046 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 6 0 0 0 1 6 1 0 0 0 0 1 9 1 0 0 0 0 2 3 1 0 0 0 0 3 4 1 0 0 0 0 3 5 2 0 0 0 0 6 7 1 0 0 0 0 6 8 2 0 0 0 0 9 10 1 0 0 0 0 M END > <DATABASE_ID> YMDB00810 > <DATABASE_NAME> YMDB > <SMILES> CC(=O)N[C@@H](CO)C(O)=O > <INCHI_IDENTIFIER> InChI=1S/C5H9NO4/c1-3(8)6-4(2-7)5(9)10/h4,7H,2H2,1H3,(H,6,8)(H,9,10)/t4-/m0/s1 > <INCHI_KEY> JJIHLJJYMXLCOY-BYPYZUCNSA-N > <FORMULA> C5H9NO4 > <MOLECULAR_WEIGHT> 147.1293 > <EXACT_MASS> 147.053157781 > <JCHEM_ACCEPTOR_COUNT> 4 > <JCHEM_ATOM_COUNT> 19 > <JCHEM_AVERAGE_POLARIZABILITY> 13.426636456180455 > <JCHEM_BIOAVAILABILITY> 1 > <JCHEM_DONOR_COUNT> 3 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> (2S)-2-acetamido-3-hydroxypropanoic acid > <ALOGPS_LOGP> -1.36 > <JCHEM_LOGP> -1.8067746783333332 > <ALOGPS_LOGS> -0.24 > <JCHEM_MDDR_LIKE_RULE> 0 > <JCHEM_NUMBER_OF_RINGS> 0 > <JCHEM_PHYSIOLOGICAL_CHARGE> -1 > <JCHEM_PKA> 12.997357799160714 > <JCHEM_PKA_STRONGEST_ACIDIC> 3.611000903600003 > <JCHEM_PKA_STRONGEST_BASIC> -2.0355996977858735 > <JCHEM_POLAR_SURFACE_AREA> 86.63 > <JCHEM_REFRACTIVITY> 31.4848 > <JCHEM_ROTATABLE_BOND_COUNT> 3 > <JCHEM_RULE_OF_FIVE> 1 > <ALOGPS_SOLUBILITY> 8.46e+01 g/l > <JCHEM_TRADITIONAL_IUPAC> acetylserine > <JCHEM_VEBER_RULE> 0 > <YMDB_ID> YMDB00810 > <GENERIC_NAME> N-Acetyl-DL-serine > <SYNONYMS> DL-Serine, N-acetyl-; N-acetylserine; Serine, N-acetyl-, DL- $$$$