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AB141108

SN 38, DNA topoisomerase I inhibitor

SN 38, DNA topoisomerase I inhibitor

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(4 Publications)

MW 392.4 Da, Purity >99%. Active metabolite of CPT-11 (Irinotecan) (ab141107). Inhibits DNA topoisomerase I (IC50 values are 0.74 and 1.9 μM in P388 and Ehrlich cells respectively) and DNA and RNA synthesis (IC50 values are 77 nM and 1.3 μM respectively). Shows potent antitumor activity, causes S- and G2 cell cycle arrest and induces apoptosis. Active in vivo.

別名を表示する

DNA topoisomerase 1, DNA topoisomerase I, NUP98 fusion gene, TOP I, TOP1_HUMAN, Topoisomerase (DNA) I, Topoisomerase 1, TopoisomeraseI, Type I DNA topoisomerase

2 Images
Immunocytochemistry/ Immunofluorescence - SN 38, DNA topoisomerase I inhibitor (AB141108)
  • ICC/IF

Unknown

Immunocytochemistry/ Immunofluorescence - SN 38, DNA topoisomerase I inhibitor (AB141108)

ab2893 staining γH2A.X in HeLa cells treated with SN 38 (ab141108), by ICC/IF. Increase of γH2A.X nuclear expression correlates with increased concentration of SN 38, as described in literature.
The cells were incubated at 37°C for 6 hours in media containing different concentrations of ab141108 (SN 38) in DMSO, fixed with 100% methanol for 5 minutes at -20°C and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab2893 (5 µg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight® 488 anti-rabbit polyclonal antibody (ab96899) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.

Chemical Structure - SN 38, DNA topoisomerase I inhibitor (AB141108)
  • Chemical Structure

Lab

Chemical Structure - SN 38, DNA topoisomerase I inhibitor (AB141108)

2D chemical structure image of ab141108, SN 38, DNA topoisomerase I inhibitor

Key facts

CAS番号

86639-52-3

精製度

>99%

製品の状態

Solid

form

分子量

392.4 Da

分子式

C<sub>2</sub><sub>2</sub>H<sub>2</sub><sub>0</sub>N<sub>2</sub>O<sub>5</sub>

PubChem

104842

由来

Synthetic

溶解性

Soluble in DMSO to 100 mM

化学名

7-Ethyl-10-hydroxycamptothecin

生物学的記述

Active metabolite of CPT-11 (Irinotecan) (ab141107). Inhibits DNA topoisomerase I (IC50 values are 0.74 and 1.9 μM in P388 and Ehrlich cells respectively) and DNA and RNA synthesis (IC50 values are 77 nM and 1.3 μM respectively). Shows potent antitumor activity, causes S- and G2 cell cycle arrest and induces apoptosis. Active in vivo.

Canonical smiles

CCC1=C2CN3C(=CC4=C(C3=O)COC(=O)C4(CC)O)C2=NC5=C1C=C(C=C5)O

Isomeric smiles

CCC1=C2CN3C(=CC4=C(C3=O)COC(=O)[C@@]4(CC)O)C2=NC5=C1C=C(C=C5)O

InChi

InChI=1S/C22H20N2O5/c1-3-12-13-7-11(25)5-6-17(13)23-19-14(12)9-24-18(19)8-16-15(20(24)26)10-29-21(27)22(16,28)4-2/h5-8,25,28H,3-4,9-10H2,1-2H3/t22-/m0/s1

InChiKey

FJHBVJOVLFPMQE-QFIPXVFZSA-N

IUPAC名

(19S)-10,19-diethyl-7,19-dihydroxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(21),2,4(9),5,7,10,15(20)-heptaene-14,18-dione

出荷温度及び保存条件

出荷温度
Ambient - Can Ship with Ice
短期保存温度
-20°C
長期保存温度
-20°C
保管に関する情報
Store under desiccating conditions|The product can be stored for up to 12 months

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

Topoisomerase I also known as DNA topoisomerase I or Topo I is an important enzyme in the unwinding of the DNA double helix during processes such as replication and transcription. This enzyme has a molecular mass of approximately 91 kDa and functions by creating transient single-strand breaks in the DNA allowing relaxation of supercoils. Topoisomerase I is widely expressed in both proliferating and non-proliferating cells with higher levels seen in tissues with rapid cell division like the gastrointestinal tract and some immune cells.
Biological function summary

Topoisomerase I plays a significant role in the modulation of DNA topology ensuring proper chromosomal functions during cellular proliferation. It serves as a single polypeptide and does not require a companion for its activity unlike other topoisomerases that may function in complexes. The enzyme’s ability to relieve torsional stress in DNA is essential for maintaining genomic stability and facilitating the smooth progression of the replication fork.

Pathways

Topoisomerase I is vital for DNA replication and transcription processes. It works in concert with other proteins such as helicases and ligases to ensure efficient unwinding and rewinding of DNA strands. The enzyme participates in the DNA damage response pathway where it interacts with proteins like PARP1 to coordinate repair processes. Its action is important in both the S phase of the cell cycle where DNA synthesis occurs and in the G0 phase where cells are in a quiescent state.

Topoisomerase I is heavily implicated in oncogenesis with significant associations to colorectal and ovarian cancers. Its heightened activity can lead to genomic instability a hallmark of cancer development. The enzyme also relates to chemotherapeutic resistance where mutations in topoisomerase I lead to reduced drug efficacy. Furthermore inhibitors targeting topoisomerase I such as camptothecin-based drugs exploit its role in cancer aiming to induce DNA damage selectively in rapidly dividing cells. Connections to other proteins like BRCA1 are apparent in these pathways as they both contribute to the DNA repair processes in cells.

製品プロトコール

文献 (4)

Recent publications for all applications. Explore the full list and refine your search

International journal of molecular sciences 24: PubMed37511490

2023

TP5: A Novel Therapeutic Approach Targeting Aberrant and Hyperactive CDK5/p25 for the Treatment of Colorectal Carcinoma.

Applications

Unspecified application

Species

Unspecified reactive species

Niranjana Amin,Herui Wang,Qi Song,Manju Bhaskar,Sharda Prasad Yadav,Mark R Gilbert,Harish Pant,Emeline Tabouret,Zhengping Zhuang

Journal of clinical and translational hepatology 11:614-625 PubMed36969901

2023

Topoisomerase I Inhibition Radiosensitizing Hepatocellular Carcinoma by RNF144A-mediated DNA-PKcs Ubiquitination and Natural Killer Cell Cytotoxicity.

Applications

Unspecified application

Species

Unspecified reactive species

Chiao-Ling Tsai,Po-Sheng Yang,Feng-Ming Hsu,Ann-Lii Cheng,Wan-Ni Yu,Jason Chia-Hsien Cheng

British journal of cancer 124:951-962 PubMed33339894

2020

SLFN11 informs on standard of care and novel treatments in a wide range of cancer models.

Applications

Unspecified application

Species

Unspecified reactive species

Claudia Winkler,Joshua Armenia,Gemma N Jones,Luis Tobalina,Matthew J Sale,Tudor Petreus,Tarrion Baird,Violeta Serra,Anderson T Wang,Alan Lau,Mathew J Garnett,Patricia Jaaks,Elizabeth A Coker,Andrew J Pierce,Mark J O'Connor,Elisabetta Leo

Nucleic acids research 44:e162 PubMed27587582

2016

Cell-based high-throughput compound screening reveals functional interaction between oncofetal HMGA2 and topoisomerase I.

Applications

Unspecified application

Species

Unspecified reactive species

Sabrina Peter,Haojie Yu,Roland Ivanyi-Nagy,Peter Dröge
View all publications

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