Pyrroles
eMolecules 821794-90-5 | Medchem Express | CMK | 2mg | 446271303 | HY-52101 | MFCD18379168 | 358.83 | C18H19ClN4O2
Medchem Express | CMK | 2mg | 446271303 | HY-52101 | 821794-90-5 | MFCD18379168 | 358.830 | C18H19ClN4O2
eMolecules 1632006-28-0 | Medchem Express | Esaxerenone | 1mg | 446255549 | HY-100471 | 466.48 | C22H21F3N2O4S
Medchem Express | N-deacetylated BMS-202 | 5mg | 446270231 | HY-19745A | 2310135-18-1 | MFCD31382120 | 377.488 | C23H27N3O2
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Medchemexpress LLC Az-PFKFB3-67 | 1704741-11-6 | MFCD30536361 | 97.0% | 455.51 | C26H25N5O3 | 10 MG
A potent, selective small-molecule inhibitor of PFKFB3 for biochemical and cellular research. It is supplied as a white to off-white solid (C26H25N5O3, 455.51 g/mol) with reported purity of ~97% and high solubility in DMSO, intended for in vitro studies of glycolytic regulation.
- Potent inhibition of PFKFB3 (IC50 11 nM).
- Selective activity versus related isoforms (PFKFB2 IC50 159 nM; PFKFB1 IC50 1130 nM).
- Suitable for biochemical and cellular assays.
- High solubility in DMSO, enabling concentrated stock solutions.
- Stable as a powder at -20°C for long-term storage.
- Available in small research pack sizes for assay development.
Medchemexpress LLC Ripk1-in-10 | 2682889-51-4 | MFCD34676845 | 98.3% | 574.58 g/mol | C30H28F2N6O4 | 5 MG
RIPK1-IN-10 is a research-grade small-molecule inhibitor of receptor-interacting protein kinase 1 (RIPK1), described as example 37 in patent WO2021160109. The compound is supplied as a purified solid for in vitro research, with reported purity of approximately 98.3%, molecular weight 574.58 g/mol, and CAS 2682889-51-4.
Medchemexpress LLC HY-18971 5mg Medchemexpress, TG4-155 CAS:1164462-05-8 Purity:>98%
Medchemexpress, HY-18971 5mg TG4-155 CAS:1164462-05-8 TG4-155 is a potent, brain-permeant and selective EP2 receptor antagonist with a K i of 9.9 nM [1] [2] . TG4-155 shows low nanomolar antagonist activity against only EP2 and DP1 [1] . TG4-155 has an EP2 Schild K B of 2.4 nM and displays 550-4750-fold selectivity for EP2 over EP1, EP3, EP4 and IP, but only 14-fold selectivity against the DP1 receptor [2] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
![Medchemexpress LLC 2-methyl-N-([1-(4-phenylpiperazin-1-yl)cyclohexyl]methyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxami | 1428327-35-8 | MFCD34676648 | 98.2% | 446.63 | C28H38N4O | 5MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000237944.png-250.jpg)
Medchemexpress LLC 2-methyl-N-([1-(4-phenylpiperazin-1-yl)cyclohexyl]methyl)-1,2,3,4-tetrahydroisoquinoline-5-carboxami | 1428327-35-8 | MFCD34676648 | 98.2% | 446.63 | C28H38N4O | 5MG
JNJ-42253432 is a centrally penetrant, high-affinity, orally active P2X7 receptor antagonist used as a research tool to study P2X7-mediated neuroinflammation and brain receptor occupancy. It exhibits high potency in preclinical assays and has documented in vivo brain occupancy at low systemic doses.
Medchemexpress LLC TLR7/8 agonist 3 | 642473-95-8 | 100.0% | 50 MG
A potent agonist for TLR7 and TLR8, this compound is derived from patent WO2016057618 (compound of formula (II)) and is intended for research use only. It induces IFN-α and TNF-α in PBMC with EC50 values of 0.12 μM and 0.37 μM, respectively.
- Potent agonist for TLR7 and TLR8.
- Induces IFN-α and TNF-α.
- Suitable for in vitro research applications.
Medchemexpress LLC HY-101971 10mg Medchemexpress, AZ PFKFB3 26 CAS:1704740-52-2 Purity:>98%
Medchemexpress, HY-101971 10mg AZ PFKFB3 26 CAS:1704740-52-2 AZ PFKFB3 26 is a potent and selective inhibitor of the metabolic kinase PFKFB3 with an IC50 of 23 nM. AZ PFKFB3 26 inhibits PFKFB1 and PFKFB2 with IC50s of 2.06 and 0.384 μM, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.