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PredicateValue (sorted: default)
rdfs:label
"1,4-Deoxy-4-((5-Hydroxymethyl-2,3,4-Trihydroxycyclohex-5-Enyl)Amino)Fructose"
rdf:type
ns1:description
" experimental This compound belongs to the aminocyclitols and derivatives. These are cyclitols with at least one hydroxyl group replace by an amino group. Aminocyclitols and Derivatives Organic Compounds Organooxygen Compounds Alcohols and Polyols Cyclic Alcohols and Derivatives Oxanes Secondary Alcohols 1,2-Aminoalcohols 1,2-Diols Ethers Dialkylamines Primary Alcohols Polyamines oxane 1,2-diol 1,2-aminoalcohol secondary alcohol polyol polyamine secondary amine primary alcohol ether secondary aliphatic amine amine organonitrogen compound logP -2.1 ALOGPS logS -0.27 ALOGPS Water Solubility 1.64e+02 g/l ALOGPS logP -3.7 ChemAxon IUPAC Name (1R,2S,3R,6R)-6-{[(2R,3R,4S,5S)-4,5-dihydroxy-2-methyloxan-3-yl]amino}-4-(hydroxymethyl)cyclohex-4-ene-1,2,3-triol ChemAxon Traditional IUPAC Name (1R,2S,3R,6R)-6-{[(2R,3R,4S,5S)-4,5-dihydroxy-2-methyloxan-3-yl]amino}-4-(hydroxymethyl)cyclohex-4-ene-1,2,3-triol ChemAxon Molecular Weight 305.3242 ChemAxon Monoisotopic Weight 305.147452095 ChemAxon SMILES C[C@H]1OC[C@H](O)[C@@H](O)[C@H]1N[C@@H]1C=C(CO)[C@@H](O)[C@H](O)[C@@H]1O ChemAxon Molecular Formula C13H23NO7 ChemAxon InChI InChI=1S/C13H23NO7/c1-5-9(12(19)8(16)4-21-5)14-7-2-6(3-15)10(17)13(20)11(7)18/h2,5,7-20H,3-4H2,1H3/t5-,7-,8+,9+,10-,11-,12-,13+/m1/s1 ChemAxon InChIKey InChIKey=LTAGIBUDYBSPEG-HCDBHUNCSA-N ChemAxon Polar Surface Area (PSA) 142.64 ChemAxon Refractivity 71.75 ChemAxon Polarizability 29.99 ChemAxon Rotatable Bond Count 3 ChemAxon H Bond Acceptor Count 8 ChemAxon H Bond Donor Count 7 ChemAxon pKa (strongest acidic) 12.65 ChemAxon pKa (strongest basic) 7.04 ChemAxon Physiological Charge 1 ChemAxon Number of Rings 2 ChemAxon Bioavailability 1 ChemAxon PubChem Compound 46936908 PubChem Substance 46504993 ChemSpider 3819398 PDB DAF BE0001625 Alpha-amylase Pseudoalteromonas haloplanktis # 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 Alpha-amylase Carbohydrate transport and metabolism Endohydrolysis of 1,4-alpha-D-glucosidic linkages in oligosaccharides and polysaccharides amy Cytoplasmic None 4.7 73268.0 Pseudoalteromonas haloplanktis GenBank Gene Database X58627 GenBank Protein Database 2879820 UniProtKB P29957 UniProt Accession AMY_PSEHA 1,4-alpha-D-glucan glucanohydrolase Alpha-amylase precursor EC 3.2.1.1 >Alpha-amylase precursor MKLNKIITTAGLSLGLLLPSIATATPTTFVHLFEWNWQDVAQECEQYLGPKGYAAVQVSP PNEHITGSQWWTRYQPVSYELQSRGGNRAQFIDMVNRCSAAGVDIYVDTLINHMAAGSGT GTAGNSFGNKSFPIYSPQDFHESCTINNSDYGNDRYRVQNCELVGLADLDTASNYVQNTI AAYINDLQAIGVKGFRFDASKHVAASDIQSLMAKVNGSPVVFQEVIDQGGEAVGASEYLS TGLVTEFKYSTELGNTFRNGSLAWLSNFGEGWGFMPSSSAVVFVDNHDNQRGHGGAGNVI TFEDGRLYDLANVFMLAYPYGYPKVMSSYDFHGDTDAGGPNVPVHNNGNLECFASNWKCE HRWSYIAGGVDFRNNTADNWAVTNWWDNTNNQISFGRGSSGHMAINKEDSTLTATVQTDM ASGQYCNVLKGELSADAKSCSGEVITVNSDGTINLNIGAWDAMAIHKNAKLNTSSASSTE SDWQRTVIFINAQTQSGQDMFIRGGIDHAYANANLGRNCQTSNFECAMPIRHNNLKNVTT SPWKANDNYLDWYGIENGQSSEAEGSATDWTTNVWPAGWGAEKTVNTDGFGVTPLNIWGE HYWMLDVDMDCSKAVNGWFELKAFIKNGQGWETAIAQDNAPYTSTNHMAQCGKINKFEFN NSGVVIRSF >2010 bp ATGAAACTCAATAAAATAATCACCACCGCAGGTTTAAGCCTAGGGTTGCTCTTACCTAGC ATTGCGACTGCTACGCCCACCACATTTGTACATTTGTTTGAATGGAATTGGCAAGATGTA GCGCAAGAATGTGAGCAATACCTAGGACCAAAAGGCTACGCTGCAGTACAGGTCTCGCCA CCTAATGAGCACATTACAGGAAGCCAATGGTGGACACGTTATCAGCCAGTAAGTTATGAA CTGCAAAGTCGTGGCGGAAACCGTGCACAGTTTATCGATATGGTAAATCGCTGTAGTGCA GCTGGGGTTGATATTTACGTTGATACGCTTATTAACCATATGGCAGCAGGAAGTGGCACA GGCACGGCGGGAAATAGCTTTGGTAATAAAAGCTTTCCTATTTATAGCCCACAAGATTTT CATGAAAGTTGTACCATTAATAACTCTGATTATGGCAACGATCGCTACCGAGTACAAAAC TGTGAACTAGTTGGACTTGCCGATTTAGATACCGCTTCAAACTATGTGCAAAATACCATT GCAGCATATATTAACGACTTACAAGCTATTGGCGTAAAAGGCTTTCGGTTTGATGCTTCT AAACATGTTGCAGCAAGCGATATCCAAAGTTTAATGGCCAAAGTAAATGGCTCGCCAGTG GTTTTTCAAGAAGTGATCGATCAAGGTGGGGAGGCTGTTGGTGCCTCTGAATATTTAAGC ACAGGTTTAGTAACTGAATTTAAATATAGCACTGAGCTTGGTAACACTTTTAGAAACGGC TCGCTTGCATGGCTGAGTAATTTTGGCGAAGGGTGGGGCTTTATGCCAAGCTCTTCTGCG GTGGTTTTTGTAGACAATCACGACAATCAGCGCGGGCACGGCGGCGCTGGCAATGTTATT ACCTTTGAAGATGGCCGCTTATATGACTTAGCCAATGTATTTATGTTGGCTTATCCGTAC GGTTATCCAAAAGTAATGTCGAGTTATGATTTTCATGGTGATACAGATGCTGGTGGGCCA AATGTACCGGTACATAATAATGGTAACTTAGAGTGTTTTGCGAGTAATTGGAAGTGTGAG CATCGCTGGTCATATATTGCAGGCGGGGTCGATTTTAGAAATAACACCGCCGACAACTGG GCAGTAACAAATTGGTGGGATAACACAAATAATCAAATTTCATTTGGCCGAGGTAGCTCG GGTCATATGGCTATTAACAAAGAAGACTCAACACTTACTGCAACTGTGCAAACCGATATG GCGTCAGGGCAATACTGTAATGTGCTAAAAGGCGAACTGTCAGCTGATGCTAAAAGTTGT AGTGGTGAGGTTATAACGGTTAATTCCGACGGTACTATTAATCTTAATATTGGCGCTTGG GATGCGATGGCAATTCATAAAAATGCCAAGTTAAATACCAGTTCTGCCTCAAGCACTGAA AGTGACTGGCAGCGAACGGTTATTTTTATTAATGCACAAACACAAAGCGGACAAGATATG TTTATCCGTGGTGGAATTGACCACGCTTATGCAAACGCAAACCTTGGTCGAAATTGCCAA ACAAGTAATTTTGAGTGTGCAATGCCTATTCGTCATAACAATTTAAAAAATGTCACAACA AGCCCTTGGAAAGCAAATGATAACTACCTTGATTGGTATGGTATAGAAAATGGGCAAAGT AGCGAAGCAGAAGGTTCTGCTACCGACTGGACAACGAACGTTTGGCCAGCAGGTTGGGGC GCTGAAAAAACGGTAAACACAGATGGTTTTGGTGTGACACCTTTAAATATATGGGGCGAA CACTATTGGATGCTTGATGTAGATATGGATTGCAGTAAAGCGGTTAATGGATGGTTTGAA CTAAAAGCATTCATTAAAAATGGCCAAGGATGGGAGACTGCCATTGCACAAGACAATGCA CCTTATACAAGTACTAATCATATGGCGCAATGCGGAAAAATTAATAAATTTGAGTTTAAT AATTCAGGTGTAGTAATTCGTAGTTTTTAA PF00128 Alpha-amylase PF02806 Alpha-amylase_C function catalytic activity function hydrolase activity function hydrolase activity, acting on glycosyl bonds function hydrolase activity, hydrolyzing O-glycosyl compounds function amylase activity function alpha-amylase activity process physiological process process metabolism process macromolecule metabolism process carbohydrate metabolism "
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