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Filtered Search Results
Medchemexpress LLC HY-18776 100mg Medchemexpress, A2AR-agonist-1 CAS:41552-95-8 Purity:98%
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Medchemexpress,HY-18776 100mg A2AR-agonist-1 CAS:41552-95-8 Formula:C20H22N6O4 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 MEDCHEMEXPRESS LLC
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5000380770 HDHODH-IN-1 100MG
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Medchemexpress LLC Famciclovir | 104227-87-4 | ≥98% | 321.33 | 500 MG
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Famciclovir (BRL 42810) is an orally active nucleoside analogue and an antiviral agent with potent activities against HBV, HSV and VZV. It can be used for the research of herpesvirus infection. It effectively cures necrotic hepatitis in mice.
- Orally active nucleoside analogue
- Antiviral agent with potent activities against HBV, HSV and VZV
- Used for the research of herpesvirus infection
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Medchemexpress LLC HY-103181 10mg Medchemexpress, N6-Cyclopentyladenosine CAS:41552-82-3 Purity:>98%
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Medchemexpress, HY-103181 10mg N6-Cyclopentyladenosine CAS:41552-82-3 N6-Cyclopentyladenosine (CPA) is a selective Adenosine A1 receptor agonist, with Ki values of 2.3 nM, 790 nM and 43 nM for human A1, A2A and A3 receptors, respectively. 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 2408840-41-3 | Medchem Express | Imlunestrant (tosylate) | 5mg | 783660502 | HY-145572A | 696.71 | C36H32F4N2O6S
Ambeed | 5-Bromo-3-methyl-1H-pyrazole | 250mg | 525109251 | A192183 | 5744-68-3 | MFCD00233969 | 161.002 | C4H5BrN2
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Medchemexpress LLC CDDO-dhTFEA | 1191265-33-4 | 99.6% | 574.72 | 100 MG
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CDDO-dhTFEA | 1191265-33-4 | 99.6% | 574.72 | 100 MG
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eMolecules 121032-29-9 | Medchem Express | Nelarabine | 5mg | 446263353 | HY-13701 | 297.271 | C11H15N5O5
Medchem Express | Neticonazole (hydrochloride) | 25mg | 518571083 | HY-128365 | 130773-02-3 | 338.890 | C17H23ClN2OS
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Medchemexpress LLC YM-244769 hydrochlor 25mg | 837424-39-2 | 25MG
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YM-244769 hydrochloride is a potent selective and orally active Na /Ca2 exchanger (NCX) inhibitor YM-244769 hydrochloride preferentially inhibits NCX3 and suppresses the unidirectional outward NCX current (Ca2 entry mode) with IC50s of 18 nM and 50 nM respectively YM-244769 hydrochloride efficiently protects against hypoxia/reoxygenation-induced SH-SY5Y neuronal cell damage YM-244769 hydrochloride can also increase urine volume and urinary excretion of electrolytes in mice[1 [2 [3
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Medchemexpress LLC Rad16-I hydrochloride | 2100275-49-6 | 98.9% | 10 MG
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RAD16-I hydrochloride is a soft nanofibrous self-assembling peptide. It provides a suitable microenvironment for the proliferation and differentiation of human mesenchymal stem cells (hMSC) into chondrocytes. It is also an ionic complementary peptide that has been used as a model to investigate the potential amyloid-like staining properties of Self-Assembling Peptide Nanofibers (SAPNFs).
- Provides a suitable microenvironment for human mesenchymal stem cells' (hMSC) proliferation and differentiation into chondrocytes.
- Used to check potential amyloid-like staining properties of SAPNFs.
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Medchemexpress LLC 2-Pyrimidinamine, 5-[8-methyl-9-(1-methylethyl)-2-(4-morpholinyl)-9H-purin-6-yl]- | 1246560-33-7 | 98.7% | 354.41 | 100 MG
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VS-5584 is a pan-PI3K/mTOR kinase inhibitor that simultaneously blocks both mTORC2 and mTORC1. This ATP-competitive inhibitor selectively targets PI3K/mTOR signaling with low nanomolar potency against all human Class I PI3K isoforms and mTOR kinase. It preferentially inhibits cancer stem cells in HMLE breast cancer cells, reducing Aldefluor-positive cancer stem cells. In vivo, it reduces cancer stem cells in breast cancer tumors and induces tumor regression in Docetaxel-resistant models. Rapidly absorbed with a tmax of 0.9 hours and an elimination half-life of 10 hours, it leads to significant tumor growth inhibition.
- Pan-PI3K/mTOR kinase inhibitor
- Blocks mTORC2 and mTORC1
- Selectively inhibits PI3K/mTOR signaling
- Inhibits cancer stem cells
- Induces tumor regression
- Rapidly absorbed, long half-life
- Leads to tumor growth inhibition
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eMolecules 120972-66-9 | 2-(4-Aminophenyl)isoindolin-1-one | Combi-Blocks | MFCD16300498 | 224.263 | C14H12N2O | 95.000 | Nc1ccc(cc1)N1Cc2ccccc2C1=O | 1g | 537624792
2-(4-Aminophenyl)isoindolin-1-one | Combi-Blocks | 120972-66-9 | MFCD16300498 | 224.263 | C14H12N2O | 95.000 | Nc1ccc(cc1)N1Cc2ccccc2C1=O | 1g | 537624792
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Medchemexpress LLC Tenofovir amibufenamide | 1571076-26-0 | 99.67% | 490.49 | 100 MG
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Tenofovir amibufenamide (HS-10234) is a Tenofovir prodrug, functioning as an orally active antiviral agent. It effectively inhibits HBV and is utilized in studies concerning chronic hepatitis B (CHB). This compound also regulates hepatocyte metabolism.
- Inhibits HBV DNA replication
- Corrects metabolic disorders caused by HBV infection
- Regulates hepatocyte metabolism
- Used for chronic hepatitis B (CHB) study
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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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