Mrv1652309272007392D 7 6 0 0 0 0 999 V2000 0.7145 0.9281 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.7145 0.1031 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4289 -0.3094 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 0.0000 -0.3094 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.0000 -1.1344 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 -0.7145 0.1031 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.4289 -0.3094 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 2 1 2 0 0 0 0 3 2 1 0 0 0 0 4 2 1 0 0 0 0 4 5 1 1 0 0 0 6 4 1 0 0 0 0 7 6 1 0 0 0 0 M END > <DATABASE_ID> CDB000131 > <DATABASE_NAME> CDB > <SMILES> N[C@@H](CO)C(O)=O > <INCHI_IDENTIFIER> InChI=1S/C3H7NO3/c4-2(1-5)3(6)7/h2,5H,1,4H2,(H,6,7)/t2-/m0/s1 > <INCHI_KEY> MTCFGRXMJLQNBG-REOHCLBHSA-N > <FORMULA> C3H7NO3 > <MOLECULAR_WEIGHT> 105.0926 > <EXACT_MASS> 105.042593095 > <JCHEM_ACCEPTOR_COUNT> 4 > <JCHEM_ATOM_COUNT> 14 > <JCHEM_AVERAGE_POLARIZABILITY> 9.386631521233841 > <JCHEM_BIOAVAILABILITY> 1 > <JCHEM_DONOR_COUNT> 3 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> (2S)-2-amino-3-hydroxypropanoic acid > <ALOGPS_LOGP> -3.42 > <JCHEM_LOGP> -3.8877352328917727 > <ALOGPS_LOGS> 0.66 > <JCHEM_MDDR_LIKE_RULE> 0 > <JCHEM_NUMBER_OF_RINGS> 0 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA> 15.166073878847005 > <JCHEM_PKA_STRONGEST_ACIDIC> 2.033990015469951 > <JCHEM_PKA_STRONGEST_BASIC> 8.931303956589883 > <JCHEM_POLAR_SURFACE_AREA> 83.55 > <JCHEM_REFRACTIVITY> 22.040999999999997 > <JCHEM_ROTATABLE_BOND_COUNT> 2 > <JCHEM_RULE_OF_FIVE> 1 > <ALOGPS_SOLUBILITY> 4.80e+02 g/l > <JCHEM_TRADITIONAL_IUPAC> L-serine > <JCHEM_VEBER_RULE> 0 > <Cannabis Database ID> CDB000131 > <GENERIC_NAME> L-Serine $$$$