- Carbazole oxime ester compound and synthetic method and application thereof
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The invention discloses a carbazole oxime ester compound shown as in general formula I that is shown in the description; the carbazole oxime ester compound with the structure of general formula I has the advantages of good solubility, thermal stability, high photosensitive activity and low toxicity; a photoinitiator has excellent applicability and very high photosensitivity, exhibits very high photosensitive activity when exposed to LEDs, LDI (Liniarc direct/indirect) and other light sources, the production efficiency of photosensitive compositions such as in the preparation of color filters and other application fields is significantly improved, and the efficiency is significantly better than that of existing products.
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Paragraph 0144; 0145; 0146
(2017/09/13)
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- AMINO-PROPYLENE-GLYCOL DERIVATIVES, PREPARATION METHOD AND PHARMACEUTICAL COMPOSITION AND USE THEREOF
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Immune-modulators of formula (I) below are prepared: A pharmaceutical composition contains the immune-modulators. The pharmaceutical composition is used as a drug, especially as an immune-modulating drug. The compound can be used in treatment of immune disorders and for immune suppression. Thus, for example, the compound can be used in treating hypo-immunity, rejection after organ transplantation and auto-immune disease.
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Paragraph 0128; 0129; 0344; 0345
(2014/11/11)
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- AMINO-PROPYLENE-GLYCOL DERIVATIVES, PREPARATION METHOD AND PHARMACEUTICAL COMPOSITION AND USE THEREOF
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Disclosed are immune-modulators of formula (I), the preparation method thereof, a pharmaceutical composition containing the immune-modulators, and the use of the pharmaceutical composition as a drug, especially as an immune-modulating drug. The compound can be used in immune disorders and immune suppression, and can be used in treating hypo-immunity, rejection after organ transplantation and auto-immune disease.
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Paragraph 0087-0088
(2014/10/16)
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- N-(4-Substituted-thiazolyl)oxamic Acid Derivatives, a New Series of Potent, Orally Actve Antiallergy Agents
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A series of N-(4-substituted-thiazolyl)oxamic acid derivatives were synthesized and tested for antiallergy activity in the rat PCA model.These compounds were conveniently prepared by treatment of the appropriate acetophenone with thiourea and iodine or by reaction of the chloroacetylbenzene with thiourea to give the corresponding aminothiazoles; subsequent condensation with ethyloxalyl chloride gave the thiazolyloxamates.Many of the analogues showed a 50percent inhibition at oxamic acid ethanolamine salt (61, PRH-836-EA), has been selected for further pharmacological evaluation.
- Hargrave, Karl D.,Hess, Friedrich K.,Oliver, James T.
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p. 1158 - 1163
(2007/10/02)
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