Inhibitor
| Cat.No. | Name | Information |
|---|---|---|
| M10346 | Glutamic acid (L-Glutamic acid) | L-Glutamic acid acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). |
| M18309 | p-Hydroxy-cinnamic acid | p-Hydroxy-cinnamic acid inhibits platelet activity, with IC50s of 371 μM, 126 μM for thromboxane B2 production and lipopolysaccharide-induced prostaglandin E2 generation, respectively. |
| M6687 | Docosahexaenoic acid (Oil) | Docosahexaenoic Acid (DHA) is an omega-3 fatty acid abundantly present brain and retina. Docosahexaenoic acid is a RXR agonist. |
| M9953 | Taurocholic acid | Taurocholic acid (N-Choloyltaurine) is a bile acid, which can be used in the emulsification of fats. |
| M10168 | L-Lactic acid | L-Lactic acid is an organic acid, which can be used as a precursor for the production of the bioplastic polymer poly-lactic acid. |
| M2547 | Cyromazine | Cyromazine is a triazine insect growth regulator used as an insecticide and an acaricide. |
| M2486 | Calcium Gluceptate | Calcium gluconate is a calcium salt used in the study and prevention of hypocalcemia and as an electrolyte supplement. |
| M2443 | Benzoic Acid | Benzoic acid is a colorless crystalline solid and a simple aromatic carboxylic acid, used as a food preservative. Benzoic acid is an aromatic alcohol existing naturally in many plants and is a common additive to food, drinks, cosmetics and other products. It acts as preservatives through inhibiting both bacteria and fungi. |
| M2359 | 4-Aminohippuric Acid | 4-Aminohippuric acid is a typical substrate of organic anion transport systems. 4-Aminohippuric acid is a diagnostic agent, useful in medical tests involving the kidney, used in the measurement of renal plasma flow. |
| M2086 | Ribitol | Ribitol (Adonitol) is a crystalline pentose alcohol formed by the reduction of ribose. |
| M1590 | 3-HYDROXYACETAMINOPHEN | 3-hydroxy-acetaminophen is a metabolite of Acetaminophen, which is a pain medicine. |
| M1589 | Hydroxy Iloperidone | Hydroxy Iloperidone is a metabolite of Iloperidone, which is an atypical antipsychotic. |
| M1588 | Duloxetine Phenolic Impurity | Para-Naphthol Duloxetine is a metabolite of Duloxetine, which is a serotonin-norepinephrine reuptake inhibitor (SNRI). |
| M1583 | Omeprazole sulfone | Omeprazole sulfone is a metabolite of Omeprazole, which is a proton pump inhibitor. |
| M1580 | 4-Hydroxy phenyl carvedilol | 4-Hydroxyphenyl Carvedilol is a metabolite of Carvedilol, which is a nonselective beta blocker/alpha-1 blocker. |
| M1573 | Desthiazolylmethyloxycarbonyl Ritonavir | Desthiazolylmethyloxycarbonyl Ritonavir is a metabolite of Ritonavir, which is a HIV protease inhibitor. |
| M1554 | N-Desmethyl Imatinib | N-Desmethyl Imatinib |
| M58521 | Testosterone sulfate (pyridinium) | Testosterone sulfate pyridinium is a Testosterone sulfate with a pyridinium. Testosterone sulfate is the metabolite of Testosterone. |
| M58502 | 4-Hydroxyestrone | 4-Hydroxyestrone (4-OHE1) is an estrone metabolite, it has strong neuroprotective effect against oxidative neurotoxicity. 4-Hydroxyestrone increases cytoplasmic translocation of p53 resulting from SIRT1-mediated deacetylation of p53. |
| M58378 | Taurodeoxycholic acid | Taurodeoxycholic acid, a bile acid, stabilizes the mitochondrial membrane, decreases free radical formation. Taurodeoxycholic acid inhibits apoptosis by blocking a calcium-mediated apoptotic pathway as well as caspase-12 activation. |
| M58364 | 3-Hydroxyphenylacetic acid | 3-Hydroxyphenylacetic acid (3-HPAA) is an intestinal metabolite of the dietary flavonoid quercetin flavonoid quercetin. 3-Hydroxyphenylacetic acid has antimicrobial properties. |
| M58182 | Ulodesine | Ulodesine is a purine nucleoside phosphorylase (PNP) inhibitor. Ulodesine inhibits PNP with IC50 value of 2.293 nM/L. |
| M56678 | DL-AP3 | DL-AP3 is a competitive mGluR1 and mGluR5 antagonist. |
| M56677 | SY-640 | SY-640 is an Acetamide derivative and has potent hepatoprotective effect. |
| M56676 | Teglicar | Teglicar is a selective and reversible orally active liver isoform of carnitine palmitoyl-transferase 1 (L-CPT1) inhibitor with an IC50 value of 0.68 μM and a Ki value of 0.36 μM. |
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