436372

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Aromatic polyimides.

Bower GM and Frost LW.

Journal of Polymer Science Part A: Polymer Chemistry, 1(10), 3135-3150 (1963)

Quantum wire and dot formation by chemical vapor deposition and molecular layer deposition of one-dimensional conjugated polymer.

Yoshimura T, et al.

Applied Physics Letters, 60(3), 268-270 (1992)

Synergistic enhancement of thyroid tumor induction by 2,4-diaminoanisole sulfate, N,N'-diethylthiourea and 4,4'-thiodianiline in male F344 rats.

R Hasegawa et al.

Carcinogenesis, 12(8), 1515-1518 (1991-08-01)

Three thyroid carcinogens, 2,4-diaminoanisole sulfate (DAAS), N,N'-diethylthiourea (DETU) and 4,4'-thiodianiline (TDA), were simultaneously administered in the diet to male F344 rats at one-third the concentration of the reported TD50 levels (610, 200 and 46 p.p.m. respectively) for 52 weeks. The

4,4'-Thiodianiline.

Report on carcinogens : carcinogen profiles, 11, III248-III249 (2004-01-01)

Toxicity of aromatic disulphides. III. In vivo haemolytic activity of aromatic disulphides.

R Munday et al.

Journal of applied toxicology : JAT, 5(6), 414-417 (1985-12-01)

Diphenyl disulphide, 4,4'-diaminodiphenyl disulphide, 2,2'-diaminodiphenyl disulphide, 4,4'-dimethyldiphenyl disulphide and 4,4'-dinitrodiphenyl disulphide, when administered orally to rats, induced haematological and pathological changes indicative of erythrocyte destruction in vivo. No evidence of haemolysis was detected, however, in animals receiving diphenyl disulphide-2,2'-dicarboxylic acid

The enzymatic formation of sulfoxides: the oxidation of chlorpromazine and 4,4'-diaminodiphenyl sulfide by guinea pig liver microsomes.

J R GILLETTE et al.

The Journal of pharmacology and experimental therapeutics, 130, 262-267 (1960-11-01)

4,4'-Thiodianiline.

IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 27, 147-154 (1982-04-01)

Synthesis and characterization of novel, soluble sulfur-containing copolyimides with high refractive indices.

Dusselberg D, et al.

J. Mater. Sci., 46(14), 4872-4879 (2011)

Polycondensation of pyridine-2,6-dicarboxylic acid with some di-and tetraamino compounds.

Banihashemi A and Eghbali M.

Journal of Polymer Science, 14(11), 2659-2664 (1976)

Carcinogenic effect of combined administration of 2,4-diaminoanisole sulfate, 4,4'-thiodianiline and N,N'-diethylthiourea in male Wistar rats.

L Pomorski et al.

Neoplasma, 49(4), 247-250 (2002-10-17)

Male Wistar rats were divided into two groups. Rats of group 1 were fed basal powdered diet containing 610 ppm 2,4- diaminoanisole sulfate (DAAS), 46 ppm 4,4'-thiodianiline (TDA) and 200 ppm N,N'-diethylthiourea (DETU) for 52 weeks (DTD treatment). Rats of

4,4'-Thiodianiline.

Report on carcinogens : carcinogen profiles, 12, 404-405 (2011-08-25)

DNA fragmentation and DNA repair synthesis induced in rat and human thyroid cells by four rat thyroid carcinogens.

Francesca Mattioli et al.

Toxicology and applied pharmacology, 203(2), 99-105 (2005-02-16)

Four chemicals that are known to induce in rats thyroid follicular-cell adenomas and carcinomas were assayed for their ability to induce DNA damage and DNA repair synthesis in primary cultures of human thyroid cells. Significant dose-dependent increases in the frequency

Development of QSAR models for predicting hepatocarcinogenic toxicity of chemicals.

Ilaria Massarelli et al.

European journal of medicinal chemistry, 44(9), 3658-3664 (2009-03-11)

A dataset comprising 55 chemicals with hepatocarcinogenic potency indices was collected from the Carcinogenic Potency Database with the aim of developing QSAR models enabling prediction of the above unwanted property for New Chemical Entities. The dataset was rationally split into

Toxicity of aromatic disulphides. II. Intraerythrocytic hydrogen peroxide formation and oxidative damage by aromatic disulphides.

R Munday

Journal of applied toxicology : JAT, 5(6), 409-413 (1985-12-01)

Diphenyl disulphide has been shown to generate hydrogen peroxide in erythrocytes in vitro. It also induces oxidative damage (reversible and irreversible haemoglobin oxidation, depletion of non-protein and protein-bound thiols) in these cells. Such changes were also recorded in erythrocytes exposed

In vivo evaluation of diaminodiphenyls: anticonvulsant agents with minimal acute neurotoxicity.

David R Worthen et al.

Bioorganic & medicinal chemistry letters, 19(17), 5012-5015 (2009-07-28)

Several diaminodiphenyl analogs were assessed in vivo for their capacity to inhibit seizure induction and propagation in rodents. Both 3,4'- and 4,4'-diaminodiphenyl compounds prevented seizures for as long as 4h after maximal electric shock induction. 4,4'-Diphenyl compounds bridged by a

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