Local view for "http://wifo5-04.informatik.uni-mannheim.de/drugbank/resource/drugs/DB03704"

PredicateValue (sorted: none)
drugbank:description
" 505-95-3 experimental This compound belongs to the fatty alcohols. These are aliphatic alcohols consisting of a chain of 8 to 22 carbon atoms. Fatty Alcohols Organic Compounds Lipids Fatty Alcohols Straight Chain Fatty Acids Polyamines Primary Alcohols Enolates Carboxylic Acids carboxylic acid derivative enolate carboxylic acid polyamine primary alcohol alcohol logP 3.5 ALOGPS logS -3 ALOGPS Water Solubility 2.14e-01 g/l ALOGPS logP 3.04 ChemAxon IUPAC Name 12-hydroxydodecanoic acid ChemAxon Traditional IUPAC Name 12-hydroxydodecanoic acid ChemAxon Molecular Weight 216.3172 ChemAxon Monoisotopic Weight 216.172544634 ChemAxon SMILES OCCCCCCCCCCCC(O)=O ChemAxon Molecular Formula C12H24O3 ChemAxon InChI InChI=1S/C12H24O3/c13-11-9-7-5-3-1-2-4-6-8-10-12(14)15/h13H,1-11H2,(H,14,15) ChemAxon InChIKey InChIKey=ZDHCZVWCTKTBRY-UHFFFAOYSA-N ChemAxon Polar Surface Area (PSA) 57.53 ChemAxon Refractivity 60.61 ChemAxon Polarizability 26.85 ChemAxon Rotatable Bond Count 11 ChemAxon H Bond Acceptor Count 3 ChemAxon H Bond Donor Count 2 ChemAxon pKa (strongest acidic) 4.95 ChemAxon pKa (strongest basic) -2 ChemAxon Physiological Charge -1 ChemAxon Number of Rings 0 ChemAxon Bioavailability 1 ChemAxon Rule of Five true ChemAxon Ghose Filter true ChemAxon ChEBI 10616 PubChem Compound 79034 PubChem Substance 46507831 KEGG Compound C08317 ChemSpider 71366 PDB 12H BE0000009 Alcohol dehydrogenase class-3 Human # 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 # 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 Alcohol dehydrogenase class-3 Energy production and conversion Class-III ADH is remarkably ineffective in oxidizing ethanol, but it readily catalyzes the oxidation of long-chain primary alcohols and the oxidation of S-(hydroxymethyl) glutathione ADH5 4q21-q25 Cytoplasm None 7.54 39593.0 Human HUGO Gene Nomenclature Committee (HGNC) HGNC:253 GenAtlas ADH5 GeneCards ADH5 GenBank Gene Database M30471 GenBank Protein Database 178134 UniProtKB P11766 UniProt Accession ADHX_HUMAN Alcohol dehydrogenase class chi chain Alcohol dehydrogenase class III EC 1.1.1.1 EC 1.1.1.284 FDH Glutathione- dependent formaldehyde dehydrogenase S- (hydroxymethyl)glutathione dehydrogenase >Alcohol dehydrogenase class 3 chi chain ANEVIKCKAAVAWEAGKPLSIEEIEVAPPKAHEVRIKIIATAVCHTDAYTLSGADPEGCF PVILGHEGAGIVESVGEGVTKLKAGDTVIPLYIPQCGECKFCLNPKTNLCQKIRVTQGKG LMPDGTSRFTCKGKTILHYMGTSTFSEYTVVADISVAKIDPLAPLDKVCLLGCGISTGYG AAVNTAKLEPGSVCAVFGLGGVGLAVIMGCKVAGASRIIGVDINKDKFARAKEFGATECI NPQDFSKPIQEVLIEMTDGGVDYSFECIGNVKVMRAALEACHKGWGVSVVVGVAASGEEI ATRPFQLVTGRTWKGTAFGGWKSVESVPKLVSEYMSKKIKVDEFVTHNLSFDEINKAFEL MHSGKSIRTVVKI >1125 bp ATGGCGAACGAGGTTATCAAGTGCAAGGCTGCAGTTGCTTGGGAGGCTGGAAAGCCTCTC TCCATAGAGGAGATAGAGGTGGCACCCCCAAAGGCTCATGAAGTTCGAATCAAGATCATT GCCACTGCGGTTTGCCACACCGATGCCTATACCCTGAGTGGAGCTGATCCTGAGGGTTGT TTTCCAGTGATCTTGGGACATGAAGGTGCTGGAATTGTGGAAAGTGTTGGTGAGGGAGTT ACTAAGCTGAAGGCGGGTGACACTGTCATCCCACTTTACATCCCACAGTGTGGAGAATGC AAATTTTGTCTAAATCCTAAAACTAACCTTTGCCAGAAGATAAGAGTCACTCAAGGGAAA GGATTAATGCCAGATGGTACCAGCAGATTTACTTGCAAAGGAAAGACAATTTTGCATTAC ATGGGAACCAGCACATTTTCTGAATACACAGTTGTGGCTGATATCTCTGTTGCTAAAATA GATCCTTTAGCACCTTTGGATAAAGTCTGCCTTCTAGGTTGTGGCATTTCAACCGGTTAT GGTGCTGCTGTGAACACTGCCAAGTTGGAGCCTGGCTCTGTTTGTGCCGTCTTTGGTCTG GGAGGAGTCGGATTGGCAGTTATCATGGGCTGTAAAGTGGCTGGTGCTTCCCGGATCATT GGTGTGGACATCAATAAAGATAAATTTGCAAGGGCCAAAGAGTTTGGAGCCACTGAATGT ATTAACCCTCAGGATTTTAGTAAACCCATCCAGGAAGTGCTCATTGAGATGACCGATGGA GGAGTGGACTATTCCTTTGAATGTATTGGTAATGTGAAGGTCATGAGAGCAGCACTTGAG GCATGTCACAAGGGCTGGGGCGTCAGCGTCGTGGTTGGAGTAGCTGCTTCAGGTGAAGAA ATTGCCACTCGTCCATTCCAGCTGGTAACAGGTCGCACATGGAAAGGCACTGCCTTTGGA GGATGGAAGAGTGTAGAAAGTGTCCCAAAGTTGGTGTCTGAATATATGTCCAAAAAGATA AAAGTTGATGAATTTGTGACTCACAATCTGTCTTTTGATGAAATCAACAAAGCCTTTGAA CTGATGCATTCTGGAAAGAGCATTCGAACTGTTGTAAAGATTTAA PF08240 ADH_N PF00107 ADH_zinc_N function oxidoreductase activity function ion binding function cation binding function transition metal ion binding function zinc ion binding function binding function catalytic activity "
owl:sameAs
rdfs:label
"12-Hydroxydodecanoic Acid"
rdf:type

All properties reside in the graph file:///home/swish/src/ClioPatria/guidelines2/drugbank_small.nt

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