atractylenolide ii Search Results


90
MedChemExpress atractylenolide ii
Atractylenolide Ii, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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atractylenolide ii - by Bioz Stars, 2026-02
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90
ChengDu Biopurify Phytochemicals Ltd atractylenolide ii
Atractylenolide Ii, supplied by ChengDu Biopurify Phytochemicals Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Chengdu Herbpurify CO atractylenolide iii (lot.b-034-171217)
HPLC analysis of Zhen-wu-tang (ZWT). (1) 6-gingerol, (2) paeoniflorin, (3) benzoylaconine, (4) benzoylhypacoitine, (5) <t>atractylenolide</t> <t>III,</t> (6) pachymic acid, and (7) atractylenolide II.
Atractylenolide Iii (Lot.B 034 171217), supplied by Chengdu Herbpurify CO, 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.b-034-171217)/product/Chengdu Herbpurify CO
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90
Baoji Titanium Industry Co Ltd atractylenolide ii
HPLC analysis of Zhen-wu-tang (ZWT). (1) 6-gingerol, (2) paeoniflorin, (3) benzoylaconine, (4) benzoylhypacoitine, (5) <t>atractylenolide</t> <t>III,</t> (6) pachymic acid, and (7) atractylenolide II.
Atractylenolide Ii, supplied by Baoji Titanium Industry 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 ii/product/Baoji Titanium Industry Co Ltd
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atractylenolide ii - by Bioz Stars, 2026-02
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90
BioMimetic Therapeutics atractylenolide ii
The transformation of <t>atractylenolide</t> I, II, and III in biosynthetic pathway (ref. ).
Atractylenolide Ii, supplied by BioMimetic Therapeutics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
TargetMol atractylenolide ii
The transformation of <t>atractylenolide</t> I, II, and III in biosynthetic pathway (ref. ).
Atractylenolide Ii, 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
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Image Search Results


HPLC analysis of Zhen-wu-tang (ZWT). (1) 6-gingerol, (2) paeoniflorin, (3) benzoylaconine, (4) benzoylhypacoitine, (5) atractylenolide III, (6) pachymic acid, and (7) atractylenolide II.

Journal: Frontiers in Pharmacology

Article Title: Zhen-Wu-Tang Protects IgA Nephropathy in Rats by Regulating Exosomes to Inhibit NF-κB/NLRP3 Pathway

doi: 10.3389/fphar.2020.01080

Figure Lengend Snippet: HPLC analysis of Zhen-wu-tang (ZWT). (1) 6-gingerol, (2) paeoniflorin, (3) benzoylaconine, (4) benzoylhypacoitine, (5) atractylenolide III, (6) pachymic acid, and (7) atractylenolide II.

Article Snippet: The standards of paeoniflorin (Lot.S-010-180416), benzoylaconine (Lot.B-010-190814), benzoylmesaconine (Lot.B-016-180606), atractylenolide II (Lot.B-034-181216), atractylenolide III (Lot.B-034-171217), 6-gingerol (Lot.J-038-180515) and pachymic acid (Lot.F-006-191014) were provided by Chengdu Herbpurify CO., LTD (purity > 98%, Chengdu, China).

Techniques:

Herbal sources and retention times of seven components in Zhen-wu-tang (ZWT).

Journal: Frontiers in Pharmacology

Article Title: Zhen-Wu-Tang Protects IgA Nephropathy in Rats by Regulating Exosomes to Inhibit NF-κB/NLRP3 Pathway

doi: 10.3389/fphar.2020.01080

Figure Lengend Snippet: Herbal sources and retention times of seven components in Zhen-wu-tang (ZWT).

Article Snippet: The standards of paeoniflorin (Lot.S-010-180416), benzoylaconine (Lot.B-010-190814), benzoylmesaconine (Lot.B-016-180606), atractylenolide II (Lot.B-034-181216), atractylenolide III (Lot.B-034-171217), 6-gingerol (Lot.J-038-180515) and pachymic acid (Lot.F-006-191014) were provided by Chengdu Herbpurify CO., LTD (purity > 98%, Chengdu, China).

Techniques:

The transformation of atractylenolide I, II, and III in biosynthetic pathway (ref. ).

Journal: RSC Advances

Article Title: Catalytic approach to in vivo metabolism of atractylenolide III using biomimetic iron–porphyrin complexes

doi: 10.1039/d1ra05014a

Figure Lengend Snippet: The transformation of atractylenolide I, II, and III in biosynthetic pathway (ref. ).

Article Snippet: In our previous study a biomimetic iron( iv )-oxo porphyrin π-cation radical complex (known as compound I) model has shown that AT-III was oxidised from atractylenolide II (C 15 H 20 O , MW = 232.32 g mol −1 ) and dehydrated to atractylenolide I (C 15 H 18 O , MW = 230.3 g mol −1 ) via an intrinsic biosynthetic pathway in A. japonica ( ).

Techniques: Transformation Assay

(a) Mean relative area ratio–time profiles of atractylenolide III (AT-III) and (b) oxygenated atractylenolide III (AT-III–O) after administration of AT-III single or with acetaminophen (APAP). Relative area ratio = the peak area of target compound/the peak area of IS. Differences of relative area ratios between single and combinative administration groups were not statistically significant.

Journal: RSC Advances

Article Title: Catalytic approach to in vivo metabolism of atractylenolide III using biomimetic iron–porphyrin complexes

doi: 10.1039/d1ra05014a

Figure Lengend Snippet: (a) Mean relative area ratio–time profiles of atractylenolide III (AT-III) and (b) oxygenated atractylenolide III (AT-III–O) after administration of AT-III single or with acetaminophen (APAP). Relative area ratio = the peak area of target compound/the peak area of IS. Differences of relative area ratios between single and combinative administration groups were not statistically significant.

Article Snippet: In our previous study a biomimetic iron( iv )-oxo porphyrin π-cation radical complex (known as compound I) model has shown that AT-III was oxidised from atractylenolide II (C 15 H 20 O , MW = 232.32 g mol −1 ) and dehydrated to atractylenolide I (C 15 H 18 O , MW = 230.3 g mol −1 ) via an intrinsic biosynthetic pathway in A. japonica ( ).

Techniques: