20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T21919 | UCF 101 | Apoptosis | |
UCF 101 is a specific inhibitor of HtrA2 and reduces apoptosis in PC12 cells. | |||
T40024 | Pomalidomide-PEG1-CO2H | Pomalidomide-PEG1-C2-COOH | E3 Ligase Ligand-Linker Conjugate |
Pomalidomide-PEG1-CO2H is a synthetic E3 ligase ligand-linker conjugate containing a Pomalidomide-based cereblon ligand and a 2-unit PEG linker. | |||
T28437L | Pomisartan 2HCl | Pomisartan 2HCl(144702-17-0 Free base),BIBR363 2HCL | RAAS |
Pomisartan 2HCl (BIBR363 2HCL) is a small molecule AT1R antagonist used to study heart failure and hypertension. | |||
T0818 | Decamethonium bromide | Decacuran,Syncurine | AChR , AChE |
Decamethonium bromide (Syncurine) is a neuromuscular blocker and nicotinic AChR partial agonist. | |||
T23524 | W-84 dibromide | HDMPPA | AChR |
W-84 dibromide (HDMPPA) is a M2-receptor selective modulator. | |||
T1219 | Sisomicin Sulfate | Pathomycin,Extramycin | Antibacterial , Antibiotic |
Sisomicin Sulfate (Pathomycin) is the sulfate salt form of sisomicin, a broad-spectrum aminoglycoside antibiotic isolated from Micromonospora inyoensis. Sisomicin is structurally similar to gentamicin but has a unique un... | |||
T6547 | Ipratropium Bromide | Sch 1000,Itrop,Atrovent | AChR |
Ipratropium Bromide (Sch 1000) is a synthetic anticholinergic agent that is used as an inhalant for treatment of acute bronchospasm due to chronic bronchitis and emphysema. | |||
T33846 | Oxyphenonium bromide | Spasmophen,Oxifenon,Oxyfenon,Atrenyl,Oxyphenon | Others |
Oxyphenonium bromide (Oxyfenon) shows anticholinergic activity and can be used for research on the treatment of gastric and duodenal ulcers and for the relief of visceral spasms. | |||
T7534 | Teriflunomide | A 77-1726 | Others |
Teriflunomide (A 77-1726) is the principal active metabolite of leflunomide, an approved therapy for rheumatoid arthritis and multiple sclerosis. | |||
T9389 | Thalidomide-PEG4-Propargyl | Thalidomide-O-PEG4-Propargyl | E3 Ligase Ligand-Linker Conjugate |
Thalidomide-PEG4-Propargyl (Thalidomide-O-PEG4-Propargyl) is a synthetic E3 ligase ligand-linker conjugate containing a Thalidomide-based cereblon ligand and a linker which can be used in PROTAC technology[1]. | |||
T1522 | Iopromide | Iopromidum,Ultravist | Others |
Iopromide (Iopromidum) is a low osmolar, non-ionic contrast agent for intravascular use. | |||
T9291 | Thalidomide-5-OH | 2-(2,6-dioxopiperidin-3-yl)-5-hydroxyisoindoline-1,3-dione | Others , Ligand for E3 Ligase |
Thalidomide-5-OH (2-(2,6-dioxopiperidin-3-yl)-5-hydroxyisoindoline-1,3-dione) is the Thalidomide-based cereblon ligand that used in the recruitment of CRBN protein. It can be connected to the ligand for protein by a link... | |||
T24730 | Roslin 2 bromide | Roslin-2,Benzylhexamethylenetetramine bromide,Roslin2 | FAK , p53 |
Roslin 2 bromide (Benzylhexamethylenetetramine bromide) is a p53 reactivator that disrupts the binding of FAK and p5. Roslin 2 bromide exhibits anticancer effects. | |||
T0413 | Cinromide | trans-3-Bromo-N-ethylcinnamamide | Others |
Cinromide (trans-3-Bromo-N-ethylcinnamamide) is used as a novel anticonvulsant agent. | |||
T2395L | Vortioxetine hydrobromide | Vortioxetine (Lu AA21004) HBr,Vortioxetine HBr,Lu AA21004 hydrobromide | 5-HT Receptor , Serotonin Transporter |
Vortioxetine hydrobromide (Lu AA21004 hydrobromide) is a serotonin (5-HT) modulator and stimulator (SMS), inhibits 5-HT1A/1B/3A/7 receptor and SERT (IC50: 15/33/3.7/19/1.6 nM). | |||
T19839 | Oxatomide | Oxatomida | P2X Receptor , Calcium Channel , 5-HT Receptor , Histamine Receptor |
Oxatomide (Oxatomida) is a potent and orally active dual H1 histamine receptor and P2X7 receptor antagonist with antihistamine and antiallergic activity.Oxatomide can be used to block ATP-induced currents in the human P2... | |||
T0780 | Pyridostigmine bromide | Mestinon | AChE |
Pyridostigmine bromide (Mestinon) is a cholinesterase inhibitor with a slightly longer duration of action than NEOSTIGMINE. It is used in the treatment of myasthenia gravis and to reverse the actions of muscle relaxants. | |||
T10765 | Eragidomide | CC-90009,Cereblon modulator 1 | Apoptosis , Ligand for E3 Ligase , Molecular Glues |
Eragidomide (CC-90009; Cereblon modulator 1) is a cereblon (CRBN) E3 ligase modulator. Eragidomide specifically binds to CRBN, thereby affecting the activity of the ubiquitin E3 ligase complex. | |||
T17918 | Thalidomide-O-amido-PEG2-C2-NH2 TFA | E3 Ligase Ligand-Linker Conjugates 24 TFA,Cereblon Ligand-Linker Conjugates 10 TFA | Others , E3 Ligase Ligand-Linker Conjugate |
Thalidomide-O-amido-PEG2-C2-NH2 TFA (E3 Ligase Ligand-Linker Conjugates 24 TFA) is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-O-amido-PEG2-C2-NH2 TFA incorporates the Thalidomide based cereblon ligand a... | |||
T26644 | Apomine | SK&F-99085,APB-231-A2,APB-231-A-2,SR-9223i,SK&F-99085,SR-45023A | HMG-CoA Reductase |
Apomine (SR-9223i), an inhibitor of HMG-CoA-reductase, promotes apoptosis of myeloma cells in vitro and has been implicated in the regulation of myeloma in vivo. Apomine accelerates the degradation of 3-hydroxy-3-methylg... |