| Cat.No. | Name | Information |
|---|---|---|
| M2206 | TH-302 (Evofosfamide) | TH-302 is a highly potent and selective hypoxia-activated procompound targeting hypoxic regions of solid tumors with IC50 of 19 nM. |
| 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 |
| M40894 | Sodium sulfate | Sodium sulfate is a ubiquitous salt used to enhance the binding of phenolics to sulfate and can be used in studies related to hypercalcemia. |
| M40890 | Di-tert-butyl dicarbonate | Di-tert-butyl dicarbonate is a carboxylic acid ester derivative used for amino protection of amino acids, as well as in pharmaceuticals, protein, and peptide synthesis. |
| M40888 | HOAT | HOAT inhibits the production of racemization in peptide condensation and can also be used in fragment condensation. |
| M40887 | 6-Chloro-1-hydroxibenzotriazol | 6-Chloro-1-hydroxibenzotriazol is a non-toxic reagent that inhibits peptide-coupled racemization and is also used in the preparation of fusidic acid A cyclic aminothiazole derivatives. |
| M40884 | Fmoc-1,4-trans-achc-oh | Fmoc-1,4-trans-achc-oh |
| M40883 | 3-Mercapto-1-propanol | 3-Mercapto-1-propanol can be used for the preparation of hydrophilic self-assembled monolayers and as a non-marking linker molecule for chemical and enzymatic synthesis of oligosaccharides. |
| M40881 | Cuprous iodide | Cuprous iodide is a commonly used cuprous halide used as an animal feed additive. |
| M40880 | tert-Butyl 2,2,2-trichloroacetimidate | tert-Butyl 2,2,2-trichloroacetimidate is a copper chelating ligand that acts as a transamidate in biochemical reactions and has antitumor and antimicrobial activities. |
| M40872 | AFM32a hydrochloride | AFM32a hydrochloride is a benzimidazole-based derivative and a potent and selective protein arginine deiminase 2 (PAD2) inhibitor.AFM32a hydrochloride is more selective for PAD2 than PAD4 (95-fold) and PAD3 (79-fold). |
| M40871 | AFM32a | AFM32a is a benzimidazole-based derivative and a potent and selective protein arginine deiminase 2 (PAD2) inhibitor.AFM32a is more selective for PAD2 than PAD4 (95-fold) and PAD3 (79-fold). |
| M40862 | Plaunotol | Plaunotol is an acyclic diterpenoid extracted from the stems and leaves of the Croton plant and can be used in studies related to gastric ulcers. |
| M40813 | JNT-517 | JNT-517 is a potentially first-in-class, orally active, variant SLCA6A19 inhibitor for phenylketonuria-related studies. |
| M40763 | 4A7C-301 | 4A7C-301 is a compound that activates the Nurr1 protein, binds to Nurr1, and increases its ability to increase its levels in cells exposed to MPP +. In addition, 4A7C-301 ameliorated motor and olfactory deficits in mice modeled with Parkinson's disease and possessed neuroprotective as well as brain permeability activities. |
| M40762 | BIA 28-6156 | BIA 28-6156 is an orally active beta-glucocerebrosidase (GCase) variant activator that improves lysosomal function through activation of GCase and can be used in studies related to Parkinson's disease (PD) with GBA gene mutations. |
| M40694 | RIG012 | RIG012 is a potent RIG-I antagonist that blocks RIG-I-initiated signaling, inhibits transcriptional induction of CXCL10, IFN-β 1, and IRF9, and reduces IL6 mRNA levels. The IC50 was 0.71 μM when assayed with NADH-coupled ATPase. |
| M40681 | KM04416 | KM04416 is an isothiazolone derivative and a potent 3-phosphoglycerol dehydrogenase (GPD2) inhibitor that significantly inhibits PNT1A cell proliferation. |
| M40677 | Seongsanamide D | Seongsanamide D is a bicyclic peptide isolated from Bacillus maritimus, a member of the phylum Porifera, containing isodityrosine-bonded residues with antiallergic activity. |
| M40676 | Seongsanamide C | Seongsanamide C is a bicyclic peptide isolated from Bacillus maritimus, a member of the phylum Porifera, containing isodityrosine-bonded residues with antiallergic activity. |
| M40675 | Seongsanamide B | Seongsanamide B is a bicyclic peptide isolated from Bacillus maritimus, a member of the phylum Porifera, containing isodityrosine-bonded residues with antiallergic activity. |
| M40674 | Seongsanamide A | Seongsanamide A is a bicyclic peptide isolated from Bacillus maritimus, a member of the phylum Porifera, containing isodityrosine-bonded residues with antiallergic activity. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
