Abstract: This invention relates to 2-pyridine derivatives substituted in the 4-position with a dialkylamino- or piperidinyl- or pyrrolidinylallyl group. The compounds have histamine H.sub.2 -antagonist activity.
Type:
Grant
Filed:
October 31, 1985
Date of Patent:
July 19, 1988
Assignee:
Smith Kline & French Laboratories Limited
Abstract: This invention relates to tricyclic pyridazinone compounds, pharmaceutical compositions containing the compounds, and a method of stimulating cardiac activity in a mammal by administering an effective amount of the compound. A compound of the invention is 7-carboxamido-4,4a-dihydro-4a-methyl-[5H]-indeno[1,2-c]-pyridazin-3[2H]-on e.
Type:
Grant
Filed:
September 22, 1987
Date of Patent:
July 5, 1988
Assignee:
Smith Kline & French Laboratories Limited
Abstract: This invention relates to intermediates of Mannich-alkynyl aminothiadiazole oxides having histamine H.sub.2 -antagonist activity. A particular final product of this invention is 3-amino-4-[7-piperidinohept-5-ynylamino]-1,2,5-thiadiazole-1-oxide.
Type:
Grant
Filed:
December 8, 1986
Date of Patent:
March 22, 1988
Assignee:
Smith Kline & French Laboratories Limited
Abstract: New 3,4-diamino-1,2,5-thiadiazole oxide derivatives which are histamine H.sub.1 -antagonists. A specific compound of this invention is 3-[3-[N-(4-fluorobenzyl)-N-pyrid-2-yl-amino]propylamino]-4-[pyrimidin-4-yl -methylamino]-1,2,5-thiadiazole-1-oxide.
Type:
Grant
Filed:
February 4, 1986
Date of Patent:
March 1, 1988
Assignee:
Smith Kline & French Laboratories Limited
Abstract: This invention relates to 5-oxypyrimidinone compounds having H.sub.2 -antagonist activity. A particular compound of the invention is 2-[3-(3-piperidinomethyl)phenoxy)propyl]-5-benzyloxypyrimidin-4-one.
Type:
Grant
Filed:
August 15, 1985
Date of Patent:
September 15, 1987
Assignee:
Smith Kline & French Laboratories Limited
Abstract: New 3,4-diamino-1,2,5-thiadiazole oxide derivatives which are histamine H.sub.1 -antagonists. A specific compound of this invention is 3-[3-(N-propyl-N-2-pyridylamino)-propylamino]-4-(4-pyridylmethyl)amino-1,2 ,5-thiadiazole-1-oxide.
Type:
Grant
Filed:
March 12, 1986
Date of Patent:
September 8, 1987
Assignee:
Smith Kline & French Laboratories Limited
Abstract: This invention relates to aminoalkylphenoxyalkyl substituted heterocycles. These compounds antagonize the action of histamine on histamine H.sub.2 -receptors in the brain. A compound of the invention is 2-[3-[3-(piperidinomethyl)phenoxy]propylamino]benzthiazole.
Type:
Grant
Filed:
October 17, 1985
Date of Patent:
July 21, 1987
Assignee:
Smith Kline & French Laboratories Limited
Inventors:
Thomas H. Brown, Robert C. Mitchell, Ian R. Smith, Rodney C. Young
Abstract: This invention relates to (isopropyl and tertiary butyl-amino-2-hydroxypropoxy)phenyl-3[2H]-pyridazinones which have .beta.-adrenoceptor antagonist activity.
Type:
Grant
Filed:
August 13, 1986
Date of Patent:
July 7, 1987
Assignee:
Smith Kline & French Laboratories Limited
Inventors:
Anthony M. Roe, William J. Coates, Robert A. Slater, Stephen P. Breukelman, George D. Meakins
Abstract: This invention describes tricyclic derivatives which are useful as histamine H.sub.1 -antagonists. A particular compound of this invention is 3-[3-(pyrido[3,2-b][1,4]-benzothiazin-10-yl)propylamino]-4-(pyrid-4-ylmeth ylamino)-1,2,5-thiadiazole-1-oxide.
Type:
Grant
Filed:
April 23, 1986
Date of Patent:
May 26, 1987
Assignee:
Smith Kline & French Laboratories Limited
Abstract: The invention describes 5-halo-3-amino-2-pyridyl derivatives which are useful as histamine H.sub.1 -antagonists. Particular compounds described are 2-[4-(5-bromo-3-aminopyrid-2-yl)butylamino]-5-(6-methylpyrid-3-ylmethyl)-4 -pyrimidone and 2-[4-(5-bromo-3-aminopyrid-2-yl)butylamino]-5-(N-oxopyrid-4-ylmethyl)-4-py rimidone.
Type:
Grant
Filed:
July 11, 1984
Date of Patent:
May 12, 1987
Assignee:
Smith Kline & French Laboratories Limited
Abstract: This invention relates to 2-amino-3-hydroxy, and 3-carboxy pyridine derivatives, in which the amino group is substituted by a methylthioethyl, butyl or oxypropyl group bearing a terminal heterocyclic group. The compounds have histamine H.sub.2 -antagonist activity. A specific compound of this invention is 2-[2-(2-guanidino-4-thiazolylmethylthio)ethyl]amino pyridine 3-carboxylic acid.
Type:
Grant
Filed:
July 12, 1985
Date of Patent:
March 24, 1987
Assignee:
Smith Kline & French Laboratories Limited
Abstract: The compounds are substituted pyrimidine compounds which are histamine H.sub.2 -antagonists. A specific compound of the present invention is 2-[2-(5-dimethylaminomethyl)-2-furylmethylthio)ethylamino]-5-(3-pyridylmet hyl)-4-pyrimidone.
Type:
Grant
Filed:
June 21, 1985
Date of Patent:
March 10, 1987
Assignee:
Smith Kline & French Laboratories Limited
Abstract: The invention describes a pharmaceutical dosage unit suitable for oral administration with at least one face having a recess, which recess extends from one edge across and into the face; the recess being so shaped as to accommodate at least the tip of the user's tongue.
Type:
Grant
Filed:
December 21, 1984
Date of Patent:
March 3, 1987
Assignee:
Smith Kline & French Laboratories Limited
Abstract: The compounds are isoureas and isothioureas which have an O- or S-alkylpyrimidone substituent and which are histamine H.sub.2 -antagonists and antiinflammatory agents.A specific compound of this invention is 2-[5-(O-isoureido)pentylamino]-5-(6-methyl-3-pyridylmethyl)-4-pyrimidone.
Type:
Grant
Filed:
May 1, 1985
Date of Patent:
January 27, 1987
Assignee:
Smith Kline & French Laboratories Limited
Inventors:
Charon R. Ganellin, Robert J. Ife, David A. A. Owen