| 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 |
| 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. |
| M42936 | PBR28 | PBR28 is an TSPO modulator, which can be used for prevention research of Pulmonary Arterial Hypertension (PAH). |
| M42935 | DNA polymerase-IN-4 | DNA polymerase-IN-4, a coumarin derivative, has antiretroviral activity with IC50 value of 134.22 μM. |
| M42934 | JH-131e-153 | JH-131e-153, a diacylglycerol (DAG)-lactone, is a small molecule activator of Munc13-1, targeting the C1 domain. |
| M42933 | Isoxaben | Isoxaben, a herbicide, inhibits incorporation of radiolabeled glucose into an acid insoluble cell wall fraction. |
| M42932 | Triptoquinone H | Triptoquinone H is a class of natural product isolated from traditional Chinese medicine Tripterygium hypoglaucu. |
| M42931 | AC-099 hydrochloride | AC-099 hydrochloride is a selective NPFF2R full agonist (EC50=1189 nM) and NPFF1R partial agonist (EC50=2370 nM). |
| M42930 | PI5P4Ks-IN-3 | PI5P4Ks-IN-3 is a covalent inhibitor of PI5P4K with IC50s of 1.34 μM (PI5P4Kα), and 9.9 μM (PI5P4Kβ), respectively. |
| M42929 | 9-Deazaguanine | 9-Deazaguanine is a nucleoside analog with potent inhibitory activity against purine nucleoside phosphorylase (PNP). |
| M42928 | Serine Hydrolase inhibitor-21 | Serine Hydrolase inhibitor-21, a pyridine, is a serine hydrolase inhibitor with a Ki of 429 nM for BuChE. |
| M42927 | Merodantoin | Merodantoin has significant antitumor activity in vitro and in vivo, and has less toxicity to normal cells and tissues. |
| M42926 | Lofepramine | Lofepramine (Lopramine) is a potent tricyclic antidepressant and is extensively metabolised to Desipramine. Lofepramine may also potentiate serotoninergic neurotransmission by inhibition of the neuronal uptake of serotonin and the enzyme tryptophan pyrrolase. |
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