Irinotecan (hydrochloride trihydrate)

$66$198

Products Details

Product Description

– Irinotecan hydrochloride trihydrate ((+)-Irinotecan hydrochloride trihydrate) is a topoisomerase I inhibitor with antitumor activity[1].

Web ID

– HY-16568

Storage Temperature

– 4°C (Powder, sealed storage, away from moisture)

Shipping

– Room Temperature

Applications

– Cancer-programmed cell death

Molecular Formula

– C33H45ClN4O9

Citations

– J Mol Med (Berl). 2019 Aug;97(8):1183-1193.|Apoptosis. 2016 Feb;21(2):130-42. |Biochem Pharmacol. 2023 Aug 25;115752.|Biomaterials. 16 September 2022.|Biomed Pharmacother. 2020 Aug;128:110262.|Biomed Pharmacother. 2023 Apr 25;163:114751.|bioRxiv. 2019 Dec.|Cancer Lett. 2022 Nov 30;216028.|Cell Biosci. 2023 Nov 25;13(1):215.|Cell Death Dis. 2019 Nov 25;10(12):887. |Cell Discov. 2022 Sep 14;8(1):92.|Cell Rep Med. 2023 Jan 10;100911.|Cell. 2022 Sep 1;185(18):3356-3374.e22.|Clin Cancer Res. 2023 Sep 19.|EBioMedicine. 2023 May 9;92:104594.|Eur J Pharm Biopharm. 2022 Jan 5;S0939-6411(21)00272-1.|Eur J Pharmacol. 2023 Apr 11;949:175718.|Gastroenterology. 2021 Nov;161(5):1601-1614.e23.|Gene. 2019 Mar 10;688:1-6. |Genome Med. 2016 Oct 31;8(1):116.|Heliyon. 2023 Apr 21.|INT J PHARMACEUT. 2020 May.|J Mol Med (Berl). 2019 Aug;97(8):1183-1193.|J Pharm Pharmacol. 2023 Mar 1;rgad007.|Life Sci. 2019 Aug 15;231:116529. |Lung Cancer. 2023 Mar 8;178:237-246.|Mol Biol Cell. 2023 Mar 29;mbcE22110518.|Mol Cancer Ther. 2021 Oct 28.|Mol Cancer Res. 2020 Mar;18(3):414-423.|Patent. US20210009719A1.|Pharmacol Res. 2021 Jan;163:105232.|PLoS Biol. 2022 Feb 24;20(2):e3001517.|PLoS Pathog. 2020 Mar 24;16(3):e1008429.|Signal Transduct Target Ther. 2021 May 28;6(1):188.|Theranostics. 2019 May 31;9(13):3732-3753.|Apoptosis. 2019 Apr;24(3-4):312-325.|Cancers (Basel). 2023 Sep 6, 15(18), 4442.|Front Immunol. 2018 Jan 5;8:1919.|J Mol Med (Berl). 2019 Aug;97(8):1183-1193.|Ruperto Carola University Heidelberg. Natural Sciences and Mathematics. 18 March 2022.

References

– [1]Morales C, et al. Antitumoral effect of irinotecan (CPT-11) on an experimental model of malignant neuroectodermal tumor. J Neurooncol. 2002 Feb;56(3):219-26.|[2]Pavillard V, et al. Determinants of the cytotoxicity of irinotecan in two human colorectal tumor cell lines. Cancer Chemother Pharmacol. 2002 Apr;49(4):329-35. Epub 2002 Jan 30.|[3]Allegrini G, et al. Thrombospondin-1 plus irinotecan: a novel antiangiogenic-chemotherapeutic combination that inhibits the growth of advanced human colon tumor xenografts in mice. Cancer Chemother Pharmacol. 2004 Mar;53(3):261-6. Epub 2003 Dec 5.

CAS Number

– 136572-09-3

Molecular Weight

– 677.18

Compound Purity

– 99.89

SMILES

– [H]Cl.O=C(N1CCC(N2CCCCC2)CC1)OC3=CC=C4N=C5C(CN6C(C(COC([C@@]7(CC)O)=O)=C7C=C65)=O)=C(CC)C4=C3.O.O.O

Clinical Information

– Launched

Research Area

– Cancer

Solubility

– DMSO : 50 mg/mL (ultrasonic)|Ethanol : 3.33 mg/mL (ultrasonic)|H2O : 1.52 mg/mL (ultrasonic;warming)

Target

– Autophagy;Topoisomerase

Isoform

– Topo I

Pathway

– Autophagy;Cell Cycle/DNA Damage

Product type

– Reference compound

Disclaimer: All products are for Research use only unless clearly stated otherwise on the product datasheet. Datasheets provided on the website are drafts for reference purpose only and you are requested to always refer to the hard copy included in the kit for your experimentation. Agdia Products are available for delivery only in Canada.

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