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399572-22-6

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399572-22-6 Usage

Application

Pharmaceutical industry

Purpose

Potential antitumor agent

Properties

Cytotoxic and antiproliferative

Function

Inhibits the growth of cancer cells

Stage of Research

Preclinical studies

Potential

Promising candidate for the development of new anticancer drugs

Unique Feature

Chemical structure valuable for the development of new drug candidates and the study of structure-activity relationships in medicinal chemistry

Future Impact

Holds the potential to contribute to the advancement of cancer treatment and improve patient outcomes

Chemical Classification

9CI (Chemical Abstracts Service Registry Number)

Check Digit Verification of cas no

The CAS Registry Mumber 399572-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,9,5,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 399572-22:
(8*3)+(7*9)+(6*9)+(5*5)+(4*7)+(3*2)+(2*2)+(1*2)=206
206 % 10 = 6
So 399572-22-6 is a valid CAS Registry Number.

399572-22-6Downstream Products

399572-22-6Relevant articles and documents

Structure of the molecular complexes of 18-crown-6 with 1,2,5-oxadiazole derivatives

Fonar,Simonov,Kravtsov,Lipkowski,Javolowski,Ganin

, p. 459 - 469 (2001)

This paper reports on an X-ray diffraction analysis of host-guest type molecular complexes of 18-crown-6 with 1,2,5-oxadiazole derivatives: ethyl 4-amino-1,2,5-oxadiazole-3-carboxylic ether (1:1) (complex I), 4-(2-chloroethylamino)-1,2,5-oxadiazole-3-carboxylic acid hydrazide (1:2) (complex II), and 4-amino-1,2,5-oxadiazole-3-carboxylic acid amide monohydrate (1:1:1) (complex III). Crystals I are monoclinic with cell parameters a = 8.960(2), b = 18.118(4), c = 14.405(3) A, β = 106.9(3)°, space group P21/n, R = 0.054 for 4082 reflections. The 18-crown-6 and guest molecules are linked by hydrogen bonds of NH...O(crown) and CH...O(crown) types based on the "head-to-tail" principle, alternating in infinite chains along the y axis in the crystal. Crystals II are triclinic with cell parameters a = 8.615(2), b = 9.249(2), c = 10.987(2) A, α = 106.86(3), β = 95.25(3), γ = 97.74(3)°, space group P1, R = 0.046 for 3006 reflections. The guest molecules are united into dimers by N-H...O=C hydrogen bonds. The 18-crown-6 molecules and the dimer associates of the guest form chains along [110] in the crystal. Crystals III are monoclinic with cell dimensions a = 13.238(3), b = 19.004(4), c = 8.485(2) A, β = 100.75(3)°, space group Cc, R = 0.051 for 2032 reflections. The crown ether molecule is disordered over two positions. The NH...O=C and NH...N type hydrogen bonds link the guest molecules into chains. The water molecules serve to bridge the chains with crown ether molecules, forming ribbons whose axis lies along the z direction in the crystal.

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