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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T28276 | OV-potentiator-28 | OV potentiator 28 | |
OV-potentiator-28 is a potentiator of cancer virotherapy. OV-potentiator-28 significantly enhances virus replication-associated luciferase expression, specifically in tumors. | |||
T25173 | Bradykinin potentiator-5 | BPP-5a\,BPP 5a\,BPP5a\ | |
Bradykinin potentiator-5 is a peptide inflammatory mediator, causes blood vessels to dilate (enlarge), and therefore causes blood pressure to fall. | |||
T76505 | Bradykinin potentiator B | ||
Bradykinin Potentiator B (also known as Bradykinin Potentiating Peptide B), derived from the venom of Agkistrodon halys blomhoffi, serves as a potent ACE inhibitor. It effectively inhibits the activity of bradykinin inhi... | |||
T76507 | Bradykinin potentiator C | ||
Bradykinin Potentiator C, a potent inhibitor of angiotensin-converting enzyme (ACE) with an inhibitory concentration (IC 50) of 7.1 μM for rabbit lung ACE, is regarded as a prototype for functional peptides [1]. | |||
T63003 | NMDA receptor potentiator-1 | ||
NMDA receptor potentiator-1 (Compound 1368) is a subunit-selective NMDA receptor enhancer with IC50 values of 4 μM and 5 μM for NR2C and NR2D expression, respectively. | |||
T23172 | Polygodial | Tadeonal | Antifungal |
Polygodial (Tadeonal) is an antifungal potentiator and an antibiotic, particularly against Saccharomyces cerevisiae, Candida utilis, and Sclerotinia libertiana. | |||
T23515 | VU-29 | VU 29 | GluR |
VU-29 is a positive allosteric mGlu5 receptor modulator with EC50=9 nM and Ki=244 nM for rmGluR5. It is selective for mGluR5 relative to other mGluR subtypes (EC50: rmGluR1/rmGluR2=557 nM/1.5 μM; hmGluR4=154 nM). | |||
T15820 | Mibampator | LY451395 | iGluR |
Mibampator (LY451395) is an effective and selective AMPA receptor potentiator. | |||
TQ0289 | LY450108 | iGluR | |
LY450108 is a potentiator of the AMPA receptor that can be used in Parkinson's disease studies. | |||
T17238 | VU0152100 | VU152100 | AChR |
VU0152100 is an effective and selective allosteric potentiator of M4 mAChR (EC50: 380 ± 93 nM). | |||
T9499 | Icenticaftor | QBW251 | CFTR |
Icenticaftor (QBW251) is an orally active potentiator of CFTR channel. | |||
T2588 | Ivacaftor | Ivacaftor (VX-770),VX-770 | CFTR , Autophagy |
Ivacaftor (VX-770) (VX-770) is a potentiator of CFTR targeting G551D-CFTR (EC50: 100 nM) and F508del-CFTR (EC50: 25 nM) in Fisher rat thyroid cells, respectively. | |||
T23513 | VU10010 | VU 10010 | AChR |
VU10010 (VU 10010) is allosteric potentiator of M4 acetylcholine receptors. | |||
T29123 | VU0152099 | VU 0152099,VU-0152099 | AChR |
VU0152099 is a potent and selective M4 mAChR allosteric potentiator(EC50 = 380 ± 93 nM). | |||
T7083 | GLPG1837 | ABBV-974 | CFTR , Autophagy |
GLPG1837 (ABBV-974) is an effective CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively. | |||
T14971 | CIQ | NMDAR | |
CIQ is a subunit-selective potentiator of NMDA receptors containing the NR2C or NR2D subunit. EC50 value: 2.7 μM for NR2C and 2.8 μM for NR2D. | |||
T0086 | Galanthamine hydrobromide | Galantamine hydrobromide,Galanthamine HBr | AChR , AChE |
Galanthamine hydrobromide (Galantamine hydrobromide), a long-acting and centrally active AChE inhibitor (IC50:410 nM), is an allosteric potentiator at neuronal nicotinic ACh receptors. | |||
T4573 | Cyclothiazide | GluR | |
Cyclothiazide is a benzothiadiazide that acts as a potentiator of AMPA receptorsthat potently inhibits AMPA receptor desensitization, positively modulating its response to glutamic acid (EC50 = 3.8 M). | |||
T8890 | 653-47 hydrochloride | Epigenetic Reader Domain | |
653-47 hydrochloride is a potentiator, significantly potentiates the cAMP-response element binding protein (CREB) inhibitory activity of 666-15. It is also a very weak CREB inhibitor with IC50 of 26.3 μM. | |||
T61301 | Chromenone 1 | TGF-beta/Smad | |
Chromenone 1 is a potent potentiator of osteogenic bone morphogenetic protein (BMP). Chromenone 1 induces a pronounced, kinase-independent, negative TGFβ feedback that enhances nuclear BMP-Smad signaling outputs. |