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1-[4-(Trimethylamino)phenyl]-6-phenylhexa-1,3,5-triene: synthesis, fluorescence properties, and use as a fluorescence probe of lipid bilayers
1-[4-(Trimethylamino)phenyl]-6-phenylhexa-1,3,5-triene: synthesis, fluorescence properties, and use as a fluorescence probe of lipid bilayers
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1-[4-(Trimethylamino)phenyl]-6-phenylhexa-1,3,5-triene: synthesis, fluorescence properties, and use as a fluorescence probe of lipid bilayers

Prendergast, F G ; Haugland, R P ; Callahan, P J

Biochemistry (Easton), 1981-12, Vol.20 (26), p.7333-7338 [Periódico revisado por pares]

United States

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2
1 alpha-hydroxy-25-fluorovitamin D3: a potent analogue of 1 alpha,25-dihydroxyvitamin D3
1 alpha-hydroxy-25-fluorovitamin D3: a potent analogue of 1 alpha,25-dihydroxyvitamin D3
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1 alpha-hydroxy-25-fluorovitamin D3: a potent analogue of 1 alpha,25-dihydroxyvitamin D3

Napoli, J L ; Fivizzani, M A ; Schnoes, H K ; DeLuca, H F

Biochemistry (Easton), 1978-06, Vol.17 (12), p.2387-2392 [Periódico revisado por pares]

United States

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3
1 alpha-hydroxylation of 24-hydroxyvitamin D2 represents a minor physiological pathway for the activation of vitamin D2 in mammals
1 alpha-hydroxylation of 24-hydroxyvitamin D2 represents a minor physiological pathway for the activation of vitamin D2 in mammals
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1 alpha-hydroxylation of 24-hydroxyvitamin D2 represents a minor physiological pathway for the activation of vitamin D2 in mammals

Horst, R.L ; Koszewski, N.J ; Reinhardt, T.A

Biochemistry (Easton), 1990-01, Vol.29 (2), p.578-582 [Periódico revisado por pares]

United States

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4
1-Aminocyclopropanephosphonate: time-dependent inactivation of 1-aminocyclopropanecarboxylate deaminase and Bacillus stearothermophilus alanine racemase by slow dissociation behavior
1-Aminocyclopropanephosphonate: time-dependent inactivation of 1-aminocyclopropanecarboxylate deaminase and Bacillus stearothermophilus alanine racemase by slow dissociation behavior
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1-Aminocyclopropanephosphonate: time-dependent inactivation of 1-aminocyclopropanecarboxylate deaminase and Bacillus stearothermophilus alanine racemase by slow dissociation behavior

Erion, Mark D ; Walsh, Christopher T

Biochemistry (Easton), 1987-06, Vol.26 (12), p.3417-3425 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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5
(1-Aminoethyl)boronic acid: a novel inhibitor for Bacillus stearothermophilus alanine racemase and Salmonella typhimurium D-alanine:D-alanine ligase (ADP-forming)
(1-Aminoethyl)boronic acid: a novel inhibitor for Bacillus stearothermophilus alanine racemase and Salmonella typhimurium D-alanine:D-alanine ligase (ADP-forming)
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(1-Aminoethyl)boronic acid: a novel inhibitor for Bacillus stearothermophilus alanine racemase and Salmonella typhimurium D-alanine:D-alanine ligase (ADP-forming)

Duncan, Kenneth ; Faraci, W. Stephen ; Matteson, Donald S ; Walsh, Christopher T

Biochemistry (Easton), 1989-04, Vol.28 (8), p.3541-3549 [Periódico revisado por pares]

United States: American Chemical Society

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6
1,10-Phenanthroline Inhibits Glycosylphosphatidylinositol Anchoring by Preventing Phosphoethanolamine Addition to Glycosylphosphatidylinositol Anchor Precursors
1,10-Phenanthroline Inhibits Glycosylphosphatidylinositol Anchoring by Preventing Phosphoethanolamine Addition to Glycosylphosphatidylinositol Anchor Precursors
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1,10-Phenanthroline Inhibits Glycosylphosphatidylinositol Anchoring by Preventing Phosphoethanolamine Addition to Glycosylphosphatidylinositol Anchor Precursors

Mann, Karl J ; Sevlever, Daniel

Biochemistry (Easton), 2001-03, Vol.40 (12), p.3758-3758 [Periódico revisado por pares]

American Chemical Society

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7
1,10-Phenanthroline Inhibits Glycosylphosphatidylinositol Anchoring by Preventing Phosphoethanolamine Addition to Glycosylphosphatidylinositol Anchor Precursors
1,10-Phenanthroline Inhibits Glycosylphosphatidylinositol Anchoring by Preventing Phosphoethanolamine Addition to Glycosylphosphatidylinositol Anchor Precursors
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1,10-Phenanthroline Inhibits Glycosylphosphatidylinositol Anchoring by Preventing Phosphoethanolamine Addition to Glycosylphosphatidylinositol Anchor Precursors

Mann, Karl J ; Sevlever, Daniel

Biochemistry (Easton), 2001-02, Vol.40 (5), p.1205-1213 [Periódico revisado por pares]

United States: American Chemical Society

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8
1,2-Dithiolan-3-one 1-Oxides:  A Class of Thiol-Activated DNA-Cleaving Agents That Are Structurally Related to the Natural Product Leinamycin
1,2-Dithiolan-3-one 1-Oxides:  A Class of Thiol-Activated DNA-Cleaving Agents That Are Structurally Related to the Natural Product Leinamycin
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1,2-Dithiolan-3-one 1-Oxides:  A Class of Thiol-Activated DNA-Cleaving Agents That Are Structurally Related to the Natural Product Leinamycin

Behroozi, Saeid J ; Kim, Woongki ; Dannaldson, Jeffrey ; Gates, Kent S

Biochemistry (Easton), 1996-02, Vol.35 (6), p.1768-1774 [Periódico revisado por pares]

United States: American Chemical Society

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9
1,2-naphthalene oxide as an intermediate in the microsomal hydroxylation of naphthalene
1,2-naphthalene oxide as an intermediate in the microsomal hydroxylation of naphthalene
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1,2-naphthalene oxide as an intermediate in the microsomal hydroxylation of naphthalene

Jerina, D M ; Daly, J W ; Witkop, B ; Zaltzman-Nirenberg, P ; Udenfriend, S

Biochemistry (Easton), 1970-01, Vol.9 (1), p.147-156 [Periódico revisado por pares]

United States

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10
1,2,3-Thiadiazole:  A Novel Heterocyclic Heme Ligand for the Design of Cytochrome P450 Inhibitors
1,2,3-Thiadiazole:  A Novel Heterocyclic Heme Ligand for the Design of Cytochrome P450 Inhibitors
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1,2,3-Thiadiazole:  A Novel Heterocyclic Heme Ligand for the Design of Cytochrome P450 Inhibitors

Babu, Boga Ramesh ; Vaz, Alfin D. N

Biochemistry (Easton), 1997-06, Vol.36 (23), p.7209-7216 [Periódico revisado por pares]

United States: American Chemical Society

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