Local view for "http://wifo5-04.informatik.uni-mannheim.de/drugbank/resource/drugs/DB07518"

PredicateValue (sorted: none)
rdf:type
drugbank:description
" experimental This compound belongs to the sulfuric acid monoesters. These are organic compounds containing the sulfuric acid monoester functional group. Sulfuric Acid Monoesters Organic Compounds Organic Acids and Derivatives Organic Sulfuric Acids and Derivatives Sulfuric Acid Monoesters Polyamines polyamine logP 0.93 ALOGPS logS -2.5 ALOGPS Water Solubility 7.21e-01 g/l ALOGPS logP 2.56 ChemAxon IUPAC Name {[(2R)-2-ethylhexyl]oxy}sulfonic acid ChemAxon Traditional IUPAC Name [(2R)-2-ethylhexyl]oxysulfonic acid ChemAxon Molecular Weight 210.291 ChemAxon Monoisotopic Weight 210.092579754 ChemAxon SMILES [H][C@@](CC)(CCCC)COS(O)(=O)=O ChemAxon Molecular Formula C8H18O4S ChemAxon InChI InChI=1S/C8H18O4S/c1-3-5-6-8(4-2)7-12-13(9,10)11/h8H,3-7H2,1-2H3,(H,9,10,11)/t8-/m1/s1 ChemAxon InChIKey InChIKey=MHGOKSLTIUHUBF-MRVPVSSYSA-N ChemAxon Polar Surface Area (PSA) 63.6 ChemAxon Refractivity 50.4 ChemAxon Polarizability 22.47 ChemAxon Rotatable Bond Count 7 ChemAxon H Bond Acceptor Count 3 ChemAxon H Bond Donor Count 1 ChemAxon pKa (strongest acidic) -1.2 ChemAxon Physiological Charge -1 ChemAxon Number of Rings 0 ChemAxon Bioavailability 1 ChemAxon Rule of Five true ChemAxon Ghose Filter true ChemAxon PubChem Compound 5496779 PubChem Substance 99443989 ChemSpider 4593490 PDB C26 BE0003185 Putative alkylsulfatase Pseudomonas putida # Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/10592235 unknown Putative alkylsulfatase Involved in oxidoreductase activity atsK None 7.06 33202.0 Pseudomonas putida GenBank Gene Database AF126201 UniProtKB Q9WWU5 UniProt Accession Q9WWU5_PSEPU >Putative alkylsulfatase MSNAALATAPHALELDVHPVAGRIGAEIRGVKLSPDLDAATVEAIQAALVRHKVIFFRGQ THLDDQSQEGFAKLLGEPVAHPTVPVVDGTRYLLQLDGAQGQRANSWHTDVTFVEAYPKA SILRSVVAPASGGDTVWANTAAAYQELPEPLRELADKLWAVHSNEYDYASLKPDIDPAKL ERHRKVFTSTVYETEHPVVRVHPISGERALQLGHFVKRIKGYSLADSQHLFAVLQGHVTR LENTVRWRWEAGDVAIWDNRATQHYAVDDYGTQPRIVRRVTLAGEVPVGVDGQLSRTTRK G >906 bp TCAGCCTTTACGCGTAGTACGGCTCAGTTGGCCATCCACGCCCACCGGCACTTCACCGGC CAGCGTTACCCGGCGCACGATACGTGGCTGGGTCCCATAATCATCCACCGCGTAGTGCTG TGTCGCACGGTTATCCCAGATAGCCACATCGCCCGCCTCCCAGCGCCAGCGCACGGTGTT CTCAAGGCGCGTGACATGCCCTTGCAGCACCGCGAACAAGTGCTGCGAATCGGCCAGCGA ATAGCCCTTGATGCGTTTGACGAAATGCCCCAGCTGCAGCGCCCGCTCACCGCTGATCGG GTGCACTCGCACCACCGGGTGCTCGGTCTCATACACCGTCGAGGTGAACACTTTGCGATG ACGCTCGAGTTTGGCAGGGTCGATATCGGGCTTGAGGCTGGCATAGTCGTACTCGTTGCT GTGCACCGCCCACAGCTTGTCGGCCAGCTCGCGCAGGGGCTCGGGCAACTCCTGATAGGC CGCAGCGGTATTGGCCCATACAGTATCGCCGCCCGACGCAGGGGCCACCACACTGCGCAG GATCGAGGCCTTGGGGTAGGCCTCTACGAAGGTCACATCGGTGTGCCAGGAGTTGGCCCG CTGCCCTTGGGCGCCATCGAGCTGGAGCAGGTAGCGGGTACCGTCGACCACTGGCACGGT GGGGTGAGCGACCGGCTCGCCCAGCAGCTTGGCAAAACCTTCCTGGCTTTGATCGTCCAG GTGGGTCTGGCCACGGAAGAAGATGACCTTGTGCCGCACCAACGCAGCCTGGATGGCCTC GACTGTGGCGGCATCGAGGTCGGGGGACAGTTTGACCCCGCGTATTTCGGCGCCGATACG GCCGGCGACCGGGTGGACATCAAGTTCGAGGGCGTGCGGCGCGGTGGCCAGTGCAGCGTT GCTCAT PF02668 TauD function oxidoreductase activity function catalytic activity process metabolism process cellular metabolism process generation of precursor metabolites and energy process electron transport process physiological process "
rdfs:label
"(2R)-2-ETHYL-1-HEXANESULFONIC ACID"

All properties reside in the graph file:///home/swish/src/ClioPatria/guidelines3/drugbank_small.nt

The resource does not appear as an object

Context graph