Levothyroxine acyl glucuronide (Thyroxine Acyl-β-D-glucuronide), an endogenous metabolite, is the acyl glucuronide formation of thyroxine (T4)[1].
IC50 Target
Endogenous metabolite[1]
体外研究 (In Vitro)
Levothyroxine acyl glucuronide is a metabolite of T4 glucuronides after hydrolysis with β-glucuronidase[1].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
952.99
Formula
C21H19I4NO10
CAS 号
909880-81-5
中文名称
左旋甲状腺素酰基葡糖苷酸
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Tong Z, et al. In vitro glucuronidation of thyroxine and triiodothyronine by liver microsomes and recombinant human UDP-glucuronosyltransferases. Drug Metab Dispos. 2007 Dec;35(12):2203-10.
Cholesterol glucuronide is an endogenous metabolite of lipid generated in the liver by UDP glucuonyltransferase[1][2].
IC50 Target[1]
Human Endogenous Metabolite
;
体内研究 (In Vivo)
The content of Cholesterol glucuronide in the normal liver is higher than the reported value for plasma (18 μg/g vs 6 μg/mL). Cholesterol glucuronide is synthesized in the liver and some of it enters the bloodstream. Probably the rest goes into the bile, like the other glucuronides[1].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
562.78
Formula
C33H54O7
CAS 号
17435-78-8
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Hara A, et al. Isolation and determination of cholesterol glucuronide in human liver. Lipids. 1982 Aug;17(8):515-8.
[2]. Wade AP. The estimation of cholesterol sulphate and cholesterol glucuronide in plasma. Clin Chim Acta. 1970 Jan;27(1):109-16.
T3 Acyl glucuronide 是一种内源性代谢物,是三碘甲状腺氨酸 (T3) 的酰基葡萄糖醛酸形式。
T3 Acyl glucuronide Chemical Structure
CAS No. : 910907-23-2
规格
是否有货
5 mg
询价
10 mg
询价
25 mg
询价
* Please select Quantity before adding items.
生物活性
T3 Acyl glucuronide, an endogenous metabolite, is the acyl glucuronide formation of triiodothyronine (T3)[1].
IC50 Target
Endogenous metabolite[1]
体外研究 (In Vitro)
T3 Acyl glucuronide is a metabolite of T3 glucuronides after hydrolysis with β-glucuronidase[1].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
827.10
Formula
C21H20I3NO10
CAS 号
910907-23-2
中文名称
T3酰基葡萄糖醛酸
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Tong Z, et al. In vitro glucuronidation of thyroxine and triiodothyronine by liver microsomes and recombinant human UDP-glucuronosyltransferases. Drug Metab Dispos. 2007 Dec;35(12):2203-10.
Tricin 7-O-glucuronide is an Alfalfa (Medicago sativa L.) flavonoid[1].
分子量
506.41
Formula
C23H22O13
CAS 号
32769-02-1
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献
[1]. Li C, et al. Simultaneous determination of seven flavonoids, two phenolic acids and two cholesterines in Tanreqing injection by UHPLC-MS/MS. J Pharm Biomed Anal. 2019 Jan 30;163:105-112.
Apigenin-7-glucuronide could inhibit Matrix Metalloproteinases (MMP) activities, with IC50s of 12.87, 22.39, 17.52, 0.27 μM for MMP-3, MMP-8, MMP-9, MMP-13, respectively.
IC50 & Target
MMP-3
12.87 μM (IC50)
MMP-8
22.39 μM (IC50)
MMP-9
17.52 μM (IC50)
MMP13
0.27 μM (IC50)
体外研究 (In Vitro)
Apigenin-7-Oglucuronide could inhibit Matrix Metalloproteinases (MMP) activities, with IC50s of 12.87, 22.39, 17.52, 0.27 μM for MMP-3, MMP-8, MMP-9, MMP-13, respectively [1]. Scutellarin A also inhibits the migrated capacity of ACHN and 786-O cells in a dose-dependent manner. It is also revealed that after treatment with Scutellarin A (30, 60, and 90 μM) for 24 h, the apoptosis rates in ACHN and 786-O cells are remarkably enhanced dose-dependently when compared to the control groups[2].
Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
446.36
Formula
C21H18O11
CAS 号
29741-09-1
运输条件
Room temperature in continental US; may vary elsewhere.
将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
*以上所有助溶剂都可在 Shanghai Jinpan Biotech Co Ltd 网站选购。
参考文献
[1]. Crascì L, et al. Correlating In Vitro Target-Oriented Screening and Docking: Inhibition of Matrix Metalloproteinases Activities by Flavonoids. Planta Med. 2017 Jul;83(11):901-911.
[2]. Deng W, et al. Scutellarin inhibits human renal cancer cell proliferation and migration via upregulation of PTEN. Biomed Pharmacother. 2018 Nov;107:1505-1513.
Luteolin-3-O-beta-D-glucuronide Chemical Structure
CAS No. : 53527-42-7
规格
价格
是否有货
数量
5 mg
¥1900
In-stock
10 mg
¥3450
In-stock
25 mg
¥6750
In-stock
50 mg
询价
100 mg
询价
* Please select Quantity before adding items.
Luteolin-3-O-beta-D-glucuronide 相关产品
•相关化合物库:
Natural Product Library Plus
Bioactive Compound Library Plus
Immunology/Inflammation Compound Library
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Glycoside Compound Library
Phenols Library
Flavonoids Library
生物活性
Luteolin-3-O-beta-D-glucuronide is a luteolin glucosiduronic acid consisting of luteolin having a beta-D-glucosiduronic acid residue attached at the 3′-position.
分子量
462.36
Formula
C21H18O12
CAS 号
53527-42-7
运输条件
Room temperature in continental US; may vary elsewhere.
Gypsogenin-3-O-glucuronide is a ubiquitous saponin precursor in plants of the genus Gypsophila[1].
体外研究 (In Vitro)
Treatment of suspended G. paniculata cells with gypsogenin 3,O-glucuronide 24 hours before administration of [14C]acetate results in a marked reduction in the incorporation of radioactivity into saponins and their precursors but not into sterols and steryl glucosides[1].
Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
660.83
Formula
C37H56O10
CAS 号
96553-02-5
中文名称
丝石竹皂苷元3-O-Β-D-葡萄糖醛酸甲酯
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. MaxHenry, et al. Effect of gypsogenin 3,O-glucuronide pretreatment of Gypsophila paniculata and Saponaria officinalis cell suspension cultures on the activities of microsomal 2,3-oxidosqualene cycloartenol and amyrin cyclases. Volume 31, Issue 11, 1992, Pages 3855-3859.
[1]. Crascì L, et al. Correlating In Vitro Target-Oriented Screening and Docking: Inhibition of Matrix Metalloproteinases Activities by Flavonoids. Planta Med. 2017 Jul;83(11):901-911.
Miquelianin (Quercetin 3-O-glucuronide) is a metabolite of quercetin and a type of natural flavonoid.
IC50 Target
Human Endogenous Metabolite
;
体外研究 (In Vitro)
Miquelianin shows an antioxidant effect in human plasma. At 50 μM, miquelianin suppresses the consumption of the three antioxidants lycopene, β-carotene and α-tocopherol significantly[1]. In vitro studies indicate that miquelianin is able to reach the central nervous system from the small intestine[2]. Miquelianin significantly reduces the generation of β-amyloid (Aβ) peptides by primary neuron cultures generated from the Tg2576 AD mouse model. It is also capable of interfering with the initial protein-protein interaction of Aβ1–40 and Aβ1–42 that is necessary for the formation of neurotoxic oligomeric Aβ species[3]. Treatment with 0.1 μM miquelianin suppresses ROS generation, cAMP and RAS activation, phosphorylation of ERK1/2 and the expression of HMOX1, MMP2, and MMP9 genes. Miquelianin suppresses invasion of MDA-MB-231 breast cancer cells and MMP-9 induction, and inhibits the binding of [3H]-NA to b2-AR. Miquelianin may function to suppress invasion of breast cancer cells by controlling b2-adrenergic signaling, and may be a dietary chemopreventive factor for stress-related breast cancer[4].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究 (In Vivo)
Miquelianin treatment, compared to vehicle-control treatment, significantly improves AD-type deficits in hippocampal formation basal synaptic transmission and long-term potentiation[3]. A flavonoid fraction obtained from a crude extract of Hypericum perforatum (St. John’s wort) is remarkably active in the forced swimming test. Miquelianin is one of the compound separated from the fraction[5].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
478.36
Formula
C21H18O13
CAS 号
22688-79-5
中文名称
槲皮素-3-O-葡萄糖醛酸苷
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Terao J, e al. Protection by quercetin and quercetin 3-O-beta-D-glucuronide of peroxynitrite-induced antioxidant consumption in human plasma low-density lipoprotein. Free Radic Res. 2001 Dec;35(6):925-31.
[2]. Juergenliemk G, et al. In vitro studies indicate that miquelianin (quercetin 3-O-beta-D-glucuronopyranoside) is able to reach the CNS from the small intestine. Planta Med. 2003 Nov;69(11):1013-7.
[3]. Butterweck V, et al. Flavonoids from Hypericum perforatum show antidepressant activity in the forced swimming test. Planta Med. 2000 Feb;66(1):3-6.
[4]. Yamazaki S, et al. Quercetin-3-O-glucuronide inhibits noradrenaline-promoted invasion of MDA-MB-231 human breast cancer cells by blocking β-adrenergic signaling. Arch Biochem Biophys. 2014 Sep 1;557:18-27.
[5]. Ho L, et al. Identification of brain-targeted bioactive dietary quercetin-3-O-glucuronide as a novel intervention for Alzheimer’s disease. FASEB J. 2013 Feb;27(2):769-81.
Animal Administration [5]
Rats: Miquelianin is administered orally using the gavage techniques. The rats are treated with 0.6 mg/kg miquelianin for 12 days. Antidepressant activity is performed using the Forced Swimming Test[5].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
参考文献
[1]. Terao J, e al. Protection by quercetin and quercetin 3-O-beta-D-glucuronide of peroxynitrite-induced antioxidant consumption in human plasma low-density lipoprotein. Free Radic Res. 2001 Dec;35(6):925-31.
[2]. Juergenliemk G, et al. In vitro studies indicate that miquelianin (quercetin 3-O-beta-D-glucuronopyranoside) is able to reach the CNS from the small intestine. Planta Med. 2003 Nov;69(11):1013-7.
[3]. Butterweck V, et al. Flavonoids from Hypericum perforatum show antidepressant activity in the forced swimming test. Planta Med. 2000 Feb;66(1):3-6.
[4]. Yamazaki S, et al. Quercetin-3-O-glucuronide inhibits noradrenaline-promoted invasion of MDA-MB-231 human breast cancer cells by blocking β-adrenergic signaling. Arch Biochem Biophys. 2014 Sep 1;557:18-27.
[5]. Ho L, et al. Identification of brain-targeted bioactive dietary quercetin-3-O-glucuronide as a novel intervention for Alzheimer’s disease. FASEB J. 2013 Feb;27(2):769-81.
Oroxylin A-7-O-glucuronide (Oroxyloside; Oroxylin A-7-O-β-D-glucuronide) is a flavonoid glucuronide isolated from the dried root of Scutellaria baicalensis, with prolyl oligopeptidase (POP) inhibitory activity[1].
分子量
460.39
Formula
C22H20O11
CAS 号
36948-76-2
运输条件
Room temperature in continental US; may vary elsewhere.