Cytochalasin B, actin polymerization inhibitor
5
(1 Review)
|
(3 Publications)
MW 479.6 Da, Purity >97%. Cell permeable actin polymerization inhibitor. Reversible KV1.5 blocker (IC50 = 4 μM). Inhibits I(Kur). Cytochalasin A (ab143481) analog. Inhibits transport of monosaccharides across the cell membrane. Shows antitumor effects in vivo. .
View Alternative Names
AI838772, AW493413, Cytosolic NADP-isocitrate dehydrogenase, Epididymis luminal protein 216, Epididymis secretory protein Li 26, FLJ11090, HEL-216, HEL-S-26, ICDH, IDCD, IDH, IDH1, IDHC_HUMAN, IDP, IDPC, Isocitrate dehydrogenase (NADP(+)) 1 cytosolic, Isocitrate dehydrogenase 1 (NADP+) soluble, Isocitrate dehydrogenase [NADP] cytoplasmic, MGC104252, MGC112732, NADP dependent isocitrate dehydrogenase cytosolic, NADP dependent isocitrate dehydrogenase peroxisomal, NADP(+)-specific ICDH, Oxalosuccinate decarboxylase, PICD, RP24-311F12.2, SCAN1, TYDP, TYDP1_HUMAN, Tyr-DNA phosphodiesterase 1, Tyrosyl-DNA phosphodiesterase 1
- Chemical Structure
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Chemical Structure - Cytochalasin B, actin polymerization inhibitor (AB143482)
2D chemical structure image of ab143482, Cytochalasin B, actin polymerization inhibitor
Properties and storage information
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Supplementary information
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Biological function summary
This enzyme is involved in the repair of single-strand breaks by excising the protein residues linked to DNA particularly important for maintaining genome stability. TDP1 forms part of the DNA damage response machinery. In addition to its standalone function it interacts with various other proteins in the DNA repair complex. TDP1 works alongside other repair proteins such as PARP1 to address DNA lesions and maintain cellular integrity.
Pathways
TDP1 significantly contributes to the base excision repair pathway. It aids in counteracting the effects of topoisomerase I inhibitors which are often used in cancer therapy. TDP1 cooperates with SMARCA1 a chromatin remodeler to ensure efficient DNA repair and cellular recovery post-damage. Within this context TDP1's activity is important to both preserving cellular health and conferring resistance to DNA-damaging agents.
Publications (3)
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FEMS microbes 4:xtad019 PubMed37900578
2023
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EMBO reports 22:e52006 PubMed34096155
2021
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Scientific reports 8:15585 PubMed30348987
2018
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