| 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. |
| M56777 | Y-29794 tosylate | Y-29794 tosylate is a selective, orally active inhibitor for non-peptide prolyl endopeptidase (PREP), with an IC50 of 3 nM and a Ki of 0.95 nM. |
| M56729 | 4-(6-Bromo-2-benzothiazolyl)benzenamine | 4-(6-Bromo-2-benzothiazolyl)benzenamine is a β-amyloid PET (positron emission tomography) tracer that can be used in the diagnosis of neurological diseases, such as Alzheimer's and Down's syndrome. |
| M56728 | Candoxatril | Candoxatril is a neutral endopeptidase (NEP) inhibitor. |
| M56705 | Galloflavin potassium | Galloflavin potassium is a novel lactate dehydrogenase inhibitor that can be used for the research of cancer. |
| M56692 | SSM3 tetraTFA | SSM3 tetraTFA is a potent synthetic furin inhibitor with an EC50 and a Ki of 54 nM and 12 nM, respectively. |
| M56609 | Indoluidin E | Indoluidin E selectively inhibits DHODH and suppresses cancer cell growth. |
| M56603 | Nitecapone | Nitecapone (OR-462) is an orally active and short-acting catechol-O-methyltransferase (COMT) inhibitor with gastroprotective and antioxidant properties. |
| M56602 | SACLAC | SACLAC, a Ceramide analog, is a potent and covalent acid ceramidase (ASAH1; AC) inhibitor with a Ki of 97.1 nM. |
| M56601 | Acid Ceramidase-IN-1 | Acid Ceramidase-IN-1 is a potent and oral bioavailable acid ceramidase (AC, ASAH-1) inhibitor (hAC IC50=0.166 μM). |
| M56599 | 2-MPPA | 2-MPPA (GPI-5693) is an orally active and selective glutamate carboxypeptidase II (GCP II; PSMA) inhibitor with an IC50 of 90 nM. |
| M56596 | Carboxylesterase-IN-2 | Carboxylesterase-IN-2 is a potent inhibitor of Carboxylesterase Notum with an IC50 less than or equal to 10 nM. |
| M56590 | GlyRS-IN-1 | GlyRS-IN-1 is a glycyl-tRNA synthase (GlyRS) inhibitor. |
| M56583 | UT-B-IN-1 | UT-B-IN-1 (UTBINH-14) is a reversible, competitive and selective urea transporter-B (UT-B) inhibitor with IC50 values of 10 and 25 nM for human and mouse UT-B, respectively. |
| M56519 | Benzamil | Benzamil (Benzylamiloride), an Amiloride analogue, is a Na+/Ca2+ exchanger (NCX) inhibitor (IC50~100 nM). |
| M56466 | CRAC intermediate 2 | CRAC intermediate 2 is a intermediate compound for CRAC inhibitor synthesis. |
| M56464 | RO2959 monohydrochloride | RO2959 monohydrochloride is a potent and selective CRAC channel inhibitor with an IC50 of 402 nM. |
| M56460 | Encecalinol | Encecalinol, extracted from aerial parts of Ageratina grandifolia, is a potent inhibitor of calmodulin inhibitor. |
| M56459 | Beauverolide Ja | Beauverolide Ja, a cyclotetradepsipeptide, is a potent calmodulin (CaM) inhibitor with a Kd of 0.078 μM and a Ki of 0.39 μM for Ca2+-CaM. |
| M56439 | MLKL-IN-2 | MLKL-IN-2 is a MLKL inhibitor. |
| M56391 | KF38789 | KF38789 is a selective inhibitor of P-selectin-PSGL-1 binding. |
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