| 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 |
| M42958 | BMS-195270 | BMS-195270 is a small molecule that inhibits Carbachol-evoked tonicity of isolated rat bladder strips. |
| M42957 | Isoindigo | Isoindigo is the acceptor of donor-acceptor (D-A) conjugated polymer, as well as an Indigo series dye. |
| M42956 | 3-Fluoro-L-tyrosine | 3-Fluoro-L-tyrosine is a tyrosine analogue, inhibits transamination by tyrosine aminotransferase (TAT). |
| M42955 | L-Arginine butanoate | L-Arginine butanoate ((S)-(+)-Arginine butanoate) is a compound consisting of L-Arginine and butanoate. |
| M42954 | Fosigotifator | Fosigotifator is modulates the integrated stress response (ISR) for inhibition of ISR-related diseases. |
| M42952 | Squalene synthase-IN-1 | Squalene synthase-IN-1 is a potent antihyperlipidemic agent acting through Squalene Synthase inhibition. |
| M42951 | Dilaurylglycerosulfate sodium | Dilaurylglycerosulfate sodium is a co-emulsifier in the diagnostic test for the determination of lipase. |
| M42949 | Methyl 2-acetoxybenzoate | Methyl 2-acetoxybenzoate (Methyl acetylsalicylate) is a safe and simple anti-inflammatory aspirin precursor. |
| M42948 | α-Amylase-IN-4 | α-Amylase-IN-4 show maximum inhibition of amylase activity with IC50 value 17.83 ± 0.14 μg/mL. |
| M42947 | Fecosterol | Fecosterol is a metabolite of Saccharomyces cerevisiae and can be used in the research of phytosterolemia. |
| M42946 | Viloxazine hydrochloride | Viloxazine hydrochloride is the inactive isomer of Viloxazine, and can be used as an experimental control. |
| M42945 | Decyclohexanamine-Exatecan | Decyclohexanamine-Exatecan is a Camptothecin derivative, compound a, extracted from patent WO2020219287 A1. |
| M42944 | hGAPDH-IN-1 | hGAPDH-IN-1, a 3-bromo-4,5-dihydroisoxazole derivative, is a specific and potent hGAPDH covalent inhibitor. |
| M42943 | Deoxyharringtonine | Deoxyharringtonine is an alkaloid isolated from Cephalotaxus genus with significant anti-leukemic activity. |
| M42942 | PG-11047 tetrahydrochloride | PG-11047 (CGC-11047), a polyamine analogue, is a nonfunctional competitor of the natural polyamine spermine. |
| M42941 | TINK-IN-1 | TINK-IN-1 is a potent and selective Traf2- and Nck-interacting kinase (TNIK) inhibitor with an IC50 of 8 nM. |
| M42940 | ARTD3/PARP3-IN-1 | ARTD3/PARP3-IN-1 is an unselective inhibitor of diphtheria toxin-like ADP-ribosyltransferase 3 (ARTD3)/PARP3. |
| M42939 | Furegrelate | Furegrelate (U-63557A free acid) is a potent, orally available, and selective thromboxane synthase inhibitor. |
| M42938 | Zuclopenthixol decanoate | Zuclopenthixol decanoate is a long-acting agent for schizophrenia and other serious mental illnesses research. |
| M42937 | CVM-05-002 | CVM-05-002 is a PI5P4K inhibitor, with IC50 values of 0.27 μM and 1.7 μM for PI5P4Kα and PI5P4Kβ, respectively. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.
