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Cat.No.  Name Information
M39416 Fmoc-Arg(Pbf)-OH Fmoc-Arg(Pbf)-OH is an arginine derivative containing amine protecting group Fmoc. Fmoc-Arg(Pbf)-OH is a building block for the introduction of Arg into SPPS (Solid-Phase Peptide Synthesis).
M39361 H-Phe-OMe.hydrochloride H-Phe-OMe.hydrochloride is a phenylalanine derivative.
M39348 Boc-L-2-aminobutanoic acid Boc-L-2-aminobutanoic acid is an alanine derivative.
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.

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