JPS55335A - Pantethine homologue and its preparation - Google Patents

Pantethine homologue and its preparation

Info

Publication number
JPS55335A
JPS55335A JP7361378A JP7361378A JPS55335A JP S55335 A JPS55335 A JP S55335A JP 7361378 A JP7361378 A JP 7361378A JP 7361378 A JP7361378 A JP 7361378A JP S55335 A JPS55335 A JP S55335A
Authority
JP
Japan
Prior art keywords
formula
amino
phthalyl
group
pantethine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP7361378A
Other languages
Japanese (ja)
Other versions
JPS617190B2 (en
Inventor
Usao Nakamura
Sueo Horiuchi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hamari Chemicals Ltd
Original Assignee
Hamari Chemicals Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hamari Chemicals Ltd filed Critical Hamari Chemicals Ltd
Priority to JP7361378A priority Critical patent/JPS55335A/en
Publication of JPS55335A publication Critical patent/JPS55335A/en
Publication of JPS617190B2 publication Critical patent/JPS617190B2/ja
Granted legal-status Critical Current

Links

Abstract

NEW MATERIAL:A bis-(N-D-pantoyl-γ-aminobutyryl-2-aminoethyl) disulfide shown by the formula I.
USE: Reagents, medicine, and a precursor of coenzyme A. Its chemical structure has a characteristic wherein γ-amino-n-butyric acid residue is substituted for β-alanine residue in pantethine and homo-pantothenyl group as a partial structure.
PROCESS: For example, a novel bis-(γ-amino-n-butyl-2-aminoethyl)-disulfide shown by the formula II is condensed with D-pantolactone to give the desired compound shown by the formula I. For example, phtalyl-γ-amino-n-butyric acid (phthalyl- GABA) is reacted with cystamine so that amino group of cystamine is acylated by phthalyl-GABA reside and phthalyl group is removed to give the raw material compound shown by the formula II.
COPYRIGHT: (C)1980,JPO&Japio
JP7361378A 1978-06-16 1978-06-16 Pantethine homologue and its preparation Granted JPS55335A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7361378A JPS55335A (en) 1978-06-16 1978-06-16 Pantethine homologue and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7361378A JPS55335A (en) 1978-06-16 1978-06-16 Pantethine homologue and its preparation

Publications (2)

Publication Number Publication Date
JPS55335A true JPS55335A (en) 1980-01-05
JPS617190B2 JPS617190B2 (en) 1986-03-04

Family

ID=13523351

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7361378A Granted JPS55335A (en) 1978-06-16 1978-06-16 Pantethine homologue and its preparation

Country Status (1)

Country Link
JP (1) JPS55335A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4298678A (en) * 1980-08-14 1981-11-03 E. I. Du Pont De Nemours And Company Photosensitive compositions and elements containing substituted hydroxylamine
FR2669329A1 (en) * 1990-11-09 1992-05-22 Oreal Aminomercaptoalkylamides, process for their preparation and their use in a reducing (reductive) cosmetic composition in the permanent deforming (waving) of hair
EP0514282A1 (en) * 1991-05-17 1992-11-19 L'oreal Alkylamino mercaptoalkylamides or salts thereof acceptable for cosmetic use, their use as a reducing agent and a process for the permanent deformation of hair

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4298678A (en) * 1980-08-14 1981-11-03 E. I. Du Pont De Nemours And Company Photosensitive compositions and elements containing substituted hydroxylamine
FR2669329A1 (en) * 1990-11-09 1992-05-22 Oreal Aminomercaptoalkylamides, process for their preparation and their use in a reducing (reductive) cosmetic composition in the permanent deforming (waving) of hair
EP0514282A1 (en) * 1991-05-17 1992-11-19 L'oreal Alkylamino mercaptoalkylamides or salts thereof acceptable for cosmetic use, their use as a reducing agent and a process for the permanent deformation of hair
FR2676441A1 (en) * 1991-05-17 1992-11-20 Oreal NOVEL ALKYLAMINO-MERCAPTOALKYLAMIDES OR ONE OF THEIR COSMETICALLY ACCEPTABLE SALTS, AND THEIR USE AS REDUCING AGENTS, IN A METHOD OF PERMANENT DEFORMATION OF THE HAIR.

Also Published As

Publication number Publication date
JPS617190B2 (en) 1986-03-04

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