| Cat.No. | Name | Information |
|---|---|---|
| M39330 | N-tert-Butoxycarbonyl-D-alanine | N-tert-Butoxycarbonyl-D-alanine is an alanine derivative. |
| M39292 | (2S,3S)-2-Acetamido-3-methylpentanoic acid | (2S,3S)-2-Acetamido-3-methylpentanoic acid is an isoleucine derivative. |
| M39220 | Dendrophenol | Dendrophenol (Moscatilin) acts as a NF-κB inhibitor. Antineoplastic activity. |
| M39218 | Kamebakaurin | Kamebakaurin is a natural compound isolated from Rabdosia excisa. Kamebakaurin is a potent inhibitor of NF-κB activation by directly targeting DNA-binding activity of p50. |
| M39215 | Eurycomalactone | Eurycomalactone is a potent NF-κB inhibitor with an IC50 value of 0.5 μM. Eurycomalactone inhibits protein synthesis and depletes cyclin D1. Eurycomalactone enhances radiosensitivity through arrest cell cycle at G2/M phase and delayed DNA double-strand break repair. |
| M39213 | Dehydromiltirone | Dehydromiltirone (1,2-Didehydromiltirone) is a diterpenoid quinone with an anti-inflammatory effect. Dehydromiltirone prevents liver injury by modifying the MAPK and NF-κB signaling pathways, reducing neuroinflammatory responses, and inhibiting platelet aggregation. |
| M39208 | Artemisitene | Artemisitene, a natural derivative of Artemisinin, is a Nrf2 activator with antioxidant and anticancer activities. Artemisitene activates Nrf2 by decreasing Nrf2 ubiquitination and increasing its stability. |
| M39203 | Hydroxyamine hydrochloride | Hydroxyamine hydrochloride is a selective monoamine oxidase (MAO) inhibitor used for inhibiting of platelet aggregation. Hydroxyamine hydrochloride is an intermediate of organic synthesis. |
| M39192 | Chikusetsusaponin Ib | Chikusetsusaponin Ib has anti-Alzheimer's disease activity and is a potent AChE inhibitor. |
| M39187 | 5-Methoxytryptamine | 5-Methoxytryptamine, a metabolite of Melatonin, is a nonselective 5-HT receptor agonist. 5-Methoxytryptamine has no affinity for the 5-HT3 receptor. 5-Methoxytryptamine is also a potent antioxidant and has radioprotective action. |
| M39168 | Limocitrin | Limocitrin is a natural product that can be isolated from the buds of P. acerifolia and P. orientalis. Limocitrin suppresses estradiol-dependent proliferation of MCF7 cells weakly but estradiol-induced AlkP (alkaline phosphatase) expression only marginally. |
| M39164 | (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane | (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane increases the level of alkaline phosphatase (ALP) activity. (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane promotes mesenchymal stem cells (MSCs) osteogenesis, but cannot enhance MSCs proliferation. |
| M39154 | Isomalt | Isomalt (Palatinitol) stabilizes lactate dehydrogenase (LDH) moderately during freeze-drying, and performs better during storage. Isomalt is traditionally used as a sweetening agent in the food industry. |
| M39151 | Pongamol | Pongamol (Lanceolatin C) is potent α-glucosidase inhibitor (IC50=103.5 μM) and has free-radical (DPPH) scavenging,antihyperglycemic, and antihyperglycemic activities. |
| M39148 | Resveratroloside | Resveratroloside (Resveratrol glycoside) is a competitive inhibitior of α-glucosidase with an IC50 of 22.9 μM. Resveratroloside has the ability to regulate PBG (postprandial blood glucose) levels. Resveratroloside exhibits cardioprotective effect. |
| M39144 | 4-Nitrophenyl a-D-glucopyranoside | 4-Nitrophenyl a-D-glucopyranoside is a chromogenic substrate for α-glucosidase. 4-Nitrophenyl a-D-glucopyranoside can be used to measure of α-glucosidase activity. |
| M39137 | Betaine | Betaine (Trimethylglycine) is a natural compound found in many foods and also an active methyl-donor which can maintain normal DNA methylation patterns. |
| M39131 | Myricanone | Myricanone is a compound isolated from the bark of Myrica rubra. |
| M39126 | L-Norvaline | L-Norvaline is an endogenous metabolite. |
| M39121 | Ochratoxin B | Ochratoxin B, a secondary metabolite of Aspergillus ochraceus, is the nonchlorinated analogue of the mycotoxin Ochratoxin A. Ochratoxin B has been shown to reduce the toxic effects of Ochratoxin A, and it is one of the most potent renal carcinogens in rodents. |
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