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Z-Ser-OH - 98%, high purity , CAS No.1145-80-8
Basic Description Synonyms (2S)-2-(benzyloxycarbonylamino)-3-hydroxy-propanoic acid | New Coccine Extra Conc. A Export | Sodium 5-(2,4-diamino-5-(2-hydroxy-5-nitrophenylazo)phenylazo)naphthalene-1-sulphonate | A803201 | AC-7344 | Carbobenzyloxy-L-serine | N-Carbobenzoxy-L-serine | Specifications & Purity ≥98% Shipped In Normal
Associated Targets(non-human) Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Names and Identifiers Pubchem Sid 488187205 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488187205 IUPAC Name (2S)-3-hydroxy-2-(phenylmethoxycarbonylamino)propanoic acid INCHI InChI=1S/C11H13NO5/c13-6-9(10(14)15)12-11(16)17-7-8-4-2-1-3-5-8/h1-5,9,13H,6-7H2,(H,12,16)(H,14,15)/t9-/m0/s1 InChi Key GNIDSOFZAKMQAO-VIFPVBQESA-N Canonical SMILES C1=CC=C(C=C1)COC(=O)NC(CO)C(=O)O Isomeric SMILES C1=CC=C(C=C1)COC(=O)N[C@@H](CO)C(=O)O WGK Germany 3 PubChem CID 100310 Molecular Weight 239.22 Beilstein 2058314 Reaxy-Rn 2058314
Certificates(CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Specific Rotation[α] 6.1 ° (C=6, AcOH) Melt Point(°C) 118°C Molecular Weight 239.220 g/mol XLogP3 0.400 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 6 Exact Mass 239.079 Da Monoisotopic Mass 239.079 Da Topological Polar Surface Area 95.900 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 263.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
Safety and Hazards(GHS) WGK Germany 3 Reaxy-Rn 2058314
References 1. Jay M West, Nikolai Zvonok, Kyle M Whitten, Subramanian K Vadivel, Anna L Bowman, Alexandros Makriyannis,. (2012-09-07) Biochemical and mass spectrometric characterization of human N-acylethanolamine-hydrolyzing acid amidase inhibition.. PloS one, 7 ((8)): ( e43877-e43877 ). [PMID:22952796 ]
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