Over 62% Carbon Patents (Class 424/122)
  • Patent number: 4933180
    Abstract: This disclosure describes a novel antibiotic designated Vermisporin produced in a microbiological fermentation using, for example, a new strain of Ophiobolus Vermisporus L-8. This novel antibiotic is an active antibacterial, especially anti-anaerobic bacterial agent.
    Type: Grant
    Filed: February 2, 1988
    Date of Patent: June 12, 1990
    Assignees: Mitsubishi Kasei Corporation, Meiji Seika Kaisha, Limited
    Inventors: Takashi Mikawa, Noriko Takahashi, Haruyuki Ohkishi, Yoshikazu Sato, Shinji Miyadoh, Masaji Sezaki
  • Patent number: 4920215
    Abstract: The antibiotic of the formula: ##STR1## wherein R is ##STR2## The antibiotic is useful for the treatment of swine dysentery and for promoting growth and/or increasing the efficiency of food utilization in poultry, swine and ruminants.
    Type: Grant
    Filed: December 16, 1987
    Date of Patent: April 24, 1990
    Assignee: Pfizer Inc.
    Inventors: Kelvin S. Holdom, John C. Ruddock, Junsuke Tone, Hiroshi Maeda, Martin R. Jefson
  • Patent number: 4885171
    Abstract: Methods for using rapamycin in the treatment of certain cancers or tumors are disclosed.
    Type: Grant
    Filed: March 22, 1984
    Date of Patent: December 5, 1989
    Assignee: American Home Products Corporation
    Inventors: Sehgal N. Surendra, Claude Vezina
  • Patent number: 4882142
    Abstract: The invention concerns a method for suppressing bone marrow which comprises administering to a mammal at least one bone marrow suppressing complex of a radionuclide selected from the group consisting of Samarium-153, Gadolinium-159, and Holmium-166 and 1,4,7,10-tetraazacyclododecanetetramethylenephosphonic acid a physiologically acceptable salt thereof. Suitable compositions for use in this method are also provided.
    Type: Grant
    Filed: December 19, 1988
    Date of Patent: November 21, 1989
    Assignee: The Dow Chemical Company
    Inventors: Jaime Simon, Joseph R. Garlich, David A. Wilson, Kenneth McMillan
  • Patent number: 4877776
    Abstract: A K-252 compound represented by the formula: ##STR1## wherein R.sup.1 and R.sup.2 are independently H or OH; X represents COOH, COOR or CH.sub.2 OH; Y represents H, R or COR; and Z represents OH, OR or SR, wherein R represents lower alkyl has C-kinase inhibitory activity and is expected to be useful as an active ingredient of anti-tumor agents, etc.
    Type: Grant
    Filed: December 22, 1988
    Date of Patent: October 31, 1989
    Assignee: Kyowa Hakko Kogyo Co., Ltd.
    Inventors: Chikara Murakata, Akira Sato, Masaji Kasai, Eiji Kobayashi, Makoto Morimoto, Shiro Akinaga
  • Patent number: 4869901
    Abstract: The present invention relates to methods and compositions for the control and prevention of helmintic, arthropod ectoparasitic and acaridal infections, in warm-blooded animals, such as meat-producing animals, and poultry, by administering to said animals a therapeutically or prophylactically-effective amount of new agents designated LL-F28249.alpha., .beta., .gamma., .delta., .epsilon., .zeta., .eta., .theta., .iota. and .omega., or mixtures thereof. The invention also relates to methods for the control of plant nematode infestations. These novel agents are produced via a controlled conditioned microbiological fermentation using Streptomyces sp. LL-F28249, having deposit accession number NRRL 15773.
    Type: Grant
    Filed: June 5, 1984
    Date of Patent: September 26, 1989
    Assignee: American Cyanamid Company
    Inventors: Irwin B. Wood, John A. Pankavich
  • Patent number: 4803074
    Abstract: This invention relates to a compound, FR-900848, having antimicrobial activity against various microorganisms, to a process for the preparation of same and to a pharmaceutical composition comprising same.
    Type: Grant
    Filed: March 30, 1988
    Date of Patent: February 7, 1989
    Assignee: Fujisawa Pharmaceutical Co., Ltd.
    Inventors: Masaru Yoshida, Koki Horikoshi
  • Patent number: 4792522
    Abstract: A novel complex designated herein as rigolettone complex is produced by fermentation of Streptomyces aburaviensis strain C-38,242 (ATCC 39290). The complex and its purified bioactive components, jildamycin and mantuamycin, exhibit antitumor activity in mouse tumor systems.
    Type: Grant
    Filed: August 22, 1985
    Date of Patent: December 20, 1988
    Assignee: Bristol-Myers Company
    Inventors: Donald E. Nettleton, Jr., Stanley W. Bray, James A. Bush, William T. Bradner
  • Patent number: 4759928
    Abstract: Two strains of Streptomyces were identified as Streptomyces albovinaceous. Both isolates produced an antibiotic when grown in liquid culture medium containing homogenized oats. The antibiotic (Treponemycin) was isolated from the culture broth by solvent extraction and purified. The antibiotic showed inhibitory activity against several species of bacteria, especially Treponema hyodysenteriae, the causative agent of swine dysentery. In view of the oral 50% lethal dose of 400 mg/kg and its low MIC against four strains of T. hyodysenteriae, the antibiotic has value as a swine dysentery therapeutic. The antibiotic lends itself readily to production of a tetrahydro derivative, a primary amine, a dimethyl ester and a hydrochloride esters and salts of these compounds, and hydrates of these compounds and of the esters or salts can also be produced for pharmaceutical usages.
    Type: Grant
    Filed: January 31, 1986
    Date of Patent: July 26, 1988
    Assignee: Washington State University Research Foundation
    Inventors: Sarangamat Gurusiddaiah, Shrikrishna Singh
  • Patent number: 4753798
    Abstract: This invention relates to methods and compositions for the control of protozoal infections in warm-blooded animals by administering to said animals a protozoacidally-effective amount of a new antibiotic designated LL-E19020.alpha., LL-E19020.beta. or a pharmaceutically and prophylactically acceptable salt thereof. The new antibiotics are produced by microbiological fermentation under controlled conditions using a new strain of Streptomyces lydicus subspecies tanzanius or mutants thereof.
    Type: Grant
    Filed: June 30, 1986
    Date of Patent: June 28, 1988
    Assignee: American Cyanamid Company
    Inventors: Sidney Kantor, Robert L. Kennett, Jr.
  • Patent number: 4746349
    Abstract: The present invention relates to methods for suppressing the nitrification of ammonium nitrogen in plant growth medium or soil and compositions which conserve soil nitrogen and supply soil nitrogen requirements necessary for plant nutrition.
    Type: Grant
    Filed: August 6, 1986
    Date of Patent: May 24, 1988
    Assignee: American Cyanamid Company
    Inventor: Robert H. Becker
  • Patent number: 4705688
    Abstract: This invention relates to antibiotic LL-E19020.alpha. and LL-E19020.beta. derived from the microorganism Streptomyces lydicus subspecies tanzanius NRRL 18036, which are useful as an antibacterial agent.
    Type: Grant
    Filed: June 30, 1986
    Date of Patent: November 10, 1987
    Assignee: American Cyanamid Company
    Inventors: Guy T. Carter, Michael Greenstein, Joseph J. Goodman, Donald B. Borders, William M. Maiese, Raymond T. Testa
  • Patent number: 4704276
    Abstract: This invention provides methods for increasing the growth rate of meat producing animals, for improving the efficiency of feed utilization by said meat producing animals, and for increasing lactation in lactating ruminant animals. The invention also relates to novel animal feed compositions and parenteral compositions useful in obtaining the above-described desired results.
    Type: Grant
    Filed: June 30, 1986
    Date of Patent: November 3, 1987
    Assignee: American Cyanamid Company
    Inventor: Sidney Kantor
  • Patent number: 4692310
    Abstract: A new substance K-259-2 having a molecular formula of C.sub.21 H.sub.18 O.sub.7, a molecular weight of 382 and an elemental analysis (%) of H: 4.50, C: 65.53 and N: 0. This substance is of interest in providing a new vasodilating agent in view of its ability to dilate the blood vessel, particularly the artery, of mammals. This substance may be obtained by fermentation of a microorganism Micromonospora sp. K-259 (FERM BP 569).
    Type: Grant
    Filed: April 16, 1986
    Date of Patent: September 8, 1987
    Assignee: Kyowa Hakko Kogyo Kabushiki Kaisha
    Inventors: Hiroshi Kase, Yuzuru Matsuda, Isao Kawamoto, Kozo Asano, Kunikatsu Shirahata, Tohru Yasuzawa, Koji Yamada
  • Patent number: 4692333
    Abstract: New antibiotic substances arbitrarily designated M 9026 complex, antibiotic M 9026 factor 1, antibiotic M 9026 factor 2, and antibiotic M 9026 factor 3, produced by fermentation of a strain of the Micromonospora genus. The antibiotics of the invention are antimicrobial and antitumor agents.
    Type: Grant
    Filed: August 4, 1983
    Date of Patent: September 8, 1987
    Assignee: Gruppo Lepetit S.p.A.
    Inventors: Giorgio Pirali, Maria Grandi, Hermes Pagani, Manuela Paternoster, Giorgio Tamoni, Giovanni Cassani
  • Patent number: 4692334
    Abstract: Orally administered compositions for altering lipid metabolism are described herein, these compositions containing an effective dose of cryptocidin. Also the method of altering lipid metabolism including reducing and controlling the blood cholesterol level, is described herein.
    Type: Grant
    Filed: August 29, 1984
    Date of Patent: September 8, 1987
    Assignee: Schmid Laboratories
    Inventor: Harry W. Gordon
  • Patent number: 4680178
    Abstract: The invention relates to a pharmaceutical composition for treating lymphocytic leukemia, melanoma or mammary carcinoma comprising an effective amount of FR-900216.
    Type: Grant
    Filed: July 16, 1984
    Date of Patent: July 14, 1987
    Assignee: Fujisawa Pharmaceutical Co., Ltd.
    Inventors: Sumio Kiyoto, Masakuni Okuhara, Eiko Kino, Hirokazu Tanaka, Hatsuo Aoki, Masanobu Kohsaka, Hiroshi Imanaka
  • Patent number: 4670260
    Abstract: A novel antibiotic for combating bacteria and promoting animal growth is obtained by cultivating Streptomyces strain BA 9.
    Type: Grant
    Filed: November 27, 1985
    Date of Patent: June 2, 1987
    Assignee: Bayer Aktiengesellschaft
    Inventors: Erwin Bischoff, Hartwig Muller, Olga Salcher, Friedrich Berschauer, Martin Scheer, Anno de Jong, Klaus Frobel
  • Patent number: 4666715
    Abstract: An antibiotic AM-5344-A.sub.2 substance, and a process for the preparation of the antibiotic AM-5344-A.sub.2 substance are described. The antibiotic AM-5344-A.sub.2 substance is prepared by cultivating an AM-5344-A.sub.2 substance-producing strain belonging to the genus Streptomyces, for example, Streptomyces sp. Am-5344 in a nutrient medium, and recovering the Am-5344-A.sub.2 substance from the culture.
    Type: Grant
    Filed: June 24, 1983
    Date of Patent: May 19, 1987
    Assignee: Kitasato Institute
    Inventors: Satoshi Omura, Yuzuru Iwai, Kiyoizumi Hinotozawa, Atsushi Hirano
  • Patent number: 4588588
    Abstract: A novel antifungal antibiotic which has been designated EM5487 is prepared by cultivating Lysobacter gummosus A.T.C.C. No. 39472 under submerged aerobic conditions in an aqueous nutrient medium containing an assimilable carbohydrate and nitrogen source.
    Type: Grant
    Filed: December 5, 1983
    Date of Patent: May 13, 1986
    Assignee: E. R. Squibb & Sons, Inc.
    Inventors: Edward Meyers, Raymond Cooper
  • Patent number: 4555402
    Abstract: A novel physiologically active substance K-252 having an antiallergic action is produced by culturing a microorganism of the genus Nocardiopsis.
    Type: Grant
    Filed: August 10, 1984
    Date of Patent: November 26, 1985
    Assignee: Kyowa Hakko Kogyo Co. Ltd.
    Inventors: Yuzuru Matsuda, Kazuyuki Iwahashi, Takao Iida, Noriaki Hirayama, Kozo Asano, Katsuichi Shuto, Koji Yamada, Kunikatsu Shirahata, Hiroshi Kase
  • Patent number: 4550021
    Abstract: Antibiotic 81-484 of the following physico-chemical properties:(1) elementary analysis: C.sub.33 H.sub.48 O.sub.7 (high resolution mass spectrum);(2) molecular weight: 556 [Field desorption (FD) mass spectrum];(3) melting point: not clear (oily at 10.degree.-100.degree. C.);(4) specific rotation: [.alpha.].sub.D.sup.20 =-151.degree. (c=0.1, methanol);(5) ultraviolet absorption spectrum: shown in FIG. 1 (in methanol);(6) infrared absorption spectrum: shown in FIG. 2 (KBr tablet);(7) solubility: insoluble in hexane and water, soluble in diethyl ether, methanol, ethanol, dichloromethane, chloroform, ethyl acetate, butyl acetate, acetone and benzene;(8) nuclear magnetic resonance spectrum: shown in FIG. 3 (CDCl.sub.3, TMS);(9) nature: acidic substance;(10) color reaction:negative for ninhydrin, anthrone-H.sub.2 SO.sub.
    Type: Grant
    Filed: June 5, 1984
    Date of Patent: October 29, 1985
    Assignee: The Kitasato Institute
    Inventors: Iwao Umezawa, Kanki Komiyama
  • Patent number: 4548814
    Abstract: Novel antibiotics didemnins A, B and C (didemnins), and nordidemnins A, B and C (nordidemnins) which can be obtained from a marine organism. These antibiotics are active against a variety of DNA and RNA viruses; thus, they can be used in various environments to control or eradicate these viruses. Further, these antibiotics can be used to treat animals and humans hosting a neoplastic disease.
    Type: Grant
    Filed: September 8, 1981
    Date of Patent: October 22, 1985
    Assignee: The Board of Trustees of the University of Illinois
    Inventor: Kenneth L. Rinehart, Jr.
  • Patent number: 4534970
    Abstract: This disclosure describes four new antibacterial agents designated LL-CO8078.alpha..sub.1, LL-CO8078.alpha..sub.2, LL-CO8078.alpha..sub.3 and LL-CO8078.beta. produced in a microbiological fermentation under controlled conditions using a new strain of a new species of the genus Streptomyces called Streptomyces majorciensis Labeda, sp. nov., and mutants thereof. These new antibacterial agents are active against a variety of microorganisms and thus are useful in inhibiting the growth of such bacteria wherever they may be found. In addition, these agents are active as growth promotants in warm-blooded animals.
    Type: Grant
    Filed: June 23, 1983
    Date of Patent: August 13, 1985
    Assignee: American Cyanamid Company
    Inventors: David P. Labeda, Joseph J. Goodman, Donald B. Borders, Raymond T. Testa, John H. E. J. Martin, deceased
  • Patent number: 4533547
    Abstract: A novel antiviral antibiotic AM-2722 is described represented by the molecular formula C.sub.19 H.sub.26 NO.sub.3 Cl, and having the following physicochemical properties:(1) specific rotary power: [.alpha.].sub.D.sup.20 -0.5 (C-1, chloroform);(2) the UV spectrum shown in FIG. 1; and(3) the IR spectrum shown in FIG. 2.Also described is a process for producing the antiviral antibiotic AM-2722, wherein a microorganism of Streptomyces which has the ability to produce the antibiotic AM-2722 is cultured aerobically in a nutrient medium and the antibiotic AM-2722 accumulated in the medium and the microorganism cells is recovered.
    Type: Grant
    Filed: May 11, 1981
    Date of Patent: August 6, 1985
    Assignee: The Kitasato Institute
    Inventors: Satoshi Omura, Akira Nakagawa, Hiroshi Hashimoto, Yasuhiko Kojima, Yuzuru Iwai, Ruiko Oiwa, Atsushi Hirano
  • Patent number: 4517178
    Abstract: This invention relates to a novel antibiotic 76-11; process for the production thereof which comprises culturing an antibiotic 76-11 producing microorganism belonging to the genus Actinomadura to separate and collect the antibiotic; an anticoccidiosis agent comprising the antibiotic as an effective ingredient; and a growth accelerating and feed efficiency increasing agent for domestic animals and fowls comprising the antibiotic as an effective ingredient.
    Type: Grant
    Filed: June 13, 1983
    Date of Patent: May 14, 1985
    Assignees: Rikagaku Kenkyusho, Kaken Kagaku Kabushiki Kiasha
    Inventors: Kiyoshi Isono, Goto Nakamura, Shigeo Fujita
  • Patent number: 4512976
    Abstract: This invention relates to the antibiotic stubomycin and process for producing same by culturing streptomyces sp KG - 2245 FERM-P No.
    Type: Grant
    Filed: September 25, 1981
    Date of Patent: April 23, 1985
    Assignee: The Kitasato Institute
    Inventors: Iwao Umezawa, Kanki Komiyama, Hideo Takeshima
  • Patent number: 4512975
    Abstract: Macbecin derivatives are produced by cultivating a microorganism of the genus Actinosynnema in a culture medium.The Macbecin derivatives are useful as antibacterial, antifungal or antiprotozoal agent.
    Type: Grant
    Filed: September 14, 1983
    Date of Patent: April 23, 1985
    Assignee: Takeda Chemical Industries, Ltd.
    Inventors: Toru Hasegawa, Masayuki Muroi, Seiichi Tanida
  • Patent number: 4482540
    Abstract: Orally administered compositions for altering lipid metabolism are described herein, these compositions containing an effective dose of endomycin. Also the method of altering lipid metabolism including reducing and controlling the blood cholesterol level, is described herein.
    Type: Grant
    Filed: June 8, 1981
    Date of Patent: November 13, 1984
    Assignee: Schmid Laboratories
    Inventors: Harry W. Gordon, Carl P. Schaffner
  • Patent number: 4427776
    Abstract: Novel antibiotic U-64,815 producible in a fermentation under controlled conditions using a biologically pure culture of the microorganism Streptomyces microspinus, NRRL 12524. This antibiotic is active against various Gram-positive bacteria, for example, Staphylococcus aureus. It is also active against Haemophilus influenzae. Thus, antibiotic U-64,815 can be used in various environments to eradicate or control such bacteria.
    Type: Grant
    Filed: September 21, 1981
    Date of Patent: January 24, 1984
    Assignee: The Upjohn Company
    Inventors: Howard A. Whaley, William C. Snyder, John C. Greenfield, John H. Coats
  • Patent number: 4421687
    Abstract: Macbecin derivatives are produced by cultivating a microorganism of the genus Actinosynnema in a culture medium.The Macbecin derivatives are useful as antibacterial, antifungal or antiprotozoal agent.
    Type: Grant
    Filed: September 2, 1982
    Date of Patent: December 20, 1983
    Assignee: Takeda Chemical Industries, Limited
    Inventors: Toru Hasegawa, Masayuki Muroi, Seiichi Tanida
  • Patent number: 4375463
    Abstract: Ravidomycin is produced by culturing Streptomyces ravidus NRRL 11,300 in an aqueous nutrient medium. Ravidomycin is useful as an antibacterial and antitumor agent. Methods for its preparation and use are disclosed.
    Type: Grant
    Filed: March 13, 1981
    Date of Patent: March 1, 1983
    Assignee: Ayerst, McKenna & Harrison, Inc.
    Inventors: Surendra N. Sehgal, Claude Vezina
  • Patent number: 4375464
    Abstract: Antibiotic AY24,668 is producible by culturing Streptomyces hygroscopicus NRRL 5491 in an aqueous nutrient medium. AY24,668 has antifungal properties. Methods for its preparation and use are disclosed.
    Type: Grant
    Filed: November 19, 1981
    Date of Patent: March 1, 1983
    Assignee: Ayerst, McKenna & Harrison Inc.
    Inventors: Surendra N. Sehgal, Claude Vezina
  • Patent number: 4342750
    Abstract: Orally administered compositions for treating benign prostatic hypertrophy are described herein. These compositions contain an effective dose of N-acyl amphotericin B. Also, the method of treating benign prostatic hypertrophy with such compositions is described herein.
    Type: Grant
    Filed: June 8, 1979
    Date of Patent: August 3, 1982
    Assignee: Schmid Labs., Inc.
    Inventor: Harry W. Gordon
  • Patent number: 4331658
    Abstract: Method and compositions for treatment of swine dysentery with antibiotic A-32887 (K-41). Antibiotic A-32887 is produced by submerged aerobic fermentation of Streptomyces albus NRRL 11109.
    Type: Grant
    Filed: February 22, 1980
    Date of Patent: May 25, 1982
    Assignee: Eli Lilly and Company
    Inventors: Robert L. Hamill, Marvin M. Hoehn
  • Patent number: 4331659
    Abstract: Novel antibiotic U-62,162 producible in a fermentation under controlled conditions using a man-made biologically pure culture of the microorganism Streptomyces verdensis, Dietz and Li sp.n., NRRL 12256. This antibiotic is strongly active against various Gram-positive bacteria, for example, Staphylococcus aureus. Thus, antibiotic U-62,162 can be used in various environments to eradicate or control such bacteria.
    Type: Grant
    Filed: September 10, 1980
    Date of Patent: May 25, 1982
    Assignee: The Upjohn Company
    Inventors: Herman Hoeksema, Libor Slechta
  • Patent number: 4316885
    Abstract: Disclosed are monoacyl and diacyl derivatives of rapamycin, processes for their preparation, methods of using the derivatives and pharmaceutical compositions of the derivatives. The derivatives are useful, inter alia, as antifungal antibiotics.
    Type: Grant
    Filed: August 25, 1980
    Date of Patent: February 23, 1982
    Assignee: Ayerst, McKenna and Harrison, Inc.
    Inventor: Sumanas Rakhit
  • Patent number: 4311693
    Abstract: The antibiotic MSD A63A, having antibacterial and growth-permittant activity, is produced by fermentation of Streptoverticillum hiroshimense MA4845 (ATCC 31586), in a suitable nutrient media.
    Type: Grant
    Filed: November 17, 1980
    Date of Patent: January 19, 1982
    Assignee: Merck & Co., Inc.
    Inventors: Sebastian Hernandez, Sheldon B. Zimmerman, Vincent P. Gullo, Ray S. Dewey
  • Patent number: 4303647
    Abstract: Methods and compositions for treatment of coccidiosis in poultry with antibiotic A-32887 (K-41). Antibiotic A-32887 is produced by submerged aerobic fermentation of Streptomyces albus NRRL 11109.
    Type: Grant
    Filed: February 22, 1980
    Date of Patent: December 1, 1981
    Assignee: Eli Lilly and Company
    Inventors: Robert L. Hamill, Marvin M. Hoehn
  • Patent number: 4292310
    Abstract: Orally administered compositions for altering liquid metabolism are described herein, these compositions containing an effective dose of n-acyl amphotericin B. Also the method of altering lipid metabolism including reducing and controlling the blood cholesterol level, is described herein.
    Type: Grant
    Filed: April 12, 1979
    Date of Patent: September 29, 1981
    Inventors: Harry W. Gordon, Carl P. Schaffner
  • Patent number: 4291021
    Abstract: A novel microorganism species belonging to the genus Micromonospora, i.e. Micromonospora sp. A 11725 is found to be capable of producing novel macrolide antibiotics A 11725 I, A 11725 II and A 11725 III. Novel antibiotics A 11725 Ia and A 11725 IIa are also found to be derived by chemical modification of the antibiotics A 11725 I and A 11725 II, respectively. All of these antibiotics or salts thereof exhibit excellent antibacterial and anti-mycoplasmal activities against various microorganisms such as Staphylococcus or Mycoplasma, and therefore useful for various purposes including medicaments.
    Type: Grant
    Filed: May 10, 1979
    Date of Patent: September 22, 1981
    Assignee: Toyo Jozo Company, Ltd.
    Inventors: Masaru Otani, Shuzo Satoi, Naoki Muto, Tetsu Saito, Tadashiro Fujii, Seiji Katsumata, Mitsuo Hayashi, Masaru Ono
  • Patent number: 4289757
    Abstract: A method of treating inflammation comprising topical administration to mammals suffering from an inflammatory condition not associated with amicrobial component, employing selected antibiotics as the anti-inflammatory agent.
    Type: Grant
    Filed: November 28, 1979
    Date of Patent: September 15, 1981
    Assignee: The Upjohn Company
    Inventor: E. Myles Glenn
  • Patent number: 4283390
    Abstract: Antibiotic A-39183 complex, comprising microbiologically active, related factors A, B, C, D, and E, is produced by submerged, aerobic fermentation of a new microorganism Streptomyces sp., NRRL 12049. The A-39183 antibiotics are closely related antibiotics. The individual A-39183 factors are separated by chromatography. The A-39183 factors are antibacterial agents which have activity against Staphylococcus and Streptococcus species that are penicillin resistant. The A-39183 factors are also active against both gram-positive and gram-negative anaerobic bacteria, and are ionophores.
    Type: Grant
    Filed: November 1, 1979
    Date of Patent: August 11, 1981
    Assignee: Eli Lilly and Company
    Inventors: Kay F. Koch, Ralph E. Kastner
  • Patent number: 4283391
    Abstract: A new antibiotic named pamamycin is derived from S. alboniger. The antibiotic compound is neutral and terpene-like as derived from S. alboniger. The antibiotic is produced in conjunction with substances which either stimulate or inhibit the transition of substrate to aerial mycelia. Pamamycin may be separated by thin layer chromatography. The antibiotic displays particular R.sub.f values in thin layer chromatography as well as a particular antimicrobial spectrum for its use. The molecular formula is 621 and the elemental formula thereof is C.sub.36 H.sub.63 NO.sub.7 as determined by mass spectroscopy. The structure is believed to be a saturated alkane and terpene-like. In vivo tests with Staphylococcus aureus indicate that pamamycin is a potent inhibitor of both DNA and RNA synthesis and this antibiotic has present utility in a 1% solution to degerminate hospital walls.
    Type: Grant
    Filed: July 16, 1979
    Date of Patent: August 11, 1981
    Assignee: St. Louis, University
    Inventors: Burton M. Pogell, Pamela A. McCann
  • Patent number: 4279894
    Abstract: The invention relates to a novel metabolite, M.139603, of the empirical formula C.sub.35 H.sub.53 O.sub.8 Na, which is obtained from the aerobic fermentation of a novel Streptomyces species, NCIB 11426, and to the corresponding free acid form thereof, C.sub.35 H.sub.54 O.sub.8. M.139,603 reduces the proportion of methane produced by the "digestion" of food in the rumen of ruminant animals and increases the proportion of propionate to acetate in the rumen contents. The compound is therefore useful for increasing the growth rate of ruminant animals, and/or for increasing their efficiency of food conversion. The compound also possesses activity against Gram positive micro-organisms, and against coccidia, for example Eimeria tenella.
    Type: Grant
    Filed: July 25, 1979
    Date of Patent: July 21, 1981
    Assignee: Imperial Chemical Industries Limited
    Inventors: David H. Davies, Geoffrey L. F. Norris
  • Patent number: 4275062
    Abstract: Cephalosporins of the formula ##STR1## R represents hydrogen, sodium, potassium, or certain ester groups, R.sub.1 is in the .alpha.-configuration and is hydrogen or methoxy, X represents hydrogen ##STR2## R.sub.3 represents hydrogen or lower alkyl, R.sub.4 is hydrogen, lower alkyl, ##STR3## or --(CH.sub.2).sub.n --N--(lower alkyl).sub.2, R.sub.5 represents hydrogen, sodium or potassium, and n represents an integer from 1 to 4. These compounds are useful as antibacterial agents.
    Type: Grant
    Filed: September 19, 1979
    Date of Patent: June 23, 1981
    Assignee: E. R. Squibb & Sons, Inc.
    Inventors: Hermann Breuer, Theodore Denzel, Uwe D. Treuner
  • Patent number: 4261978
    Abstract: Carriomycin and physiologically acceptable salts thereof are effective for the treatment and prophylaxis of swine dysentery.
    Type: Grant
    Filed: July 13, 1979
    Date of Patent: April 14, 1981
    Assignee: Takeda Chemical Industries, Ltd.
    Inventors: Toshihiko Kanzaki, Toshiyuki Yamazaki
  • Patent number: 4260599
    Abstract: An antifibrotic substance P-1894B is produced by cultivating a microorganism belonging to the genus Streptomyces and being capable of producing P-1894B in a culture medium to have Antifibrotic substance P-1894B elaborated and accumulated in the cultured broth and recovering the substance.P-1894B is effective for the prophylaxis or treatment of the fibrosis due to excessive collagen accumulation in mammal.
    Type: Grant
    Filed: July 26, 1979
    Date of Patent: April 7, 1981
    Assignee: Takeda Chemical Industries, Ltd.
    Inventors: Hisayoshi Okazaki, Tsuneo Kanamaru, Kazuhiko Ohta
  • Patent number: 4251511
    Abstract: Novel antibiotic U-59,761 producible in a fermentation under controlled conditions using a biologically pure culture of the microorganism Saccharopolyspora hirsuta strain 367, NRRL 12045. This antibiotic is active against various microorganisms, for example, Staphylococcus aureus, Streptococcus pyogenes, Sarcina lutea, Klebsiella pneumoniae, Mycobacterium avium, and Bacteroides fragilis. Thus, antibiotic U-59,761 can be used in various environments to eradicate or control such bacteria.
    Type: Grant
    Filed: October 2, 1979
    Date of Patent: February 17, 1981
    Assignee: The Upjohn Company
    Inventors: Howard A. Whaley, John H. Coats
  • Patent number: 4248863
    Abstract: Antibiotic substances named saframycins A, B, C, D and E having antibacterial activity and activity against transplantable tumors. It is produced by cultivation of Streptomyces lavendulae strain No. 314.
    Type: Grant
    Filed: September 6, 1978
    Date of Patent: February 3, 1981
    Inventor: Tadashi Arai