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Filtered Search Results
eMolecules EMOLECULES INC
5000474042 2 4-DICHLORO-7H-PYRROLO 2 25MG
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eMolecules EMOLECULES INC
5000474043 2 4-DICHLORO-7H-PYRROLO 2 50MG
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Medchemexpress LLC B7-H6 Human HEK293 50ug
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B7-H6 a distinctive monomeric protein uniquely triggers NCR3-dependent natural killer (NK) cell activation specifically interacting with NCR3 while avoiding engagement with other NK cell-activating receptors (NCR1 NCR2 and KLRK1) This specificity underscores B7-H6 s unique role in initiating NK cell responses through the NCR3 pathway within the intricate network of NK cell activation mechanisms B7-H6 Protein Human (HEK293 Fc) is the recombinant human-derived B7-H6 protein expressed by HEK293 with C-hFc labeled tag
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Medchemexpress LLC B7-H6 Human HEK293 5ug
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B7-H6 a distinctive monomeric protein uniquely triggers NCR3-dependent natural killer (NK) cell activation specifically interacting with NCR3 while avoiding engagement with other NK cell-activating receptors (NCR1 NCR2 and KLRK1) This specificity underscores B7-H6 s unique role in initiating NK cell responses through the NCR3 pathway within the intricate network of NK cell activation mechanisms B7-H6 Protein Human (HEK293 Fc) is the recombinant human-derived B7-H6 protein expressed by HEK293 with C-hFc labeled tag
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eMolecules EMOLECULES INC
5000473854 2 4-DICHLORO-7H-PYRROLO 2 25MG
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Sigma Aldrich Fine Chemicals Biosciences MCF 7/S0.5 Human Breast Ca
Estrogen receptor-positive breast cancer is the most common type of breast cancer. About 80% of all breast cancers express the estrogen receptor (ER) and depend on estrogen to support the growth and spread of the cancer cells. Hormonal therapy such as tamoxifen may help slow or stop the growth of ER breast cancers by blocking the actions of estrogen. Primary or acquired tamoxifen resistance poses a major clinical challenge in the treatment of ER breast cancer. The MCF-7/S0.5 is the parental line from which many tamoxifen-resistant cell lines have been derived and is utilized as a parental control to its derivative cell lines in parallel experiments.The presence of hormones in the serum required in tissue culture media complicates the demonstration of specific hormone and antihormone effects. The MCF-7/S0.5 human breast cancer cells have been adapted to long-term growth in low serum concentration (0.5% fetal bovine serum) by a stepwise reduction of the medium serum content from 5% to
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Medchemexpress LLC HY-13417 500mg , AICAR Acadesine;AICA Riboside CAS:2627-69-2 Purity:98%
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Medchemexpress, HY-13417 500mg AICAR Acadesine;AICA Riboside CAS:2627-69-2 Formula:C9H14N4O5 AMPK Purity:98% AICAR is an activator of AMP-activated protein kinase ( AMPK ), down-regulates the insulin receptor expression in HepG2 cells. 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 EMOLECULES INC
5000492806 2 9-DICHLORO-1 10-PHENANTHR 1G
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Medchemexpress LLC M-89 | 2363165-42-6 | 99.1% | 657.87 g/mol | C37H47N5O4S | 5 MG
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M-89 is a potent, selective menin-MLL interaction inhibitor supplied as a research compound for preclinical biochemical and cellular studies. It is used to disrupt the menin-MLL protein-protein interaction in epigenetic and leukemia research.
- Potent menin-MLL protein-protein interaction inhibitor (Kd 1.4 nM).
- High purity (99.1%) suitable for biochemical assays.
- Soluble in DMSO at approximately 7.35 mg/mL with ultrasonic assistance.
- Available in small research quantities for exploratory studies.
- Stable when stored as powder at low temperatures for long-term use.
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Medchemexpress LLC (1R)-tenofovir amibufenamide | 1571076-15-7 | 98.1% | C22H31N6O5P | 10MG
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(1R)-Tenofovir amibufenamide is an investigational antiviral prodrug of tenofovir provided for research use. It is active against hepatitis B virus and HIV pathways and is supplied as a solid reagent for in vitro and preclinical studies; not for human or clinical use. Chemical identifiers include CAS 1571076-15-7, molecular formula C22H31N6O5P, and molecular weight 490.49 g/mol.
- High purity 98.13%.
- Molecular weight 490.49 g/mol.
- Molecular formula C22H31N6O5P.
- Active against HBV and HIV in preclinical assays.
- Provided in milligram-scale quantities suitable for research.
- Intended for in vitro and preclinical research, not for human use.
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![Medchemexpress LLC N-[(3-aminophenyl)methyl]-6-[4-[(3-fluorophenyl)methoxy]phenoxy]pyridine-3-carboxamide | 838819-70-8 | MFCD28160863 | 99.2% | C26H22FN3O3 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000260319.png-250.jpg)
Medchemexpress LLC N-[(3-aminophenyl)methyl]-6-[4-[(3-fluorophenyl)methoxy]phenoxy]pyridine-3-carboxamide | 838819-70-8 | MFCD28160863 | 99.2% | C26H22FN3O3 | 10MG
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YM-244769 is a potent, selective, orally active Na+/Ca2+ exchanger (NCX) inhibitor with preferential activity against NCX3, used in research to investigate NCX function and calcium handling in cellular and in vivo studies.
- Potent and selective NCX inhibitor with preference for NCX3.
- High purity: 99.2%.
- Solid, off-white to light yellow appearance.
- Soluble in DMSO (≈120 mg/mL); suitable for in vitro use and for formulation in vivo studies.
- Storage: sealed at 4°C; solutions stable at -80°C for up to 6 months.
- Available in small research pack sizes to support experimental workflows.
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Sigma Aldrich Fine Chemicals Biosciences Candesartan cilexetil European Pharmacopoeia (EP) Reference Standard | 145040-37-5 | MFCD00871371 |
Candesartan cilexetil European Pharmacopoeia (EP) Reference Standard | Mol Wt: 610.66 | 145040-37-5 | MFCD00871371 |
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Sigma Aldrich Fine Chemicals Biosciences Candesartan cilexetil for system suitability European Pharmacopoeia (EP) Reference Standard | 145040-37-5 | MFCD00871371 |
Candesartan cilexetil for system suitability European Pharmacopoeia (EP) Reference Standard | Mol Wt: 610.66 | 145040-37-5 | MFCD00871371 |
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![Medchemexpress LLC 5-[(E)-2-thiophen-2-ylethenyl]-1H-pyrazole | 1070881-42-3 | 99.9% | C9H8N2S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000258416.png-250.jpg)
Medchemexpress LLC 5-[(E)-2-thiophen-2-ylethenyl]-1H-pyrazole | 1070881-42-3 | 99.9% | C9H8N2S | 10MG
Terevalefim (ANG-3777) is a small-molecule hepatocyte growth factor (HGF) mimetic that selectively activates the c-Met receptor. It has been used in preclinical studies to decrease apoptosis, increase cellular proliferation, and promote organ repair and function. For research use only; not for clinical use or sale to patients.
- Selectively activates the c-Met receptor in cellular assays.
- Demonstrated to decrease apoptosis and promote proliferation in preclinical models.
- High chemical purity suitable for research applications.
- Solid, white to light brown appearance for convenient handling and storage.
- Soluble in DMSO at high concentration; ultrasonic agitation recommended.
- Stable when stored under recommended cryogenic conditions.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Sigma Aldrich Fine Chemicals Biosciences Etomidate >98% (HPLC), powder | Purity: >98% (HPLC) | Mol Wt: 244.29 | 33125-97-2 | MFCD00869295 | 10MG
Etomidate >98% (HPLC), powder | Purity: >98% (HPLC) | Mol Wt: 244.29 | 33125-97-2 | MFCD00869295 | 10MG
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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