| 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. |
| M57061 | BMPO | BMPO (BocMPO) is a cell-permeable superior spin trap with favorable chemical and spectroscopic features. |
| M57060 | MASM7 | MASM7 is a mitofusin activator, and can achieve mitochondrial fusion via mitofusins. |
| M57057 | CQ211 | CQ211 is a potent and selective RIOK2 inhibitor with a Kd of 6.1 nM. |
| M57037 | MK-6240 | MK-6240 is a tau positron emission tomography (PET) tracer for neurofibrillary tangles (NFTs), exhibiting high specificity and selectivity for binding to NFTs. |
| M57017 | LDN-27219 | LDN-27219 is a reversible, slow-binding inhibitor of TGase. |
| M56993 | ACSS2-IN-2 | ACSS2-IN-2 is an acyl-CoA synthetase short-chain family member 2 (ACSS2) inhibitor. |
| M56974 | Thermospermine | Thermospermine, a structural isomer of Spermine, is synthesized by a thermospermine synthase designated ACAULIS5 (ACL5). |
| M56953 | GPR132 antagonist 1 | GPR132 antagonist 1 (GPR132-B-160, Compound 25) is a GPR132 antagonist with an EC50 value of 0.075 μM. |
| M56847 | Naphthol AS-BI phosphate | Naphthol AS-BI phosphate is a substrate for acid and alkaline phosphatase and can be used in fluorescence assays. |
| M56836 | Bathocuproine disulfonate disodium | Bathocuproine disulfonate disodium (BCS) is an organic compound used as a highly sensitive colorimetric reagent for copper ions in biochemical and analytical applications. |
| M56792 | 3FAx-Neu5Ac | 3FAx-Neu5Ac, a Sialic acid peracetylated analog, is a sialyltransferase inhibitor. |
| M56598 | GCPII-IN-1 | GCPII-IN-1 is a glutamate carboxypeptidase II (GCPII, or PSMA) inhibitor scaffold with a Ki of 44.3 nM. |
| M56597 | GCPII-IN-1 TFA | GCPII-IN-1 TFA is a glutamate carboxypeptidase II (GCPII, or PSMA) inhibitor scaffold with a Ki of 44.3 nM. |
| M56465 | RO2959 hydrochloride | RO2959 hydrochloride is a potent and selective CRAC channel inhibitor with an IC50 of 402 nM. |
| M56355 | FEN1-IN-4 | FEN1-IN-4 is a human flap endonuclease-1 (hFEN1) inhibitor. |
| M56336 | 15(S)-HPETE | 15(S)-HPETE is a monohydroperoxy polyunsaturated fatty acid (PUFA) produced by the action of 15-lipoxygenase (15-LO) on arachidonic acid. |
| M56333 | hGPR91 antagonist 1 | hGPR91 antagonist 1 is a potent and selective GPR91 antagonist with an IC50 of 7 nM for human GPR91. |
| M56164 | α-NETA | α-NETA is a potent and noncompetitive choline acetyltransferase (ChA) inhibitor with an IC50 of 9 μM. |
| M55790 | Braco-19 | Braco-19 is a potent telomerase/telomere inhibitor, preventing the capping and catalytic action of telomerase. |
| M55695 | 6-O-Methylcerevisterol | 6-O-Methylcerevisterol is a natural steroid found in the fungus Ganoderma lucidum. 6-O-Methylcerevisterol has antitubercular and anti-tumor activities. 6-O-Methylcerevisterol can also inhibit Epstein-barr Virus. |
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