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Filtered Search Results
OMICRON BIOCHEMICALS INC A A -1 1-2H2 TREHALOSE 0.050G
NC3717191 A A -1 1-2H2 TREHALOSE 0.050G
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SANTA CRUZ BIOTECHNOLOGY 3-O-METHYL-D-GLUCOPYRANOSIDE
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NC3432117 3-O-METHYL-D-GLUCOPYRANOSIDE
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AGILENT TECHNOLOGIES BETA-N-ACETYLHEXOSAMINIDASE 1
NC2960616 BETA-N-ACETYLHEXOSAMINIDASE 1
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AVANTI POLAR LIPIDS INC MAL TRIDECAN 2YLOXY MALTOSIDE
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NC3382997 MAL TRIDECAN 2YLOXY MALTOSIDE
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OMICRON BIOCHEMICALS INC A A-UL-13C12 TREHALOSE .5GR
NC3567014 A A-UL-13C12 TREHALOSE .5GR
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Boston Bioproducts Inc IPTG - 5x5g
IPTG - 5x5g (For Research Use and Further Manufacturing Only)
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TARGETMOL CHEMICALS INC TUROFEXORATE ISOPROPYL 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Turofexorate Isopropyl (XL335) is a potent selective and orally bioavailable FXR agonist with EC50 of 4 nMpurity: 99%
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Chem-Impex International, Inc. 5-Azacytidine | 320-67-2 | MFCD00006539 | 5G
5-Azacytidine, 320-67-2, MFCD00006539, 5G
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Medchemexpress LLC 3-Deazaadenosine | 6736-58-9 | ≥99.0% | 266.26 | 10 MG
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3-Deazaadenosine is an inhibitor of S-adenosylhomocysteine hydrolase, with a Ki of 3.9 μM. It exhibits anti-inflammatory, anti-proliferative, and anti-HIV activity.
- Inhibits S-adenosylhomocysteine hydrolase
- Ki of 3.9 μM
- Anti-inflammatory activity
- Anti-proliferative activity
- Anti-HIV activity
- Inhibits p24 antigen in PBMCs infected with HIV-1 isolates
- Inhibits LPS-induced TNF-α mRNA expression
- Enhances nuclear translocation of NF-κB but blocks LPS-induced NF-κB transcriptional activity
- Inhibits phosphorylation of Raf, ERK, protein-dependent kinase 1, protein kinase B (Akt), and forkhead transcription factor FoxO1a
- Suppresses vascular smooth muscle cell (VSMC) proliferation via interfering with Ras signaling
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Medchemexpress LLC 1,2,4-triazin-5(2H)-one, 3,4-dihydro-2-β-D-ribofuranosyl-3-thioxo | 27089-56-1 | MFCD00006473 | 97.0% | 261.26 g/mol | C8H11N3O5S | 100 MG
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2-Thio-6-azauridine is a thio-substituted azauridine nucleoside provided for research and biochemical assay use. It serves as a modified nucleoside reagent for molecular biology and biochemical studies; identity and purity are supported by analytical data from the certificate of analysis.
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Medchemexpress LLC 3-Deazaadenosine hydrochloride | 86583-19-9 | 99.7% | 302.72 | 10 MG
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3-Deazaadenosine hydrochloride is a chemical compound known as an inhibitor of S-adenosylhomocysteine hydrolase (SAHH), with a reported Ki of 3.9 μM. It exhibits a range of biological activities including anti-inflammatory, anti-proliferative, and anti-HIV effects. This compound is suitable for various research applications studying its inhibitory actions and biological impacts.
- Inhibits S-adenosylhomocysteine hydrolase (SAHH)
- Demonstrates anti-inflammatory activity
- Shows anti-proliferative effects
- Exhibits anti-HIV activity
- Inhibits p24 antigen in PBMCs infected with HIV-1 isolates
- Suppresses vascular smooth muscle cell proliferation
- Interferes with Ras signaling pathways
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Medchemexpress LLC 6-AZURIDINE 1G
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6-AZURIDINE 1G
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Medchemexpress LLC 1,2,4-triazin-5(2H)-one, 3,4-dihydro-2-β-D-ribofuranosyl-3-thioxo- | 27089-56-1 | MFCD00006473 | 97.0% | 261.26 g/mol | C8H11N3O5S | 50 MG
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2-Thio-6-azauridine is a biochemical assay reagent used in research applications. It is a thio analog of 6-azauridine (C8H11N3O5S) with a molecular weight of 261.26 g/mol, supplied as a high-purity solid for laboratory assays. Store under recommended conditions and use for research purposes only.
- High purity (97.0%).
- Molecular formula C8H11N3O5S; molecular weight 261.26 g/mol.
- Intended for biochemical assays and research use only.
- Storage: solid at 4°C; in solvent, store under nitrogen at -80°C (6 months) or -20°C (1 month).
- Supplied as a solid for convenient handling in laboratory workflows.
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Apexbio Technology LLC 3-Deazaadenosine hydrochloride(Synonyms: 3-Deazaadenosine HCl, C3-Deazaadenosine hydrochloride, 3-Deaza-adenosine hydrochloride), 5mg, CAS: 86583-19-9.
3-Deazaadenosine hydrochloride (CAS 86583-19-9) is a selective inhibitor of S-adenosylhomocysteine hydrolase (SAHH) exhibiting inhibition with a Ki value around 3 9 M It disrupts SAHH-dependent methyl metabolism pathways thereby altering intracellular methyltransferase reactions Due to this biochemical activity it serves as a research agent for studying inflammation cell proliferation and HIV infection as well as investigations into enzyme-mediated methylation processes and related pathological mechanisms
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eMolecules 673-04-1 | N2,N4-Diethyl-6-methoxy-1,3,5-triazine-2,4-diamine | MFCD01311011 | 250mg
Ambeed | N2,N4-Diethyl-6-methoxy-1,3,5-triazine-2,4-diamine | 250mg | 589771500 | A692646 | 673-04-1 | MFCD01311011 | 197.242 | C8H15N5O
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