UCE1022, a new antitumor antibiotic with topoisomerase I mediated DNA cleavage activity, from Paecilomyces. 1994

N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano

UI MeSH Term Description Entries
D009279 Naphthacenes Polyacenes with four ortho-fused benzene rings in a straight linear arrangement. This group is best known for the subclass called TETRACYCLINES. Tetracenes,Benz(b)Anthracenes
D009284 Naphthols Naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position. They are often used in dyes and pigments, as antioxidants for rubber, fats, and oils, as insecticides, in pharmaceuticals, and in numerous other applications. Hydroxynaphthalene,Hydroxynaphthalenes,Naphthol
D010143 Paecilomyces A mitosporic fungal genus occasionally causing human diseases such as pulmonary infections, mycotic keratitis, endocarditis, and opportunistic infections. Its teleomorph is BYSSOCHLAMYS. Paecilomyce
D002166 Camptothecin An alkaloid isolated from the stem wood of the Chinese tree, Camptotheca acuminata. This compound selectively inhibits the nuclear enzyme DNA TOPOISOMERASES, TYPE I. Several semisynthetic analogs of camptothecin have demonstrated antitumor activity. Camptothecine
D002627 Chemistry, Physical The study of CHEMICAL PHENOMENA and processes in terms of the underlying PHYSICAL PHENOMENA and processes. Physical Chemistry,Chemistries, Physical,Physical Chemistries
D004249 DNA Damage Injuries to DNA that introduce deviations from its normal, intact structure and which may, if left unrepaired, result in a MUTATION or a block of DNA REPLICATION. These deviations may be caused by physical or chemical agents and occur by natural or unnatural, introduced circumstances. They include the introduction of illegitimate bases during replication or by deamination or other modification of bases; the loss of a base from the DNA backbone leaving an abasic site; single-strand breaks; double strand breaks; and intrastrand (PYRIMIDINE DIMERS) or interstrand crosslinking. Damage can often be repaired (DNA REPAIR). If the damage is extensive, it can induce APOPTOSIS. DNA Injury,DNA Lesion,DNA Lesions,Genotoxic Stress,Stress, Genotoxic,Injury, DNA,DNA Injuries
D004264 DNA Topoisomerases, Type I DNA TOPOISOMERASES that catalyze ATP-independent breakage of one of the two strands of DNA, passage of the unbroken strand through the break, and rejoining of the broken strand. DNA Topoisomerases, Type I enzymes reduce the topological stress in the DNA structure by relaxing the superhelical turns and knotted rings in the DNA helix. DNA Nicking-Closing Protein,DNA Relaxing Enzyme,DNA Relaxing Protein,DNA Topoisomerase,DNA Topoisomerase I,DNA Topoisomerase III,DNA Topoisomerase III alpha,DNA Topoisomerase III beta,DNA Untwisting Enzyme,DNA Untwisting Protein,TOP3 Topoisomerase,TOP3alpha,TOPO IIIalpha,Topo III,Topoisomerase III,Topoisomerase III beta,Topoisomerase IIIalpha,Topoisomerase IIIbeta,DNA Nicking-Closing Proteins,DNA Relaxing Enzymes,DNA Type 1 Topoisomerase,DNA Untwisting Enzymes,DNA Untwisting Proteins,Topoisomerase I,Type I DNA Topoisomerase,III beta, Topoisomerase,III, DNA Topoisomerase,III, Topo,III, Topoisomerase,IIIalpha, TOPO,IIIalpha, Topoisomerase,IIIbeta, Topoisomerase,Topoisomerase III, DNA,Topoisomerase, TOP3,beta, Topoisomerase III
D006367 HeLa Cells The first continuously cultured human malignant CELL LINE, derived from the cervical carcinoma of Henrietta Lacks. These cells are used for, among other things, VIRUS CULTIVATION and PRECLINICAL DRUG EVALUATION assays. Cell, HeLa,Cells, HeLa,HeLa Cell
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000903 Antibiotics, Antineoplastic Chemical substances, produced by microorganisms, inhibiting or preventing the proliferation of neoplasms. Antineoplastic Antibiotics,Cytotoxic Antibiotics,Antibiotics, Cytotoxic

Related Publications

N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
October 1990, The Journal of antibiotics,
N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
July 1992, The Journal of antibiotics,
N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
February 1993, The Journal of antibiotics,
N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
November 1999, The Journal of antibiotics,
N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
May 1992, Cancer research,
N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
November 2005, The Journal of biological chemistry,
N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
February 1993, Cancer research,
N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
August 1989, Cancer research,
N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
April 2007, The Journal of antimicrobial chemotherapy,
N Fujii, and Y Yamashita, and K Ando, and T Agatsuma, and Y Saitoh, and K Gomi, and Y Nishiie, and H Nakano
July 1990, The Journal of biological chemistry,
Copied contents to your clipboard!