Thiomyristoyl
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| Drug class | Sirtuin 2 (SIRT2) inhibitor |
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| Formula | C34H51N3O3S |
| Molar mass | 581.86 g·mol−1 |
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Thiomyristoyl is a drug which acts as a potent sirtuin 2 (SIRT2) inhibitor. It inhibits SIRT2 with an IC50 of 28 nM, though its activity at other SIRT subtypes has not been well characterized. It has beneficial effects in an animal model of ulcerative colitis,[1] and is also used for studying the role of SIRT2 in cancer progression.[2][3]
See also
References
- ^ Xu Y, Cai R, Zhao Z, Zhou L, Zhou Q, Hassan S, et al. (January 2021). "Thiomyristoyl ameliorates colitis by blocking the differentiation of Th17 cells and inhibiting SIRT2-induced metabolic reprogramming". International Immunopharmacology. 90 107212. doi:10.1016/j.intimp.2020.107212. PMID 33310666.
- ^ Xu L, Wang L, Zhou L, Dorfman RG, Pan Y, Tang D, et al. (May 2019). "The SIRT2/cMYC Pathway Inhibits Peroxidation-Related Apoptosis In Cholangiocarcinoma Through Metabolic Reprogramming". Neoplasia. 21 (5): 429–441. doi:10.1016/j.neo.2019.03.002. PMC 6441712. PMID 30933885.
- ^ Lin R, Yang Y, Wu E, Zhou M, Wang S, Zhang Q (January 2023). "SIRT2 promotes cell proliferation and migration through mediating ERK1/2 activation and lactosylceramide accumulation in prostate cancer". The Prostate. 83 (1): 71–81. doi:10.1002/pros.24437. PMID 36082450.