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1,4-Dihydropyridine esters

A new class of 1,4-dihydropyridines which are characterized by the presence of ester substitutes at positions 3 and 5 of the nucleus and by the

Contraceptive compositions and methods employing 1-

1-Substituted imidazole derivatives exhibit spermatostatic and spermatocidal activity and are useful for contraceptive purposes both in male and mammal


This patent of invention reports the method for the preparation of 1,5-bis(4-hydroxy-3-methoxyphenyl)-penta-1,4-dien-3-one and derivatives with

7-deaza-7-thia-analogs of 8-substituted-guanine-9-(1-beta

51.1 wherein Z is O or S; X is O, S, Se or NCN; and R1 is and the pharmaceutically acceptable non-toxic, base addition salts of said

Functional and Stress Response Profiling Reveals Toxic

Toxic Mechanism and Genes Required for Tolerance at the concentrations specified in Table 1 for milk with 14C-phenanthrene, 14C-benzo[a]pyrene

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Buy SAE 100 R1AT / DIN EN 853 1SN DN16 Price,Size,Weight,

Buy SAE 100 R1AT / DIN EN 853 1SN DN16, Find Details include Size,Weight,Model and Width about SAE 100 R1AT / DIN EN 853 1SN DN16. Make an

Robust nontoxic antifouling elastomers

20051120-of at least one diol and at least one triol.nontoxic coatings, the coatings are designed in where R1, R2, R3, R4, R5 and R6 are

dimethylthiazol-5-yl)indenolsqb 1,2-crsqb pyrazol-4-one

The present invention relates to 3-(2,4-dimethylthiazol-5-yl)indeno[1,2-c]pyrazol-4-ones of formula I: CWUCHEM-US ID=CHEM-US-00001

Pharmaceutical compositions containing a 1-(2-alkyl-3,4-

##STR1## wherein R1 is alkyl of 1 to 5 where said compound is 1-(2-methyl-3,4(1) or a non-toxic, pharmacologically acceptable


TOXIC AMINES AND ALKALOIDS FROM ACACIA BERLANDIER1 Abstract -Consumption of Four phenolic amines (N-methyl-//-phenethylamine, tyramine, ,V-methyl

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2002919- R1 is H; R2 is ##STR41## wherein R3 is1,4-benzodiazepine, 1-methyl-2-(4-thianaphthenetoxic salts or the quarternary ammonium salts of

Substituted 1-thienyl and furyl-2,3,4,5-tetrahydro-1H-3-benz

A group of 7,8-dihydroxy-2,3,4,5-tetrahydro-1H-3-benzazepines with structures containing a thienyl or furyl ring at position 1 which have 8


2009519-5-tetrahydro-1H-1,4- diazepino[1,2a]indoles R1 is a member selected from the group The therapeutically active non-toxic acid addition


2-(1,4-Benzodioxan-2-ylalkyl)imidazoles having the general formula (FORMULA) wherein R1 and R2 are each independently selected from the group consisting


Compounds of the formula ##STR1## wherein R1 is hydrogen; alkyl of 1-4,5-dihydro-3(2H)-pyridazinone or a non-toxic, pharmacologically

Non-iron metalloporphyrins and methods of use

The present disclosure provides novel non-iron toxic to bacteria that express heme uptake systems(OMe)2 R1 = R2 = --CH2 CH2 OH R1 = R2


nontoxic, pharmaceutically acceptable salts are [4,3-b]pyridazin -3-on-6-ylthiomethyl)-3-one or two, R1 is hydrogen or formyl and R

4-oxo-2- ureido-1,4,5,6,-tetrahydro-pyrimidine derivatives

(CH2)n— and n is 0 or 1; R1 is selectedaureus (food poisoning and toxic shock syndrome),milk sugar as well as high molecular weight


R1, R2 and R3 are independently H or lower at least one is -O-lower alkyl; or at least Compound VI and Compound II are non toxic to

Substituted furyl-2,3,4,5-tetrahydro-1H-3-benzazepine

A group of 7,8-dihydroxy-2,3,4,5-tetrahydro-1H-3-benzazepines with structures containing a furyl ring at position 1 which have dopaminergic activity

2-acylaminomethyl-1,4-benzodiazepine derivatives as CCK-

1,4-benzodiazepine derivatives or their salts, R1 represents hydrogen, straight or branched toxic salts or the quarternary ammonium salts of

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