| 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. |
| M9272 | S107 | S107 is a Type 1 ryanodine receptor (RyR1) stabilizer. |
| M9246 | HUHS015 | HUHS015 is a potent PCA-1/ALKBH3 inhibitor, which continuously administering HUHS015 significantly suppressed the growth of DU145 cells. |
| M9244 | 1-methoxy PMS | 1-methoxy PMS is stable electron-transport mediator between NAD(P)H and tetrazolium dyes. |
| M9207 | Tributylammonium pyrophosphate | Tributylammonium pyrophosphate |
| M9191 | Sodium pyrophosphate | Sodium pyrophosphate is a colorless transparent crystalline chemical compound with the formula Na4P2O7. |
| M9171 | Sodium succinate | Sodium succinate is an important metabolite at the cross-road of several metabolic pathways. |
| M9102 | Palosuran | Palosuran, also known as ACT-058362, is a Urotensin-II receptor antagonist with an IC50 of 3.6±0.2 nM. |
| M9038 | Photochlor | Photochlor is a lipophilic, second-generation, chlorin-based photosensitizer. |
| M9031 | 6-Methylcoumarin | 6-Methylcoumarin belongs to the class of organic compounds known as coumarins and derivatives. |
| M9002 | ML281 | ML-281 is a potent ans selective STK33 inhibitor with IC50 value of 14 nM. |
| M8965 | 2,6-Diaminopurine | 2, 6-diaminopurine is a compound used to study leukemia. |
| M8935 | EXP-3174 | EXP-3174 is a potent AT1 antagonist with Kis of 0.57 and 0.67 nM for rat and human forms, respectively. |
| M8907 | Acecainide HCl | Acecainide HCl, also known as N-acetylprocainamide and ASL 601, is the N-acetylated metabolite of procainamide. |
| M8905 | EBE-A22 | EBE-A22 is a derivative of PD 153035, has no effect on EGF-R TK but maintains a high cytotoxic profile. |
| M8894 | GJ-103 | GJ-103 is an active analog of the read-through compound GJ072. |
| M8878 | Inositol Nicotinate | Inositol Nicotinate is a formulation of niacin, which is also called vitamin B3, an essential human nutrient. |
| M8838 | UBP302 | UBP302 is a selective GluR5 antagonist. |
| M8820 | Tyrphostin RG 14620 | Non-phenolic tyrphostin-class tyrosine kinase inhibitor. |
| M8819 | TOFA | TOFA is an allosteric inhibitor of acetyl-CoA carboxylase-α (ACCA). TOFA can inhibit the anorectic effect of subcutaneous tamoxifen (TMX) on food intake during refeeding experiments in rats. |
| M8811 | Triparanol | Triparanol (MER-29) is a potent cholesterol biosynthesis inhibitor blocking the 24-dehydrocholesterol reductase (24-DHCR). |
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