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Filtered Search Results
Selleck Chemical LLC Nitrofural S1644-2mg
Nitrofural (Nitrofurazone) is a topical anti-infective agent with an IC50 of 22 83 1 2 M (Rat LD50 590 mg/kg)
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Selleck Chemical LLC Taladegib (LY2940680) S2157-5mg
Taladegib (LY2940680) binds to the Smoothened (Smo) receptor and potently inhibits Hedgehog (Hh) signaling Phase 1/2
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eMolecules 108319-06-8 | Medchem Express | Temafloxacin | 5mg | 632896554 | HY-16487 | MFCD00864828 | 417.388 | C21H18F3N3O3
Pharmablock | 5-bromo-2-fluoro-3-nitro-benzoic acid | 250mg | 783661891 | PBT4018 | 1153279-80-1 | MFCD12173024 | 264.006 | C7H3BrFNO4
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Medchemexpress LLC HY-112564 5mg Medchemexpress, JNJ-632 CAS:1572510-42-9 Purity:>98%
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Medchemexpress, HY-112564 5mg JNJ-632 CAS:1572510-42-9 JNJ-632 is a hepatitis B virus (HBV) capsid assembly modulator (CAM). 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 VACUOLIN-1 5MG
VACUOLIN-1 5MG APEXBIO TECHNOLOGIES
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eMolecules 1292821-90-9 | Medchem Express | K-80003 | 5mg | 415690801 | HY-U00458 | 336.406 | C22H21FO2
Ambeed | 3-Oxo-3-(piperidin-1-yl)propanenitrile | 10g | 600845652 | A685211 | 15029-30-8 | MFCD00006487 | 152.197 | C8H12N2O
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Medchemexpress LLC Neo 376 (SPI-376) | 496921-73-4 | 99.2% | 357.88 g/mol | C20H24ClN3O | 25 MG
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NEO 376 (SPI-376) is a small-molecule research compound described as a selective modulator of 5-HT1, GABA, and dopamine receptors with reported antipsychotic activity. Supplied as a white to off-white solid for preclinical research use; available in multiple pack sizes and solution formats.
- Selective modulator of 5-HT1, GABA, and dopamine receptors.
- High purity (99.23%) suitable for research applications.
- Chemical formula C20H24ClN3O; molecular weight 357.88 g/mol.
- Readily soluble in DMSO; manufacturer provides in vivo formulation protocols.
- Available as solids (multiple mg sizes) and 10 mM DMSO solutions for convenience.
- Storage recommendations provided to maintain stability of powder and solutions.
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eMolecules 3,3'-(Isopropylazanediyl)bis(1-(4-((2-isopropoxyethoxy)methyl)phenoxy)propan-2-ol) | Toronto Research Chemicals |591.786 | C33H53NO8CC(C)OCCOCc1ccc(OCC(O)CN(CC(O)COc2ccc(COCCOC(C)C)cc2)C(C)C)cc1 | 50mg | 601597334
3,3'-(Isopropylazanediyl)bis(1-(4-((2-isopropoxyethoxy)methyl)phenoxy)propan-2-ol) | Toronto Research Chemicals |591.786 | C33H53NO8CC(C)OCCOCc1ccc(OCC(O)CN(CC(O)COc2ccc(COCCOC(C)C)cc2)C(C)C)cc1 | 50mg | 601597334
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Medchemexpress LLC Cbp/p300-in-8 | 2304416-91-7 | 99.9% | C27H31N3O4 | 10MG
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CBP/p300-IN-8 is a small-molecule inhibitor that targets the bromodomains of the CBP/p300 family and is used in epigenetic research. It inhibits CBP at low-nanomolar concentrations and exhibits activity against BRD4, and is supplied as a high-purity solid reagent for laboratory studies.
- Potent inhibitor of CBP/p300 bromodomains.
- CBP IC50 0.01-0.1 μM; BRD4 IC50 1-1000 μM.
- Molecular formula C27H31N3O4; molecular weight 461.55.
- High purity (99.94%).
- White to off-white solid for analytical and biological assays.
- Available in small research pack sizes with room-temperature shipping options.
- Storage: powder at -20°C (up to 3 years) or 4°C (up to 2 years); in solvent at -80°C (6 months) or -20°C (1 month).
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eMolecules 618070-67-0 | 5-Amino-1-(4-fluorophenyl)-1H-pyrazole-4-carbohydrazide | Chem-Impex | MFCD03934813 | 235.222 | C10H10FN5O | 98.000 | NNC(=O)c1cnn(c1N)-c1ccc(F)cc1 | 1g | 386899521
5-Amino-1-(4-fluorophenyl)-1H-pyrazole-4-carbohydrazide | Chem-Impex | 618070-67-0 | MFCD03934813 | 235.222 | C10H10FN5O | 98.000 | NNC(=O)c1cnn(c1N)-c1ccc(F)cc1 | 1g | 386899521
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Medchemexpress LLC BSJ-02-162 (CDK4/6-IN-11) | 2139329-47-6 | 98.1% | 831.92 g/mol | C43H49N11O7 | 5 MG
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BSJ-02-162 is a proteolysis-targeting chimera (PROTAC) small molecule for research use that induces degradation of cyclin-dependent kinases CDK4 and CDK6. It links an E3 ligase ligand to a CDK4/6-targeting ligand via a chemical linker to promote targeted proteasomal degradation in biochemical and cell-based studies. Not for human or clinical use.
- Induces selective degradation of CDK4 and CDK6 in cell-based assays.
- Suitable for biochemical and cell-based research into cell cycle pathways.
- Available as solid powder and as a DMSO solution for flexible dosing.
- High reported purity supports reproducible experimental results.
- Compatible with common assay formats and routine handling.
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Medchemexpress LLC HY-107337 5mg Medchemexpress, Delapril (hydrochloride) CAS:83435-67-0 Purity:>98%
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Medchemexpress, HY-107337 5mg Delapril (HCl) CAS:83435-67-0 Delapril is an angiotensin-converting enzyme (ACE) inhibitor for the treatment of cardiovascular diseases. 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 1334921-03-7 | Medchem Express | TAI-1 | 5mg | 779715204 | HY-B0790 | MFCD28348371 | 431.51 | C24H21N3O3S
ChemScene | 3-Bromo-n-(2-biphenylyl)carbazole | 100mg | 632304357 | CS-0161041 | 1609267-04-0 | MFCD30536717 | 398.303 | C24H16BrN
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eMolecules 935467-97-3 | Medchem Express | TH-237A | 5mg | 446259830 | HY-11054 | 333.335 | C18H17F2NO3
Medchem Express | TH-237A | 5mg | 446259830 | HY-11054 | 935467-97-3 | 333.335 | C18H17F2NO3
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Medchemexpress LLC AGI-41998 | 2377492-26-5 | 99.94% | C22H16BrF3N4O2 | 50 MG
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AGI-41998 is a potent and orally active inhibitor of methionine adenosyltransferase 2A (MAT2A) that effectively penetrates the blood-brain barrier. It shows inhibitory activities against MAT2A and S-adenosyl methionine (SAM) in HCT-116 MTAP-null cells with IC50s of 22 nM and 34 nM respectively. AGI-41998 significantly inhibits the proliferation of HCT-116 cells and tumor growth, and can be used to study the role of SAM regulation in the central nervous system (CNS) and colon cancer.
- Potent and orally active inhibitor of MAT2A
- Effectively penetrates the blood-brain barrier
- Exhibits inhibitory activities against MAT2A and SAM in HCT-116 MTAP-null cells
- Significantly inhibits proliferation of HCT-116 cells and tumor growth
- Can be used for research on SAM regulation in the CNS and colon cancer
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