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" 1745-81-9 experimental This compound belongs to the phenylpropenes. These are compounds containing a phenylpropene moeity, which consists of a propene substituent bound to a phenyl group. Phenylpropenes Organic Compounds Benzenoids Benzene and Substituted Derivatives Phenylpropenes Phenols and Derivatives Polyamines Enols phenol derivative polyamine enol logP 2.4 ALOGPS logS -1.6 ALOGPS Water Solubility 3.06e+00 g/l ALOGPS logP 2.77 ChemAxon IUPAC Name 2-(prop-2-en-1-yl)phenol ChemAxon Traditional IUPAC Name 2-allylphenol ChemAxon Molecular Weight 134.1751 ChemAxon Monoisotopic Weight 134.073164942 ChemAxon SMILES OC1=CC=CC=C1CC=C ChemAxon Molecular Formula C9H10O ChemAxon InChI InChI=1S/C9H10O/c1-2-5-8-6-3-4-7-9(8)10/h2-4,6-7,10H,1,5H2 ChemAxon InChIKey InChIKey=QIRNGVVZBINFMX-UHFFFAOYSA-N ChemAxon Polar Surface Area (PSA) 20.23 ChemAxon Refractivity 42.33 ChemAxon Polarizability 14.83 ChemAxon Rotatable Bond Count 2 ChemAxon H Bond Acceptor Count 1 ChemAxon H Bond Donor Count 1 ChemAxon pKa (strongest acidic) 9.33 ChemAxon pKa (strongest basic) -6 ChemAxon Physiological Charge 0 ChemAxon Number of Rings 1 ChemAxon Bioavailability 1 ChemAxon Rule of Five true ChemAxon Melting Point -6 °C PhysProp Boiling Point 220 °C PhysProp PubChem Compound 15624 PubChem Substance 46508761 ChemSpider 14864 PDB 2LP BE0001248 Lysozyme Enterobacteria phage T4 # Overington JP, Al-Lazikani B, Hopkins AL: How many drug targets are there? Nat Rev Drug Discov. 2006 Dec;5(12):993-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17139284 # Imming P, Sinning C, Meyer A: Drugs, their targets and the nature and number of drug targets. Nat Rev Drug Discov. 2006 Oct;5(10):821-34. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/17016423 unknown Lysozyme Involved in lysozyme activity Helps to release the mature phage particles from the cell wall by breaking down the peptidoglycan E Cytoplasmic None 10.08 18636.0 Enterobacteria phage T4 GenBank Gene Database X04567 GenBank Protein Database 15261 UniProtKB P00720 UniProt Accession LYS_BPT4 EC 3.2.1.17 Endolysin Lysis protein Muramidase >Lysozyme MNIFEMLRIDEGLRLKIYKDTEGYYTIGIGHLLTKSPSLNAAKSELDKAIGRNCNGVITK DEAEKLFNQDVDAAVRGILRNAKLKPVYDSLDAVRRCALINMVFQMGETGVAGFTNSLRM LQQKRWDEAAVNLAKSRWYNQTPNRAKRVITTFRTGTWDAYKNL >495 bp ATGAATATATTTGAAATGTTACGTATAGATGAACGTCTTAGACTTAAAATCTATAAAGAC ACAGAAGGCTATTACACTATTGGCATCGGTCATTTGCTTACAAAAAGTCCATCACTTAAT GCTGCTAAATCTGAATTAGATAAAGCTATTGGGCGTAATTGCAATGGTGTAATTACAAAA GATGAGGCTGAAAAACTCTTTAATCAGGATGTTGATGCTGCTGTTCGCGGAATTCTGAGA AATGCTAAATTAAAACCGGTTTATGATTCTCTTGATGCGGTTCGTCGCTGTGCATTGATT AATATGGTTTTCCAAATGGGAGAAACCGGTGTGGCAGGATTTACTAACTCTTTACGTATG CTTCAACAAAAACGCTGGGATGAAGCAGCAGTTAACTTAGCTAAAAGTATATGGTATAAT CAAACACCTAATCGCGCAAAACGAGTCATTACAACGTTTAGAACTGGCACTTGGGACGCG TATAAAAATCTATAA PF00959 Phage_lysozyme function hydrolase activity function hydrolase activity, acting on glycosyl bonds function hydrolase activity, hydrolyzing O-glycosyl compounds function lysozyme activity function catalytic activity process metabolism process cell wall catabolism process peptidoglycan catabolism process macromolecule metabolism process carbohydrate metabolism process cellular carbohydrate metabolism process peptidoglycan metabolism process physiological process process catabolism process cellular catabolism "
rdfs:label
"2-Allylphenol"

All properties reside in the graph file:///home/swish/src/ClioPatria/guidelines/drugbank_small.nt

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