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Filtered Search Results
Medchemexpress LLC Darbufelone mesylate | 139340-56-0 | 99.7% | 428.57 | C19H28N2O5S2 | 25 MG
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Darbufelone mesylate is a research-grade small molecule inhibitor that suppresses cellular production of PGF2α and LTB4. It potently inhibits PGHS-2 (IC50 = 0.19 μM) with substantially lower activity against PGHS-1 (IC50 = 20 μM), and is provided as the methanesulfonate salt for assay and cell-based studies.
- Potent PGHS-2 inhibition (IC50 = 0.19 μM).
- Marked selectivity over PGHS-1 (IC50 = 20 μM).
- High purity, suitable for analytical and biological use (≈99.7%).
- Provided as the mesylate salt for improved handling and stability.
- Characterized molecular weight 428.57 and formula C19H28N2O5S2.
- Intended for research use in biochemical and cell-based assays.
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Medchemexpress LLC Darbufelone mesylate | 139340-56-0 | MFCD00906463 | 99.7% | 428.57 | C19H28N2O5S2 | 50 MG
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Darbufelone mesylate is a research-grade small molecule that inhibits cellular production of prostaglandin F2α and leukotriene B4, with preferential activity against PGHS-2. It is supplied as a solid, high-purity salt suitable for in vitro pharmacology and assay development.
- Dual inhibitor of PGF2α and LTB4 production.
- Potent PGHS-2 inhibition (IC50 = 0.19 μM).
- High-purity solid suitable for research applications.
- Available in small pack sizes for assay development.
- Datasheet, COA, and SDS available for quality and safety information.
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Medchemexpress LLC Cl2a-sn-38 | 1279680-68-0 | 1480.61 | C73H97N11O22 | 50 MG
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CL2A-SN-38 is a drug-linker conjugate composed of the DNA topoisomerase I inhibitor SN-38 linked via a hydrolyzable CL2A linker, intended for antibody-drug conjugate (ADC) research and development. It releases active SN-38 within tumor cells and the tumor microenvironment, producing bystander antitumor effects.
- Drug-linker conjugate designed for ADC development.
- Releases SN-38 within tumor cells and tumor microenvironment.
- Camptothecin-class topoisomerase I inhibitor mechanism.
- Molecular formula C73H97N11O22; molecular weight 1480.61.
- Soluble in DMSO (100 mg/mL) and in documented in vivo formulations.
- Store at -20°C under nitrogen; in solution -80°C (6 months) or -20°C (1 month).
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eMolecules PHENOL, 4-(3-AMINOPROPYL)-2,6-BIS(1,1-DIMETHYLETHYL)- | 19510-14-6 | MFCD13192453 | 0.25g
AstaTech | PHENOL, 4-(3-AMINOPROPYL)-2,6-BIS(1,1-DIMETHYLETHYL)- | 0.25g | 335881740 | P16807 | 95.000 | 19510-14-6 | MFCD13192453 | 263.425 | C17H29NO
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000454352 RUTIN TRIHYDRATE 100MG
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eMolecules Medchem Express / Rotigotine / 10mg / 446271448 / HY-75502 / / 99755-59-6 / MFCD00870193 / 315.480 / C19H25NOS
Medchem Express / Rotigotine / 10mg / 446271448 / HY-75502 / / 99755-59-6 / MFCD00870193 / 315.480 / C19H25NOS
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Medchemexpress LLC HY-100962 50mg Medchemexpress, (E)-AG 99 CAS:122520-85-8 Purity:>98%
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Medchemexpress, HY-100962 50mg (E)-AG 99 CAS:122520-85-8 (E)-AG 99 ((E)-Tyrphostin 46; (E)-Tyrphostin AG 99) is a potent EGFR inhibitor [1] . 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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Selleck Chemical LLC Combretastatin A4-10mg
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Combretastatin A4 is a microtubule-targeting agent that binds β-tubulin with Kd of 0.4 μM.Phase 3.
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eMolecules 2,8-Dimethyl-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole dihydrochloride | 33162-17-3 | MFCD00444963 | 1g
Apollo Scientific | 2,8-Dimethyl-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole dihydrochloride | 1g | 562458260 | OR953929 | | 33162-17-3 | MFCD00444963 | 275.220 | C13H20Cl2N2
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Selleck Chemical LLC TBHQ-100mg
Tert-butylhydroquinone (TBHQ) is an antioxidant compound which is used to prevent lipid peroxidation and shows multiple cytoprotective actions. It is an activator of Nrf2.
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Medchemexpress LLC Theaflavin-3-gallate | 30462-34-1 | MFCD29918450 | 99.9% | 716.60 g/mol | C36H28O16 | 10 MG
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Theaflavin-3-gallate is a polyphenolic theaflavin monomer derived from black tea, supplied as a research-grade reagent for studies of apoptosis, oxidative stress, and DNA damage signaling. It acts as a pro-oxidant in some cancer cell models and can induce p53-dependent cell-cycle arrest and DNA damage via the ATM/Chk/p53 pathway.
- Purity 99.9%.
- Molecular weight 716.60 g/mol.
- Used to study apoptosis and p53-dependent mechanisms.
- Induces oxidative stress and DNA damage in cell-based assays.
- Available in small milligram sizes suitable for analytical work.
- For research use only; not for human or diagnostic use.
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Medchemexpress LLC HY-10358 10mg Medchemexpress, MK-2206 (dihydrochloride) CAS:1032350-13-2 Purity:>98%
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Medchemexpress, HY-10358 10mg MK-2206 (dihydrochloride) CAS:1032350-13-2 MK-2206 dihydrochloride (MK-2206 (2HCl)) is an orally active allosteric AKT inhibitor with IC50s of 5 nM, 12 nM, and 65 nM for AKT1, AKT2, and AKT3, respectively. MK-2206 dihydrochloride induces autophagy. 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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Frontier Specialty Chemicals 5G POTASSIUM 3-TRIFLUOROBORATO
Potassium 3-trifluoroboratopropionate methyl ester
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eMolecules Medchem Express / Mulberroside C / 5mg / 589794234 / HY-N0620 / / 102841-43-0 / MFCD20527296 / 458.463 / C24H26O9
Medchem Express / Mulberroside C / 5mg / 589794234 / HY-N0620 / / 102841-43-0 / MFCD20527296 / 458.463 / C24H26O9
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Medchemexpress LLC HY-102081 2mg Medchemexpress, 2OH-BNPP1 CAS:833481-73-5 Purity:>98%
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Medchemexpress, HY-102081 2mg 2OH-BNPP1 CAS:833481-73-5 2OH-BNPP1 is an inhibitor of BUB1 kinase, a Ser/Thr kinase, used for the treatment of cancer. 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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