专利号:US-4760068-A 优先权日:1982-06-14 标题:Certain pyridyl alkenoic acid derivatives which inhibit the action of thromboxane A2 synthetase 发明人:TERAO SHINJI; NISHIKAWA KOHEI 权利人:TAKEDA CHEMICAL INDUSTRIES LTD 摘要:Novel compound of the formula: ##STR1## wherein R 1 is pyridyl group, R 2 is a phenyl group, a thienyl group, a furyl group, a naphthyl group, a benzothienyl group or pyridyl group, which may optionally have a lower alkoxy group, a lower alkyl group, a halogen atom, trifluoromethyl group, a lower alkenyl group or methylenedioxy group, R 3 is hydrogen atom or a lower alkyl group, and n is an integer of 0 to 6, Y is sulphur atom, methylene group or a group of the formula: ##STR2## wherein R 4 is hydrogen atom or acetyl group, and m is 0 or 1, and their pharmaceutically acceptable salts having an inhibitory action on bio-synthesis of thromboxane A 2 (TXA 2 ) and an effect of accelerating the productivility of prostaglandin I 2 (PGI 2 ), and can be used for mammals to the prophylaxis or therapy of thrombosis caused by platelet aggregation or ischemic diseases caused by vasospasms in cardiac, cerebral and peripheral circulatory system (e.g. cardiac infarction, apoplexy, infarct of blood vessels in kidney, lung and other organs, pectic ulcer, etc.).
专利号:WO-2023137518-A1 优先权日:2022-01-21 标题 :Platinum complexes 发明人:ALDRICH-WRIGHT JANICE; GORDON CHRISTOPHER; DEO KRISHANT M; KHOURY ALEEN; MCGHIE BRONDWYN; APUTEN ANGELICO; PLATTEN-MENTI MARIA; RASHID FATIN; JURISINEC ASHLEY; SOLIMAN SARAH 权利人:WESTERN SYDNEY UNIV 摘要:The present disclosure relates to platinum complexes, and in particular platinum(II) and platinum(IV) complexes. The present disclosure also relates to synthesis of the platinum complexes, and to intermediates for the synthesis of the platinum complexes. The present disclosure also relates to methods and use of the platinum complexes for treating cancer.
专利号:US-6531614-B2 优先权日:1993-12-15 标题 :Method of prostaglandin synthesis 发明人:CONROW RAYMOND E 权利人:ALCON MFG LTD 摘要:Methods of synthesizing 9-Halo-13,14-dihydroprostaglandins useful in the treatment of glaucoma and ocular hypertension are disclosed. Also disclosed are ophthalmic, pharmaceutical compositions comprising such prostaglandins.
专利号:US-4536505-A 优先权日:1983-05-17 标 题:Certain N-(pyridyl) indoles 发明人:BROWNE LESLIE J 权利人:CIBA GEIGY CORP 摘要:Disclosed are compounds of formula I ##STR1## wherein Ar is 3- or 4-pyridyl or 3- or 4-pyridyl substituted by lower alkyl; n R 1 is hydrogen, halogen, trifluoromethyl, lower alkyl, hydroxy, acylated or etherified hydroxy, lower alkyl-(thio, sulfinyl or sulfonyl), or two of R 1 on adjacent carbon atoms represent alkylenedioxy; n p is 1 or 2; n R 2 represents hydrogen or lower alkyl; one of R 3 and R 4 represents hydrogen and the other of R 3 and R 4 represents the group A-B in which n A represents alkylene of 1 to 12 carbon atoms, alkynylene or alkenylene of 2 to 12 carbon atoms each, lower alkylene-phenylene, lower alkylene-(thio or oxy)-lower alkylene, lower alkylene-(thio or oxy)-phenylene, lower alkylenephenylene-lower (alkylene or alkenylene), or alkadienylene or 4 to 12 carbon atoms; and n B represents carboxy, esterified carboxy, carbamoyl, mono- or di-lower alkylcarbamoyl, cyano, hydroxycarbamoyl, or 5-tetrazolyl; the pyridyl-N-oxides thereof; and pharmaceutically acceptable salts thereof; methods for their synthesis and pharmaceutical compositions thereof. These compounds are useful as selective thromboxane synthetase inhibitors for the treatment of diseases such as cerebral ischaemia, shock, thrombosis and ischaemic heart disease.
专利号:US-6344581-B1 优先权日:1993-12-15 标题 :Method of prostaglandin synthesis
专利号:US-2002107414-A1 优先权日:1993-12-15 标 题:Method of prostaglandin synthesis
参考标题:Asymmetric Hydrogenation Of Tetrasubstituted Cyclic Enones To Chiral Cycloalkanols With Three Contiguous Stereocenters 作者:Yun-Ting Liu,Ji-Qiang Chen,Lin-Ping Li,Xin-Yang Shao,Jian-Hua Xie,Qi-Lin Zhou |发布日期:2017.6.16 摘要:A Highly Efficient Iridium-Catalyzed Asymmetric Hydrogenation Of Tetrasubstituted Cyclic Enones Has Been Developed For The Enantioselective Synthesis Of Chiral Cycloalkanols With Three Contiguous Stereocenters. The C═o And C═c Bonds Of The Enone Substrates Were Hydrogenated Sequentially In One Pot With Excellent Enantioselectivity (92 To >99% Ee) And Diastereoselectivity (Dr 95:5 To >99:1). The Reaction
合成参考文献
参考文献:10.1016/j.ejmech.2023.115973 摘要:Li T, He X, Tao W, Zhang R, He Q, Gong H, Liu Y, Luo D, Zhang M, Zou C, Zhang S, He Y. Development of membrane-targeting TPP+-chloramphenicol conjugates to combat methicillin-resistant staphylococcus aureus (MRSA) infections. European Journal of Medicinal Chemistry. 2024 Jan;264():115973. doi: 10.1016/j.ejmech.2023.115973.