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86
Cambridge Crystallographic compounds 3a
Unless otherwise noted, reactions were carried out with 1 (0.2 mmol) and 2 (6 mmol) in MeCN (2 mL), suspensions of E. coli expressing BacFre-K474F/I500L (OD 600 = 10) in MOPS buffer (18 mL, 50 mM, pH 9). Reactions were conducted at room temperature under air for 12 h. Isolated yield. a E . coli expressing BacFre-K474F/I500L (OD 600 = 20). b Nitroalkanes 2 (2 mmol). cReaction for 24 h. The absolute configuration of <t>3a</t> <t>and</t> <t>4d</t> was determined by X-ray crystallographic analysis. All other products were assigned by analogy. Std con: standard condition.
Compounds 3a, supplied by Cambridge Crystallographic, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Ambeed Inc compound c 3b compound c 3a
Unless otherwise noted, reactions were carried out with 1 (0.2 mmol) and 2 (6 mmol) in MeCN (2 mL), suspensions of E. coli expressing BacFre-K474F/I500L (OD 600 = 10) in MOPS buffer (18 mL, 50 mM, pH 9). Reactions were conducted at room temperature under air for 12 h. Isolated yield. a E . coli expressing BacFre-K474F/I500L (OD 600 = 20). b Nitroalkanes 2 (2 mmol). cReaction for 24 h. The absolute configuration of <t>3a</t> <t>and</t> <t>4d</t> was determined by X-ray crystallographic analysis. All other products were assigned by analogy. Std con: standard condition.
Compound C 3b Compound C 3a, supplied by Ambeed Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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97
ATCC compounds 3a 3e against methicillin
Unless otherwise noted, reactions were carried out with 1 (0.2 mmol) and 2 (6 mmol) in MeCN (2 mL), suspensions of E. coli expressing BacFre-K474F/I500L (OD 600 = 10) in MOPS buffer (18 mL, 50 mM, pH 9). Reactions were conducted at room temperature under air for 12 h. Isolated yield. a E . coli expressing BacFre-K474F/I500L (OD 600 = 20). b Nitroalkanes 2 (2 mmol). cReaction for 24 h. The absolute configuration of <t>3a</t> <t>and</t> <t>4d</t> was determined by X-ray crystallographic analysis. All other products were assigned by analogy. Std con: standard condition.
Compounds 3a 3e Against Methicillin, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
Bruker Corporation compound 3a
Unless otherwise noted, reactions were carried out with 1 (0.2 mmol) and 2 (6 mmol) in MeCN (2 mL), suspensions of E. coli expressing BacFre-K474F/I500L (OD 600 = 10) in MOPS buffer (18 mL, 50 mM, pH 9). Reactions were conducted at room temperature under air for 12 h. Isolated yield. a E . coli expressing BacFre-K474F/I500L (OD 600 = 20). b Nitroalkanes 2 (2 mmol). cReaction for 24 h. The absolute configuration of <t>3a</t> <t>and</t> <t>4d</t> was determined by X-ray crystallographic analysis. All other products were assigned by analogy. Std con: standard condition.
Compound 3a, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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97
ATCC compounds 3a
Absorption and photoluminescence spectra ( λ ex = 440 nm) of compounds <t>3a</t> ( a , d <t>),</t> <t>3b</t> ( b , e ) and 3c ( c , f ) (100 μM) in pH buffers.
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97
ATCC compounds 3a 3e
Photophysical and redox behavior of carbazole derivatives. (A) UV/vis absorption spectra of <t>3a</t> – <t>3e</t> in chloroform (50 μM). (B) UV/vis absorption spectra of 6a , 6b, and 7 in chloroform (50 μM). (C) UV/vis absorption spectra of 10a – 10c in chloroform (50 μM). (D) UV/vis absorption spectra of 11 and 12 in chloroform (50 μM). (E) Tauc plot of compound 3a . (F) The cyclic voltammetry profile of 3a in MeCN with n -Bu 4 NPF 6 (0.1 M) using Fc/Fc + as the internal reference.
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97
ATCC analogous compound 3a
Photophysical and redox behavior of carbazole derivatives. (A) UV/vis absorption spectra of <t>3a</t> – <t>3e</t> in chloroform (50 μM). (B) UV/vis absorption spectra of 6a , 6b, and 7 in chloroform (50 μM). (C) UV/vis absorption spectra of 10a – 10c in chloroform (50 μM). (D) UV/vis absorption spectra of 11 and 12 in chloroform (50 μM). (E) Tauc plot of compound 3a . (F) The cyclic voltammetry profile of 3a in MeCN with n -Bu 4 NPF 6 (0.1 M) using Fc/Fc + as the internal reference.
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97
ATCC compounds 3a e
Photophysical and redox behavior of carbazole derivatives. (A) UV/vis absorption spectra of <t>3a</t> – <t>3e</t> in chloroform (50 μM). (B) UV/vis absorption spectra of 6a , 6b, and 7 in chloroform (50 μM). (C) UV/vis absorption spectra of 10a – 10c in chloroform (50 μM). (D) UV/vis absorption spectra of 11 and 12 in chloroform (50 μM). (E) Tauc plot of compound 3a . (F) The cyclic voltammetry profile of 3a in MeCN with n -Bu 4 NPF 6 (0.1 M) using Fc/Fc + as the internal reference.
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97
ATCC compounds 3a o
Photophysical and redox behavior of carbazole derivatives. (A) UV/vis absorption spectra of <t>3a</t> – <t>3e</t> in chloroform (50 μM). (B) UV/vis absorption spectra of 6a , 6b, and 7 in chloroform (50 μM). (C) UV/vis absorption spectra of 10a – 10c in chloroform (50 μM). (D) UV/vis absorption spectra of 11 and 12 in chloroform (50 μM). (E) Tauc plot of compound 3a . (F) The cyclic voltammetry profile of 3a in MeCN with n -Bu 4 NPF 6 (0.1 M) using Fc/Fc + as the internal reference.
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Image Search Results


Unless otherwise noted, reactions were carried out with 1 (0.2 mmol) and 2 (6 mmol) in MeCN (2 mL), suspensions of E. coli expressing BacFre-K474F/I500L (OD 600 = 10) in MOPS buffer (18 mL, 50 mM, pH 9). Reactions were conducted at room temperature under air for 12 h. Isolated yield. a E . coli expressing BacFre-K474F/I500L (OD 600 = 20). b Nitroalkanes 2 (2 mmol). cReaction for 24 h. The absolute configuration of 3a and 4d was determined by X-ray crystallographic analysis. All other products were assigned by analogy. Std con: standard condition.

Journal: bioRxiv

Article Title: Multicopper oxidase mediated single-carbon insertion for skeletal remodeling

doi: 10.64898/2026.03.28.714988

Figure Lengend Snippet: Unless otherwise noted, reactions were carried out with 1 (0.2 mmol) and 2 (6 mmol) in MeCN (2 mL), suspensions of E. coli expressing BacFre-K474F/I500L (OD 600 = 10) in MOPS buffer (18 mL, 50 mM, pH 9). Reactions were conducted at room temperature under air for 12 h. Isolated yield. a E . coli expressing BacFre-K474F/I500L (OD 600 = 20). b Nitroalkanes 2 (2 mmol). cReaction for 24 h. The absolute configuration of 3a and 4d was determined by X-ray crystallographic analysis. All other products were assigned by analogy. Std con: standard condition.

Article Snippet: The structures of compounds 3a (CCDC: 2481996), 4d (CCDC: 2481997) in this article have been deposited in the Cambridge Crystallographic Data Center.

Techniques: Expressing, Isolation

Absorption and photoluminescence spectra ( λ ex = 440 nm) of compounds 3a ( a , d ), 3b ( b , e ) and 3c ( c , f ) (100 μM) in pH buffers.

Journal: Molecules

Article Title: New Benzimidazole-Based pH-Sensitive Fluorescent Probes

doi: 10.3390/molecules30234622

Figure Lengend Snippet: Absorption and photoluminescence spectra ( λ ex = 440 nm) of compounds 3a ( a , d ), 3b ( b , e ) and 3c ( c , f ) (100 μM) in pH buffers.

Article Snippet: Compounds 3a and 3b at all concentrations studied and compound 3b at concentrations ranging from 10 −7 to 10 −5 M exhibited a weak toxic effect on cellular proteins. and (in ESI) present data on the effect of the studied substances on the biofilm biomass, the number of viable cells, and the metabolic activity of bacterial cells of the E. coli CDC F-50 and S. aureus ATCC 6538-P FDA 209-P strains.

Techniques:

The dependence curve of the fluorescence intensity at the maximum on the pH and pKa value for compounds 3a ( a ), 3b ( b ), and 3c ( c ).

Journal: Molecules

Article Title: New Benzimidazole-Based pH-Sensitive Fluorescent Probes

doi: 10.3390/molecules30234622

Figure Lengend Snippet: The dependence curve of the fluorescence intensity at the maximum on the pH and pKa value for compounds 3a ( a ), 3b ( b ), and 3c ( c ).

Article Snippet: Compounds 3a and 3b at all concentrations studied and compound 3b at concentrations ranging from 10 −7 to 10 −5 M exhibited a weak toxic effect on cellular proteins. and (in ESI) present data on the effect of the studied substances on the biofilm biomass, the number of viable cells, and the metabolic activity of bacterial cells of the E. coli CDC F-50 and S. aureus ATCC 6538-P FDA 209-P strains.

Techniques: Fluorescence

Toxicity of compounds 3a – c at concentrations of 10 −8 –10 −4 M using the V. aquamarinus strain VKPM B-11245. The dotted lines in the diagram indicate the boundaries of the zones of acceptable toxicity, toxicity, and high toxicity. * Differences from the control are statistically significant, t -test; p < 0.05.

Journal: Molecules

Article Title: New Benzimidazole-Based pH-Sensitive Fluorescent Probes

doi: 10.3390/molecules30234622

Figure Lengend Snippet: Toxicity of compounds 3a – c at concentrations of 10 −8 –10 −4 M using the V. aquamarinus strain VKPM B-11245. The dotted lines in the diagram indicate the boundaries of the zones of acceptable toxicity, toxicity, and high toxicity. * Differences from the control are statistically significant, t -test; p < 0.05.

Article Snippet: Compounds 3a and 3b at all concentrations studied and compound 3b at concentrations ranging from 10 −7 to 10 −5 M exhibited a weak toxic effect on cellular proteins. and (in ESI) present data on the effect of the studied substances on the biofilm biomass, the number of viable cells, and the metabolic activity of bacterial cells of the E. coli CDC F-50 and S. aureus ATCC 6538-P FDA 209-P strains.

Techniques: Control

Changes in the toxicity of compounds 3a ( a ), 3b ( b ), 3c ( c ), depending on concentrations (10 −8 –10 −4 M). The dotted line in the diagram indicates the boundary between weak and moderate toxicity. * Differences from the control are statistically significant, t -test; p < 0.05.

Journal: Molecules

Article Title: New Benzimidazole-Based pH-Sensitive Fluorescent Probes

doi: 10.3390/molecules30234622

Figure Lengend Snippet: Changes in the toxicity of compounds 3a ( a ), 3b ( b ), 3c ( c ), depending on concentrations (10 −8 –10 −4 M). The dotted line in the diagram indicates the boundary between weak and moderate toxicity. * Differences from the control are statistically significant, t -test; p < 0.05.

Article Snippet: Compounds 3a and 3b at all concentrations studied and compound 3b at concentrations ranging from 10 −7 to 10 −5 M exhibited a weak toxic effect on cellular proteins. and (in ESI) present data on the effect of the studied substances on the biofilm biomass, the number of viable cells, and the metabolic activity of bacterial cells of the E. coli CDC F-50 and S. aureus ATCC 6538-P FDA 209-P strains.

Techniques: Control

The effect of compounds 3a – c on the biomass, metabolic activity, and viable cell count of bacterial biofilms of E. coli CDC F-50 and S. aureus ATCC 6538-P FDA 209-P strains, depending on concentration (10 −8 –10 −4 M). * Differences from control are statistically significant, t -test; p < 0.05.

Journal: Molecules

Article Title: New Benzimidazole-Based pH-Sensitive Fluorescent Probes

doi: 10.3390/molecules30234622

Figure Lengend Snippet: The effect of compounds 3a – c on the biomass, metabolic activity, and viable cell count of bacterial biofilms of E. coli CDC F-50 and S. aureus ATCC 6538-P FDA 209-P strains, depending on concentration (10 −8 –10 −4 M). * Differences from control are statistically significant, t -test; p < 0.05.

Article Snippet: Compounds 3a and 3b at all concentrations studied and compound 3b at concentrations ranging from 10 −7 to 10 −5 M exhibited a weak toxic effect on cellular proteins. and (in ESI) present data on the effect of the studied substances on the biofilm biomass, the number of viable cells, and the metabolic activity of bacterial cells of the E. coli CDC F-50 and S. aureus ATCC 6538-P FDA 209-P strains.

Techniques: Activity Assay, Cell Counting, Concentration Assay, Control

Photophysical and redox behavior of carbazole derivatives. (A) UV/vis absorption spectra of 3a – 3e in chloroform (50 μM). (B) UV/vis absorption spectra of 6a , 6b, and 7 in chloroform (50 μM). (C) UV/vis absorption spectra of 10a – 10c in chloroform (50 μM). (D) UV/vis absorption spectra of 11 and 12 in chloroform (50 μM). (E) Tauc plot of compound 3a . (F) The cyclic voltammetry profile of 3a in MeCN with n -Bu 4 NPF 6 (0.1 M) using Fc/Fc + as the internal reference.

Journal: ACS Omega

Article Title: Antimicrobial, Structural, Optical, and Redox Profiling of 7 H ‑Benzo[ c ]carbazol-10-ol Derivatives: An Integrated Experimental and Computational Study

doi: 10.1021/acsomega.5c08465

Figure Lengend Snippet: Photophysical and redox behavior of carbazole derivatives. (A) UV/vis absorption spectra of 3a – 3e in chloroform (50 μM). (B) UV/vis absorption spectra of 6a , 6b, and 7 in chloroform (50 μM). (C) UV/vis absorption spectra of 10a – 10c in chloroform (50 μM). (D) UV/vis absorption spectra of 11 and 12 in chloroform (50 μM). (E) Tauc plot of compound 3a . (F) The cyclic voltammetry profile of 3a in MeCN with n -Bu 4 NPF 6 (0.1 M) using Fc/Fc + as the internal reference.

Article Snippet: Compounds 3a – 3e (except 3d ) and 7 , which are typical 7 H -benzo [ c ] carbazol-10-ols, demonstrated good antibacterial activity against S. aureus ATCC-6538 and P. aeruginosa ATCC-9027, with inhibition zones up to 17 mm for 3e .

Techniques: