| 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. |
| M66433 | Catumaxomab | Catumaxomab, a trifunctional IgG2 antibody, is composed of mouse and rat heavy and light chains and binds to human EpCAM and human CD 3 receptors. |
| M66432 | ML-SI1 | ML-SI1, a racemic mixture of diastereomers, is a TRPML inhibitor with an IC 50 value of 15 μM for TRPML1. |
| M66431 | NHC-triphosphate tetraammonium | NHC-triphosphate tetraammonium is an active phosphorylated intracellular metabolite of β-d-N4-Hydroxycytidine (NHC) as a triphosphate form. |
| M66430 | Sasanlimab | Sasanlimab is a humanized IgG4 isotype anti- PD-1 antibody. Sasanlimab blocks PD-1 interaction with PD-L1 / PD-L2 , reverses PD-1-mediated inhibitory T-cell signaling. |
| M66429 | VUF11207 | VUF11207 is a CXCR7 agonist and a high-potency CXCR7 (pK i of 8.1) ligand that induces recruitment of β-arrestin2 (pEC 50 of 8.8) and subsequent internalization (pEC 50 of 7.9) of CXCR7 . |
| M66428 | ZK159222 | ZK159222, a 25-carboxylic ester analogue of 1α,25-(OH)2D3, is a potent 1α,25-(OH)2D3 receptor (VDR) antagonist. |
| M66427 | QD394 | QD394 is a reactive oxygen species (ROS) inducer that can induce lipid peroxidation, increase intracellular ROS accumulation, inhibit STAT3 phosphorylation, and induce ferroptosis. |
| M66426 | HOIPIN-8 | HOIPIN-8 is a potent inhibitor of linear ubiquitin chain assembly complex (LUBAC) with an IC 50 of 11 nM. |
| M66424 | Tobevibart | Tobevibart (VIR-3434) is a human IgG1 lambda monoclonal antibody against hepatitis B virus (HBV) surface antigen (HBsAg). |
| M66423 | BAY 59-9435 | BAY 59-9435 is a potent and selective inhibitor of Hormone Sensitive Lipase (HSL), with an IC 50 of 0.023 μM. |
| M66422 | Pulsatilla saponin D | Pulsatilla saponin D (SB365), isolated from the root of Pulsatilla chinensis , is an anti-tumor agent. |
| M66421 | Risedronic acid | Risedronic acid (Risedronate) is a bisphosphonate and potent antiresorptive agent. Risedronic acid induces Apoptosis. |
| M66420 | ECI830 | ECI830 (CDK2-IN-37) is an orally active, ATP-competitive and highly selective CDK2 inhibitor. ECI830 shows high selectivity over other CDK family members. |
| M66419 | RMC-9945 | RMC-9945 (RM-044) is a KRAS inhibitor and selective, covalent, orally active RAS (ON) G12D inhibitor. RMC-9945 increases β-Catenin/TCF transcriptional activity. |
| M66418 | Allyl methyl sulfide | Allyl methyl sulfide is an orally active organic sulfide. Allyl methyl sulfide is one of the main active ingredients in garlic volatile metabolites. Allyl methyl sulfide can be extracted from garlic. |
| M66417 | LM11A-31 | LM11A-31, a non-peptide p75 NTR (neurotrophin receptor p75) modulator, is an orally active and potent proNGF (nerve growth factor) antagonist. |
| M66416 | Dimethyl malonate | Dimethyl malonate is a competitive inhibitor of succinate dehydrogenase (SDH). Dimethyl malonate is able to cross the blood-brain barrier and hydrolyse to malonate. |
| M66415 | MKC9989 | MKC9989 is a Hydroxy aryl aldehydes (HAA) inhibitor and also inhibits IRE1α with an IC 50 of 0.23 to 44 μM. |
| M66414 | L-Glutamine-13C5 | L-Glutamine - 13 C 5 is the 13 C-labeled L-Glutamine. L-Glutamine is an orally active nutritional agent and cellular metabolism regulator. |
| M66413 | Oveporexton | Oveporexton (TAK-861) is an orally active and selective orexin receptor 2 (OX2R) agonist with an EC 50 of 2.5 nM. Oveporexton exhibits 3000-fold selectivity for OX2R over OX1R. |
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