| 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 |
| M45365 | Lobatoside C | Lobatoside C, a triterpenoid saponin isolated from hyoscyamus with arabinose terminal sugar, inhibited SW-620, SK-MEL-5, and UO-31 cell lines with GI50 values of 8.91, 4.17, and 6.03, respectively. |
| M45364 | MB-104 | MB-104 is a SLAM family member-7 (SLAMF7) modulator that can be used in a variety of cancer-related studies. |
| M45250 | DCSZ11 | DCSZ11 is a monoclonal antibody targeting CD93 for studies related to solid tumors. |
| M45249 | DCBY02 | DCBY02 is a monoclonal antibody targeting CD93 for studies related to solid tumors. |
| M45247 | INTH 454 | INTH 454 is an inhibitor targeting CBP/p300 for studies related to solid tumors. |
| M45241 | Ecallantide | Ecallantide is a potent, selective inhibitor of recombinant plasma kinin releasing enzyme that inhibits bradykinin production. |
| M45240 | OK-101 | OK-101 is a lipid-coupled chemokine peptide agonist of the ChemR23 g-protein-coupled receptor that can be used in studies related to neuropathic corneal pain (NCP). |
| M45237 | AUR107 | AUR107 is an inhibitor targeting CBP/p300 for studies related to solid tumors. |
| M45230 | Carboxymethyl cellulose | Carboxymethyl cellulose is a carboxymethyl group substitution product of cellulose. Depending on its molecular weight or degree of substitution, it can be a completely soluble or insoluble multimer, the latter of which can be used as a weakly acidic cation exchanger to separate neutral or basic proteins. |
| M45227 | DLX-001 | DLX-001 is a novel compound that can be used in studies related to depression. |
| M45225 | NPX887 | NPX887 is a monoclonal antibody targeting the co-stimulatory molecule B7H7, which can be used in studies related to solid tumors. |
| M45214 | ABSK051 | ABSK051 is a novel, selective small molecule CD73 inhibitor with strong inhibitory effect on CD73 enzyme activity, which can be used for solid tumor related studies. |
| M45165 | AGX87 | AGX87 is a neurotyrosine kinase receptor (NTRK) inhibitor, as well as a proto-oncogene tyrosine protein kinase (ROS1) inhibitor, and may be used in studies related to solid tumors. |
| M45132 | Palopegteriparatide | Palopegteriparatide is a long-acting precursor compound of parathyroid hormone (PTH), as well as a calcium-sensitive receptor (CaSR) antagonist, and a parathyroid hormone receptor (PTH1R) modulator, and may be used in studies related to hypoparathyroidism (HP). |
| M45122 | Al-3d | Al-3d directly binds to Aster-B and Aster-C proteins, thereby inhibiting cholesterol absorption. |
| M45108 | yGsy2p-IN-H23 | yGsy2p-IN-H23 is a first-in-class, potent inhibitor of yeast glycogen synthase 2 (yGsy2p) that binds within the glucose-binding pocket of uridine diphosphate of yGsy2p, with an IC50 value of 875 µM for human glycogen synthase 1 (hGYS1). it can be used in studies related to glycogen accumulation diseases (GSDs). |
| M45103 | ML-290 | ML-290 is a first-in-class, potent relaxin/glucagon-like peptide receptor (RXFP1) agonist and anti-fibrotic gene activator with an EC50 value of 94 nM. |
| M45099 | I942 | I942 is a first-in-class selective non-cyclic nucleotide (NCN) EPAC1 agonist that attenuates pro-inflammatory cytokine signaling commonly associated with cardiovascular disease. |
| M45094 | (S)-Subasumstat | (S)-Subasumstat is the inactive isomer of Subasumstat and serves as a control compound in experiments.Subasumstat is a first-in-class, selective inhibitor of the SUMOylation enzymatic reaction with potential immune-activating and antitumor activity. |
| M45056 | RLS-0071 | RLS-0071RLS-0071 is a dual-targeted peptide that modulates humoral and cellular immunity by inhibiting neutrophil effectors, including myeloperoxidase and neutrophil extracellular net trap (NET) formation. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
