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Filtered Search Results
eMolecules 199864-88-5 | Ambeed | 4-(4-Fluoronaphthalen-1-yl)-6-isopropylpyrimidin-2-amine maleate | 100mg | 595927932 | A123169 | MFCD22628775 | 397.406 | C21H20FN3O4
Medchem Express | TRPM4-IN-1 | 10mg | 592903570 | HY-122605 | 351424-20-9 | MFCD01930120 | 340.160 | C15H11Cl2NO4
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Medchemexpress LLC Milvexian | 1802425-99-5 | 99.9% | 626.44 g/mol | C28H23Cl2F2N9O2 | 5MG
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Milvexian is an orally bioavailable, reversible small-molecule inhibitor of coagulation factor XIa intended for research use in antithrombotic and coagulation studies. The compound is supplied as a solid (white to off-white) and is accompanied by analytical documentation to support its use in preclinical and mechanistic experiments.
- Orally bioavailable, reversible factor XIa inhibitor.
- Molecular formula C28H23Cl2F2N9O2 and molecular weight 626.44 g/mol.
- Reported purity 99.93%.
- Provided as a solid, white to off-white powder.
- Supplied in small research quantities, for example 5 mg packages.
- Documentation available: datasheet, certificate of analysis, HNMR, LC-MS, and safety data sheet.
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eMolecules 84558-03-2 | 2-(4-ISOPROPYLPHENYL)ETHANAMINE | MFCD06212662 | 5g
WuXi ChemSupply | 2-(4-ISOPROPYLPHENYL)ETHANAMINE | 5g | 599168871 | LN01803386 | 95.000 | 84558-03-2 | MFCD06212662 | 163.264 | C11H17N
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Medchemexpress LLC Calcium-Sensing receptor antagonist I | 478963-79-0 | 98.95% | C23H24N2O2 | 50 MG
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Calcium-Sensing receptor antagonist I (HY-50713) is a click chemistry reagent containing an Alkyne group. It is designed for research use and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Contains an alkyne group
- Enables copper-catalyzed azide-alkyne cycloaddition
- Antagonist of calcium-sensing parathyroid hormone receptors
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eMolecules 118414-82-7 | Medchem Express | MK-886 | 5mg | 446263888 | HY-14166 | MFCD00876710 | 472.08 | C27H34ClNO2S
ChemScene | (S)-tert-Butyl 2-(5-(4-iodophenyl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate | 100mg | 768994374 | CS-0618211 | 1242094-29-6 | MFCD30489068 | 439.297 | C18H22IN3O2
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Medchemexpress LLC RO-3 | 1026582-88-6 | 97.3% | 302.37 | 5 MG
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RO-3 is a potent, and orally active P2X3 and P2X2/3 antagonist with pIC50s of 5.9 and 7.0 for human homomultimeric P2X3 and heteromultimeric P2X2/3 receptors, respectively. It shows selectivity for P2X3 and P2X2/3 over all other functional homomultimeric P2X receptors (IC50 >10 μM at P2X1,2,4,5,7).
- Reduces afferent nerve activity induced by distension or α,β-meATP in guinea pig ureter-afferent nerve and mouse bladder-pelvic nerve preparations.
- Has activity in several rodent models of pain, as well as in cystometry models optimized to measure various parameters associated with sensory regulation of the micturition reflex.
- Exhibits moderate to high metabolic stability in rat and human hepatocytes and liver microsomes, is highly permeable, orally bioavailable (14%), and has a reasonable in vivo plasma half-life (t1/2=0.41 h) in rats.
- Appearance: Solid.
- Color: Yellow to orange.
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eMolecules 27465-52-7 | 1-(4-Isopropylphenyl)propan-1-one | Combi-Blocks | MFCD01095865 | 176.259 | C12H16O | 97.000 | CCC(=O)c1ccc(cc1)C(C)C | 25g | 439371923
1-(4-Isopropylphenyl)propan-1-one | Combi-Blocks | 27465-52-7 | MFCD01095865 | 176.259 | C12H16O | 97.000 | CCC(=O)c1ccc(cc1)C(C)C | 25g | 439371923
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Medchemexpress LLC HY-101441A 5mg Medchemexpress, ST-193 (hydrochloride) CAS: Purity:>98%
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Medchemexpress, HY-101441A 5mg ST-193 (hydrochloride) CAS: ST-193 hydrochloride is a potent broad-spectrum arenavirus inhibitor; inhibits Guanarito, Junin, Lassa and Machupo virus with IC 50 values of 0.44, 0.62, 1.4 and 3.1 nM, 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.
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Apexbio Technology LLC GSK 4716 101574-65-6 10mg
GSK 4716 (CAS 101574-65-6) is a small-molecule agonist targeting estrogen-related receptors ERR and ERR It is designed to activate these nuclear receptors thereby modulating mitochondrial function and cellular energy metabolic processes GSK 4716 exerts its biological activity primarily through nuclear receptor-mediated gene regulation pathways Based on these pharmacological properties GSK 4716 holds research potential in investigating mitochondrial bioenergetics metabolic regulation and pathophysiological conditions related to metabolic disorders
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Medchemexpress LLC Foropafant | 136468-36-5 | 99.9% | 50 MG
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Foropafant (SR27417) is a highly potent, competitive, selective, and orally active antagonist of the platelet-activating factor (PAF) receptor. It exhibits a Ki value of 57 pM for [3H]PAF binding, which is at least 5-fold lower than that of unlabeled PAF itself, and potently inhibits PAF-induced aggregation of rabbit and human platelets. This product is for research use only.
- Highly potent
- Competitive, selective, and orally active antagonist of the platelet-activating factor (PAF) receptor
- Ki value of 57 pM for [3H]PAF binding
- Potently inhibits PAF-induced aggregation of rabbit and human platelets
- Intended for research use only
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eMolecules 80225-53-2 | Medchem Express | Rosmanol | 5mg | 434310730 | HY-N5015 | MFCD12031636 | 346.423 | C20H26O5
Medchem Express | Rosmanol | 5mg | 434310730 | HY-N5015 | 80225-53-2 | MFCD12031636 | 346.423 | C20H26O5
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Medchemexpress LLC Denudatin B | 87402-88-8 | 5 MG
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Denudatin B is an antiplatelet agent that relaxes vascular smooth muscle by inhibiting Ca2+ influx through voltage-gated and receptor-operated Ca2+ channels. It exhibits a nonspecific antiplatelet action.
- Antiplatelet agent
- Relaxes vascular smooth muscle
- Inhibits Ca2+ influx through voltage-gated and receptor-operated Ca2+ channels
- Nonspecific antiplatelet action
- Molecular formula: C21H24O5
- Molecular weight: 356.41
- Target: Calcium channel
- Pathway: Membrane transporter/ion channel; neuronal signaling
- Soluble in DMSO (50 mg/mL)
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Medchemexpress LLC Tetrahydropiperine | 23434-88-0 | MFCD17167032 | 99.4% | 289.37 g·mol-1 | C17H23NO3 | 10 MG
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Tetrahydropiperine is a research-grade small molecule used to probe inflammatory and survival signaling pathways in cellular and biochemical studies. It acts on NF-κB and MAPK signaling and modulates the PI3K/Akt/mTOR pathway.
- Selective inhibitor of NF-κB and MAPKs, useful for pathway studies.
- Modulates PI3K/Akt/mTOR signaling for research on cell survival.
- High purity solid, suitable for analytical and cellular assays.
- Available in small research pack sizes for screening and mechanism-of-action work.
- Molecular weight approximately 289.37 g·mol-1 and formula C17H23NO3.
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Frontier Specialty Chemicals 250MG 1,3-BIS(2,6-DIISOPROPYLP
1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene copper(I) chloride; CAS: 578743-87-0; 250mg
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eMolecules 317319-10-1 | 2-(4-HYDROXY-2-METHYLPHENOXY)-ACETIC ACID METHYL ESTER | MFCD07778439 | 1g
Ambeed | 1144771010-Octamethyl-2347891012-octahydro-1H-dibenzo[bh]fluorene | 250mg | 525017491 | A119735 | 77308-48-6 | MFCD23135524 | 386.623 | C29H38
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