atractylenolide iii Search Results


atl iii  (MedChemExpress)
93
MedChemExpress atl iii
Atl Iii, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
atl iii - by Bioz Stars, 2026-05
93/100 stars
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atractylenolide iii  (ChromaDex)
90
ChromaDex atractylenolide iii
The chemical structures of 11 marker compounds of Jaeumganghwa-tang. (1) 5-Hydroxymethylfurfural, (2) mangiferin, (3) paeoniflorin, (4) nodakenin, (5) naringin, (6) hesperidin, (7) decursinol, (8) berberine, (9) glycyrrhizin, (10) <t>atractylenolide</t> <t>III</t> and (11) decursin
Atractylenolide Iii, supplied by ChromaDex, 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/result/atractylenolide iii/product/ChromaDex
Average 90 stars, based on 1 article reviews
atractylenolide iii - by Bioz Stars, 2026-05
90/100 stars
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atractylenolide iii (lot no. wen2356)  (FUJIFILM)
90
FUJIFILM atractylenolide iii (lot no. wen2356)
The chemical structures of 11 marker compounds of Jaeumganghwa-tang. (1) 5-Hydroxymethylfurfural, (2) mangiferin, (3) paeoniflorin, (4) nodakenin, (5) naringin, (6) hesperidin, (7) decursinol, (8) berberine, (9) glycyrrhizin, (10) <t>atractylenolide</t> <t>III</t> and (11) decursin
Atractylenolide Iii (Lot No. Wen2356), 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/result/atractylenolide iii (lot no. wen2356)/product/FUJIFILM
Average 90 stars, based on 1 article reviews
atractylenolide iii (lot no. wen2356) - by Bioz Stars, 2026-05
90/100 stars
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atractylenolide iii  (TSUMURA)
90
TSUMURA atractylenolide iii
The chemical structures of 11 marker compounds of Jaeumganghwa-tang. (1) 5-Hydroxymethylfurfural, (2) mangiferin, (3) paeoniflorin, (4) nodakenin, (5) naringin, (6) hesperidin, (7) decursinol, (8) berberine, (9) glycyrrhizin, (10) <t>atractylenolide</t> <t>III</t> and (11) decursin
Atractylenolide Iii, supplied by TSUMURA, 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/result/atractylenolide iii/product/TSUMURA
Average 90 stars, based on 1 article reviews
atractylenolide iii - by Bioz Stars, 2026-05
90/100 stars
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atractylenolide iii  (Tauto Biotech Co. Ltd)
90
Tauto Biotech Co. Ltd atractylenolide iii
Conformational analysis of sesquiterpene lactones. (A) 2D chemical structures of alantolactone and <t>atractylenolide</t> I. (B) Geometry optimized 3D structures of alantolactone (green) and atractylenolide I (cyan) were aligned based on their lactone rings. (C) Schematic diagram for determining the torsion angle between sesquiterpene skeleton-lactone ring (S-L torsion angle). We calculated Van der Waals (VdW) strains in SH2 binding pocket for alantolactone (D) and atractylenolide I (E). Putative VdW strains were visualized as red flat cylinders. (F) Geometry optimized 3D structures of sesquiterpene lactones were aligned based on their lactone rings. Sesquiterpene lactones, namely alantolactone, isoalantolactone, and parthenolide, which demonstrated over 50% inhibitory effects on STAT3 activation, are shown in green. (G) Correlation between S-L torsion angles and relative p-STAT3 at 10 μM of nine sesquiterpene lactones.
Atractylenolide Iii, supplied by Tauto Biotech Co. Ltd, 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/result/atractylenolide iii/product/Tauto Biotech Co. Ltd
Average 90 stars, based on 1 article reviews
atractylenolide iii - by Bioz Stars, 2026-05
90/100 stars
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atractylenolide iii  (Beijing Solarbio Science)
90
Beijing Solarbio Science atractylenolide iii
Conformational analysis of sesquiterpene lactones. (A) 2D chemical structures of alantolactone and <t>atractylenolide</t> I. (B) Geometry optimized 3D structures of alantolactone (green) and atractylenolide I (cyan) were aligned based on their lactone rings. (C) Schematic diagram for determining the torsion angle between sesquiterpene skeleton-lactone ring (S-L torsion angle). We calculated Van der Waals (VdW) strains in SH2 binding pocket for alantolactone (D) and atractylenolide I (E). Putative VdW strains were visualized as red flat cylinders. (F) Geometry optimized 3D structures of sesquiterpene lactones were aligned based on their lactone rings. Sesquiterpene lactones, namely alantolactone, isoalantolactone, and parthenolide, which demonstrated over 50% inhibitory effects on STAT3 activation, are shown in green. (G) Correlation between S-L torsion angles and relative p-STAT3 at 10 μM of nine sesquiterpene lactones.
Atractylenolide Iii, supplied by Beijing Solarbio Science, 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/result/atractylenolide iii/product/Beijing Solarbio Science
Average 90 stars, based on 1 article reviews
atractylenolide iii - by Bioz Stars, 2026-05
90/100 stars
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atractylenolide iii  (Verlag GmbH)
90
Verlag GmbH atractylenolide iii
Conformational analysis of sesquiterpene lactones. (A) 2D chemical structures of alantolactone and <t>atractylenolide</t> I. (B) Geometry optimized 3D structures of alantolactone (green) and atractylenolide I (cyan) were aligned based on their lactone rings. (C) Schematic diagram for determining the torsion angle between sesquiterpene skeleton-lactone ring (S-L torsion angle). We calculated Van der Waals (VdW) strains in SH2 binding pocket for alantolactone (D) and atractylenolide I (E). Putative VdW strains were visualized as red flat cylinders. (F) Geometry optimized 3D structures of sesquiterpene lactones were aligned based on their lactone rings. Sesquiterpene lactones, namely alantolactone, isoalantolactone, and parthenolide, which demonstrated over 50% inhibitory effects on STAT3 activation, are shown in green. (G) Correlation between S-L torsion angles and relative p-STAT3 at 10 μM of nine sesquiterpene lactones.
Atractylenolide Iii, supplied by Verlag 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/result/atractylenolide iii/product/Verlag GmbH
Average 90 stars, based on 1 article reviews
atractylenolide iii - by Bioz Stars, 2026-05
90/100 stars
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atractylenolide iii  (FUJIFILM)
90
FUJIFILM atractylenolide iii
Conformational analysis of sesquiterpene lactones. (A) 2D chemical structures of alantolactone and <t>atractylenolide</t> I. (B) Geometry optimized 3D structures of alantolactone (green) and atractylenolide I (cyan) were aligned based on their lactone rings. (C) Schematic diagram for determining the torsion angle between sesquiterpene skeleton-lactone ring (S-L torsion angle). We calculated Van der Waals (VdW) strains in SH2 binding pocket for alantolactone (D) and atractylenolide I (E). Putative VdW strains were visualized as red flat cylinders. (F) Geometry optimized 3D structures of sesquiterpene lactones were aligned based on their lactone rings. Sesquiterpene lactones, namely alantolactone, isoalantolactone, and parthenolide, which demonstrated over 50% inhibitory effects on STAT3 activation, are shown in green. (G) Correlation between S-L torsion angles and relative p-STAT3 at 10 μM of nine sesquiterpene lactones.
Atractylenolide Iii, 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/result/atractylenolide iii/product/FUJIFILM
Average 90 stars, based on 1 article reviews
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atractylenolide iii cfs201701  (ChemFaces Biochemical Co Ltd)
90
ChemFaces Biochemical Co Ltd atractylenolide iii cfs201701
Conformational analysis of sesquiterpene lactones. (A) 2D chemical structures of alantolactone and <t>atractylenolide</t> I. (B) Geometry optimized 3D structures of alantolactone (green) and atractylenolide I (cyan) were aligned based on their lactone rings. (C) Schematic diagram for determining the torsion angle between sesquiterpene skeleton-lactone ring (S-L torsion angle). We calculated Van der Waals (VdW) strains in SH2 binding pocket for alantolactone (D) and atractylenolide I (E). Putative VdW strains were visualized as red flat cylinders. (F) Geometry optimized 3D structures of sesquiterpene lactones were aligned based on their lactone rings. Sesquiterpene lactones, namely alantolactone, isoalantolactone, and parthenolide, which demonstrated over 50% inhibitory effects on STAT3 activation, are shown in green. (G) Correlation between S-L torsion angles and relative p-STAT3 at 10 μM of nine sesquiterpene lactones.
Atractylenolide Iii Cfs201701, supplied by ChemFaces Biochemical Co Ltd, 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/result/atractylenolide iii cfs201701/product/ChemFaces Biochemical Co Ltd
Average 90 stars, based on 1 article reviews
atractylenolide iii cfs201701 - by Bioz Stars, 2026-05
90/100 stars
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atractylenolide iii  (BOC Sciences)
N/A
Atractylenolide III is a major component of Atractylodes rhizome, which can induce apoptosis of the lung carcinoma cells.
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Image Search Results


The chemical structures of 11 marker compounds of Jaeumganghwa-tang. (1) 5-Hydroxymethylfurfural, (2) mangiferin, (3) paeoniflorin, (4) nodakenin, (5) naringin, (6) hesperidin, (7) decursinol, (8) berberine, (9) glycyrrhizin, (10) atractylenolide III and (11) decursin

Journal: Pharmacognosy Magazine

Article Title: Simultaneous determination of 11 bioactive compounds in Jaeumganghwa-tang by high performance liquid chromatography-diode array detection

doi: 10.4103/0973-1296.133267

Figure Lengend Snippet: The chemical structures of 11 marker compounds of Jaeumganghwa-tang. (1) 5-Hydroxymethylfurfural, (2) mangiferin, (3) paeoniflorin, (4) nodakenin, (5) naringin, (6) hesperidin, (7) decursinol, (8) berberine, (9) glycyrrhizin, (10) atractylenolide III and (11) decursin

Article Snippet: Decursinol was purchased from Elcomscience Co., Ltd. Paeoniflorin was purchased from Wako Co., Ltd. 5-HMF was purchased from Sigma Aldrich Co., Ltd. Mangiferin was purchased from Fluka Co., Ltd. Atractylenolide III was purchased from Chromadex Co., Ltd.

Techniques: Marker

(a) Chromatograms of Jaeumganghwa-tang standard mixture and (b) sample. (1) 5-Hydroxymethylfurfural, (2) mangiferin, (3) paeoniflorin, (4) nodakenin, (5) naringin, (6) hesperidin, (7) decursinol, (8) berberine, (9) glycyrrhizin, (10) atractylenolide III and (11) decursin

Journal: Pharmacognosy Magazine

Article Title: Simultaneous determination of 11 bioactive compounds in Jaeumganghwa-tang by high performance liquid chromatography-diode array detection

doi: 10.4103/0973-1296.133267

Figure Lengend Snippet: (a) Chromatograms of Jaeumganghwa-tang standard mixture and (b) sample. (1) 5-Hydroxymethylfurfural, (2) mangiferin, (3) paeoniflorin, (4) nodakenin, (5) naringin, (6) hesperidin, (7) decursinol, (8) berberine, (9) glycyrrhizin, (10) atractylenolide III and (11) decursin

Article Snippet: Decursinol was purchased from Elcomscience Co., Ltd. Paeoniflorin was purchased from Wako Co., Ltd. 5-HMF was purchased from Sigma Aldrich Co., Ltd. Mangiferin was purchased from Fluka Co., Ltd. Atractylenolide III was purchased from Chromadex Co., Ltd.

Techniques:

Liquid chromatography-mass spectrometry spectra of maker compound in Jaeumganghwa-tang. (1) 5-Hydroxymethylfurfural, (2) mangiferin, (3) paeoniflorin, (4) nodakenin, (5) naringin, (6) hesperidin, (7) decursinol, (8) berberine, (9) glycyrrhizin, (10) atractylenolide III and (11) decursin

Journal: Pharmacognosy Magazine

Article Title: Simultaneous determination of 11 bioactive compounds in Jaeumganghwa-tang by high performance liquid chromatography-diode array detection

doi: 10.4103/0973-1296.133267

Figure Lengend Snippet: Liquid chromatography-mass spectrometry spectra of maker compound in Jaeumganghwa-tang. (1) 5-Hydroxymethylfurfural, (2) mangiferin, (3) paeoniflorin, (4) nodakenin, (5) naringin, (6) hesperidin, (7) decursinol, (8) berberine, (9) glycyrrhizin, (10) atractylenolide III and (11) decursin

Article Snippet: Decursinol was purchased from Elcomscience Co., Ltd. Paeoniflorin was purchased from Wako Co., Ltd. 5-HMF was purchased from Sigma Aldrich Co., Ltd. Mangiferin was purchased from Fluka Co., Ltd. Atractylenolide III was purchased from Chromadex Co., Ltd.

Techniques: Liquid Chromatography, Mass Spectrometry

Conformational analysis of sesquiterpene lactones. (A) 2D chemical structures of alantolactone and atractylenolide I. (B) Geometry optimized 3D structures of alantolactone (green) and atractylenolide I (cyan) were aligned based on their lactone rings. (C) Schematic diagram for determining the torsion angle between sesquiterpene skeleton-lactone ring (S-L torsion angle). We calculated Van der Waals (VdW) strains in SH2 binding pocket for alantolactone (D) and atractylenolide I (E). Putative VdW strains were visualized as red flat cylinders. (F) Geometry optimized 3D structures of sesquiterpene lactones were aligned based on their lactone rings. Sesquiterpene lactones, namely alantolactone, isoalantolactone, and parthenolide, which demonstrated over 50% inhibitory effects on STAT3 activation, are shown in green. (G) Correlation between S-L torsion angles and relative p-STAT3 at 10 μM of nine sesquiterpene lactones.

Journal: Biomolecules & Therapeutics

Article Title: Unraveling Stereochemical Structure-Activity Relationships of Sesquiterpene Lactones for Inhibitory Effects on STAT3 Activation

doi: 10.4062/biomolther.2023.210

Figure Lengend Snippet: Conformational analysis of sesquiterpene lactones. (A) 2D chemical structures of alantolactone and atractylenolide I. (B) Geometry optimized 3D structures of alantolactone (green) and atractylenolide I (cyan) were aligned based on their lactone rings. (C) Schematic diagram for determining the torsion angle between sesquiterpene skeleton-lactone ring (S-L torsion angle). We calculated Van der Waals (VdW) strains in SH2 binding pocket for alantolactone (D) and atractylenolide I (E). Putative VdW strains were visualized as red flat cylinders. (F) Geometry optimized 3D structures of sesquiterpene lactones were aligned based on their lactone rings. Sesquiterpene lactones, namely alantolactone, isoalantolactone, and parthenolide, which demonstrated over 50% inhibitory effects on STAT3 activation, are shown in green. (G) Correlation between S-L torsion angles and relative p-STAT3 at 10 μM of nine sesquiterpene lactones.

Article Snippet: Alantolactone, isoalantolactone, costunolide, dehydrocostus lactone, parthenolide, atractylenolide I, atractylenolide II, atractylenolide III, and sclareolide, were purchased from Tauto Biotech (Shanghai, China).

Techniques: Binding Assay, Activation Assay