| 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. |
| M7804 | 5-Fluoro-2′-deoxycytidine | 5-Fluoro-2′-deoxycytidine is a mechanism based DNMT (DNA cytosine-5 methyltransferase) inhibitor, that forms a covalent link with the cysteine residue in the active site of DNMT. |
| M7802 | Fadrozole hydrochloride | Fadrozole is a nonsteroidal aromatase inhibitor. |
| M7773 | dPPA | Selective activator of PKC beta. |
| M7761 | Diacylglycerol Kinase Inhibitor II | Diacylglycerol kinase inhibitor. |
| M7746 | Dexrazoxane | Dexrazoxane (ICRF-187, ADR-529, DXZ) is an iron chelator that can be used to prevent DOX-induced cardiotoxicity. |
| M7741 | DNQX | DNQX is a competitive kainate, quisqualate (non-NMDA) glutamate receptor antagonist. |
| M7720 | Caerulomycin A | Caerulomycins produced by Streptomyces caeruleus are bipyridinic molecules endowed with antibiotic properties. |
| M7696 | Choline bitartrate | Choline bitartrate is a precursor of the neurotransmitter acetylcholine and acts as a methyl donor in various metabolic processes and lipid metabolism. |
| M7644 | GF 109203X hydrochloride | Inhibitor of protein kinase C; potent inhibitor of GSK-3. |
| M7643 | Bongkrekic acid solution | An antiapoptotic agent, it protects against NMDA receptor induced neuronal apoptosis, extends cell survival in cells undergoing apoptosis following infection with viral vectors and abrogates apoptosis induced by hydrogen peroxide in T-cells. |
| M7639 | BF-170 hydrochloride | BF-170 is a new probe for neurofibrillary tangles (tau fibrils). |
| M7621 | Auraptene | Auraptene is an estrogen receptor modulator that also acts as an ACAT inhibitor. |
| M7610 | Ancitabine hydrochloride | Antineoplastic. |
| M7602 | Acepromazine maleate | Acepromazine is a phenothiazine antipsychotic compound commonly used as a veterinary drug (horse, dog, and cat). |
| M7596 | 4′-Aminomethyltrioxsalen hydrochloride | 4′-Aminomethyltrioxsalen hydrochloride is used to inactivate DNA and RNA viruses, including HIV-1, by nucleic acid cross-linking followed by UV irradiation. |
| M7580 | GJ103 sodium salt | GJ103 sodium salt is an active analog of the read-through compound GJ072. |
| M7571 | PCI-27483 | PCI-27483 is a FVIIa/tissue factor inhibitor, with antitumour effects. |
| M7564 | PF-06282999 | PF-06282999 is a potent and selective myeloperoxidase inhibitor which is potential useful for the treatment of cardiovascular diseases. |
| M7556 | G007-LK | G007-LK is a potent and selective inhibitor of TNKS1 and TNKS2, with IC50s of 46 nM and 25 nM, respectively. |
| M7543 | TP-808 | TP808 is a useful intermediate for the synthesis of diverse tetracycline antibiotics. |
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