About 11 results found for searched term "70-26-8" (0.053 seconds)
Cat.No. | Name | Target |
---|---|---|
M5753 | L-Ornithine | Metabolite/Endogenous Metabolite |
(S)-2,5-Diaminopentanoic acid | ||
L-ornithine has an antifatigue effect by increasing the efficiency of energy consumption and promoting the excretion of ammonia. It is one of the key reactants in the urea cycle. | ||
M6243 | Vorapaxar Sulfate | PAR |
Vorapaxar is a first-in-class, potent and orally-active protease-activated receptor 1 (PAR-1) antagonist that blocks thrombin-mediated platelet activation without interfering with thrombin-mediated fibrin deposition. | ||
M6483 | AZD 9272 | Others |
AZD 9272 is a potent and selective mGlu 5 antagonist; brain penetrant. | ||
M6627 | CP 775146 | Others |
CP 775146 is a selective, high affinity PPARα agonist. | ||
M6739 | G10 | STING |
G10 is a activator of STING-dependent signaling. | ||
M8060 | CP-868388 | Others |
CP-868388 is a potent PPARα agonist with a Ki of 10. | ||
M8135 | Rhodblock 1a | Others |
Rhodblock 1a is an inhibitor of the Rho Kinase pathway. | ||
M44826 | Cyclo(L-Phe-L-Pro) | Antifungal |
Cyclo(L-Phe-L-Pro), isolated from Pseudomonas fluorescens and Pseudomonas alcaligenes cell-free culture supernatants is an antifungal cyclic dipeptide. | ||
M56734 | PTP1B-IN-3 diammonium | Phosphatase |
PTP1B-IN-3 diammonium is a potent and orally active PTP1B inhibitor with IC50s of 120 nM for both PTP1B and TCPTP. | ||
M56154 | Ronacaleret hydrochloride | Others |
Ronacaleret hydrochloride (SB 751689A) is an orally active, potent, and selective calcium-sensing receptor (CaSR) antagonist that stimulates endogenous parathyroid hormone release from the parathyroid glands. | ||
M56024 | PRT062607 acetate | Others |
PRT062607 (P505-15) acetate is an orally available Syk inhibitor (IC50: 1 nM) that inhibits inflammation and induction Apoptosis. |
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