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Application of the comprehensive analysis of pollution of the Kacha river by oil products in the information and analytical system

Journal of physics. Conference series, 2021-11, Vol.2094 (5), p.52003

2021

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Sarafotoxin S6c: An agonist which distinguishes between endothelin receptor subtypes

Biochemical and biophysical research communications, 1991-03, Vol.175 (2), p.556-561

1991

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Pharmacology of L-754,142, a highly potent, orally active, nonpeptidyl endothelin antagonist

The Journal of pharmacology and experimental therapeutics, 1995-12, Vol.275 (3), p.1518

1995

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A peripherally acting alpha-2 adrenoceptor antagonist: L-659,066

The Journal of pharmacology and experimental therapeutics, 1988-04, Vol.245 (1), p.32

1988

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Identification of an orally active, nonpeptidyl oxytocin antagonist

The Journal of pharmacology and experimental therapeutics, 1993-01, Vol.264 (1), p.308

1993

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Nonpeptide oxytocin antagonists: Analogs of L-371,257 with improved potency

Bioorganic & medicinal chemistry letters, 1999-05, Vol.9 (9), p.1311-1316

1999

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Nonpeptide oxytocin antagonists: Potent, orally bioavailable analogs of L-371,257 containing A 1- R-(pyridyl)ethyl ether terminus

Bioorganic & medicinal chemistry letters, 1998-11, Vol.8 (21), p.3081-3086

1998

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In vitro pharmacological profile of a novel structural class of oxytocin antagonists

The Journal of pharmacology and experimental therapeutics, 1991-01, Vol.256 (1), p.304

1991

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Benzodiazepines as Potent and Selective Bradykinin B1 Antagonists

Journal of medicinal chemistry, 2003-05, Vol.46 (10), p.1803-1806

2003

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Antagonism of oxytocin in rats and pregnant rhesus monkeys by the novel cyclic hexapeptides, L-366,682 and L-366,948

The Journal of pharmacology and experimental therapeutics, 1991-03, Vol.256 (3), p.827

1991

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Pharmacology of L-744,453, a novel nonpeptidyl endothelin antagonist

Life sciences (1973), 1996-03, Vol.58 (14), p.1149-1157

1996

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L-368,899, a potent orally active oxytocin antagonist for potential use in preterm labor

Drug development research, 1993-11, Vol.30 (3), p.129-142

1993

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Bradykinin agonist activity of a novel, potent oxytocin antagonist

European journal of pharmacology, 1991-04, Vol.196 (3), p.233-237

1991

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STUDY OF THE CHEMICAL COMPOSITION OF CONES AND SEEDS OF CONIFEROUS SPECIES OF SIBERIA

Хвойные бореальной зоны, 2023, Vol.41 (1), p.95-100

2023

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The effects of deleting the mouse neurotensin receptor NTR1 on central and peripheral responses to neurotensin

The Journal of pharmacology and experimental therapeutics, 2002-01, Vol.300 (1), p.305-313

2002

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Hypotensive action of 8-hydroxy-2-(di-N-propylamino)tetralin (8-OH-DPAT) in spontaneously hypertensive rats

Archives internationales de pharmacodynamie et de thérapie, 1985-02, Vol.273 (2), p.251

1985

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Development of browser game for student’s vocational guidance

Educational resources and technology, 2016, p.25-29

2016

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Development of Orally Active Oxytocin Antagonists: Studies on 1-(1-{4-[1-(2-Methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2- methoxybenzoyl}piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and Related Pyridines

Journal of medicinal chemistry, 1998-06, Vol.41 (12), p.2146-2163

1998

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Benzodiazepines as Potent and Selective Bradykinin B 1 Antagonists

Journal of medicinal chemistry, 2003-05, Vol.46 (10), p.1803-1806

2003

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1-{1-[4-[(N-acetyl-4-piperidinyl)oxy]-2-methoxybenzoyl]piperidin-4-yl}-4H-3,1-benzoxazin-2(1H)-one (L-371,257) : a new, orally bioavailable, non-peptide oxytocin antagonist

Journal of medicinal chemistry, 1995-11, Vol.38 (23), p.4634-4636

1995

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Pharmacological evaluation of d(CH2)5Tyr(Me)AVP as an antagonist of vasopressin-induced contraction of the isolated rat caudal artery

Archives internationales de pharmacodynamie et de thérapie, 1986-11, Vol.284 (1), p.72

1986

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Development of orally active oxytocin antagonists : Studies on 1-(1-{4-[1-(2-methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2-methoxybenzo yl}piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and related pyridines

Journal of medicinal chemistry, 1998, Vol.41 (12), p.2146-2163

1998

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1-(1-[4-[(N-acetyl-4-piperidinyl)oxy]-2-methoxybenzoyl]piperidin-4- yl)-4H-3,1-benzoxazin-2(1H)-one (L-371,257): a new, orally bioavailable, non-peptide oxytocin antagonist

Journal of medicinal chemistry, 1995-11, Vol.38 (23), p.4634-4636

1995

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Progress in the development of oxytocin antagonists for use in preterm labor

Advances in experimental medicine and biology, 1995, Vol.395, p.601

1995

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ChemInform Abstract: 1-(1-(4-((N-Acetyl-4-piperidinyl)oxy)-2-methoxybenzoyl)piperidin-4-yl)- 4H-3,1-benzoxazin-2(1H)-one (L-371,257): A New, Orally Bioavailable, Non-Peptide Oxytocin Antagonist

ChemInform, 1996-03, Vol.27 (11), p.no-no

1996

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Application of the comprehensive analysis of pollution of the Kacha river by oil products in the information and analytical system

Sarafotoxin S6c: An agonist which distinguishes between endothelin receptor subtypes

Pharmacology of L-754,142, a highly potent, orally active, nonpeptidyl endothelin antagonist

A peripherally acting alpha-2 adrenoceptor antagonist: L-659,066

Identification of an orally active, nonpeptidyl oxytocin antagonist

Nonpeptide oxytocin antagonists: Analogs of L-371,257 with improved potency

Nonpeptide oxytocin antagonists: Potent, orally bioavailable analogs of L-371,257 containing A 1- R-(pyridyl)ethyl ether terminus

In vitro pharmacological profile of a novel structural class of oxytocin antagonists

Benzodiazepines as Potent and Selective Bradykinin B1 Antagonists

Antagonism of oxytocin in rats and pregnant rhesus monkeys by the novel cyclic hexapeptides, L-366,682 and L-366,948

Pharmacology of L-744,453, a novel nonpeptidyl endothelin antagonist

L-368,899, a potent orally active oxytocin antagonist for potential use in preterm labor

Bradykinin agonist activity of a novel, potent oxytocin antagonist

STUDY OF THE CHEMICAL COMPOSITION OF CONES AND SEEDS OF CONIFEROUS SPECIES OF SIBERIA

The effects of deleting the mouse neurotensin receptor NTR1 on central and peripheral responses to neurotensin

Hypotensive action of 8-hydroxy-2-(di-N-propylamino)tetralin (8-OH-DPAT) in spontaneously hypertensive rats

Development of browser game for student’s vocational guidance

Development of Orally Active Oxytocin Antagonists: Studies on 1-(1-{4-[1-(2-Methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2- methoxybenzoyl}piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and Related Pyridines

Benzodiazepines as Potent and Selective Bradykinin B 1 Antagonists

1-{1-[4-[(N-acetyl-4-piperidinyl)oxy]-2-methoxybenzoyl]piperidin-4-yl}-4H-3,1-benzoxazin-2(1H)-one (L-371,257) : a new, orally bioavailable, non-peptide oxytocin antagonist

Pharmacological evaluation of d(CH2)5Tyr(Me)AVP as an antagonist of vasopressin-induced contraction of the isolated rat caudal artery

Development of orally active oxytocin antagonists : Studies on 1-(1-{4-[1-(2-methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2-methoxybenzo yl}piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and related pyridines

1-(1-[4-[(N-acetyl-4-piperidinyl)oxy]-2-methoxybenzoyl]piperidin-4- yl)-4H-3,1-benzoxazin-2(1H)-one (L-371,257): a new, orally bioavailable, non-peptide oxytocin antagonist

Progress in the development of oxytocin antagonists for use in preterm labor

ChemInform Abstract: 1-(1-(4-((N-Acetyl-4-piperidinyl)oxy)-2-methoxybenzoyl)piperidin-4-yl)- 4H-3,1-benzoxazin-2(1H)-one (L-371,257): A New, Orally Bioavailable, Non-Peptide Oxytocin Antagonist

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