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| Product | Description | |
|---|---|---|
| Urolithin A | ?97% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Urolithin A | Urolithin A, a gut-microbial metabolite of ellagic acid, exerts anti-inflammatory, antiproliferative, and antioxidant properties. Urolithin A induces autophagy and apoptosis , suppresses cell cycle progression, and inhibits DNA synthesis [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 1143-70-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100599. |  |
| Urolithin A | Urolithin A Inhibitor. Uses: Scientific use. Product Category: T7174. CAS No. 1143-70-0. |  |
| Urolithin A | Urolithin A is a major metabolite of ellagitannin and exhibits anti-inflammatory and antioxidant properties. Group: Biochemicals. Alternative Names: 3,8-Hydroxydibenzo-α-pyrone; 3,8-Dihydroxyurolithin; 2,7-Dihydroxy-3,4-benzocoumarin; δ-Lactone 2,4,4-Trihydroxy-2-biphenylcarboxylic Acid. Grades: Highly Purified. CAS No. 1143-70-0. Pack Sizes: 50mg. Molecular Formula: C??H?O?. US Biological Life Sciences. |  Worldwide |
| Urolithin A | Urolithin A is a urolithin, a type of microflora human metabolite of dietary ellagic acid derivatives, such as ellagitannins.During intestinal metabolism by bacteria, ellagitannins and punicalagins are converted to urolithins, which have unknown biological activity in vivo.Urolithin A glucuronide is found in plasma at low concentrations. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Uro-A;pyran-6-one.html >3,8-Dihydroxy-6H-dibenzo |  |
| Urolithin A 8-Methyl Ether | Urolithin A 8-Methyl Ether. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3-Hydroxy-8-methoxy-6H-benzo[c]chromen-6-one. Appearance: Light Beige to Very Dark Orange Solid. CAS No. 35233-17-1. Molecular formula: C14H10O4. Mole weight: 242.23. Purity: 0.98. Product ID: ACM35233171. Alfa Chemistry ISO 9001:2015 Certified. | |
| 2-Bromo-4,5-dimethoxybenzoic Acid 2,3-Dimethoxyphenyl Ester | 2-Bromo-4,5-dimethoxybenzoic Acid 2,3-Dimethoxyphenyl Ester is an intermediate in the synthesis of Urolithin D (U847020) used in biological studies to evaluate DNA gyrase inhibitory activity of ellagic acid derivatives. Group: Biochemicals. Grades: Highly Purified. CAS No. 146776-38-7. Pack Sizes: 50mg, 100mg. Molecular Formula: C17H17BrO6. US Biological Life Sciences. | Worldwide |
| 2-Hydroxy-4-methoxybenzaldehyde | 2-hydroxy-4-methoxybenzaldehyde is a potent tyrosinase inhibitor [1]. 2-Hydroxy-4-methoxybenzaldehyde, an isomer of Vanillin, could be used to synthesis Urolithin M7 [2]. Uses: Scientific research. Group: Natural products. CAS No. 673-22-3. Pack Sizes: 10 mM * 1 mL; 1 g. Product ID: HY-N0445. | |
| Dorsomorphin | Dorsomorphin (Compound C) is a selective and ATP-competitive AMPK inhibitor ( K i =109 nM in the absence of AMP). Dorsomorphin (BML-275) selectively inhibits BMP type I receptors ALK2 , ALK3 , and ALK6. Dorsomorphin can reverse autophagy activation and anti-inflammatory effect of Urolithin A (HY-100599) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Compound C; BML-275. CAS No. 866405-64-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13418A. | |
| Dorsomorphin dihydrochloride | Dorsomorphin (Compound C) dihydrochloride is a potent, selective and ATP-competitive AMPK inhibitor, with a K i of 109 nM. Dorsomorphin dihydrochloride inhibits BMP pathway by targeting the type I receptors ALK2 , ALK3 , and ALK6. Dorsomorphin dihydrochloride can reverse autophagy activation and anti-inflammatory effect of Urolithin A (HY-100599). Uses: Scientific research. Group: Signaling pathways. Alternative Names: Compound C dihydrochloride; BML-275 dihydrochloride. CAS No. 1219168-18-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 20 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13418. | |
| Urolithin B | Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK , ERK and Akt 's oxidation, and increases AMPK 's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 1139-83-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-126307. | |
| Urolithin C | Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2]. Uses: Scientific research. Group: Natural products. CAS No. 165393-06-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-135897. | |
| Urolithin C | Urolithin C is a chebulic ellagitannins metabolite with antioxidant activity. Synonyms: 6H-Dibenzo[b,d]pyran-6-one, 3,8,9-trihydroxy-. CAS No. 165393-06-6. Molecular formula: C13H8O5. Mole weight: 244.2. |  |
| Urolithin D | Urolithin D (3,4,8,9-Tetrahydroxy urolithin) is a colonic metabolite of Ellagitannins and a competitive, reversible, and selective antagonist of the EphA receptor. Urolithin D inhibits EphA2-ephrin-A1 binding with an IC50 of 0.9 ?M. Urolithin D is also a potent antioxidant that scavenges free radicals and repairs oxidized DNA damage. Additionally, Urolithin D suppresses triglyceride accumulation and promotes fatty acid oxidation by activating the AMPK signaling pathway. Urolithin D can be used for research on tumors, metabolic, and inflammatory diseases[1][2][3]. Uses: Scientific research. Group: Natural products. Alternative Names: 3,4,8,9-Tetrahydroxy urolithin. CAS No. 131086-98-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-133178. | |
| Urolithin E | Urolithin E is a biological molecule. Uses: Scientific research. Group: Signaling pathways. CAS No. 1453297-45-4. Pack Sizes: 1 mg; 5 mg. Product ID: HY-W746164. | |
| Urolithin B | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
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