2-Hydroxy-4-methoxybenzoic acid
Code | Size | Price |
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TAR-T2A2428-500mg | 500mg | £103.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here. |
Quantity:
TAR-T2A2428-1mL | 1 mL * 10 mM (in DMSO) | £107.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here. |
Quantity:
TAR-T2A2428-1g | 1g | £109.00 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here. |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃
Images
Documents
Further Information
Bioactivity:
2-hydroxy-4-methoxybenzoic acid is a predicted metabolite generated by BioTransformer1 that is produced by the metabolism of 3-(2-hydroxy-4-methoxyphenyl)propanoic acid. It is generated by unspecified-gutmicro enzyme via a beta-oxidation-of-carbxoylic-acid reaction. This beta-oxidation-of-carbxoylic-acid occurs in human gut microbiota.
CAS:
2237-36-7
Formula:
C8H8O4
Molecular Weight:
168.148
Purity:
0.9992
SMILES:
COc1ccc(C(O)=O)c(O)c1
References
1. Fimognari, C., Lenzi, M., Ferruzzi, L., Turrini, E., Scartezzini, P., & Poli, F. et al. (2011). Mitochondrial Pathway Mediates the Antileukemic Effects of Hemidesmus Indicus, a Promising Botanical Drug.?Plos ONE,?6(6), e21544. doi: 10.1371/journal.pone.0021544
2. Samy, R., Gopalakrishnakone, P., & Chow, V. (2012). Therapeutic application of natural inhibitors against snake venom phospholipase A2.?Bioinformation,?8(1), 48-57. doi: 10.6026/9732063202008048
3. Zhang, Z., Zhang, X., Zhao, Z., Yan, R., Xu, R., Gong, H., & Zhu, H. (2012). Synthesis, biological evaluation and molecular docking studies of 1,3,4-oxadiazole derivatives as potential immunosuppressive agents.?Bioorganic & Medicinal Chemistry,?20(10), 3359-3367. doi: 10.12016/j.bmc.2012.03.064