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Filtered Search Results
Medchemexpress LLC FC131 TFA | 842166-42-1 | 99.9% | 843.85 | 10 MG
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FC131 TFA is a CXCR4 antagonist that inhibits [125I]-SDF-1 binding to CXCR4 with an IC50 of 4.5 nM. It also exhibits anti-HIV activity. It is for research use only and not sold to patients.
- Inhibits [125I]-SDF-1 binding to CXCR4 with an IC50 of 4.5 nM
- Exhibits anti-HIV activity
- Appearance: solid
- Color: white to off-white
- Soluble in DMSO (100 mg/mL)
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Medchemexpress LLC DX600 | 478188-26-0 | 99.7% | 3074.33 | 10 MG
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DX600 is a selective ACE2 specific inhibitor with a KD of 1.3 nM, and it does not cross-react with ACE. It exacerbates diabetes-induced cardiovascular dysfunction and increases cardiac and renal NOX activity.
- Inhibits rhACE2 activity
- Decreases NR 8383 cell growth and increases TNF-a and IL-6 content in the supernatant
- Exacerbates diabetes-induced cardiovascular dysfunction in Streptozotocin-treated diabetic rats
- Increases thrombus weight in a thrombosis model in rats
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Medchemexpress LLC BA 1 TFA | 99.4% | 1247.32 | 5 MG
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BA 1 TFA is a potent agonist for the bombesin (BB) family of receptors. It binds with high affinity to Bombesin receptor subtype-3 (BRS3), gastrin releasing peptide receptor (GRPR), and neuromedin B receptor (NMBR) with IC50s of 6, 0.4, and 2.5 nM respectively. BA1 (0.1 μM) significantly increases FAK tyrosine phosphorylation in BRS-3 transfected NCI-H1299 cells.
- Potent agonist for bombesin (BB) family of receptors
- Binds with high affinity to BRS3 (IC50 6 nM)
- Binds with high affinity to GRPR (IC50 0.4 nM)
- Binds with high affinity to NMBR (IC50 2.5 nM)
- Significantly increases FAK tyrosine phosphorylation in BRS-3 transfected NCI-H1299 cells
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Medchemexpress LLC N-(4-chloro-3-nitrophenyl)-4-nitro-2,1,3-benzoxadiazol-5-amine | 313964-19-1 | 99.9% | 335.66 g/mol | C12H6ClN5O5 | 10 MG
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HIF-2α-IN-3 is a small-molecule allosteric inhibitor of hypoxia-inducible factor-2α (HIF-2α) used as a research reagent in studies of hypoxia signaling and oncology. Reported biochemical activity includes an IC50 of 0.4 μM and a KD of 1.1 μM; the compound is supplied as a high-purity solid for laboratory use.
- Allosteric HIF-2α inhibition with reported IC50 0.4 μM and KD 1.1 μM.
- Suitable for in vitro studies of hypoxia signaling and cancer biology.
- High purity suitable for research applications.
- Supplied as a light yellow solid for standard laboratory handling.
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Medchemexpress LLC NELOCIGUAT 10 mg
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NELOCIGUAT 10MG
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Medchemexpress LLC OD36 | 1638644-62-8 | 99.3% | 330.77 | 5 MG
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OD36 | 1638644-62-8 | 99.3% | 330.77 | 5 MG
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Medchemexpress LLC F-15599 tosylate (NLX-101 tosylate) | 955112-72-8 | 567.05 | 100 MG
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F-15599 tosylate is a highly selective G-protein biased 5-HT1A receptor agonist, with a Ki of 3.4 nM. It is intended for research use only.
- Highly selective G-protein biased 5-HT1A receptor agonist
- Ki of 3.4 nM
- Related to neurological, eye or ear disease research
- Can be found in compound screening libraries
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Medchemexpress LLC DAA-1106 | 220551-92-8 | 99.9% | 395.42 | 100 MG
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DAA1106 is a peripheral benzodiazepine receptor (PBR) agonist that is permeable to the blood-brain barrier, but has no affinity for GABAA receptors.
- Acts as a peripheral benzodiazepine receptor agonist
- Permeable to the blood-brain barrier
- No affinity for GABAA receptors
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Medchemexpress LLC Sodium 2-(3-(2,6-difluoro-4-(1H-pyrazol-4-yl)phenyl)-3-oxoprop-1-en-1-yl)-4-(1-methyl-1H-pyrazol-4-yl | 2519537-70-1 | 98.9% | 50 MG
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HOIPIN-8 is a research small-molecule inhibitor of the linear ubiquitin chain assembly complex (LUBAC) used to probe ubiquitination and NF-κB signaling in biochemical and cell-based studies. It is supplied as a sodium salt with a molecular weight of 456.38 g/mol.
- Molecular weight 456.38 g/mol
- Molecular formula C23H15F2N4NaO3
- Potent LUBAC inhibitor with IC50 of 11 nM
- Soluble in DMSO at 50 mg/mL and formulatable for in vivo dosing
- Store sealed at -20°C; in solution store at -80°C for long-term stability
- Suitable for biochemical assays and cell-based research
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Medchemexpress LLC 2-(((r)-3-(chlorophenyl)-1-((r)-1-hydroxypropan-2-yl)sulfonyl)-1-(2-hydroxypropan-2-yl)piperidin-4-yl)methanamine | 1838123-21-9 | 99.5% | 100MG
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2-(((r)-3-(chlorophenyl)-1-((r)-1-hydroxypropan-2-yl)sulfonyl)-1-(2-hydroxypropan-2-yl)piperidin-4-yl)methanamine | 1838123-21-9 | 99.5% | 100MG
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Medchemexpress LLC (Rac)-MEM 1003 | 165187-25-7 | 99.6% | 5MG
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(Rac)-MEM 1003 | 165187-25-7 | 99.6% | 5MG
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Medchemexpress LLC RORT INVERSE AGONIS 100 mg
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RORT INVERSE AGONIS 100MG
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Medchemexpress LLC AHR ANTAGONIST 2 50 mg
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AHR ANTAGONIST 2 50MG
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Medchemexpress LLC Elabela(19-32) (TFA) | 98.8% | 1821.05 | 5 MG
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Elabela(19-32) TFA is an active fragment of ELABELA (ELA) that binds to the apelin receptor (APJ). It activates the Gαi1 and β-arrestin-2 signaling pathways, induces receptor internalization, and has demonstrated effects on cardiovascular function, including reducing arterial pressure and exerting positive inotropic effects on the heart.
- Binds to apelin receptor (APJ)
- Activates Gαi1 and β-arrestin-2 signaling pathways with EC50s of 8.6 nM and 166 nM, respectively
- Induces receptor internalization with an EC50 of 36 nM in HEK293 cells
- Reduces arterial pressure
- Exerts positive inotropic effects on the heart
- Has a Ki of 0.93 nM for binding of radioligand apelin-13[Glp65, Nle75, Tyr77][125I]
- Rapidly metabolized in rat plasma (t1/2<2 min)
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Medchemexpress LLC BAM(8-22) | 412961-36-5 | 99.89% | 1971.20 | 5 MG
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BAM(8-22), a proteolytically cleaved product of proenkephalin A and sensory neuron-specific receptor (SNSR) agonist, is a potent activator of Mas-related G-protein-coupled receptors (Mrgprs), specifically MrgprC11 and hMrgprX1. It induces scratching in mice in an Mrgpr-dependent manner. Additionally, BAM(8-22) has an analgesic effect and can inhibit the activation of microglia.
- Potent activator of Mas-related G-protein-coupled receptors (Mrgprs).
- Induces scratching in mice in an Mrgpr-dependent manner.
- Has an analgesic effect.
- Inhibits the activation of microglia.
- Increases miR-184 level in LPS-treated BV-2 cells.
- Reduces Iba-1 and inflammatory cytokines in LPS-treated BV-2 cells.
- Diminishes NMDA-evoked nocifensive behaviors and hyperalgesia in rat pain models.
- Reduces NMDA-evoked expression of FLI and NADPH reactivity in the spinal dorsal horn.
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