Indisulam

Indisulam
Names
	Preferred IUPAC name N1-(3-Chloro-1H-indol-7-yl)benzene-1,4-disulfonamide
	Other names E7070
Identifiers
CAS Number	165668-41-7;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:145431;
ChEMBL	ChEMBL77517;
ChemSpider	187608;
DrugBank	DB06370;
KEGG	D04522;
PubChem CID	216468;
UNII	WJ98J3NM90;
CompTox Dashboard (EPA)	DTXSID50168008 ;
	InChI 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) Key: SETFNECMODOHTO-UHFFFAOYSA-N;
	SMILES C1=CC2=C(C(=C1)NS(=O)(=O)C3=CC=C(C=C3)S(=O)(=O)N)NC=C2Cl;
Properties
Chemical formula	C14H12ClN3O4S2
Molar mass	385.84 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Indisulam is a chloroindolyl sulfonamide cell cycle inhibitor that exhibits antitumor activity in vitro and in an animal model.^[1]^[2]^[3] This compound affects cell cycle progression in human tumor cells and is being studied for the treatment of cancers such as melanomas and blood-borne cancers such as leukemia.^[4]

References

↑ Fukuoka K, Usuda J, Iwamoto Y, et al. (2001). "Mechanisms of Action of the Novel Sulfonamide Anticancer Agent E7070 on Cell Cycle Progression in Human Non-Small Cell Lung Cancer Cells". Invest New Drugs. 19 (3): 219–27. doi:10.1023/A:1010608317361. PMID 11561678. S2CID 26100991.
↑ Ozawa Y, Sugi NH, Nagasu T, Owa T, Watanabe T, Koyanagi N, Yoshino H, Kitoh K, Yoshimatsu K (November 2001). "E7070, a Novel Sulphonamide Agent With Potent Antitumour Activity in Vitro and in Vivo". European Journal of Cancer. 37 (17): 2275–82. doi:10.1016/s0959-8049(01)00275-1. PMID 11677118.
↑ E. Raymond; W.W. ten Bokkel Huinink; J. Taïeb; J.H. Beijnen; S. Faivre; J. WandersM. Ravic; P. Fumoleau; J.P. Armand; J.H.M. Schellens (2002-08-15). "Phase I and Pharmacokinetic Study of E7070, a Novel Chloroindolyl Sulfonamide Cell-Cycle Inhibitor, Administered as a One-Hour Infusion Every Three Weeks in Patients With Advanced Cancer". Journal of Clinical Oncology. 20 (16): 3508–21. doi:10.1200/JCO.2002.09.030. PMID 12177112.
↑ Rita Assi; Hagop M. Kantarjian; Jorge E. Cortes; Tapan Kadia; Naveen Pemmaraju; Elias J. Jabbour; Nitin Jain; Naval Daver; Taisuke Uehara; Takashi Owa; Gautam Borthakur (2001). "Final Results of Phase 2, Open-Label Study of E7070, Idarubicin and Cytarabine in Patients (Pts) with Relapsed or Refractory (R/R) Acute Myeloid Leukemia (AML) and High-Risk Myelodysplastic Syndrome (MDS)". Blood. 130 (supplement 1).

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[1] Fukuoka K, Usuda J, Iwamoto Y, et al. (2001). "Mechanisms of Action of the Novel Sulfonamide Anticancer Agent E7070 on Cell Cycle Progression in Human Non-Small Cell Lung Cancer Cells". Invest New Drugs. 19 (3): 219–27. doi:10.1023/A:1010608317361. PMID 11561678. S2CID 26100991.

[2] Ozawa Y, Sugi NH, Nagasu T, Owa T, Watanabe T, Koyanagi N, Yoshino H, Kitoh K, Yoshimatsu K (November 2001). "E7070, a Novel Sulphonamide Agent With Potent Antitumour Activity in Vitro and in Vivo". European Journal of Cancer. 37 (17): 2275–82. doi:10.1016/s0959-8049(01)00275-1. PMID 11677118.

[3] E. Raymond; W.W. ten Bokkel Huinink; J. Taïeb; J.H. Beijnen; S. Faivre; J. WandersM. Ravic; P. Fumoleau; J.P. Armand; J.H.M. Schellens (2002-08-15). "Phase I and Pharmacokinetic Study of E7070, a Novel Chloroindolyl Sulfonamide Cell-Cycle Inhibitor, Administered as a One-Hour Infusion Every Three Weeks in Patients With Advanced Cancer". Journal of Clinical Oncology. 20 (16): 3508–21. doi:10.1200/JCO.2002.09.030. PMID 12177112.

[4] Rita Assi; Hagop M. Kantarjian; Jorge E. Cortes; Tapan Kadia; Naveen Pemmaraju; Elias J. Jabbour; Nitin Jain; Naval Daver; Taisuke Uehara; Takashi Owa; Gautam Borthakur (2001). "Final Results of Phase 2, Open-Label Study of E7070, Idarubicin and Cytarabine in Patients (Pts) with Relapsed or Refractory (R/R) Acute Myeloid Leukemia (AML) and High-Risk Myelodysplastic Syndrome (MDS)". Blood. 130 (supplement 1).

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