CAS: 138-60-3; 4-Oxo-1,4-Dihydropyridine-2,6-Dicarboxylic Acid

相似化合物

199926-39-1 20443-03-2 910628-19-2

上下游产品

CAS号99-32-1 白屈菜酸 | CAS号109880-40-2 methyl 6-formyl... | CAS号53389-01-8 4-氯-2,6-二吡啶甲酸乙酯 | CAS号4722-94-5 4-氯吡啶-2,6-二羧酸 | CAS号5371-70-0 4-氯-2,6-二吡啶甲酸甲酯 | CAS号184870-12-0 4-oxo-1H-pyridi... | CAS号1817-20-5 [4-chloro-6-(hy... | CAS号18986-54-4 4-phenylmethoxy... | CAS号19872-91-4 4-羟基-2,6-吡啶二甲酸二甲酯 | CAS号206647-42-9 4-bromopyridine... | CAS号126769-30-0 methyl 4-(dimet...

4-氯-2,6-二甲基吡啶置于氢氧化钾,Potassium Permanganate,Sodium Acetate,溶剂黄146体系中,化学反应生成4-氧代-1,4-二氢-2,6-吡啶二甲酸
参考文献:ochiai; Fujimoto,Pharmaceutical Bulletin,1954,Vol. 2,P. 131,136
标题:ochiai; Fujimoto,Pharmaceutical Bulletin,1954,Vol. 2,P. 131,136

专利信息

专利号:US-2004110228-A1
优先权日:2002-04-01
标 题:Combinatorial organic synthesis of unique biologically active compounds
发明人：MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

专利号:US-7109220-B2
优先权日:2003-11-19
标 题:Amino substituted pyridinyl methanone compounds useful in treating kinase disorders
发明人：LIN RONGHUI; WETTER STEVEN K; LU YANHUA; CONNOLLY PETER J; EMANUEL STUART; GRUNINGER ROBERT H; MIDDLETON STEVEN A
权利人:JANSSEN PHARMACEUTICA NV
摘要:The present invention provides amino substituted pyridinyl methanone compounds; pharmaceutical compositions comprising the compounds and methods of synthesis thereof. The compounds, which are cyclin dependent kinase (CDK) inhibitors, can be used to treat or ameliorate CDK mediated disorders. The invention thus also provides the therapeutic or prophylactic use of the compounds and/or pharmaceutical compositions to treat such disorders.

专利号:CN-1683378-A
优先权日:2004-04-13
标 题:Synthesis and preparation of nickel-chelidonamic acid film with fluorescent property

专利号:EP-1626982-B1
优先权日:2003-05-23
标 题:Metal chelate complexes immobilized on solid supports for peptide preparation
发明人：RYBKA ANDREAS; FRANK HANS-GEORG; BRACHT FRANZ-PETER; HABERL UDO
权利人:APLAGEN GMBH
摘要:Use of an activated solid phase and an anchoring part which is attached to a peptide for solid phase peptide synthesis, wherein the anchoring part is coordinatively and reversibly attached to the activated solid phase. nFurthermore provided is a process for competitively detachment of said anchoring part, for purification and refolding of said peptides. Provided are peptides with an anchoring part for coordinative and reversible attachment of said peptides to an activated solid phase.

专利号:CN-111760594-A
优先权日:2020-07-30
标 题:A kind of vanadium pyridine/TS-1 catalyst for preparing 2,5-dichlorophenol by catalytic oxidation and its synthesis method and application

专利号:CN-111760594-B
优先权日:2020-07-30
标 题 :A kind of vanadium pyridine/TS-1 catalyst for preparing 2,5-dichlorophenol by catalytic oxidation and its synthesis method and application