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Filtered Search Results
Medchemexpress LLC HY-18299 5mg Medchemexpress, Purvalanol B CAS:212844-54-7 Purity:>98%
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Medchemexpress, HY-18299 5mg Purvalanol B CAS:212844-54-7 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-18768 5mg Medchemexpress, NCT-501 CAS:1802088-50-1 Purity:>98%
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Medchemexpress, HY-18768 5mg NCT-501 CAS:1802088-50-1 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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Medchemexpress LLC HY-W004360 10mg Medchemexpress, BIBR 1087 SE CAS:212321-78-3 Purity:>98%
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Medchemexpress, HY-W004360 10mg BIBR 1087 SE CAS:212321-78-3 BIBR 1087 SE is an intermediate metabolite of dabigatran etexilate. 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 VS-5584 5MG
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501873459 VS-5584 5MG
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MEDCHEMEXPRESS LLC N6-ETHYLADENOSINE 10MG
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501872348 N6-ETHYLADENOSINE 10MG
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MEDCHEMEXPRESS LLC INOLITAZONE DIHYDROCHLORIDE
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501873083 INOLITAZONE DIHYDROCHLORIDE
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MEDCHEMEXPRESS LLC CID-2858522 5MG
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501873272 CID-2858522 5MG
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Medchemexpress LLC Contezolid (MRX-I) | 1112968-42-9 | 99.2% | 408.33 | 50 MG
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Contezolid (MRX-I) | 1112968-42-9 | 99.2% | 408.33 | 50 MG
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Medchemexpress LLC 7-BIA 10mg | 1313403-49-4 | 294.30 g/mol | C15H18O6 | 10 MG
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7-BIA is a small-molecule inhibitor of receptor-type protein tyrosine phosphatase D (PTPRD) used for biochemical and cellular research. Reported activity: PTPRD IC50 ≈ 1-3 μM; PTPRS IC50 = 40 μM. Molecular formula C15H18O6; molecular weight 294.30 g/mol; purity 98.0%.
- Potent PTPRD inhibition (IC50 ≈ 1-3 μM)
- Also inhibits PTPRS (IC50 = 40 μM)
- High stated purity of 98.0%
- Supplied as solid and solution formats for flexible use
- Suitable for biochemical and cellular research applications
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Medchemexpress LLC HY-17505 1g , Candesartan (Cilexetil) TCV-116 CAS:145040-37-5 Purity:98%
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Medchemexpress, HY-17505 1g Candesartan (Cilexetil) TCV-116 CAS:145040-37-5 Formula:C33H34N6O6 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 Upacicalcet sodium | 2052969-18-1 | 99.9% | 373.75 | 1 ML
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Upacicalcet sodium is a non-peptide calcimimetic agent that functions as a calcium-sensing receptor (CaSR) agonist. It is used in secondary hyperparathyroidism (SHPT) research due to its ability to decrease serum intact parathyroid hormone (iPTH) and calcium (Ca2+) levels, which helps reduce hypocalcemia and gastrointestinal complications. This compound also improves vascular calcification and bone disorders in models of adenine-induced SHPT and inhibits cortical pore formation and bone fibrosis in rats with chronic kidney disease (CKD).
- Functions as a CaSR agonist (EC50 = 10.8 nM)
- Increases intracellular Ca2+ and IP-1 in human CaSR-expressing cells
- Reduces serum iPTH, Ca2+, and Pi levels in rats
- Inhibits parathyroid hyperplasia in CKD rat models
- Inhibits ectopic calcification and cortical hole formation in CKD rat models
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eMolecules 25743-12-8 | NH-bis(PEG2-OH) | Broadpharm | MFCD29764330 | 281.349 | C12H27NO6 | 98.000 | OCCOCCOCCNCCOCCOCCO | 1g | 303671216
NH-bis(PEG2-OH) | Broadpharm | 25743-12-8 | MFCD29764330 | 281.349 | C12H27NO6 | 98.000 | OCCOCCOCCNCCOCCOCCO | 1g | 303671216
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Medchemexpress LLC HY-101938 1mg Medchemexpress, Sinefungin CAS:58944-73-3 Purity:>98%
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Medchemexpress, HY-101938 1mg Sinefungin CAS:58944-73-3 Sinefungin is a potent inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2'-)-methyltransferase, and viral multiplication. Sinefungin, a SET7/9 inhibitor, ameliorates renal fibrosis by inhibiting H3K4 methylation. 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 YM-244769 hydrochloride | 837424-39-2 | 99.0% | 479.93 g·mol⁻1 | C26H23ClFN3O3 | 5 MG
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YM-244769 hydrochloride is a potent, selective, and orally active Na+/Ca2+ exchanger (NCX) inhibitor used in preclinical research. It preferentially inhibits NCX3 with low-nanomolar activity and has demonstrated neuroprotective effects in cell models and effects on urine volume and electrolyte excretion in animal studies.
- Potent, selective inhibition of Na+/Ca2+ exchanger (NCX3) with low-nanomolar potency.
- Orally active pharmacology suitable for in vivo preclinical studies.
- Demonstrated neuroprotective activity in hypoxia/reoxygenation cell models.
- Shown to increase urine volume and electrolyte excretion in animal studies.
- Provided as a high-purity solid with recommended cold storage for stability.
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Medchemexpress LLC Upacicalcet (sodium) | 2052969-18-1 | 99.9% | 373.75 | 50 MG
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Upacicalcet (sodium) | 2052969-18-1 | 99.9% | 373.75 | 50 MG
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