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- Terpenoids
- Iridoids
Iridoids
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Iridoids (269)
- Formula: C11H16O4
- Molecular Weight: 212.24
1-O-Methyljatamanin D is a Iridoids product that can be isolated from the herbs of Valeriana jatamansi.
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- Formula: C20H24O12
- Molecular Weight: 456.40
15-Demethylplumieride is a Iridoids product that can be isolated from the barks of Plumeria rubra.
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- Formula: C17H24O11
- Molecular Weight: 404.37
11-Methylforsythide is a natural product.
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- Formula: C26H30O14
- Molecular Weight: 566.51
10-O-Caffeoyl deacetyldaphylloside is a Iridoids product that can be isolated from the fruits of Gardenia jasminoides.
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- Formula: C25H32O13
- Molecular Weight: 540.51
10-Hydroxyligstroside is a natural product.
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- Formula: C10H14O3
- Molecular Weight: 182.22
1,6,8-Trideoxyshanzhigenin is a Iridoids product that can be isolated from the herbs of Gardenia jasminoides.
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- Formula: C34H46O19
- Molecular Weight: 758.72
(E)-Aldosecologanin is a Iridoids product that can be isolated from the herbs of Lonicera japonica.
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- Formula: C17H24O12
- Molecular Weight: 420.37
10-Hydroxyoleoside 11-methyl ester is a natural product.
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- Formula: C43H60O22
- Molecular Weight: 928.92
Nudifloside B is a Iridoids product that can be isolated from the stems of Jasminum nudiflorum..
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- Formula: C26H38O12
- Molecular Weight: 542.57
Jasminin is a Iridoids product that can be isolated from the leaves of Jasminum primulinum HEMSL..
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- Formula: C26H38O12
- Molecular Weight: 542.57
Isojasminin is a Iridoids product that can be isolated from the stems of Jasminum nudiflorum.
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- Formula: C26H38O13
- Molecular Weight: 558.57
4''-Hydroxyisojasminin is a Iridoids product that can be isolated from the roots of Jasminum sambac.
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- Formula: C18H28O11
- Molecular Weight: 420.41
7S-O-Methylmorroniside is a natural product.
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- Formula: C21H24N2O4
- Molecular Weight: 368.43
Mitraphylline (Standard) is the analytical standard of Mitraphylline. This product is intended for research and analytical applications. Mitraphylline is the major pentacyclic oxindolic alkaloid presented in Uncaria tomentosa. Mitraphylline inhibits lipopolysaccharide-mediated activation of primary human neutrophils. Mitraphylline exhibits antiproliferative activity in human glioma and neuroblastoma cell lines. Mitraphylline can inhibit interleukin release in vivo.
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- Formula: C16H22O11
- Molecular Weight: 390.34
Secologanoside (Standard) is the analytical standard of Secologanoside. This product is intended for research and analytical applications. Secologanoside is a triterpenoid isolated from Poraqueiba sericea, weakly inhibits elastase with an IC50 of 164 μg/mL. Secologanoside is moderate cytotoxic to fibroblasts.
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- Formula: C16H24O11
- Molecular Weight: 392.36
Shanziside (Standard) is the analytical standard of Shanziside. This product is intended for research and analytical applications. Shanziside is a iridoid glucoside isolated from Phlomis tuberosa L.
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- Formula: C21H32O15
- Molecular Weight: 524.47
Melittoside (Standard) is the analytical standard of Melittoside. This product is intended for research and analytical applications.
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- Formula: C15H24O9
- Molecular Weight: 348.35
Ajugol (Standard) is the analytical standard of Ajugol (HY-N0914). This product is intended for research and analytical applications. Ajugol is an orally active iridoid glycoside found in the traditional Chinese medicine Leonurus japonicus. Ajugol is an autophagy activator. Ajugol activates TFEB-mediated autophagy and lysosomal biogenesis. Ajugol also has anti-inflammatory effects. Ajugol has great potential in the research of asthma, non-alcoholic fatty liver disease (NAFLD), and osteoarthritis.
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- Formula: C22H28O11
- Molecular Weight: 468.45
Caprarioside is an iridoid glycoside that can be isolated from Capraria biflora L..
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- Formula: C9H12O4
- Molecular Weight: 184.19
Aucubigenin, the aglycone of the iridoid glycoside aucubin, has been characterized through X-ray diffraction analysis. Its crystal structure reveals monoclinic symmetry with specific conformations adopted by its cyclopentane and pyran rings. The study also determined the absolute configurations of both aucubin and aucubigenin. Significant O-H O hydrogen bonding interactions were observed in the crystal lattices of both compounds, highlighting their structural stability and potential for intermolecular interactions.
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