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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.
M8607 Bifeprunox mesylate Bifeprunox (DU-127,090) is an atypical antipsychotic compound.
M8606 NCX 4016 NCX 4016 (nitroaspirin) is nitroderivative of aspirin that combines cyclooxygenase inhibitor with an NO donor.
M8605 NA-17 NA-17 is a fluorescent naphthalimide that induces accumulation of activated p53 in mitochondria and nuclei of NSCLC cells.
M8601 R-Ketorolac R-Ketorolac is potent and selective Rho-family GTPases Cdc42 (cell division control protein 42) and Rac1 (Ras-related C3 botulinum toxin substrate 1) allosteric inhibitor that modulates downstream GTPase-dependent physiologic responses critical to tumor metastasis.
M8599 Epiblastin A Epiblastin A is triamterene derivative that potently induces reprograming of epiblast stem cells (EpiSC) into embryonic stem cells (ESC).
M8598 ZQ-16 ZQ-16 is a potent and selective agonist for medium-chain free fatty acid receptor GPR84 (G protein-coupled receptor 84).
M8597 DHED DHED (10β, 17β-dihydroxyestra-1< WBR >, 4-dien-3-one) is an inactive precursor compound that selectively produces estrogen only in the brain.
M8596 WWL70 WWL70 is a selective inhibitor of α/β-hydrolase domain-containing 6 (ABHD6), a serine hydrolase that acts as an alternative hydrolase of the endocannabinoid 2-arachidonoylglycerol (2-AG).
M8593 Hexaminolevulinate hydrochloride Hexaminolevulinate (HAL) hydrochloride is a hexyl ester of 5-Aminolevulinic acid (ALA), a precursor to porphyrins including the photosensitizer protoporphyrin IX (PPIX).
M8588 iKIX1 iKIX1 is an antifungal agent that can re-sensitize drug-resistant Candida glabrata to azole antifungals.
M8586 Tazarotenic acid Tazarotenic acid, an active metabolite of tazarotene, is a potent and selective agonist of the retinoid receptor (RAR) that binds to RARα, RARβ, and RARγ.
M8585 Rp-8-Br-cGMPS sodium salt Rp-8-bromo-cGMPS is a cell permeable cGMP analog that blocks cGMP-dependent protein kinase (cGK, G-kinase, Protein Kinase G, PKG).
M8584 Dapiprazole hydrochloride Dapiprazole hydrochloride is an an α-adrenergic blocking agent that is used to reverse mydriasis after eye examination.
M8583 Ferutinin An ERα (estrogen receptor) agonist; phytoestrogen.
M8581 Bis(heptyl)-cognitin dihydrochloride Bis(heptyl)-cognitin (B7C) is a potent neuroprotective agent and cognitive enhancer.
M8580 Perlapine Perlapine is a potent and selective agonist of hM3Dq DREADD (Designer Receptors Exclusively Activated by Designer Drugs), which does not activate the native human M3 receptor.
M8579 CMPPE CMPPE is a GABAB receptor positive allosteric modulator (PAM).
M8578 Undecylprodigiosin hydrochloride Undecylprodigiosin is a tri-pyrolle antibiotic isolated from Streptomyces coelicolor A3 that exhibits immunosuppressive and apoptotic activities as well as antibacterial, antioxidative and UV protective properties.
M8577 BAY-678 BAY-678 is an orally available, highly potent and selective inhibitor of human neutrophil elastase (HNE).
M8574 THPN THPN is potent nuclear receptor TR3 (Nur77) antagonist that induces autophagic cell death in melanoma.




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