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PredicateValue (sorted: default)
rdfs:label
"(S)-4-Bromo-3-Hydroxy-3-Methylbutyl Diphosphate"
rdf:type
ns1:description
" experimental This compound belongs to the organic pyrophosphates. These are organic compounds containing the pyrophosphate oxoanion, with the structure OP([O-])(=O)OP(O)([O-])=O. Organic Pyrophosphates Organic Compounds Organooxygen Compounds Organic Oxoanionic Compounds Organic Pyrophosphates Organic Phosphoric Acids Organophosphate Esters Tertiary Alcohols Bromohydrins Polyamines Organobromides Alkyl Bromides phosphoric acid ester organic phosphate tertiary alcohol bromohydrin halohydrin polyamine organobromide alcohol organohalogen alkyl halide alkyl bromide logP 0.01 ALOGPS logS -1.5 ALOGPS Water Solubility 1.01e+01 g/l ALOGPS logP -0.5 ChemAxon IUPAC Name ({[(3R)-4-bromo-3-hydroxy-3-methylbutoxy](hydroxy)phosphoryl}oxy)phosphonic acid ChemAxon Traditional IUPAC Name [(3R)-4-bromo-3-hydroxy-3-methylbutoxy(hydroxy)phosphoryl]oxyphosphonic acid ChemAxon Molecular Weight 343.003 ChemAxon Monoisotopic Weight 341.926903063 ChemAxon SMILES C[C@](O)(CBr)CCO[P@](O)(=O)OP(O)(O)=O ChemAxon Molecular Formula C5H13BrO8P2 ChemAxon InChI InChI=1S/C5H13BrO8P2/c1-5(7,4-6)2-3-13-16(11,12)14-15(8,9)10/h7H,2-4H2,1H3,(H,11,12)(H2,8,9,10)/t5-/m1/s1 ChemAxon InChIKey InChIKey=YKAYCWPQDPILSA-RXMQYKEDSA-N ChemAxon Polar Surface Area (PSA) 133.52 ChemAxon Refractivity 57.8 ChemAxon Polarizability 24.12 ChemAxon Rotatable Bond Count 7 ChemAxon H Bond Acceptor Count 6 ChemAxon H Bond Donor Count 4 ChemAxon pKa (strongest acidic) 1.78 ChemAxon pKa (strongest basic) -3.2 ChemAxon Physiological Charge -2 ChemAxon Number of Rings 0 ChemAxon Bioavailability 1 ChemAxon Rule of Five true ChemAxon PubChem Compound 448012 PubChem Substance 46507951 ChemSpider 2718734 PDB SBH BE0001417 Isopentenyl-diphosphate Delta-isomerase Escherichia coli (strain K12) # 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 Isopentenyl-diphosphate Delta-isomerase Secondary metabolites biosynthesis, transport and catabolism Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) idi Cytoplasm None 6.35 20508.0 Escherichia coli (strain K12) GenBank Gene Database AF119715 GenBank Protein Database 4633513 UniProtKB Q46822 UniProt Accession IDI_ECOLI EC 5.3.3.2 IPP isomerase IPP:DMAPP isomerase Isopentenyl pyrophosphate isomerase >Isopentenyl-diphosphate Delta-isomerase MQTEHVILLNAQGVPTGTLEKYAAHTADTRLHLAFSSWLFNAKGQLLVTRRALSKKAWPG VWTNSVCGHPQLGESNEDAVIRRCRYELGVEITPPESIYPDFRYRATDPSGIVENEVCPV FAARTTSALQINDDEVMDYQWCDLADVLHGIDATPWAFSPWMVMQATNREARKRLSAFTQ LK >549 bp ATGCAAACGGAACACGTCATTTTATTGAATGCACAGGGAGTTCCCACGGGTACGCTGGAA AAGTATGCCGCACACACGGCAGACACCCGCTTACATCTCGCGTTCTCCAGTTGGCTGTTT AATGCCAAAGGACAATTATTAGTTACCCGCCGCGCACTGAGCAAAAAAGCATGGCCTGGC GTGTGGACTAACTCGGTTTGTGGGCACCCACAACTGGGAGAAAGCAACGAAGACGCAGTG ATCCGCCGTTGCCGTTATGAGCTTGGCGTGGAAATTACGCCTCCTGAATCTATCTATCCT GACTTTCGCTACCGCGCCACCGATCCGAGTGGCATTGTGGAAAATGAAGTGTGTCCGGTA TTTGCCGCACGCACCACTAGTGCGTTACAGATCAATGATGATGAAGTGATGGATTATCAA TGGTGTGATTTAGCAGATGTATTACACGGTATTGATGCCACGCCGTGGGCGTTCAGTCCG TGGATGGTGATGCAGGCGACAAATCGCGAAGCCAGAAAACGATTATCTGCATTTACCCAG CTTAAATAA PF00293 NUDIX function isomerase activity function intramolecular oxidoreductase activity function intramolecular oxidoreductase activity, transposing C=C bonds function isopentenyl-diphosphate delta-isomerase activity function catalytic activity process metabolism process primary metabolism process lipid metabolism process cellular lipid metabolism process isoprenoid metabolism process isoprenoid biosynthesis process physiological process "
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