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4',7-Dichloro-4,6-dimethoxy-6'-methylspiro[benzofuran-2(3H),1'-[3]cyclohexene]-2',3-dione is a complex organic compound with a unique chemical structure. It is characterized by the presence of a spiro ring system, which consists of a benzofuran and a cyclohexene ring connected through a spiro carbon atom. The benzofuran ring features two chlorine atoms at the 4' and 7 positions, while the cyclohexene ring has a methyl group at the 6' position. Additionally, there are two methoxy groups attached to the benzofuran ring at the 4 and 6 positions. The compound also contains a 2',3-dione group, which is a carbonyl group at both the 2' and 3 positions. This chemical is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its specific properties and reactivity.

1235-50-3

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1235-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1235-50-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1235-50:
(6*1)+(5*2)+(4*3)+(3*5)+(2*5)+(1*0)=53
53 % 10 = 3
So 1235-50-3 is a valid CAS Registry Number.

1235-50-3Upstream product

1235-50-3Downstream Products

1235-50-3Relevant academic research and scientific papers

Disparate SAR data of griseofulvin analogues for the dermatophytes Trichophyton mentagrophytes, T. rubrum, and MDA-MB-231 cancer cells

R?nnest, Mads H.,Raab, Marc S.,Anderhub, Simon,Boesen, Sven,Kr?mer, Alwin,Larsen, Thomas O.,Clausen, Mads H.

supporting information; experimental part, p. 652 - 660 (2012/04/10)

Griseofulvin and 53 analogues of this compound have been tested against the pathogenic dermatophytes Trichophyton rubrum and Trichophyton mentagrophytes as well as against the breast cancer cell line MDA-MB-231. The modifications to griseofulvin include the 4, 5, 6, 2′, 3′, and 4′ positions. The SAR of the griseofulvin analogues toward the two fungi followed the same trend with the majority being less active than griseofulvin and none had more than twice the potency of the parent compound. A comparison of the antifungal and the anticancer SAR revealed distinct differences, as the majority of analogues showed increased activity against the cancer cell line MDA-MB-231, highlighted by 2′-benzyloxy-2′-demethoxy-griseofulvin, which showed low activity against both fungi but was among the most potent compounds against MDA-MB-231 cancer cells. Tubulin has been proposed as the target of griseofulvin in both fungal and mammalian cells, but the differences revealed by this SAR study strongly suggest that the mode-of-action of the compound class toward fungi and mammalian cancer cells is different.

Synthesis and structure-activity relationship of griseofulvin analogues as inhibitors of centrosomal clustering in cancer cells

R?nnest, Mads H.,Rebacz, Blanka,Markworth, Lene,Terp, Anette H.,Larsen, Thomas O.,Kr?mer, Alwin,Clausen, Mads H.

supporting information; experimental part, p. 3342 - 3347 (2010/03/26)

Griseofulvin was identified as an inhibitor of centrosomal clustering in a recently developed assay. Centrosomal clustering is an important cellular event that enables bipolar mitosis for cancer cell lines harboring supernumerary centrosomes. We report he

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