Search Result
Results for "
aglycone
" in MedChemExpress (MCE) Product Catalog:
| Cat. No. |
Product Name |
Target |
Research Areas |
Chemical Structure |
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- HY-N2072
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Transcrocetin; trans-Crocetin
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iGluR
Apoptosis
COX
p38 MAPK
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Neurological Disease
Inflammation/Immunology
Cancer
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Crocetin (Transcrocetin) is an aglycone of crocin. Crocetin is an orally active and brain-penetrant. Crocetin shows strong NMDA receptor affinity and channel opening activity. Crocetin can downregulate the proinflammatory cytokines and COX-2 exoression. Crocetin can inhibit apoptosis and activation of MAPK. Crocetin can delay delays brain and body aging. Crocetin can be used for the researches of cancer, neurological disease and inflammation, such as cervical cancer and ischemia .
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- HY-N6833
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Others
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Metabolic Disease
Inflammation/Immunology
Cancer
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Rebaudioside M, a glycoside of the ent-kaurene diterpenoid aglycone, is a non-calorie sweetener isolated from Stevia rebaudiana. Rebaudioside M has antidiabetics, antihypertension, anti-inflammatory, antioxidant, anticaries and anticancer benefits. Rebaudioside M is more than 350 times sweeter than sucrose. Rebaudioside M can be used in food and beverage .
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- HY-13250
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Drug Derivative
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Cancer
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Silvestrol aglycone is a Silvestrol analogue, inhibits protein translation initiation in cancer cells, with EC50s of 10 and 200 nM for myc-LUC and tub-LUC luciferase reporter protein translation, respectively. Anti-cancer activity .
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- HY-W008226
-
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2,4,6-trihydroxyacetophenone; 1-(2,4,6-Trihydroxyphenyl)ethanone
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Cytochrome P450
Bacterial
Antibiotic
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Infection
Metabolic Disease
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Phloracetophenone (2,4,6-trihydroxyacetophenone) is the aglycone part of acetophenone glycoside obtained from Curcuma comosa Roxb, with cholesterol-lowering activity. Phloracetophenone enhances cholesterol 7α-hydroxylase (CYP7A1) activity . Phloracetophenone stimulats bile secretion mediated through Mrp2 .
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- HY-N2736
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Beta-lactamase
COX
Interleukin Related
Bacterial
JNK
ERK
p38 MAPK
STAT
Apoptosis
NO Synthase
Nuclear Factor of activated T Cells (NFAT)
Lactate Dehydrogenase
Reactive Oxygen Species (ROS)
SOD
Akt
Caspase
Bcl-2 Family
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Infection
Neurological Disease
Inflammation/Immunology
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3′,4′,7-Trihydroxyflavone is an orally active inhibitor of OXA-48 (IC50 = 1.89 μM) and COX-1 (IC50 = 36.37 μM). 3′,4′,7-Trihydroxyflavone exhibits antioxidant and anti-inflammatory properties, inhibiting the release of inflammatory cytokines such as IL-6, IL-8, and TNF-α. 3′,4′,7-Trihydroxyflavone inhibits H2O2-induced neuronal apoptosis and ROS accumulation, and exerts anti-neuroinflammatory effects by suppressing the JNK-STAT1 pathway. 3′,4′,7-Trihydroxyflavone exhibits antimicrobial and antibiotic-modifying activities against multidrug-resistant Gram-negative enteric bacteria. 3′,4′,7-Trihydroxyflavone inhibits RANKL-induced osteoclast formation via NFATc1. 3′,4′,7-Trihydroxyflavone activates the CREB-BDNF axis and restores scopolamine (HY-N0296)-induced memory deficits in mice .
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- HY-E70130
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Others
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Others
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Snailase, Snail gastrointestinal is an enzyme mixture composed of more than 20 enzymes, which is often used for enzymatic hydrolysis of purified flavonoid glycosides. Snailase can be obtained from the digestive tract and includes cellulase, sucrase, hemicellulase, pectinase, polygalacturonase, protease, etc .
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- HY-N0467
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Dulcoside B
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Endogenous Metabolite
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Neurological Disease
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Rebaudioside C (Dulcoside B) is an orally effective natural sweetener that cannot pass the blood-brain barrier and selectively binds to human sweet taste receptors (TAS1R2/TAS1R3). The sweetness of Rebaudioside C is about 20-30 times that of sucrose, and its sweetness activity depends on the C-16/C-17 double bond structure and specific aglycones. The glycoside structure in the Rebaudioside C molecule can bind to the sweet taste receptor, activate the taste signal transduction pathway, and produce sweetness perception .
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- HY-119323
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Fluorescent Dye
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Others
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7-Azido-4-methylcoumarin is a selective coumarin-based fluorescent probe for hydrogen sulfide (H2S). In the presence of H2S, the aromatic azido group of 7-Azido-4-methylcoumarin is selectively reduced to produce the fluorescently active 7-amino-4-methylcoumarin (AMC). 7-Azido-4-methylcoumarin binds to the coumarin/phenol-binding site of BSA, the aglycone-binding site of UGT1A6, and the substrate-binding site of SULT1A1, respectively. 7-Azido-4-methylcoumarin retains its fluorescent properties after covalent binding, acts as a fluorescent H2S probe, and does not react with cysteine, homocysteine or glutathione (Ex/Em = 340/445 nm) .
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- HY-121309
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Adriamycin aglycone; Adriamycinone
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NF-κB
TNF Receptor
Interleukin Related
Drug Derivative
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Inflammation/Immunology
Cancer
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Doxorubicinone (Adriamycin aglycone) is the aglycone of the antibiotic Doxorubicin (HY-15142A), i.e., its sugar-free parent nucleus structure. Doxorubicinone does not induce DNA damage or bind to RelA, but still downregulates the expression of pro-inflammatory cytokines (such as TNF, IL-12, etc.) regulated by the NF-κB pathway. Doxorubicinone can be used in sepsis-related research .
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- HY-N6073
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- HY-135115
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3,4-DHPEA-EA
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α-synuclein
HDAC
Adrenergic Receptor
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Inflammation/Immunology
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Oleuropein Aglycone (3,4-DHPEA-EA) is a polyphenol and the aglycone form of oleuropein (HY-N0292), formed by enzymatic, acidic or acetylated hydrolysis of oleuropein. Dietary intake of oleuropein Aglycone (50 mg/kg diet) increases the number of neuronal autophagic vesicles, reverses cognitive deficits in the TgCRND8 transgenic mouse model of Alzheimer's disease, and reduces the levels of histone deacetylase 2 (HDAC2) in the cortex and hippocampus. Oleuropein Aglycone increases urinary norepinephrine, interscapular brown adipose tissue epinephrine, and UCP1 protein levels, and reduced plasma leptin levels and total abdominal adipose tissue weight in a rat model of high-fat diet-induced obesity. Oleuropein Aglycone also reduced lung neutrophil infiltration, lipid peroxidation, and IL-1β levels in a mouse model of carrageenan-induced pleurisy.
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- HY-N0798
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20(R)-APPT
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Others
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Others
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20(R)-Protopanaxatriol is a natural aglycone of ginsenosides Re, Rf, Rg1, Rg2 and Rh.
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- HY-N3434
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Drug Derivative
Reactive Oxygen Species (ROS)
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Cancer
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Kaempferol 3,7,4'-trimethyl ether is an O-methylated kaempferol flavonol aglycone distributed in Siparuna gigantotepala, Aframomum arundinaceum and Siparuna guianensis. Kaempferol 3,7,4'-trimethyl ether exhibits antioxidant activity. Kaempferol 3,7,4'-trimethyl ether suppresses the proliferation of leukemia cells and exerts selective cytotoxicity against both drug‑sensitive and multi‑factorial drug‑resistant cancer cells. Kaempferol 3,7,4'-trimethyl ether can be applied in the research of multidrug‑resistant cancers .
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- HY-106048
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5-Hydroxy-1H-imidazole-4-carboxamide; FF-10501
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Nucleoside Antimetabolite/Analog
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Others
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Bredinin aglycone (5-Hydroxy-1H-imidazole-4-carboxamide) is a purine nucleotide analogue. Bredinin aglycone can be used to examine the efficiency of catalysts for the preparation of purine nucleotide analogues .
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- HY-N1375
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Others
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Cancer
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Qingyanshengenin (NSC 379666; compound 2), a pregnane glycoside, is a C21 steroidal aglycone isolated from the root of Cynanchumot ophyllum (Asclepiadaceae). Qingyanshengenin has anti-cancer activity .
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- HY-N6833R
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Reference Standards
Others
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Others
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Rebaudioside M (Standard) is the analytical standard of Rebaudioside M. This product is intended for research and analytical applications. Rebaudioside M, a glycoside of the ent-kaurene diterpenoid aglycone, is a non-calorie sweetener isolated from Stevia rebaudiana. Rebaudioside M is more than 350 times sweeter than sucrose .
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- HY-126941
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ERK
MMP
Reactive Oxygen Species (ROS)
NF-κB
p38 MAPK
NOD-like Receptor (NLR)
TRP Channel
TNF Receptor
Interleukin Related
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Infection
Neurological Disease
Inflammation/Immunology
Endocrinology
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Hecogenin acetate is an orally active steroid saponin aglycone with extensive biological activities. Hecogenin acetate inhibits the phosphorylation of NF-κB and p38 MAPK signaling pathways, antagonizes TRPA1/TRPM8 channels, inhibits the production of pro-inflammatory cytokines, and has anti-inflammatory and analgesic effects. Hecogenin acetate inhibits the production of ROS and the activation of NLRP3 inflammasome; downregulates the expression of MMP-2, and has neuroprotective and anti-tumor activities. Hecogenin acetate enhances gastric mucosal defense and promotes ulcer healing. Hecogenin acetate can be used in combination with certain antibiotics to regulate bacterial efflux pumps and restore antibiotic sensitivity .
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- HY-N2093
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Vicine
2 Publications Verification
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Drug Metabolite
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Cardiovascular Disease
Metabolic Disease
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Vicine, an alkaloid glycoside found mainly in fava beans, is toxic in individuals who have a hereditary loss of the enzyme glucose-6-phosphate dehydrogenase and may cause haemolytic anaemia.Vicine is an inactive compound that is hydrolysed by the intestinal microflora to a highly reactive free radical generating compound, the aglycone divicine when Vicine enters the body through food .
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- HY-N2072R
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Transcrocetin (Standard); trans-Crocetin (Standard)
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iGluR
Reference Standards
Apoptosis
COX
p38 MAPK
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Neurological Disease
Inflammation/Immunology
Cancer
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Crocetin (Standard) (TransCrocetin (Standard) ) is an aglycone of crocin. Crocetin (Standard) is orally active and brain-penetrant. Crocetin (Standard) shows strong NMDA receptor affinity and channel opening activity. Crocetin (Standard) can downregulate the proinflammatory cytokines and COX-2 exoression. Crocetin (Standard) can inhibit apoptosis and activation of MAPK. Crocetin (Standard) can delay delays brain and body aging. Crocetin (Standard) can be used for the researches of cancer, neurological disease and inflammation, such as cervical cancer and ischemia .
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- HY-N7497
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Others
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Others
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Protoescigenin is the main aglycone of horse chestnut saponin mixture known as escin. Protoescigenin is selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene .
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- HY-135738
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Drug Intermediate
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Others
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Convicine is a pyrimidine glycoside. Convicine, as well as Vicine, is the precursor of the aglycones Divicine and Isouramil. Convicine is the main factors of favism, which is a genetic condition leading to severe hemolysis after faba bean ingestion. Convicine can be isolated from the faba bean .
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- HY-121309R
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Adriamycin aglycone (Standard); Adriamycinone (Standard)
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Reference Standards
NF-κB
TNF Receptor
Interleukin Related
Drug Derivative
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Inflammation/Immunology
Cancer
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Doxorubicinone (Adriamycin aglycone) (Standard) is the analytical standard of Doxorubicinone. This product is intended for research and analytical applications. Doxorubicinone is the aglycone of the antibiotic Doxorubicin (HY-15142A), i.e., its sugar-free parent nucleus structure. Doxorubicinone does not induce DNA damage or bind to RelA, but still downregulates the expression of pro-inflammatory cytokines (such as TNF, IL-12, etc.) regulated by the NF-κB pathway. Doxorubicinone can be used in sepsis-related research.
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- HY-121125
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Others
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Others
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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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- HY-N16529
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Glycosidase
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Metabolic Disease
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1,6,8-Trihydroxy-2,7-dimethoxy-3-methylanthraquinone (Compound 2) is a anthraquinone aglycone found in Cassia obtusefolia. 1,6,8-Trihydroxy-2,7-dimethoxy-3-methylanthraquinone can inhibit α-glucosidase with an IC50 of 120.65 μg/mL. 1,6,8-Trihydroxy-2,7-dimethoxy-3-methylanthraquinone can be used for the research of diabetes .
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- HY-137970
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A-83543D aglycone
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Parasite
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Infection
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Spinosyn D aglycone is an aglycone form of the insecticide Spinosyn D (HY-125326). Unlike spinosyn D, spinosyn D aglycone is not lethal to H. virescens (tobacco budworm) neonate larvae (LC50=>64 ppm).
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- HY-156133
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Drug Derivative
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Others
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Dihydrospinosyn A aglycone (compound 2) is a derivative of spinosyn A aglycone with a hydrolyzed C9- and C17-glycosidic bond.
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- HY-N11996
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NO Synthase
NF-κB
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Others
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Aloenin aglycone (compound 13) is an NF-κB inhibitor that can be isolated from aloe exudate. Aloenin aglycone inhibits TNFα-induced NF-κB transcriptional activity (IC50: 18.7 μM). Aloenin aglycone (10 μM) also reduced inducible nitric oxide synthase (iNOS) and intercellular adhesion molecule 1 (ICAM-1) gene expression after treatment of HepG2 cells with 10 ng/mL TNFα .
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- HY-155252
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(-)-Spinosyn A aglycon
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Insecticide
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Others
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Spinosyn A aglycone ((-)-Spinosyn A aglycon) is an aglycone form of the insecticide Spinosyn A (HY-B0767). Spinosyn A aglycone is an acid degradation product produced by hydrolysis of both saccharide groups on spinosyn A .
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- HY-13250B
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Drug Isomer
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Cancer
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Silvestrol aglycone enantiomer is a cyclopenta benzofuran core phenol .
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- HY-N10257
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- HY-106048R
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5-Hydroxy-1H-imidazole-4-carboxamide (Standard); FF-10501 (Standard)
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Reference Standards
Nucleoside Antimetabolite/Analog
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Others
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Bredinin aglycone (Standard) is the analytical standard of Bredinin aglycone. This product is intended for research and analytical applications. Bredinin aglycone (5-Hydroxy-1H-imidazole-4-carboxamide) is a purine nucleotide analogue. Bredinin aglycone can be used to examine the efficiency of catalysts for the preparation of purine nucleotide analogues[1].
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- HY-160121
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Patrinoside aglycone
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Apoptosis
NO Synthase
TNF Receptor
Interleukin Related
PGE synthase
COX
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Inflammation/Immunology
Cancer
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Patrinoside aglucone (Compound 8) is an iridoid glucoside that can be isolated from the Valeriana tuberosa. Patrinoside aglucone has potent anticancer activity with G2/M phase tumor cell cycle arrest and apoptosis induction. Patrinoside aglucone also significantly inhibits the proliferation of cancer stem cells (such as MDA-MB-231 and U-251MG cells). Patrinoside aglucone has great anti-inflammatory activity by inhibiting NO release (IC50: 43.44 μM) and significantly reduces the level of TNF-α, IL-1β, IL-6, PGE2 and COX-2 .
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- HY-180463
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Drug Metabolite
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Others
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Rubradirin aglycone (Compound 7) is an aglycone of Rubradirin and can be obtained by mild acid hydrolysis of Rubradirin .
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- HY-141441
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Bacterial
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Infection
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Novobiocic acid is an aglycone form of the antibiotic Novobiocin (HY-B0425).
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- HY-N7954
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Others
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Neurological Disease
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Neopanaxadiol, an aglycone of protopanaxadiol type ginsenosides, has the potential for Alzheimer's disease research .
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- HY-N12749
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- HY-N9816
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Drug Metabolite
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Others
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Plucheoside B (Compound 7b) aglycone is an aglycone of plucheoside B with an absolute configuration of 3R, 4R, and 9R that can be isolated from the leaves of Croton cascarilloides Räuschel .
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- HY-N3932
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Others
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Others
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Garjasmin (compound 1) is a kind of iridoid aglycone. Garjasmin can be isolated from the flowers of Gardenia jasminoides Ellis .
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- HY-N3691
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-
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- HY-N13220
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Others
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Endocrinology
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Soybean Extract is a soybean extract, and its components include: Isoflavone. Soybean Extract has an increased content of isoflavone aglycones after biotransformation, which is an estrogen-like bioactive compound with effective type I collagen enhancement. .
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- HY-N0798R
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20(R)-APPT (Standard)
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Reference Standards
Others
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Others
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20(R)-Protopanaxatriol (Standard) is the analytical standard of 20(R)-Protopanaxatriol. This product is intended for research and analytical applications. 20(R)-Protopanaxatriol is a natural aglycone of ginsenosides Re, Rf, Rg1, Rg2 and Rh.
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- HY-137968
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Parasite
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Infection
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Avermectin B1a aglycon is an aglycone derivative of Avermectin B1a (HY-15308), an antiparasitic agent that paralyzes nematodes. Avermectin B1a aglycon hyperpolarizes P. crassipes muscle fibers, with a minimum effective concentration of 0.1 μM .
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- HY-N11975
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Others
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Others
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Glycyrrhizin-6′,6′′-dimethylester (compound 23) is a licorice saponin isolated from licorice root. Glycyrrhizin-6′,6′′-dimethylester can participate as an aglycone in the generation of methyl glucuronate, producing similar threshold sweetness, licorice, and bitterness .
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- HY-N6073R
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Reference Standards
Apoptosis
HSV
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Infection
Metabolic Disease
Inflammation/Immunology
Cancer
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Soyasapogenol A (Standard) is the analytical standard of Soyasapogenol A (HY-N6073). This product is intended for research and analytical applications. Soyasapogenol A is a triterpenoid aglycone of soyasaponins. Soyasapogenol A has activities such as anti-inflammation, anti-cancer, hepatoprotection and anti-HSV-1. Soyasapogenol A can be used in the research of tumors and immune inflammatory diseases .
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- HY-N11976
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Others
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Others
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Glycyrrhizin-6′′-methylester (compound 22) is a glycyrrhizin that can be isolated from licorice root. Glycyrrhizin-6′′-methylester can participate as an aglycone in the formation of methyl glucuronate, producing a sweet and licorice taste, but no bitterness. This reveals the importance of the free carboxyl group on the glycoside cone-bound glucuronic acid for natural sweetness and licorice taste .
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- HY-N7497R
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Reference Standards
Others
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Others
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Protoescigenin (Standard) is the analytical standard of Protoescigenin. This product is intended for research and analytical applications. Protoescigenin is the main aglycone of horse chestnut saponin mixture known as escin. Protoescigenin is selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene .
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- HY-129236
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Na+/K+ ATPase
Apoptosis
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Cancer
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Hellebrin is a bufadienolide compound extracted from plants that can inhibit tumor cell growth. Hellebrigenin shows potential in overcoming cancer cells' resistance to apoptosis stimuli and has also demonstrated anti-proliferation effects in multidrug-resistant (MDR) cancer cell models. Hellebrin can act on Na+/K+-ATPase to regulate intracellular signaling pathways .
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- HY-125550
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- HY-N12923
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Others
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Others
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IB-96212 aglycone (Compound 2) is the hydrolyzate of IB-96212 (HY-161239A) .
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- HY-N18227
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Others
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Others
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12β-Hydroxycimigenol (Compound 1a) is a cycloartane-type triterpene aglycone that can be isolated from the aerial parts of Cimicifuga simplex .
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- HY-N18246
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Others
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Others
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Glaucogenin B is a steroid aglycone. Glaucogenin B can be found in the dried root of Cynanchum glaucescens Hand-Mazz (Asclepiadaceae) .
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- HY-N14147
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- HY-121416
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Others
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Others
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Jurubidine is a novel and potent cyclised aglycone .
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- HY-N18323
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Others
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Others
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Toosenoside A (Compound 5) is a glycoside with a rare naturally occurring aglycone. Toosenoside A can be isolated from the fruits of Melia toosendan .
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- HY-N16989
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Others
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Others
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Neochlorogenin is a spirostan-type steroidal saponin aglycone that can be naturally extracted from the dried leaves of Solanum torvum Sw. (Indian nightshade) .
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- HY-E70104A
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- HY-N11738
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Others
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Cancer
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Aspalathin is a C-glycosyldihydrochalcone flavonoid and antioxidant.Aspalathin functions as an antimutagen.Aspalathin can be absorbed by pig intestine as a C-glycoside, and can also be cleaved into its aglycone and sugar moiety.Aspalathin is found in Aspalathus linearis (rooibos) .
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- HY-P2872A
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Endogenous Metabolite
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Metabolic Disease
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Thioglucosidase, Sinapis alba (white mustard) seed (EC 3.2.1.147) hydrolyzes the S-glucosidic bond of a glucosinolate substrate to form an unstable aglycone that rearranges with the loss of sulfate primarily to the isothiocyanate, though thiocyanates and nitriles are also formed.
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- HY-N17882
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Bupleuroside III
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Drug Derivative
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Others
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Hydroxysaikosaponin A (Bupleuroside III) is the acid hydrolysis degradation product of Saikosaponin A (HY-N0246) .
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- HY-N18046
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Drug Derivative
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Cancer
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Otophylloside Q is a pregnane glycoside (C-21 steroidal glycoside) isolated from the roots of Cynanchum otophyllum. With caudatin (HY-N1983), an anticancer agent, as its aglycone, Otophylloside Q contains a sugar chain composed of cymarose, oleandrose and glucose units .
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- HY-N18019
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Drug Metabolite
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Metabolic Disease
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Tetrahydro bellidifolin (Compound 1a) is the aglycone obtained from the hydrolysis of Tetrahydroswertianolin (HY-N18018) by β-glucosidase. Tetrahydro bellidifolin exhibits significant hepatoprotective activity and reduce serum ALT levels. Tetrahydro bellidifolin can be used for the research of liver injury .
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- HY-E71248
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Biochemical Assay Reagents
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Others
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α-Rhamnosidase 78A, Streptomyces avermitilis (EC 3.2.1.40) is a thermostable Alpha-L-Rhamnosidase (Naringinase, RhamA) that catalyzes the cleavage of the bond between terminal L (+)-rhamnose and the aglycone of rhamnose-containing glycosides. The enzyme is very active on naringin but has also substantial activity with hesperidin as substrate.
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- HY-N17637
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Drug Intermediate
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Others
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Machaeric acid is a triterpenoid and triterpene sapogenin, which serves as the aglycone of Senegaloside A; it can be isolated from the seeds of Caragana microphylla Lam. and Acacia senegal(Mimosaceae). Machaeric acid exhibits remarkable biosafety, and even at concentrations as high as 200 μM, it does not induce cytotoxicity or reduce the viability of H4IIE rat hepatoma cells .
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- HY-W750858
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Drug Derivative
Herbicide
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Others
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DIBOA-Glucoside is a glycoside derivative that can be found in cereal crops like rye, wheat, and maize. DIBOA-Glucoside is a stable, less toxic glucoside form of DIBOA. DIBOA-Glucoside, upon pest or pathogen attack, is hydrolyzed by an enzyme, releasing the toxic aglycone DIBOA and glucose, thereby deterring insects and suppressing weeds through an allelopathic effect .
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- HY-N17763
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Others
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Inflammation/Immunology
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Styraxlignolide G is a furanofuran-type lignan compound that can be isolated from the stem bark of Styrax japonica. Styraxlignolide G exhibits very weak DPPH free radical scavenging activity, while its hydrolyzed aglycone molecule possesses antioxidant activity (IC50=186.7 μM) and is involved in antioxidant-related regulation in the body. Styraxlignolide G can be used in the study of inflammatory diseases.
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- HY-E71188
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Biochemical Assay Reagents
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Others
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13-Deoxydaunorubicin hydroxylase (EC 1.14.13.181) shows broad substrate specificity for structures based on an anthracycline aglycone, but have a strong preference for 4-methoxy anthracycline intermediates (13-Deoxydaunorubicin and 13-dihydrodaunorubicin) over their 4-hydroxy analogues (13-deoxycarminomycin and 13-dihydrocarminomycin) , as well as a preference for substrates hydroxylated at the C-13 rather than the C-14 position.
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- HY-N18040
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Drug Derivative
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Others
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Esculentoside F is a triterpene saponin found in the root of Phytolacca acinosa Roxb .
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- HY-N19769
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Others
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Others
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Phenylmethyl O-β-D-glucopyranosyl-(1→3)-O-β-D-glucopyranoside (Compound 10) is a triglycoside compound. Phenylmethyl O-β-D-glucopyranosyl-(1→3)-O-β-D-glucopyranoside is isolated from the whole plant of sesame (Sesamum indicum) .
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- HY-N18021
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Others
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Others
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3-O-[α-L-Arabinopyranosyl]-30-norolean-12,20(29)-dien-28-oic acid (Compound 1) is a triterpenoid glucoside found in Stauntonia brachyanthera Hand-Mazz .
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- HY-N17505
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Others
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Others
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(1S,2R,4S)-Borneol β-D-glucopyranoside (Compound 10) is a monoterpenoid glucoside.(1S,2R,4S)-Borneol β-D-glucopyranoside can be found in the leaf of Thymus vulgaris .
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- HY-N19936
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Drug Derivative
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Cancer
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Qinyangshengenin-3-O-β-D-digitoxopyranoside is a C21 steroidal glycoside that can be found in the whole herb of Prunella vulgaris Linn. Qinyangshengenin-3-O-β-D-digitoxopyranoside can be used for research of leukemia and lung cancer .
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| Cat. No. |
Product Name |
Category |
Target |
Chemical Structure |
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- HY-N2072
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-
-
- HY-N6833
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-
-
- HY-W008226
-
-
-
- HY-N2736
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Flavonoids
Classification of Application Fields
Flavones
Leguminosae
Other Diseases
Phenols
Polyphenols
Plants
Vicia faba L.
Disease Research Fields
Source Classification
|
Beta-lactamase
COX
Interleukin Related
Bacterial
JNK
ERK
p38 MAPK
STAT
Apoptosis
NO Synthase
Nuclear Factor of activated T Cells (NFAT)
Lactate Dehydrogenase
Reactive Oxygen Species (ROS)
SOD
Akt
Caspase
Bcl-2 Family
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3′,4′,7-Trihydroxyflavone is an orally active inhibitor of OXA-48 (IC50 = 1.89 μM) and COX-1 (IC50 = 36.37 μM). 3′,4′,7-Trihydroxyflavone exhibits antioxidant and anti-inflammatory properties, inhibiting the release of inflammatory cytokines such as IL-6, IL-8, and TNF-α. 3′,4′,7-Trihydroxyflavone inhibits H2O2-induced neuronal apoptosis and ROS accumulation, and exerts anti-neuroinflammatory effects by suppressing the JNK-STAT1 pathway. 3′,4′,7-Trihydroxyflavone exhibits antimicrobial and antibiotic-modifying activities against multidrug-resistant Gram-negative enteric bacteria. 3′,4′,7-Trihydroxyflavone inhibits RANKL-induced osteoclast formation via NFATc1. 3′,4′,7-Trihydroxyflavone activates the CREB-BDNF axis and restores scopolamine (HY-N0296)-induced memory deficits in mice .
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- HY-N0467
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- HY-121309
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-
-
- HY-N6073
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-
-
- HY-N0798
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-
-
- HY-N3434
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-
-
- HY-106048
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-
-
- HY-N1375
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-
-
- HY-N6833R
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-
-
- HY-126941
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-
-
- HY-N2093
-
-
-
- HY-N2072R
-
-
-
- HY-N7497
-
-
-
- HY-135738
-
-
-
- HY-121309R
-
-
-
- HY-121125
-
-
-
- HY-N16529
-
-
-
- HY-N11996
-
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Liliaceae
Phenols
Polyphenols
Aloe vera (L.) Burm. f.
Plants
Source Classification
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NO Synthase
NF-κB
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Aloenin aglycone (compound 13) is an NF-κB inhibitor that can be isolated from aloe exudate. Aloenin aglycone inhibits TNFα-induced NF-κB transcriptional activity (IC50: 18.7 μM). Aloenin aglycone (10 μM) also reduced inducible nitric oxide synthase (iNOS) and intercellular adhesion molecule 1 (ICAM-1) gene expression after treatment of HepG2 cells with 10 ng/mL TNFα .
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-
-
- HY-N10257
-
-
-
- HY-106048R
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-
-
- HY-160121
-
-
-
- HY-N7954
-
-
-
- HY-N12749
-
-
-
- HY-N9816
-
-
-
- HY-N3932
-
-
-
- HY-N3691
-
-
-
- HY-N0798R
-
-
-
- HY-N11975
-
-
-
- HY-N6073R
-
-
-
- HY-N11976
-
|
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Glycyrrhiza glabra Linn.
Leguminosae
Ketones, Aldehydes, Acids
Plants
Source Classification
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Others
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Glycyrrhizin-6′′-methylester (compound 22) is a glycyrrhizin that can be isolated from licorice root. Glycyrrhizin-6′′-methylester can participate as an aglycone in the formation of methyl glucuronate, producing a sweet and licorice taste, but no bitterness. This reveals the importance of the free carboxyl group on the glycoside cone-bound glucuronic acid for natural sweetness and licorice taste .
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-
-
- HY-N7497R
-
|
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Triterpenes
other families
Terpenoids
Plants
Source Classification
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Reference Standards
Others
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Protoescigenin (Standard) is the analytical standard of Protoescigenin. This product is intended for research and analytical applications. Protoescigenin is the main aglycone of horse chestnut saponin mixture known as escin. Protoescigenin is selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene .
|
-
-
- HY-N12923
-
-
-
- HY-N18227
-
-
-
- HY-N18246
-
-
-
- HY-N14147
-
-
-
- HY-121416
-
-
-
- HY-N18323
-
-
-
- HY-N16989
-
-
-
- HY-N11738
-
-
-
- HY-N17882
-
-
-
- HY-N18046
-
-
-
- HY-N18019
-
-
-
- HY-N17637
-
-
-
- HY-W750858
-
-
-
- HY-N17763
-
-
-
- HY-N18040
-
-
-
- HY-N19769
-
-
- HY-N18021
-
-
- HY-N17505
-
-
- HY-N19936
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-
| Cat. No. |
Product Name |
|
Classification |
-
- HY-119323
-
|
|
|
Azide
Labeling and Fluorescence Imaging
|
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7-Azido-4-methylcoumarin is a selective coumarin-based fluorescent probe for hydrogen sulfide (H2S). In the presence of H2S, the aromatic azido group of 7-Azido-4-methylcoumarin is selectively reduced to produce the fluorescently active 7-amino-4-methylcoumarin (AMC). 7-Azido-4-methylcoumarin binds to the coumarin/phenol-binding site of BSA, the aglycone-binding site of UGT1A6, and the substrate-binding site of SULT1A1, respectively. 7-Azido-4-methylcoumarin retains its fluorescent properties after covalent binding, acts as a fluorescent H2S probe, and does not react with cysteine, homocysteine or glutathione (Ex/Em = 340/445 nm) .
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