| Cat.No. | Name | Information |
|---|---|---|
| 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 |
| M7791 | Exo-1 | Exo1 is a reversible inhibitor of exocytosis, also a Golgi ARF 1 (ADP-Ribosylation Factor) GTPase activator. |
| M2688 | Ethamivan | Ethamivan is postulated to interact with muscarinic receptors in the medulla. |
| M2685 | Estradiol valerate | Estradiol is a synthetic ester used to treat menopausal symptoms and hormone deficiencies. |
| M2656 | Dropropizine | Dropropizine is a racemic non-opiate antitussive agent, it is used as a cough suppressant. |
| M2654 | D-Phenylalanine | D-Phenylalanine, an carboxypeptidase A, endorphinase and enkephalinase inhibitor, enhances endorphin production and diminishes pain. |
| M2631 | Dibenzothiophene | Dibenzothiophene (DBT) is a model compound for organic sulfur in fossil fuels. |
| M2606 | Tirasemtiv | Tirasemtiv (CK-2017357) is a a small-molecule fast-skeletal-troponin activator, which is being developed as a potential treatment for diseases and conditions associated with aging, muscle weakness and wasting or neuromuscular dysfunction. |
| M2602 | Hydrastinine hydrochloride | Hydrastinine hydrochloride is a semisynthetic alkaloid from the hydrolysis of the alkaloid hydrastine, which was found naturally in small quantities in Hydrastis canadensis L. |
| M2599 | Methylisoindigotin | Meisoindigo, a derivative of Indigo naturalis, might induce apoptosis and myeloid differentiation of acute myeloid leukemia (AML). |
| M2589 | NSI-189 | NSI-189 is a nootropic and neurogenic research chemical derived from nicotinamide and pyrazine. |
| M2586 | AT-56 | AT-56 Inhibits the production of PGD2 from PGH2 in vitro, with no effect on PGE2 or PGF2α production. |
| M2580 | GBR 12935 dihydrochloride | GBR 12935 dihydrochloride is a potent and selective inhibitor of dopamine uptake (KD = 5.5 nM in rat striatal membranes). |
| M2579 | Catharanthine sulfate | Catharanthine inhibits nicotinic receptor mediated diaphragm contractions with IC50 of 59.6 μM. |
| M2544 | Cyclandelate | Cyclandelate is an effective inhibitor of rat hepatic acycloenzyme A: cholesterol acyltransferase (ACAT) with IC50 of 80 μM. |
| M2543 | Cyclamic acid | Cyclamic acid in the form of its sodium or calcium salt is one of the most widely used artificial sweeteners. |
| M2540 | Creatinine | Creatinine is a break-down product of creatine phosphate in muscle. |
| M2539 | Coumarin | Coumarin is a secondary phytochemical with hepatotoxic and carcinogenic properties. |
| M2534 | Closantel | Closantel is gram positive antibacterial activity inhibitor, inhibiting the KinA/Spo0F system with IC50 of 3.8 μM. |
| M2518 | Chromocarb | Chromocarb is a vasoprotectant. |
| M2498 | CCG 50014 | CCG 50014 is a potent and selective inhibitor of RGS4 with IC50 of 30 nM. |
| M2493 | Carbimazole | Carbimazole is an effective thyroid hormone inhibitor under a class of drugs known as pro-drugs. It is considered a pro-drug because it converts to methimazole after being absorbed by the body, generating an antithyroid action that works against hyperthyroidism (excessive production of thyroid hormones) and thyrotoxicosis (inflammation of the thyroid gland). |
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