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1-(2-Nitrophenyl)thiosemicarbazides: a novel class of potent, orally active non-peptide antagonist for the bradykinin B(2) receptor
1-(2-Nitrophenyl)thiosemicarbazides: a novel class of potent, orally active non-peptide antagonist for the bradykinin B(2) receptor
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1-(2-Nitrophenyl)thiosemicarbazides: a novel class of potent, orally active non-peptide antagonist for the bradykinin B(2) receptor

Dziadulewicz, E K ; Ritchie, T J ; Hallett, A ; Snell, C R ; Ko, S Y ; Wrigglesworth, R ; Hughes, G A ; Dunstan, A R ; Bloomfield, G C ; Drake, G S ; Brown, M C ; Lee, W ; Burgess, G M ; Davis, C ; Yaqoob, M ; Perkins, M N ; Campbell, E A ; Davis, A J ; Rang, H P

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.769 [Periódico revisado por pares]

United States

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2
1,25-Dihydroxyvitamin D3 effects on collagen and DNA synthesis in periosteum and periosteum-free calvaria
1,25-Dihydroxyvitamin D3 effects on collagen and DNA synthesis in periosteum and periosteum-free calvaria
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1,25-Dihydroxyvitamin D3 effects on collagen and DNA synthesis in periosteum and periosteum-free calvaria

Canalis, E ; Lian, J B

Bone (New York, N.Y.), 1985, Vol.6 (6), p.457-460 [Periódico revisado por pares]

United States

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3
13,13-Dimethyl-des-C,D analogues of (20S)-1α,25-dihydroxy-2-methylene-19-norvitamin D3 (2MD): Total synthesis, docking to the VDR, and biological evaluation
13,13-Dimethyl-des-C,D analogues of (20S)-1α,25-dihydroxy-2-methylene-19-norvitamin D3 (2MD): Total synthesis, docking to the VDR, and biological evaluation
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13,13-Dimethyl-des-C,D analogues of (20S)-1α,25-dihydroxy-2-methylene-19-norvitamin D3 (2MD): Total synthesis, docking to the VDR, and biological evaluation

Plonska-Ocypa, Katarzyna ; Sibilska, Izabela ; Sicinski, Rafal R. ; Sicinska, Wanda ; Plum, Lori A. ; DeLuca, Hector F.

Bioorganic & medicinal chemistry, 2011-12, Vol.19 (23), p.7205-7220 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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4
1,3,8-Triazaspiro[4.5]decane-2,4-diones as Efficacious Pan-Inhibitors of Hypoxia-Inducible Factor Prolyl Hydroxylase 1–3 (HIF PHD1–3) for the Treatment of Anemia
1,3,8-Triazaspiro[4.5]decane-2,4-diones as Efficacious Pan-Inhibitors of Hypoxia-Inducible Factor Prolyl Hydroxylase 1–3 (HIF PHD1–3) for the Treatment of Anemia
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1,3,8-Triazaspiro[4.5]decane-2,4-diones as Efficacious Pan-Inhibitors of Hypoxia-Inducible Factor Prolyl Hydroxylase 1–3 (HIF PHD1–3) for the Treatment of Anemia

Vachal, Petr ; Miao, Shouwu ; Pierce, Joan M ; Guiadeen, Deodial ; Colandrea, Vincent J ; Wyvratt, Matthew J ; Salowe, Scott P ; Sonatore, Lisa M ; Milligan, James A ; Hajdu, Richard ; Gollapudi, Anantha ; Keohane, Carol A ; Lingham, Russell B ; Mandala, Suzanne M ; DeMartino, Julie A ; Tong, Xinchun ; Wolff, Michael ; Steinhuebel, Dietrich ; Kieczykowski, Gerard R ; Fleitz, Fred J ; Chapman, Kevin ; Athanasopoulos, John ; Adam, Gregory ; Akyuz, Can D ; Jena, Dhirendra K ; Lusen, Jeffrey W ; Meng, Juncai ; Stein, Benjamin D ; Xia, Lei ; Sherer, Edward C ; Hale, Jeffrey J

Journal of medicinal chemistry, 2012-04, Vol.55 (7), p.2945-2959 [Periódico revisado por pares]

United States: American Chemical Society

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5
16, 16 Dimethyl prostaglandin E2 decreases the formation of collagen in fibrotic rat liver slices
16, 16 Dimethyl prostaglandin E2 decreases the formation of collagen in fibrotic rat liver slices
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16, 16 Dimethyl prostaglandin E2 decreases the formation of collagen in fibrotic rat liver slices

PETERS, K. M ; SNYDER, K. F ; RUSH, B. D ; RUWART, M. J ; HENLEY, K. S

Prostaglandins, 1989-04, Vol.37 (4), p.445-456 [Periódico revisado por pares]

Stoneham, MA: Butterworth-Heinemann

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6
17 beta-Estradiol and tamoxifen prevent the over-glycosylation of rat trabecular bone collagen induced by ovariectomy
17 beta-Estradiol and tamoxifen prevent the over-glycosylation of rat trabecular bone collagen induced by ovariectomy
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17 beta-Estradiol and tamoxifen prevent the over-glycosylation of rat trabecular bone collagen induced by ovariectomy

Moro, L ; Bettica, P ; Romanello, M ; Suarez, K N

European journal of clinical chemistry and clinical biochemistry, 1997-01, Vol.35 (1), p.29

Germany

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7
17Beta-estradiol, its metabolites, and progesterone inhibit cardiac fibroblast growth
17Beta-estradiol, its metabolites, and progesterone inhibit cardiac fibroblast growth
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17Beta-estradiol, its metabolites, and progesterone inhibit cardiac fibroblast growth

Dubey, R K ; Gillespie, D G ; Jackson, E K ; Keller, P J

Hypertension (Dallas, Tex. 1979), 1998-01, Vol.31 (1 Pt 2), p.522-528 [Periódico revisado por pares]

United States

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8
(1S, 3S)-3-Amino-4-difluoromethylenyl-1-cyclopentanoic Acid (CPP-115), a Potent γ-Aminobutyric Acid Aminotransferase Inactivator for the Treatment of Cocaine Addiction
(1S, 3S)-3-Amino-4-difluoromethylenyl-1-cyclopentanoic Acid (CPP-115), a Potent γ-Aminobutyric Acid Aminotransferase Inactivator for the Treatment of Cocaine Addiction
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(1S, 3S)-3-Amino-4-difluoromethylenyl-1-cyclopentanoic Acid (CPP-115), a Potent γ-Aminobutyric Acid Aminotransferase Inactivator for the Treatment of Cocaine Addiction

Pan, Yue ; Gerasimov, Madina R ; Kvist, Trine ; Wellendorph, Petrine ; Madsen, Karsten K ; Pera, Elena ; Lee, Hyunbeom ; Schousboe, Arne ; Chebib, Mary ; Bräuner-Osborne, Hans ; Craft, Cheryl M ; Brodie, Jonathan D ; Schiffer, Wynne K ; Dewey, Stephen L ; Miller, Steven R ; Silverman, Richard B

Journal of medicinal chemistry, 2012-01, Vol.55 (1), p.357-366 [Periódico revisado por pares]

United States: American Chemical Society

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9
2-Iminothiazolidine-4-carboxylic acid produces hippocampal CA1 lesions independent of seizure excitation and glutamate receptor activation
2-Iminothiazolidine-4-carboxylic acid produces hippocampal CA1 lesions independent of seizure excitation and glutamate receptor activation
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2-Iminothiazolidine-4-carboxylic acid produces hippocampal CA1 lesions independent of seizure excitation and glutamate receptor activation

BITNER, R. S ; YIM, G. K. W ; ISOM, G. E

Neurotoxicology (Park Forest South), 1997, Vol.18 (1), p.191-200 [Periódico revisado por pares]

Orlando, FL: Elsevier

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10
2-Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N-benzyl-N- methylamide (SDZ NKT 343), a Potent Human NK1 Tachykinin Receptor Antagonist with Good Oral Analgesic Activity in Chronic Pain Models
2-Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N-benzyl-N- methylamide (SDZ NKT 343), a Potent Human NK1 Tachykinin Receptor Antagonist with Good Oral Analgesic Activity in Chronic Pain Models
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2-Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N-benzyl-N- methylamide (SDZ NKT 343), a Potent Human NK1 Tachykinin Receptor Antagonist with Good Oral Analgesic Activity in Chronic Pain Models

Walpole, C ; Ko, S. Y ; Brown, M ; Beattie, D ; Campbell, E ; Dickenson, F ; Ewan, S ; Hughes, G. A ; Lemaire, M ; Lerpiniere, J ; Patel, S ; Urban, L

Journal of medicinal chemistry, 1998-08, Vol.41 (17), p.3159-3173 [Periódico revisado por pares]

United States: American Chemical Society

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