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PredicateValue (sorted: default)
rdfs:label
"[N-(2,4-DIAMINOPTERIDIN-6-YL)-METHYL]-DIBENZ[B,F]AZEPINE"
rdf:type
ns1:description
" experimental This compound belongs to the dibenzazepines. These are compounds with two benzene rings connected by an azepine ring. Dibenzazepines Organic Compounds Heterocyclic Compounds Benzazepines Dibenzazepines Pteridines and Derivatives Azepines Aminopyrimidines and Derivatives Primary Aromatic Amines Benzene and Substituted Derivatives Pyrazines Tertiary Amines Polyamines pteridine azepine aminopyrimidine benzene pyrazine primary aromatic amine pyrimidine tertiary amine polyamine amine primary amine organonitrogen compound logP 3.17 ALOGPS logS -3.8 ALOGPS Water Solubility 5.79e-02 g/l ALOGPS logP 3.15 ChemAxon IUPAC Name 6-{2-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3,5,7,9,11,13-heptaen-2-ylmethyl}pteridine-2,4-diamine ChemAxon Traditional IUPAC Name 6-{2-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3,5,7,9,11,13-heptaen-2-ylmethyl}pteridine-2,4-diamine ChemAxon Molecular Weight 367.4066 ChemAxon Monoisotopic Weight 367.154543579 ChemAxon SMILES NC1=NC2=C(N=C(CN3C4=CC=CC=C4C=CC4=CC=CC=C34)C=N2)C(N)=N1 ChemAxon Molecular Formula C21H17N7 ChemAxon InChI InChI=1S/C21H17N7/c22-19-18-20(27-21(23)26-19)24-11-15(25-18)12-28-16-7-3-1-5-13(16)9-10-14-6-2-4-8-17(14)28/h1-11H,12H2,(H4,22,23,24,26,27) ChemAxon InChIKey InChIKey=NXCCIJQEAKMFGW-UHFFFAOYSA-N ChemAxon Polar Surface Area (PSA) 106.84 ChemAxon Refractivity 112.22 ChemAxon Polarizability 38.49 ChemAxon Rotatable Bond Count 2 ChemAxon H Bond Acceptor Count 7 ChemAxon H Bond Donor Count 2 ChemAxon pKa (strongest acidic) 15.87 ChemAxon pKa (strongest basic) 3 ChemAxon Physiological Charge 0 ChemAxon Number of Rings 5 ChemAxon Bioavailability 1 ChemAxon Rule of Five true ChemAxon Ghose Filter true ChemAxon PubChem Compound 446744 PubChem Substance 99444877 ChemSpider 394026 PDB PMD BE0000330 Dihydrofolate reductase Human # 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 Dihydrofolate reductase Coenzyme transport and metabolism DHFR 5q11.2-q13.2 None 7.6 21322.0 Human HUGO Gene Nomenclature Committee (HGNC) HGNC:2861 GenAtlas DHFR GeneCards DHFR GenBank Gene Database J00140 GenBank Protein Database 182724 UniProtKB P00374 UniProt Accession DYR_HUMAN EC 1.5.1.3 >Dihydrofolate reductase VGSLNCIVAVSQNMGIGKNGDLPWPPLRNEFRYFQRMTTTSSVEGKQNLVIMGKKTWFSI PEKNRPLKGRINLVLSRELKEPPQGAHFLSRSLDDALKLTEQPELANKVDMVWIVGGSSV YKEAMNHPGHLKLFVTRIMQDFESDTFFPEIDLEKYKLLPEYPGVLSDVQEEKGIKYKFE VYEKND >564 bp ATGGTTGGTTCGCTAAACTGCATCGTCGCTGTGTCCCAGAACATGGGCATCGGCAAGAAC GGGGACCTGCCCTGGCCACCGCTCAGGAATGAATTCAGATATTTCCAGAGAATGACCACA ACCTCTTCAGTAGAAGGTAAACAGAATCTGGTGATTATGGGTAAGAAGACCTGGTTCTCC ATTCCTGAGAAGAATCGACCTTTAAAGGGTAGAATTAATTTAGTTCTCAGCAGAGAACTC AAGGAACCTCCACAAGGAGCTCATTTTCTTTCCAGAAGTCTAGATGATGCCTTAAAACTT ACTGAACAACCAGAATTAGCAAATAAAGTAGACATGGTCTGGATAGTTGGTGGCAGTTCT GTTTATAAGGAAGCCATGAATCACCCAGGCCATCTTAAACTATTTGTGACAAGGATCATG CAAGACTTTGAAAGTGACACGTTTTTTCCAGAAATTGATTTGGAGAAATATAAACTTCTG CCAGAATACCCAGGTGTTCTCTCTGATGTCCAGGAGGAGAAAGGCATTAAGTACAAATTT GAAGTATATGAGAAGAATGATTAA PF00186 DHFR_1 function dihydrofolate reductase activity function cofactor binding function coenzyme binding function NADP binding function binding function catalytic activity function oxidoreductase activity, acting on the CH-NH group of donors function oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor function oxidoreductase activity process glycine biosynthesis process serine family amino acid metabolism process physiological process process glycine metabolism process nucleobase, nucleoside, nucleotide and nucleic acid metabolism process metabolism process nucleotide metabolism process cellular metabolism process amino acid metabolism process amino acid and derivative metabolism process nucleotide biosynthesis "

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