Local view for "http://wifo5-04.informatik.uni-mannheim.de/drugbank/resource/drugs/DB03120"

PredicateValue (sorted: default)
rdfs:label
"Para-Toluene Sulfonate"
rdf:type
drugbank:description
" experimental This compound belongs to the toluenes. These are compounds containing a benzene ring which bears a methane group. Toluenes Organic Compounds Benzenoids Benzene and Substituted Derivatives Toluenes Sulfonyls Organic Sulfites Sulfonic Acids Polyamines sulfonyl sulfonic acid derivative organic sulfite sulfonic acid polyamine logP -0.88 ALOGPS logS -1.9 ALOGPS Water Solubility 2.30e+00 g/l ALOGPS logP 1.67 ChemAxon IUPAC Name 4-methylbenzene-1-sulfonic acid ChemAxon Traditional IUPAC Name para-toluene sulfonate ChemAxon Molecular Weight 172.202 ChemAxon Monoisotopic Weight 172.019414812 ChemAxon SMILES CC1=CC=C(C=C1)S(O)(=O)=O ChemAxon Molecular Formula C7H8O3S ChemAxon InChI InChI=1S/C7H8O3S/c1-6-2-4-7(5-3-6)11(8,9)10/h2-5H,1H3,(H,8,9,10) ChemAxon InChIKey InChIKey=JOXIMZWYDAKGHI-UHFFFAOYSA-N ChemAxon Polar Surface Area (PSA) 54.37 ChemAxon Refractivity 41.72 ChemAxon Polarizability 16.55 ChemAxon Rotatable Bond Count 1 ChemAxon H Bond Acceptor Count 3 ChemAxon H Bond Donor Count 1 ChemAxon pKa (strongest acidic) -2.1 ChemAxon Physiological Charge -1 ChemAxon Number of Rings 1 ChemAxon Bioavailability 1 ChemAxon Rule of Five true ChemAxon ChEBI 27849 PubChem Compound 6101 PubChem Substance 46507671 PDB TSU BE0003751 Lysozyme C 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 Lysozyme C LYZ Human UniProtKB P61626 UniProt Accession LYSC_HUMAN BE0003970 Pro-cathepsin H 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 Pro-cathepsin H Involved in cysteine-type endopeptidase activity Important for the overall degradation of proteins in lysosomes CTSH 15q24-q25 Lysosome None 8.19 37377.4 Human HUGO Gene Nomenclature Committee (HGNC) GNC:2535 GeneCards CTSH GenBank Gene Database X07549 GenBank Protein Database 29708 UniProtKB P09668 UniProt Accession CATH_HUMAN Cathepsin H heavy chain Cathepsin H light chain Cathepsin H mini chain >Cathepsin H MWATLPLLCAGAWLLGVPVCGAAELSVNSLEKFHFKSWMSKHRKTYSTEEYHHRLQTFAS NWRKINAHNNGNHTFKMALNQFSDMSFAEIKHKYLWSEPQNCSATKSNYLRGTGPYPPSV DWRKKGNFVSPVKNQGACGSCWTFSTTGALESAIAIATGKMLSLAEQQLVDCAQDFNNHG CQGGLPSQAFEYILYNKGIMGEDTYPYQGKDGYCKFQPGKAIGFVKDVANITIYDEEAMV EAVALYNPVSFAFEVTQDFMMYRTGIYSSTSCHKTPDKVNHAVLAVGYGEKNGIPYWIVK NSWGPQWGMNGYFLIERGKNMCGLAACASYPIPLV PF00112 Peptidase_C1 PF08246 Inhibitor_I29 function peptidase activity function endopeptidase activity function cysteine-type endopeptidase activity function cysteine-type peptidase activity function catalytic activity function hydrolase activity process protein metabolism process cellular protein metabolism process proteolysis process physiological process process metabolism process macromolecule metabolism "
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