SYNTHESIS OF SOME METHOXY- AND HYDROXY-PHENAZINE-1-CARBOXYLIC ACIDS.BROOKE PK; CHALLAND SR; FLOOD ME et al.1976; J. CHEM. SOC., PERKIN TRANS., 1; G.B.; DA. 1976; NO 21; PP. 2248-2251; BIBL. 22 REF.Article

Metabolites of microorganisms. CCXLVIII: Synthetic analogs of saphenamycinBAHNMÜLLER, U; KELLER-SCHIERLEIN, W; BRANDL, M et al.Journal of antibiotics (Tokyo. 1968). 1988, Vol 41, Num 11, pp 1552-1560, issn 0021-8820Article

DAS MASSENSPEKTROSKOPISCHE FRAGMENTIERUNGSVERHALTEN VON HYDROXY- UND METHOXYPHENAZINCARBONSAEUREN UND IHREN METHYLESTERN = FRAGMENTATION EN SPECTROMETRIE DE MASSE D'ACIDES HYDROXY- ET METHOXY PHENAZINECARBOXYLIQUES ET DE LEURS ESTERS DE METHYLEBUDZIKIEWICZ H; STOCKL D; ROMER A et al.1979; J. HETEROCYCL. CHEM.; USA; DA. 1979; VOL. 16; NO 7; PP. 1307-1312; ABS. ENG; BIBL. 28 REF.Article

Revised structure for the phenazine antibiotic from Pseudomonas fluorescens 2-79 (NRRL B-15132)BRISBANE, P. G; JANIK, L. J; TATE, M. E et al.Antimicrobial agents and chemotherapy. 1987, Vol 31, Num 12, pp 1967-1971, issn 0066-4804Article

Potential antitumor agents. LI: Synthesis and antitumor activity of substituted phenazine-1-carboxamidesREWCASTLE, G. W; DENNY, W. A; BAGULEY, B. C et al.Journal of medicinal chemistry (Print). 1987, Vol 30, Num 5, pp 843-851, issn 0022-2623Article

Phenacein: an angiotensin-converting enzyme inhibitor produced by a streptomycete. I: Taxonomy, fermentation and biological propertiesBUSH, K; HENRY, P. R; SOUSER-WOEHLEKE, M et al.Journal of antibiotics (Tokyo. 1968). 1984, Vol 37, Num 11, pp 1308-1312, issn 0021-8820Article

Role of a phenazine antibiotic from Pseudomonas fluorescens in biological control of Gaeumannomyces graminis var. triticiTHOMASHOW, L. S; WELLER, D. M.Journal of bacteriology. 1988, Vol 170, Num 8, pp 3499-3508, issn 0021-9193Article

Phenacein: an angiotensin-converting enzyme inhibitor produced by a streptomycete. II: Isolation, structure determination and synthesisWEN-CHIH LIU; PARKER, W. L; BRANDT, S. S et al.Journal of antibiotics (Tokyo. 1968). 1984, Vol 37, Num 11, pp 1313-1319, issn 0021-8820Article

2,3,9-Trihydroxyphenazin-1-carbonsäure ― ein unter Berylliumeinwirkung gebildetes neues Phenazinderivat aus Pseudomonas fluorescens = Acide trihydroxy-2,3,9 phénazinecarboxylique-1 ― un nouveau dérivé de la phénazine produit à partir de Pseudomonas fluorescens en présence de béryllium = 2,3,9-Trihydroxyphenazine-1 carboxylic acid ― a new phenazine derivative from Pseudomonas fluorescences grown under beryllium stressTARAZ, K; SCHAFFNER, E. M; BUDZIKIEWICZ, H et al.Zeitschrift für Naturforschung. B, A journal of chemical sciences. 1990, Vol 45, Num 4, pp 552-556, issn 0932-0776Article

DC-86-M, a novel antitumor antibiotic. II: Structure determination and biological activitiesTAKAHASHI, K; TAKAHASHI, I; MORIMOTO, M et al.Journal of antibiotics (Tokyo. 1968). 1986, Vol 39, Num 5, pp 624-628, issn 0021-8820Article

MOLECULE/RADICAL REACTIONS PRIOR TO IONIZATION UNDER NEGATIVE CHEMICAL IONIZATION CONDITIONSSTOECKL D; BUDZIKIEWICZ H.1982; ORG. MASS. SPECTROM.; ISSN 0030-493X; GBR; DA. 1982; VOL. 17; NO 8; PP. 376-381; BIBL. 23 REF.Article

PD 116,152, a new phenazine antitumor antibiotic structure and antitumor activitySMITKA, T. A; BUNGE, R. H; WILTON, J. H et al.Journal of antibiotics (Tokyo. 1968). 1986, Vol 39, Num 6, pp 800-803, issn 0021-8820Article

THE CHEMICAL DEGRADATION OF PHENAZINE-1-CARBOXYLIC ACID.LEVITCH ME.1976; J. NATION. MED. ASS.; U.S.A.; DA. 1976; VOL. 68; NO 6; PP. 487-491; BIBL. 4 REF.Article

CARBON-13 NUCLEAR MAGNETIC RESONANCE CHEMICAL SHIFTS OF SUBSTITUTED PHENAZINES.BREITMAIER E.1976; J. ORG. CHEM.; U.S.A.; DA. 1976; VOL. 41; NO 12; PP. 2104-2108; BIBL. 18 REF.Article