CAS: 1738-76-7; Benzyl Glycinate 4-Methylbenzenesulfonate

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CAS号104-15-4 对甲苯磺酸 | CAS号56-40-6 甘氨酸 | CAS号100-51-6 苯甲醇 | CAS号81110-58-9 2-[(benzoylthio... | CAS号98-59-9 对甲苯磺酰氯(PTSC) | CAS号1738-68-7 甘氨酸苄酯盐酸盐 | CAS号19525-53-2 benzyl 2-[(2-ph... | CAS号81477-91-0 N-二苯亚甲基甘氨酸苄酯 | CAS号16305-78-5 benzyl 2-[2-(ph... | CAS号67585-90-4 benzyl 2-[[2-[[... | CAS号686-43-1 缬氨酰-甘氨酸 | CAS号87428-99-7 benzyl 2-(2-ben... | CAS号889097-01-2 benzyl 2-(2,5-d... | CAS号954-92-7 benzyl 3,4-dime... | CAS号41995-26-0 benzyl 2-is°Cya...

2-[(Benzoylthio)Methyl]-3-Phenylpropanoic Acid 反应生成甘氨酸苄酯对甲苯磺酸盐
参考文献:Aminoacid Derivatives And Their Therapeutic Applications
标题:Aminoacid Derivatives And Their Therapeutic Applications
摘要:这项发明涉及氨基酸衍生物,以及含有该氨基酸衍生物的具有阿肽酶抑制,镇痛,止泻和降压活性的组合物,其化学式如下:##str1## 其中变量如本文所述,例如 ##str2##

专利信息

专利号:US-5945548-A
优先权日:1995-03-03
标题:Process for the synthesis of α-substituted acrylic acids and their application
发明人：DUHAMEL PIERRE; DUHAMEL LUCETTE; DANVY DENIS; MONTEIL THIERRY; LECOMTE JEANNE-MARIE; SCHWARTZ JEAN-CHARLES
权利人:BIOPROJECT SOC CIV
摘要:Process for the synthesis of α-substituted acrylic acids of general formula (I) and their application to the synthesis of N-(mercaptoacyl)aminoacid derivatives of formula (II). ##STR1##

专利号:US-5817749-A
优先权日:1993-03-29
标 题:Processes and intermediate compounds for the preparation of platelet glycoprotein IIb/IIIa inhibitors
发明人：ZHANG LIN-HUA; MA PHILIP; DEGRADO WILLIAM FRANK
权利人:DU PONT PHARM CO
摘要:This invention provides processes for the synthesis of platelet glycoprotein IIb/IIIa inhibitors and intermediate compounds useful in said processes. The compounds afforded by this invention have the formula: Formula (I)

专利号:US-3953416-A
优先权日:1971-12-20
标 题:Synthetic decapeptide having the activity of the luteinizing hormone releasing hormone and method for manufacturing the same
发明人：FOLKERS KARL; CURRIE BRUCE L; CHANG JAW-KANG; SIEVERTSSON HANS; BOGENTOFT CONNY
权利人:FOLKERS KARL; CURRIE BRUCE L; CHANG JAW KANG; SIEVERTSSON HANS; BOGENTOFT CONNY
摘要:A synthetic decapeptide, L-pglutamyl-L-histidyl-L-tryptophanyl-L-seryl-L-tyrosyl-glycyl-L-leucy l-L-arginyl-L-prolyl-glycinamide which has the hormonal activities of the luteinizing hormone releasing hormone (LRH) of the hypothalamus gland of mammals is produced by utilizing as the key starting materials, the amino acids, glutamic acid or pyroglutamic acid, histidine, tryptophan, serine, tyrosine, glycine, leucine, arginine, and proline. Synthesis of the decapeptide is accomplished by coupling, in appropriate combinations of appropriate protected forms of the amino acids, and finally deprotecting to yield the amide, L-pglutamyl-L-histidyl-L-tryptophanyl-L-seryl-L-tyrosyl-glycyl-L-leucy l-L-arginyl-L-prolyl-glycinamide.

专利号:US-2009215986-A1
优先权日:2006-03-08
标题:Solution Synthesis of Peptide Cell Growth Stimulators
发明人：EPSTEIN DAVID; KRUSZYNSKI MARIAN F; MARSH CHRISTOPHER; SCHMIDT ALBERT
权利人:EPSTEIN DAVID; KRUSZYNSKI MARIAN F; MARSH CHRISTOPHER; SCHMIDT ALBERT
摘要:A solution phase synthetic method for preparing basic tripeptides of the formula Gly-Xaa-Gly-X which have in various biological properties such as stimulating protein production when used as additives in a bioreactor. The basic tripeptides of the invention may be produced on gram or kilogram scale.

专利号:US-4416820-A
优先权日:1981-01-14
标题:Indole derivatives and a method for production of peptides
发明人：FUKUDA TSUNEHIKO; KOBAYASHI SHIGERU; FUJINO MASAHIKO
权利人:TAKEDA CHEMICAL INDUSTRIES LTD
摘要:An indole group in an amino acid or a peptide can be protected with a group shown by the formula: wherein R1 and R5 each is hydrogen, methyl or methoxy; R2 and R4 each is hydrogen or methyl; and R3 is methyl or methoxy, and said group may easily be removed without affecting the amino acid or the peptide to be derived from the protected amino acid or peptide. Thus, the present invention is useful in the synthesis of a peptide containing an indole group.

专利号:WO-0058269-A1
优先权日:1999-03-26
标题:Dtpa esters with orthogonal removable protecting groups
发明人：ACHILEFU SAMUEL I; SRINIVASAN ANANTHACHARI
权利人:MALLINCKRODT INC; ACHILEFU SAMUEL I; SRINIVASAN ANANTHACHARI
摘要:The synthesis of compounds of formula (XXXIII) wherein each R4 is a removable protecting group; R5 is a removable protecting group different from and removable separately from R4; each R6 and R8 is a linking moiety having 1 to 10 carbon atoms; and R9 is hydrogen or a C1 to C50 alkyl moiety; is disclosed. These compounds are useful intermediates in the synthesis of compounds of formula (X). These compounds are useful in the preparation of nuclear pharmaceuticals such as those used for tumor imaging or tumor therapy.