| Cat.No. | Name | Information |
|---|---|---|
| M2206 | TH-302 (Evofosfamide) | TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM. |
| M6098 | Baicalein | Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor, IC50 value of 3.12 mM. |
| M9325 | EGTA | EGTA is a specific calcium chelator with a Kd of 60.5 nM at physiological pH (7.4) and a high specificity for Ca2+ than for Mg2+.EGTA significantly inhibits the substrate adhesion capacity of inflammatory macrophages. |
| M9330 | Brij-35 | Brij-35 (Polidocanol) is a high HLB, ethoxylated, nonionic ether of lauryl alcohol with broad pH stability. |
| M6154 | 2-PMPA tetrasodium | 2-PMPA (PMPA tetrasodium salt) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC50 of 300 pM. |
| M2250 | Pamidronate disodium | Pamidronate disodium is a nitrogen containing bisphosphonate, used to the research of preventing osteoporosis. |
| M9916 | DPPH | DPPH (2,2-Diphenyl-1-picrylhydrazyl) is a stable free radical that measures the free radical scavenging activity of antioxidants. |
| M9194 | Insulin (human) | Insulin (human) is a polypeptide hormone that regulates the level of sugar (glucose) in the blood and is produced by beta cells of islets. |
| M3409 | Formestane | Formestane is a second generation selective aromatase inhibitor with an IC50 of 80 nM. |
| M9665 | N-(2-amino-2-oxoethyl)acrylamide | N-(2-Amino-2-oxoethyl)acrylamide |
| M20566 | Undecanedioic acid | Undecanedioic acid is a long-chain dicarboxylic acid that has applications in corrosion inhibitors, hot melt adhesives, high performance polyamides/Nylon, and more. |
| M20563 | 4-Pentenoic acid | 4-Pentenoic acid is an endogenous metabolite. |
| M20562 | Dodecanedioic acid | Dodecanedioic acid is a dicarboxylic acid mainly used in antiseptics, top-grade coatings, painting materials, corrosion inhibitors, surfactants, and engineering plastics. |
| M20560 | Indole-2-carboxylic acid | Indole-2-carboxylic acid is a strong inhibitor of lipid peroxidation. |
| M20559 | Brucine sulfate heptahydrate | Brucine is an alkaloid that acts as an antagonist at glycine receptors and paralyzes inhibitory neurons. |
| M20557 | 3-Indoleacetonitrile | 3-Indoleacetonitrile, a plant growth hormone, is a light-induced auxin-inhibitory substance that is isolated from light-grown cabbage (Brassica olearea L.) shoots. |
| M20556 | 2,6-Dihydroxybenzoic acid | 2,6-Dihydroxybenzoic acid is a phenolic compound which is known to have poor biological performance such as DPPH scavenging activity and microbial growth inhibition. |
| M20548 | 2,4-Pyridinedicarboxylic acid | 2,4-Pyridinedicarboxylic acid is a compound that structurally mimics 2-oxoglutarate (2-OG) and chelates zinc, thus affecting a range of enzymes. It blocks the activity of 2-OG oxygenases. |
| M20546 | D-Carnitine hydrochloride | Carnitine is biosynthesized from lysine. It might be associated with the energy production from branched chain amino acids. |
| M20542 | Ethacrynate Sodium | Ethacrynate Sodium is the sodium salt form of ethacrynic acid, which inhibits symport of sodium, potassium, and chloride primarily in the ascending limb of Henle, but also in the proximal and distal tubules. |
| M20534 | 4'-Deoxyphlorizin | 4'-Deoxyphlorizin is an inhibitor of the glucose transport system. |
| M20532 | Delapril Hydrochloride | an agonist of the RXR signaling pathway |
| M20531 | Carvedilol EP IMpurity E | Used as pharmaceutical intermediates-Intermediates |
| M20525 | Carvedilol Phosphate | Carvedilol Phosphate is the phosphate salt form of carvedilol, a racemic mixture and adrenergic blocking agent with antihypertensive activity and devoid of intrinsic sympathomimetic activity. |
| M20523 | Tropolone | Tropolone inhibits both mono-and o-dihydroxyphenolase activity of mushroom tyrosinase. |
| M20522 | Tropinone | Tropinone is an alkamine intermediate at the branch point of biosynthetic pathways leading to various tropane alkaloids. |
| M20518 | Orphenadrine Hydrochloride | A muscarinic receptor antagonist, specifically an H1 histamine receptor antagonist. This compound is a muscle relaxant. Orphenadrine has also been reported to inhibit the noradrenergic transporter and to block the NMDA receptor ion channel. |
| M20512 | Ammonium lactate | inhibit nucleocapsid/RNA interactions in Rift Valley Fever Virus |
| M20510 | Chicago Sky Blue 6B | A potent inhibitor of L-glutamate uptake via glutamate transporter (EAAT) |
| M20509 | 4,4prime-Bis(4-aminophenoxy)biphenyl | A potent Flk-1 (VEGFR2) and Tie-2 inhibitor |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
