Phenylpropanoids and polyketides
Medchemexpress LLC HY-N0014 100mg Medchemexpress, Icariin CAS:489-32-7 Purity:>98%
Medchemexpress, HY-N0014 100mg Icariin CAS:489-32-7 Icariin is a flavonol glycoside. Icariin inhibits PDE5 and PDE4 activities with IC 50 s of 432 nM and 73.50 μM, respectively. Icariin also is a PPARα activator. 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.
Medchemexpress LLC 4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-2-(4-methoxyphenyl)- | 480-36-4 | 592.55 | 20 MG
Linarin (Buddleoside) is an orally active and selective inhibitor of acetylcholinesterase (AChE). It exhibits various activities including anti-inflammatory, antioxidant, sleep aid and sedation, bone differentiation, anti-tumor, antibacterial, and antiviral properties. Linarin can be utilized in the study of diseases affecting the nervous system, osteoporosis, and cancer.
- Orally active and selective inhibitor of acetylcholinesterase (AChE).
- Anti-inflammatory properties.
- Antioxidant properties.
- Sleep aid and sedation.
- Promotes bone differentiation.
- Anti-tumor activity.
- Antibacterial properties.
- Antiviral properties.
- Useful for studying diseases such as those of the nervous system, osteoporosis, and cancer.
Medchemexpress LLC Linarin | 480-36-4 | 592.55 | 5 MG
Linarin (Buddleoside) is an orally active and selective inhibitor of acetylcholinesterase (AChE). It exhibits various activities such as anti-inflammatory, antioxidant, sleep aid, sedation, bone differentiation, anti-tumor, antibacterial, and antiviral properties. Linarin can be utilized in research for diseases like nervous system disorders, osteoporosis, and cancer.
- Orally active and selective inhibitor of acetylcholinesterase (AChE)
- Possesses anti-inflammatory activity
- Exhibits antioxidant properties
- Acts as a sleep aid and sedative
- Promotes bone differentiation
- Shows anti-tumor effects
- Demonstrates antibacterial activity
- Has antiviral properties
- Can be used to study nervous system diseases, osteoporosis, and cancer
Medchemexpress LLC (5Z,2E)-CU-3 | 1815598-71-0 | 95.0% | 1 ML
(5Z,2E)-CU-3 is a small-molecule diacylglycerol kinase (DGK) inhibitor and apoptosis inducer supplied as a ready-to-use 10 mM solution in DMSO for research applications.
- Supplied as a 10 mM solution in DMSO (1 mL).
- High purity verified at 95.0%.
- Molecular weight 392.47 g/mol and formula C16H12N2O4S3.
- Solid, yellow to brown appearance.
- Intended for apoptosis and DGK pathway research.
Apexbio Technology LLC trans-Cinnamic acid 140-10-3 20mg
trans-Cinnamic acid (140-10-3) is a small-molecule inhibitor that exerts inhibitory activity against specific enzyme targets involved in inflammation oxidative stress and microbial proliferation It modulates these biological processes thereby regulating pathways associated with inflammatory response and antimicrobial defense trans-Cinnamic acid exerts its biological activity primarily through enzyme inhibition In in vitro studies trans-Cinnamic acid demonstrates inhibitory activity with reported IC50 values typically between 50 200 M depending on the experimental conditions and cell models Based on these pharmacological properties trans-Cinnamic acid holds research potential in anti-inflammatory antimicrobial antioxidant response studies and metabolic assays in tissue culture and cell-based experimental models
Apexbio Technology LLC Icariin 489-32-7 100mg
Icariin (CAS 489-32-7) is a small-molecule inhibitor targeting phosphodiesterases notably PDE5 and PDE4 It is designed to modulate cyclic nucleotide signaling by inhibiting PDE activity thereby regulating processes such as smooth muscle relaxation and neuronal signaling Icariin exerts its biological activity primarily through the inhibition of PDE5 (IC 0 43 M) and PDE4 (IC 73 50 M) Based on these pharmacological properties icariin holds research potential in the investigation of erectile function nitric oxide synthase expression angiogenesis pathways and osteogenic differentiation in bone marrow stromal cells
eMolecules 5-Methyl-8-hydroxycoumarin | 36651-81-7 | MFCD18450566 | 1g
Synthonix - Stock | 5-Methyl-8-hydroxycoumarin | 1g | 495880208 | M64560 | | 36651-81-7 | MFCD18450566 | 176.171 | C10H8O3
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Selleck Chemical LLC AG 494
AG-494 a member of the tyrphostin family of tyrosine kinase inhibitors is a potent inhibitor of EGF receptor autophosphorylation (IC50 1 2 M) and EGF-dependent cell growth (IC50 6 M)
eMolecules 6-Hydroxychromene-3-carboxaldehyde | 134822-76-7 | MFCD03548123 | 1g
Apollo Scientific | 6-Hydroxychromene-3-carboxaldehyde | 1g | 562430702 | OR55042 | 95.000 | 134822-76-7 | MFCD03548123 | 176.171 | C10H8O3
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Cayman Chemical FerulIc AcId ethyl ester 1g
A lipophilic derivative of ferulic acid, with increased ability to cross cell membranes; less DPPH radical scavenging capacity than ferulic acid (IC50 = 66.7 μM for FAEE vs. 44.6 μM for ferulic acid); increases the expression of HO-1, Hsp70, and Hsp72, providing neuroprotection against amyloid β-peptide
Selleck Chemical LLC Sodium salicylate S3137-50mg
Sodium salicylate(2-Hydroxybenzoic acid Sodium salt Salicylic acid Sodium salt) is used in medicine as an analgesic and antipyretic
Apexbio Technology LLC BIBF 1202 894783-71-2 5mg
BIBF 1202 (CAS 894783-71-2) is a carboxylate metabolite derivative of BIBF 1120 characterized as a selective inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2) kinase In biochemical assays BIBF 1202 demonstrates inhibitory activity against VEGFR2 kinase with an IC50 of 62 nM This compound is frequently employed in studies investigating the regulation of the VEGFR2 signaling pathway and its role in endothelial cell function Additionally BIBF 1202 is utilized in preclinical models related to tumor angiogenesis and associated pharmacological research