A sulfonamide with anticancer activity
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Indisulam

Item No. 22759

Technical Information
Formal Name
N1-(3-chloro-1H-indol-7-yl)-1,4-benzenedisulfonamide
CAS Number
165668-41-7
Synonyms
  • E-7070
Molecular Formula
C14H12ClN3O4S2
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlDMSO:PBS(pH 7.2) (1:4): 0.2 mg/mlEthanol: slightly soluble
λmax
224, 272, 281 nm
SMILES
NS(C1=CC=C(S(NC2=CC=CC3=C2NC=C3Cl)(=O)=O)C=C1)(=O)=O
InChi Code
InChI=1S/C14H12ClN3O4S2/c15-12-8-17-14-11(12)2-1-3-13(14)18-24(21,22)10-6-4-9(5-7-10)23(16,19)20/h1-8,17-18H,(H2,16,19,20)
InChi Key
SETFNECMODOHTO-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    Indisulam is a sulfonamide with anticancer activity.1 In vitro, indisulam has antiproliferative effects on a wide range of human tumor lines with HCT116 colorectal being the most sensitive and NCI-H596 non-small cell lung cancer (NSCLC) the most resistant (IC50s = 0.11 and 94 μg/ml, respectively). It increases the number of P388 murine leukemia cells in the G1 phase of the cell cycle in a dose-dependent manner and exerts time-dependent cytotoxicity against HCT116 cells. In vivo, indisulam suppresses tumor growth and decreases tumor volume in murine HCT116, SW620, and HCT15 colorectal and LX-1 and PC9 lung cancer xenograft models. Indisulam induces proteasomal degradation of RNA binding motif protein 39 (RBM39) through association with the CUL4-DCAF15 E3 ubiquitin ligase in vitro.2 It is also an inhibitor of carbonic anhydrase in H. pylori (Ki = 310-562 nM).3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Ozawa, Y., Sugi, N.H., Nagasu, T., et alE7070, a novel sulphonamide agent with potent antitumour activity in vitro and in vivo. Eur. J. Cancer 37(17), 2275-2282 (2001).

    2. Han, T., Goralski, M., Gaskill, N., et alAnticancer sulfonamides target splicing by inducing RBM39 degradation via recruitment to DCAF15. Science 356(6336), (2017).

    3. Nishimori, I., Vullo, D., Minakuchi, T., et alCarbonic anhydrase inhibitors: Cloning and sulfonamide inhibition studies of a carboxyterminal truncated α-carbonic anhydrase from Helicobacter pylori. Bioorg. Med. Chem. Lett. 16(8), 2182-2188 (2006).