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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T22782 | FGIN-1-27 | Others | |
high affinity agonist of the translocator protein | |||
T1308 | Orphenadrine hydrochloride | Mebedrol,Mephenamin | Sodium Channel , NMDAR , Norepinephrine , iGluR , Histamine Receptor |
Orphenadrine hydrochloride (Mephenamin) is a muscarinic antagonist used to treat drug-induced parkinsonism and to relieve pain from muscle spasm. | |||
T6618 | Orphenadrine Citrate | Flexon,Flexoject,Banflex | AChR , iGluR |
Orphenadrine Citrate (Flexon) is a skeletal muscle relaxant, it acts in the central nervous system to produce its muscle relaxant effects. | |||
T60157 | PBRM1-BD2-IN-8 | Epigenetic Reader Domain | |
PBRM1-BD2-IN-8 (compound 34) is a potent PBRM1 Bromodomain inhibitor (PBRM1-BD2 Kd=4.4 μM, PBRM1-BD2 IC50=0.16 μM; PBRM1-BD5 Kd=25 μM). PBRM1-BD2-IN-8 shows anti-cancer activity. | |||
T60158 | PBRM1-BD2-IN-3 | Epigenetic Reader Domain | |
PBRM1-BD2-IN-3 (compound 12) is a potent inhibitor of PBRM1-BD2, exhibiting an IC50 value of 1.1 μM, and is utilized in anticancer research. | |||
T60156 | PBRM1-BD2-IN-2 | Epigenetic Reader Domain | |
PBRM1-BD2-IN-2, a selective and cell-active inhibitor of the polybromo-1 (PBRM1) bromodomain, exhibits binding affinity and inhibitory activity specifically targeting the PBRM1-BD2 domain, with Kd and IC50 values of 9.3 ... | |||
T60159 | PBRM1-BD2-IN-5 | Epigenetic Reader Domain | |
PBRM1-BD2-IN-5 is a potent inhibitor of the PBRM1 Bromodomain, demonstrating dissociation constant (Kd) values of 1.5 μM and 3.9 μM for PBRM1-BD2 and PBRM1-BD5, respectively, and boasts an inhibitory concentration 50 (IC... | |||
T60155 | PBRM1-BD2-IN-7 | Epigenetic Reader Domain | |
PBRM1-BD2-IN-7, a selective and cell-active inhibitor targeting the polybromo-1 (PBRM1) bromodomain, demonstrates inhibitory efficacy against PBRM1-BD2 with an IC50 value of 0.29 μM. This compound is utilized in cancer r... | |||
T24836 | ß-pBrPh-Glc | Beta-pBrPh-Glc,ßpBrPhGlc,p-Bromophenyl-beta-D-glucopyranoside,p-Bromophenyl-ß-D-glucopyranoside | Antioxidant |
ß-pBrPh-Glc (ßpBrPhGlc) is an inhibitor of ice recrystallization, controlling the growth of extracellular ice and inhibiting the recrystallization of intracellular ice. ß-pBrPh-Glc may be used as a cryopreservative , pos... | |||
T78076 | PBR28 | Others | |
PBR28, a TSPO modulator, holds potential for preventative research in Pulmonary Arterial Hypertension (PAH) and is instrumental in brain positron emission tomography (PET) imaging studies through its capacity for radioac... | |||
T72843 | PBRM1-BD2-IN-6 | ||
PBRM1-BD2-IN-6, a potent inhibitor of the PBRM1 bromodomain, exhibits an IC50 value of 0.22 µM and demonstrates antiproliferative activity. It holds potential for research in PBRM1-dependent cancer treatment. | |||
T70980 | PBRM | ||
PBRM is the first selective, potent, non-estrogenic, irreversible inhibitor of 17β-HSD1. | |||
T72841 | PBRM1-BD2-IN-1 | ||
PBRM1-BD2-IN-1 is a selective and cell-active inhibitor of the polybromo-1 (PBRM1) bromodomain, displaying binding affinity and inhibitory efficacy with Kd and IC50 values of 0.7 μM and 0.2 μM, respectively. This compoun... | |||
T3173 | DAA-1106 | DAA1106 | Others , GABA Receptor |
DAA-1106 is a potent and selective ligand for peripheral benzodiazepine receptor (PBR), acting as a potent and selective agonist at the peripheral benzodiazepine receptor. |