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Filtered Search Results
eMolecules 1261590-48-0 | Medchem Express | Duvelisib (R enantiomer) | 5mg | 446268210 | HY-17044A | MFCD30187518 | 416.87 | C22H17ClN6O
Ambeed | 2-Ethylhexyl 3-(35-di-tert-butyl-4-hydroxyphenyl)propanoate | 250mg | 696731383 | A1364274 | 144429-84-5 | 390.608 | C25H42O3
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eMolecules 1604810-83-4 | Medchem Express | THZ1 | 5mg | 446271624 | HY-80013 | MFCD28167785 | 566.06 | C31H28ClN7O2
Medchem Express | JI051 | 5mg | 459606917 | HY-117113 | 2234281-75-3 | 364.445 | C22H24N2O3
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eMolecules 174022-42-5 | Medchem Express | Bevirimat | 5mg | 446275447 | HY-N0842 | MFCD00954243 | 584.838 | C36H56O6
ChemScene | 7-Nitroindolin-2-one | 100mg | 572187912 | CS-0094283 | 25369-31-7 | MFCD04088356 | 178.147 | C8H6N2O3
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Cayman Chemical ANTIBODY LysoFP-NO2 25mg
A turn-on lysosome-targeted fluorescent probe for CO; transformed into the highly fluorescent derivative lysoFP-NH2 in the presence of lysosomal CO; selective for CO over reactive nitrogen, oxygen, and sulfur species; ex/em = 440/528 nm, respectively; not cytotoxic to HepG2 cells for up to five hours at 30 µM
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eMolecules 935-69-3 | Ambeed | 7-Methyl-7H-purin-6-amine | 100mg | 600851603 | A574718 | MFCD00127790 | 149.157 | C6H7N5
Ambeed | 7-Methyl-7H-purin-6-amine | 100mg | 600851603 | A574718 | 935-69-3 | MFCD00127790 | 149.157 | C6H7N5
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Medchemexpress LLC Caerulomycin A 100mg | 21802-37-9 | 100 MG
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Caerulomycin A is a natural-product antifungal and antibiotic research compound (CAS 21802-37-9) that modulates immune signaling by enhancing TGF-β-Smad3 and suppressing interferon-γ-induced STAT1 pathways. It is supplied as a solid for laboratory research with reported purity ≥98% and molecular weight 229.23 g·mol-1.
- Antifungal and antibiotic activity.
- Modulates TGF-β-Smad3 and STAT1 signaling.
- Supplied as milligram-scale solid for research use only.
- Reported purity ≥98% (HPLC where reported).
- Soluble in DMSO; store refrigerated or frozen for long-term stability.
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Medchemexpress LLC HY-112633 10mg Medchemexpress, SMN-C3 CAS:1449597-34-5 Purity:>98%
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Medchemexpress, HY-112633 10mg SMN-C3 CAS:1449597-34-5 SMN-C3 is an orally active SMN2 splicing modulator and has the potential to treat spinal muscular atrophy (SMA). 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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Medchemexpress LLC HY-18931A 5mg Medchemexpress, NSC305787 (hydrochloride) CAS:53868-26-1 Purity:>98%
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Medchemexpress, HY-18931A 5mg NSC305787 (hydrochloride) CAS:53868-26-1 NSC305787 hydrochloride is an inhibitor of ezrin with a Kd of 5.85 μM, inhibits the phosphorylation of ezrin caused by PKCΙ with an IC50 of 8.3 μM, has antitumor activity. 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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Medchemexpress LLC Chlorquinaldol | 72-80-0 | 98.7% | 500 MG
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Chlorquinaldol (Chloquinan) is an antibacterial agent with potential use in topical skin conditions and vaginal infections. It is also a β-catenin/TCF4 inhibitor, demonstrating anti-proliferation, anti-migration, and apoptosis-inducing activity in cancer cells.
- Antibacterial agent for topical skin and vaginal infections.
- Acts as a β-catenin/TCF4 inhibitor.
- Demonstrates anti-proliferation and anti-migration activity.
- Induces apoptosis in cancer cells.
- Inhibits Wnt/β-catenin signaling in colorectal cancer cells.
- Reduces β-catenin acetylation, affecting interaction with TCF4.
- Inhibits stemness of colorectal cancer cells.
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Medchemexpress LLC HY-100033 5mg Medchemexpress, NSC5844 CAS:140926-75-6 Purity:>98%
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Medchemexpress, HY-100033 5mg NSC5844 CAS:140926-75-6 NSC5844 is a 4-aminoquinoline derivative, with antitumor and antimalarial activity. 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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eMolecules 2250025-92-2 | Medchem Express | DREADD agonist 21 (dihydrochloride) | 5mg | 761506071 | HY-100234A | 351.28 | C17H20Cl2N4
Ambeed | 22-Disulfanediyldiethanamine | 250mg | 716187862 | A1114607 | 51-85-4 | MFCD01002952 | 152.270 | C4H12N2S2
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Medchemexpress LLC HY-B0548A 500mg Medchemexpress, Hydroxyzine (dihydrochloride) CAS:2192-20-3 Purity:>98%
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Medchemexpress, HY-B0548A 500mg Hydroxyzine (dihydrochloride) CAS:2192-20-3 Hydroxyzine dihydrochloride, a benzodiazepine antihistamine agent, acts as a orally active histamine H1-receptor and serotonin antagonist. Hydroxyzine dihydrochloride has anxiolytic effect and can be used forthe research of generalised anxiety disorder. 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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Medchemexpress LLC Fenbendazole-d3 | 1228182-47-5 | MFCD16652570 | 99.7% | 302.37 g/mol | C15H10D3N3O2S | 10 MG
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Fenbendazole-d3 is a deuterium-labeled analogue of fenbendazole used as an analytical reference standard and tracer in research. It is applied in pharmacokinetic and metabolism studies and shows microtubule destabilizing and antiparasitic activity, with reported antitumor effects in preclinical models.
- Deuterium-labeled reference standard for analytical studies.
- High purity: 99.7% as supplied.
- Suitable for pharmacokinetic and metabolism tracing.
- Exhibits microtubule destabilizing activity and antiparasitic effects.
- Available in small quantities for laboratory use (e.g., 10 mg).
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Medchemexpress LLC Calhex 231 hydrochloride | 2387505-78-2 | MFCD22580412 | 99.8% | 443.41 g·mol⁻¹ | C25H28Cl2N2O | 100 MG
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Calhex 231 hydrochloride is a research-grade small molecule that functions as a negative allosteric modulator of the calcium-sensing receptor (CaSR), inhibiting CaSR-mediated inositol phosphate signaling. It is supplied as a solid, high-purity material intended for in vitro research applications.
- Negative allosteric modulator of the calcium-sensing receptor (CaSR).
- Reported IC50 ≈ 0.39 μM for inhibition of CaSR-mediated inositol phosphate signaling.
- Solid powder with reported solubility in DMSO up to ~50 mM.
- High purity (≈99.8%).
- Intended for in vitro research use only.
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Medchemexpress LLC Mi-389 | 2222635-92-7 | 99.3% | 654.69 g/mol | C35H35FN6O6 | 5 MG
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MI-389 is a proteolysis-targeting chimera (PROTAC) that degrades the translation termination factor GSPT1 through recruitment of the CRL4CRBN E3 ligase. It is provided as a research-grade small molecule with reported antiproliferative activity in leukemia cell lines and is intended for in vitro and cellular studies.
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