baicalin Search Results


95
MedChemExpress ba n0197
Ba N0197, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/Baicalin/pmc11282607-60-14-10
Average 95 stars, based on 1 article reviews
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94
TargetMol baicalin
Potential medication screening for targeting SRGN protein. (A) Workflow of screening. (B) SRGN protein structure. (C) Docking pocket 1 of SRGN protein. (D) Docking pocket 2 of SRGN protein. The docking pockets and poses, and binding residues of sorafenib (E) <t>,</t> <t>daurisoline</t> (F) , regorafenib (G) , and <t>baicalin</t> (H) with SRGN protein.
Baicalin, supplied by TargetMol, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/Baicalin/pmc12080381-40-0-6
Average 94 stars, based on 1 article reviews
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91
Santa Cruz Biotechnology experimental design baicalin
Potential medication screening for targeting SRGN protein. (A) Workflow of screening. (B) SRGN protein structure. (C) Docking pocket 1 of SRGN protein. (D) Docking pocket 2 of SRGN protein. The docking pockets and poses, and binding residues of sorafenib (E) <t>,</t> <t>daurisoline</t> (F) , regorafenib (G) , and <t>baicalin</t> (H) with SRGN protein.
Experimental Design Baicalin, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/Baicalin/pm33190590-35-3-11
Average 91 stars, based on 1 article reviews
experimental design baicalin - by Bioz Stars, 2026-10
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94
MedChemExpress baicalin methyl ester
Potential medication screening for targeting SRGN protein. (A) Workflow of screening. (B) SRGN protein structure. (C) Docking pocket 1 of SRGN protein. (D) Docking pocket 2 of SRGN protein. The docking pockets and poses, and binding residues of sorafenib (E) <t>,</t> <t>daurisoline</t> (F) , regorafenib (G) , and <t>baicalin</t> (H) with SRGN protein.
Baicalin Methyl Ester, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/Baicalin+methyl+ester/pm42031733-256-12-19
Average 94 stars, based on 1 article reviews
baicalin methyl ester - by Bioz Stars, 2026-10
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94
Thermo Fisher baicalin
Potential medication screening for targeting SRGN protein. (A) Workflow of screening. (B) SRGN protein structure. (C) Docking pocket 1 of SRGN protein. (D) Docking pocket 2 of SRGN protein. The docking pockets and poses, and binding residues of sorafenib (E) <t>,</t> <t>daurisoline</t> (F) , regorafenib (G) , and <t>baicalin</t> (H) with SRGN protein.
Baicalin, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/Baicalin/pmc08790824-304-5-1
Average 94 stars, based on 1 article reviews
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93
Selleck Chemicals baicalin
Fig. 1. Investigation of transcriptional activities of rsAHR1 and rsAHR2 for 10 natural ligands. Concentration-response curves of rsAHR1 and rsAHR2 were measured for (A) 8 h-treatment group <t>with</t> <t>FICZ,</t> I3C, DIM, Quercetin, Genistein, Daidzein, <t>Baicalin,</t> Retinol, Resveratrol, and Astaxanthin and (B) 18 h-treatment group with FICZ, I3C, DIM, and Quercetin. The EC50 values were calculated from concentration-response curves of rsAHR1 and rsAHR2. Fold induction was measured using DMSO as the control. Each data point represents the average and standard deviation (SD) of fold induction from independent replicate experiments (n = 1–4).
Baicalin, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/Baicalin/pm38569320-98-11-12
Average 93 stars, based on 1 article reviews
baicalin - by Bioz Stars, 2026-10
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91
ChromaDex baicalein
Fig. 1. Investigation of transcriptional activities of rsAHR1 and rsAHR2 for 10 natural ligands. Concentration-response curves of rsAHR1 and rsAHR2 were measured for (A) 8 h-treatment group <t>with</t> <t>FICZ,</t> I3C, DIM, Quercetin, Genistein, Daidzein, <t>Baicalin,</t> Retinol, Resveratrol, and Astaxanthin and (B) 18 h-treatment group with FICZ, I3C, DIM, and Quercetin. The EC50 values were calculated from concentration-response curves of rsAHR1 and rsAHR2. Fold induction was measured using DMSO as the control. Each data point represents the average and standard deviation (SD) of fold induction from independent replicate experiments (n = 1–4).
Baicalein, supplied by ChromaDex, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/Baicalin/pmc02940884-95-5-27
Average 91 stars, based on 1 article reviews
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86
ChromaDex baicalin
Fig. 1. Investigation of transcriptional activities of rsAHR1 and rsAHR2 for 10 natural ligands. Concentration-response curves of rsAHR1 and rsAHR2 were measured for (A) 8 h-treatment group <t>with</t> <t>FICZ,</t> I3C, DIM, Quercetin, Genistein, Daidzein, <t>Baicalin,</t> Retinol, Resveratrol, and Astaxanthin and (B) 18 h-treatment group with FICZ, I3C, DIM, and Quercetin. The EC50 values were calculated from concentration-response curves of rsAHR1 and rsAHR2. Fold induction was measured using DMSO as the control. Each data point represents the average and standard deviation (SD) of fold induction from independent replicate experiments (n = 1–4).
Baicalin, supplied by ChromaDex, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/Baicalin/10__1016_slash_j__lwt__2020__109056-85-0-3
Average 86 stars, based on 1 article reviews
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90
Muegge GmbH baicalin
Fig. 1. Investigation of transcriptional activities of rsAHR1 and rsAHR2 for 10 natural ligands. Concentration-response curves of rsAHR1 and rsAHR2 were measured for (A) 8 h-treatment group <t>with</t> <t>FICZ,</t> I3C, DIM, Quercetin, Genistein, Daidzein, <t>Baicalin,</t> Retinol, Resveratrol, and Astaxanthin and (B) 18 h-treatment group with FICZ, I3C, DIM, and Quercetin. The EC50 values were calculated from concentration-response curves of rsAHR1 and rsAHR2. Fold induction was measured using DMSO as the control. Each data point represents the average and standard deviation (SD) of fold induction from independent replicate experiments (n = 1–4).
Baicalin, supplied by Muegge GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/baicalin/10__1155_slash_2024_slash_4309908-150-61-22
Average 90 stars, based on 1 article reviews
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90
FUJIFILM baicalin
HPLC chromatograms of standard compounds (A) and extract of Hwangryunhaedok-tang (B) obtained at a UV wavelength of 240 nm. <t>1,</t> <t>Geniposide;</t> 2, berberine chloride; 3, <t>baicalin;</t> 4, wogonin.
Baicalin, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/baicalin/pmc05403749-31-3-9
Average 90 stars, based on 1 article reviews
baicalin - by Bioz Stars, 2026-10
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90
Immunocellular Therapeutics baicalin
Comparisons of the autophagic effects and traditional usages of CHMs and their <t> active components. </t>
Baicalin, supplied by Immunocellular Therapeutics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/baicalin/baicalin/pmc06274228-129-2-16
Average 90 stars, based on 1 article reviews
baicalin - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


Potential medication screening for targeting SRGN protein. (A) Workflow of screening. (B) SRGN protein structure. (C) Docking pocket 1 of SRGN protein. (D) Docking pocket 2 of SRGN protein. The docking pockets and poses, and binding residues of sorafenib (E) , daurisoline (F) , regorafenib (G) , and baicalin (H) with SRGN protein.

Journal: International Journal of Biological Sciences

Article Title: SRGN-mediated reactivation of the YAP/CRISPLD2 axis promotes aggressiveness of hepatocellular carcinoma

doi: 10.7150/ijbs.108151

Figure Lengend Snippet: Potential medication screening for targeting SRGN protein. (A) Workflow of screening. (B) SRGN protein structure. (C) Docking pocket 1 of SRGN protein. (D) Docking pocket 2 of SRGN protein. The docking pockets and poses, and binding residues of sorafenib (E) , daurisoline (F) , regorafenib (G) , and baicalin (H) with SRGN protein.

Article Snippet: Baicalin and daurisoline were purchased from TargetMol (USA; T3054, T2775).

Techniques: Binding Assay

Molecular dynamics simulations of four medication monomer-SRGN complexes. (A) Sorafenib-SRGN complex. (B) Regorafenib-SRGN complex. (C) Baicalin-SRGN complex. (D) Daurisoline-SRGN complex.

Journal: International Journal of Biological Sciences

Article Title: SRGN-mediated reactivation of the YAP/CRISPLD2 axis promotes aggressiveness of hepatocellular carcinoma

doi: 10.7150/ijbs.108151

Figure Lengend Snippet: Molecular dynamics simulations of four medication monomer-SRGN complexes. (A) Sorafenib-SRGN complex. (B) Regorafenib-SRGN complex. (C) Baicalin-SRGN complex. (D) Daurisoline-SRGN complex.

Article Snippet: Baicalin and daurisoline were purchased from TargetMol (USA; T3054, T2775).

Techniques:

Fig. 1. Investigation of transcriptional activities of rsAHR1 and rsAHR2 for 10 natural ligands. Concentration-response curves of rsAHR1 and rsAHR2 were measured for (A) 8 h-treatment group with FICZ, I3C, DIM, Quercetin, Genistein, Daidzein, Baicalin, Retinol, Resveratrol, and Astaxanthin and (B) 18 h-treatment group with FICZ, I3C, DIM, and Quercetin. The EC50 values were calculated from concentration-response curves of rsAHR1 and rsAHR2. Fold induction was measured using DMSO as the control. Each data point represents the average and standard deviation (SD) of fold induction from independent replicate experiments (n = 1–4).

Journal: Ecotoxicology and environmental safety

Article Title: In Silico and In Vitro multiple analysis approach for screening naturally derived ligands for red seabream aryl hydrocarbon receptor.

doi: 10.1016/j.ecoenv.2024.116262

Figure Lengend Snippet: Fig. 1. Investigation of transcriptional activities of rsAHR1 and rsAHR2 for 10 natural ligands. Concentration-response curves of rsAHR1 and rsAHR2 were measured for (A) 8 h-treatment group with FICZ, I3C, DIM, Quercetin, Genistein, Daidzein, Baicalin, Retinol, Resveratrol, and Astaxanthin and (B) 18 h-treatment group with FICZ, I3C, DIM, and Quercetin. The EC50 values were calculated from concentration-response curves of rsAHR1 and rsAHR2. Fold induction was measured using DMSO as the control. Each data point represents the average and standard deviation (SD) of fold induction from independent replicate experiments (n = 1–4).

Article Snippet: FICZ (Enzo Life Sciences), Indole-3-carbinol (Sigma Aldrich), 3,3’- Diindolylmethane (Sigma Aldrich), Baicalin (Selleck Chemicals), Daidzein (Selleck Chemicals), Genistein (MedChemExpress), Quercetin (Sigma Aldrich), Astaxanthin (Sigma Aldrich), Retinol (Sigma Aldrich), and Resveratrol (Santacruz) were utilized in this study for investigating the transcriptional activity in rsAHR1 and rsAHR2.

Techniques: Concentration Assay, Control, Standard Deviation

HPLC chromatograms of standard compounds (A) and extract of Hwangryunhaedok-tang (B) obtained at a UV wavelength of 240 nm. 1, Geniposide; 2, berberine chloride; 3, baicalin; 4, wogonin.

Journal: World Journal of Gastroenterology

Article Title: Effects of Hwangryunhaedok-tang on gastrointestinal motility function in mice

doi: 10.3748/wjg.v23.i15.2705

Figure Lengend Snippet: HPLC chromatograms of standard compounds (A) and extract of Hwangryunhaedok-tang (B) obtained at a UV wavelength of 240 nm. 1, Geniposide; 2, berberine chloride; 3, baicalin; 4, wogonin.

Article Snippet: Geniposide, berberine chloride, baicalin, and wogonin were purchased from Wako (Japan).

Techniques:

Contents of four marker components of Hwangryunhaedok-tang by HPLC ( n = 4)

Journal: World Journal of Gastroenterology

Article Title: Effects of Hwangryunhaedok-tang on gastrointestinal motility function in mice

doi: 10.3748/wjg.v23.i15.2705

Figure Lengend Snippet: Contents of four marker components of Hwangryunhaedok-tang by HPLC ( n = 4)

Article Snippet: Geniposide, berberine chloride, baicalin, and wogonin were purchased from Wako (Japan).

Techniques: Marker, High Performance Liquid Chromatography

Comparisons of the autophagic effects and traditional usages of CHMs and their  active components.

Journal: Molecules

Article Title: New Potential Pharmacological Functions of Chinese Herbal Medicines via Regulation of Autophagy

doi: 10.3390/molecules21030359

Figure Lengend Snippet: Comparisons of the autophagic effects and traditional usages of CHMs and their active components.

Article Snippet: The two main active components, baicalin and wogonin inhibit the release of proinflammatory mediators from different immunocellular components [ , ].

Techniques: Mutagenesis, Inhibition, Activation Assay, Activity Assay, Protein-Protein interactions, Blocking Assay, Phospho-proteomics