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MW 623.1 Da, Purity >99%. Potent DNA topoisomerase I inhibitor. Displays antitumor activity against a variety of tumor types. Active metabolite SN38 (ab141108) also available.

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Images

Chemical Structure - CPT 11 (Irinotecan), DNA topoisomerase I inhibitor (AB141107), expandable thumbnail
  • Immunocytochemistry/ Immunofluorescence - CPT 11 (Irinotecan), DNA topoisomerase I inhibitor (AB141107), expandable thumbnail

Publications

Key facts

CAS number

100286-90-6

Purity

> 99%

Form

Solid

Molecular weight

623.1 Da

Molecular formula

C33H39ClN4O6

PubChem identifier

74990

Nature

Synthetic

Recommended products

MW 623.1 Da, Purity >99%. Potent DNA topoisomerase I inhibitor. Displays antitumor activity against a variety of tumor types. Active metabolite SN38 (ab141108) also available.

Key facts

Purity

> 99%

PubChem identifier

74990

Solubility

Soluble in water to 5 mM. Soluble in DMSO to 100 mM.

Biochemical name

Irinotecan hydrochloride

Biological description

Potent DNA topoisomerase I inhibitor. Displays antitumor activity against a variety of tumor types. Active metabolite SN38 (ab141108) also available.

Canonical SMILES

CCC1=C2CN3C(=CC4=C(C3=O)COC(=O)C4(CC)O)C2=NC5=C1C=C(C=C5)OC(=O)N6CCC(CC6)N7CCCCC7.Cl

Isomeric SMILES

CCC1=C2CN3C(=CC4=C(C3=O)COC(=O)[C@@]4(CC)O)C2=NC5=C1C=C(C=C5)OC(=O)N6CCC(CC6)N7CCCCC7.Cl

InChI

InChI=1S/C33H38N4O6.ClH/c1-3-22-23-16-21(43-32(40)36-14-10-20(11-15-36)35-12-6-5-7-13-35)8-9-27(23)34-29-24(22)18-37-28(29)17-26-25(30(37)38)19-42-31(39)33(26,41)4-2;/h8-9,16-17,20,41H,3-7,10-15,18-19H2,1-2H3;1H/t33-;/m0./s1

InChIKey

GURKHSYORGJETM-WAQYZQTGSA-N

IUPAC name

[(19S)-10,19-diethyl-19-hydroxy-14,18-dioxo-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)-heptaen-7-yl] 4-piperidin-1-ylpiperidine-1-carboxylate;hydrochloride

Storage

Shipped at conditions

Ambient - Can Ship with Ice

Appropriate short-term storage conditions

+4°C

Appropriate long-term storage conditions

+4°C

Storage information

The product can be stored for up to 12 months

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2 product images

  • Chemical Structure - CPT 11 (Irinotecan), DNA topoisomerase I inhibitor (ab141107), expandable thumbnail

    Chemical Structure - CPT 11 (Irinotecan), DNA topoisomerase I inhibitor (ab141107)

    2D chemical structure image of ab141107, CPT 11 (Irinotecan), DNA topoisomerase I inhibitor

  • Immunocytochemistry/ Immunofluorescence - CPT 11 (Irinotecan), DNA topoisomerase I inhibitor (ab141107), expandable thumbnail

    Immunocytochemistry/ Immunofluorescence - CPT 11 (Irinotecan), DNA topoisomerase I inhibitor (ab141107)

    Anti-gamma H2A.X (phospho S139) antibody ab2893 staining γH2A.X in HeLa cells treated with CPT 11 (Irinotecan) (ab141107), by ICC/IF. Increase of γH2A.X nuclear expression correlates with increased concentration of CPT 11 (Irinotecan), as described in literature.
    The cells were incubated at 37°C for 6 hours in media containing different concentrations of ab141107 (CPT 11 (Irinotecan)) 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 Anti-gamma H2A.X (phospho S139) antibody 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 (Goat Anti-Rabbit IgG H&L (DyLight® 488) preadsorbed ab96899) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.

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