Cinnamic acids and derivatives
Medchemexpress LLC Ferulic acid 4-O-sulfate | 86321-29-1 | 98.1% | 274.25 | 5 MG
Ferulic acid 4-O-sulfate is a metabolite of Ferulic acid. It has been shown to relax arteries and lower blood pressure in mice. This compound causes significant concentration-dependent relaxations in mouse aorta, femoral, and saphenous arteries at concentrations of 0.1-30 μM.
- Metabolite of Ferulic acid
- Relaxes arteries
- Lowers blood pressure in mice
- Causes concentration-dependent relaxations in mouse aorta, femoral, and saphenous arteries
Medchemexpress LLC 3-Methylcinnamic acid | 3029-79-6 | 99.77% | C10H10O2 | 5 G
3-Methylcinnamic acid is a drug intermediate utilized in the synthesis of various active compounds. This product is strictly for research use only and is not intended for patient administration. Careful handling and storage are recommended to maintain product integrity and safety.
- Store powder at -20°C for up to 3 years or at 4°C for 2 years.
- When in solvent, store at -80°C for 6 months or at -20°C for 1 month.
- Avoid breathing dust, fume, gas, mist, vapors, or spray.
- Wash hands thoroughly after handling.
- Use only outdoors or in a well-ventilated area.
- Wear appropriate protective equipment including gloves, clothing, and eye/face protection.
- May cause irritation to skin, eyes, and respiratory tract.
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
![Medchemexpress LLC Carbamic acid, N-[(2R,3S)-2-methyl-4-oxo-3-oxetanyl]-, 5-phenylpentyl ester | 1439366-88-7 | 99.7% | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000231161.png-250.jpg)
Medchemexpress LLC Carbamic acid, N-[(2R,3S)-2-methyl-4-oxo-3-oxetanyl]-, 5-phenylpentyl ester | 1439366-88-7 | 99.7% | 1 ML
ARN 077 (enantiomer) is the less-active stereoisomer of ARN 077 (also reported as URB913 enantiomer). It is supplied for research use and reported to inhibit rat NAAA with an IC50 of 3.53 μM for the less-active enantiomer. The compound is offered as a 10 mM solution in DMSO (1 mL) and as solid quantities for laboratory use.
- Supplied as 10 mM solution in DMSO, 1 mL, and as solids for flexibility in experiments.
- High reported purity (≈99.7%), suitable for research applications.
- Molecular formula C16H21NO4, molecular weight 291.34 g/mol.
- Reported CAS number 1439366-88-7 for unambiguous identification.
- Intended for research use only; not for human or diagnostic use.
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
Selleck Chemical LLC p-Coumaric Acid S4759-25mg
p-Coumaric acid (4-Hydroxycinnamic acid P-Hydroxycinnamic acid 4-Coumaric acid Trans-p-Coumaric acid para-Coumaric Acid) is a hydroxy derivative of cinnamic acid found in a variety of edible plants and is reported to have antioxidant anti-inflammatory and antimicrobial activity
Medchemexpress LLC α-cyano-4-hydroxycinnamic acid | 28166-41-8 | MFCD00004204 | 99.9% | 189.17 | C10H7NO3 | 1 ML
α-Cyano-4-hydroxycinnamic acid is a small-molecule inhibitor of monocarboxylate transporters commonly used in biochemical research and as a matrix in mass spectrometry. It is supplied at high purity and is available as both solid material and as a ready-to-use 10 mM solution in DMSO for laboratory use.
- High purity (99.9%) suitable for sensitive assays.
- Available as a 10 mM solution in DMSO for immediate use.
- Also available as solid in multiple sizes for flexible use.
- Effective monocarboxylate transporter inhibitor for in vitro studies.
- Suitable as a MALDI matrix for peptide analysis.
- Datasheet, certificate of analysis, and safety data sheet available.
Med Vet International Fluoxetine, 20mg, 30 Tablets
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Fluoxetine is a generic form of PROZac and is an SSRI antidepressant. It affects chemicals in the brain that may be unbalanced in people with depression, panic, anxiety, or obsessive-compulsive disorder.
Selleck Chemical LLC BLU 451-E1877-1G
BLU 451 is a central nervous system (CNS)-penetrant wild-type EGFR-sparing covalent inhibitor of epidermal growth factor receptor (EGFR) exon 20 insertion (Ex20ins) with an IC50 of 7-78 nM It also exhibits a potent anti-tumor efficacy
Selleck Chemical LLC -cyano-4-hydroxycinnamic acid(-CHCA) 200mg 28166-41-8
4-Chloro-?-cyanocinnamic acid (?-CHCA) is a classic monocarboxylate transporters (MCT) inhibitor. ?-cyano-4-hydroxycinnamate (CHC) has a 10-fold selectivity for MCT1 compared to other MCTs. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Selleck Chemical LLC Tyrphostin AG-528
Tyrphostin AG-528 (Tyrphostin B66) is a potent inhibitor of epidermal growth factor receptors (EGFR) and ErbB2/HER2 with IC50 of 4 9 M and 2 1 M respectively Tyrphostin AG-528 exhibits anticancer activity