Cinnamic acids and derivatives
Sigma Aldrich Fine Chemicals Biosciences trans-Cinnamic acid-beta,2,3,4,5,6-d6 98 atom % D | 91453-04-2 | MFCD01863724 | 250MG
trans-Cinnamic acid-beta,2,3,4,5,6-d6 98 atom % D | Mol Wt: 154.2 | 91453-04-2 | MFCD01863724 | 250MG
Cayman Chemical p-CoumarIc AcId 50g
A hydroxy derivative of cinnamic acid that can be found in a variety of edible plants that is reported to have antioxidant, anti-inflammatory, and antimicrobial activity
eMolecules 4'-(4-Fluorobenzyloxy)acetophenone | 72293-96-0 | MFCD00173651 | 25g
Oakwood Chemical | 4'-(4-Fluorobenzyloxy)acetophenone | 25g | 537669236 | 008324 | | 72293-96-0 | MFCD00173651 | 244.265 | C15H13FO2
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Cayman Chemical p-CoumarIc AcId 10g
A hydroxy derivative of cinnamic acid that can be found in a variety of edible plants that is reported to have antioxidant, anti-inflammatory, and antimicrobial activity
Medchemexpress LLC Arn 077 enantiomer | 1439366-88-7 | 99.7% | 1 MG
Arn 077 enantiomer is the less active enantiomer of ARN 077 and functions as an inhibitor of N-acylethanolamine acid amidase (NAAA); reported IC50 for rat NAAA is 3.53 μM. Supplied as a solid for research applications.
- Less active enantiomer with reported IC50 = 3.53 μM for rat NAAA.
- Chemical formula C16H21NO4; molecular weight 291.34 g/mol.
- White to off-white solid; powder storage at -20°C for long-term stability.
- High DMSO solubility (100 mg/mL); vehicle formulations reported for in vivo use at ≥ 2.5 mg/mL.
- For research use only; handle according to appropriate safety procedures.
Selleck Chemical LLC (R)-(-)-JQ1 Enantiomer S2965-5mg
(R)-(-)-JQ1 Enantiomer is the stereoisomer of ( )-JQ1 ( )-JQ1 potently decreases expression of both BRD4 target genes whereas (R)-(-)-JQ1 Enantiomer has no effect
Selleck Chemical LLC Tyrphostin AG 879 S2816-25mg
Tyrphostin AG 879 potently inhibits HER2/ErbB2 with IC50 of 1 M 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR
Selleck Chemical LLC Tyrphostin 9 S2895-25mg
Tyrphostin 9 (SF 6847 RG-50872) is firstly designed as an EGFR inhibitor with IC50 of 460 M but is also found to be more potent to PDGFR with IC50 of 0 5 M
Selleck Chemical LLC AMG-458 S2747-5mg
AMG 458 is a potent c-Met inhibitor with Ki of 1 2 nM 350-fold selectivity for c-Met than VEGFR2 in cells