公开(公告)号：DE2305998A1

公开(公告)日：1973-08-16

申请号：DE2305998

申请日：1973-02-07

Applicant: OREAL

Inventor： MANOUSSOS GEORGES ,  DOSSOU KOOVI GATIEN ,  GASCON MARTINE

IPC: A61L15/18 ,  A61F13/18

Abstract: An absorbent material for use in absorbing body fluids, has a fluid permeable outer portion impregnated with deodorizing amounts of periodic acid.

公开(公告)号：AT296944B

公开(公告)日：1972-03-10

申请号：AT445269

申请日：1968-06-21

Applicant: OREAL

Inventor： KALOPISSIS GREGOIRE ING ,  MANOUSSOS GEORGES

IPC: C07C149/24

公开(公告)号：DE1767819A1

公开(公告)日：1972-02-03

申请号：DE1767819

申请日：1968-06-20

Applicant: OREAL

Inventor： MANOUSSOS GEORGES ,  KALOPISSIS GREGOIRES

IPC: A61K8/46 ,  A61Q5/00 ,  C07C323/25 ,  C07D213/82 ,  C07K1/00 ,  A61K7/06

公开(公告)号：DE1667903A1

公开(公告)日：1972-01-05

申请号：DE1667903

申请日：1968-02-21

Applicant: OREAL

Inventor： KALOPISSIS GREGOIRE ,  MANOUSSOS GEORGES

IPC: A61K8/44 ,  A61K8/46 ,  A61K31/13 ,  A61K31/195 ,  A61K31/38 ,  A61K31/44 ,  A61Q5/00 ,  A61Q19/00 ,  C07D213/32 ,  C07D213/82 ,  C07D213/89 ,  C07D307/38 ,  C07D333/20 ,  C07D333/32 ,  A61K27/00

公开(公告)号：DE1667907A1

公开(公告)日：1971-03-11

申请号：DE1667907

申请日：1968-03-19

Applicant: OREAL

Inventor： MANOUSSOS GEORGES ,  BERREBI CLAUDINE

IPC: A61K8/98 ,  A61Q7/00

公开(公告)号：DE1947896A1

公开(公告)日：1970-09-17

申请号：DE1947896

申请日：1969-09-22

Applicant: OREAL

Inventor： BERREBI CLAUDINE ,  MANOUSSOS GEORGES

IPC: A61K8/73 ,  A61K8/98 ,  A61K35/36 ,  A61K35/50 ,  A61K35/54 ,  A61Q19/00 ,  A61Q19/06 ,  A61Q19/08

公开(公告)号：GB1163870A

公开(公告)日：1969-09-10

申请号：GB849268

申请日：1968-02-21

Applicant: OREAL

Inventor： KALOPISSIS GREGOIRE ,  MANOUSSOS GEORGES

IPC: A61K8/44 ,  A61K8/46 ,  A61K31/13 ,  A61K31/195 ,  A61K31/38 ,  A61K31/44 ,  A61Q5/00 ,  A61Q19/00 ,  C07D213/32 ,  C07D213/82 ,  C07D213/89 ,  C07D307/38 ,  C07D333/20 ,  C07D333/32

Abstract: 1,163,870. Anti-seborrhoeic compositions. L'OREAL. 21 Feb., 1968 [21 Feb., 1967], No. 8492/68. Addition to 1,051,870. Heading A5B. Anti-seborrhoeic compositions comprise as active ingredient a compound of the general formula R-S-CH 2 -CH(NHR 11 )COOR 1 where R is triphenylmethyl, diphenylmethyl, benzyl or R 1 OOC-(CH 2 ) n . R 1 is H or C 1 -C 6 alkyl, n is 1-4 and R 11 is H or -COR or SO 2 R where R is C 1 -C 6 alkyl or aryl, or a non-toxic acid addition salt thereof together with a) a solid ingestible excipient, (b) an edible syrup or (c) a flavouring agent, or (d) in an ingestible capsule.

公开(公告)号：CA1024445A

公开(公告)日：1978-01-17

申请号：CA140187

申请日：1972-04-20

Applicant: OREAL

Inventor： KALOPISSIS GREGOIRE ,  MANOUSSOS GEORGES

IPC: A61K8/46 ,  A61K8/49 ,  A61K31/10 ,  A61K31/13 ,  A61K31/195 ,  A61K31/33 ,  A61K31/395 ,  A61Q5/00 ,  A61Q5/02 ,  A61Q19/00 ,  C07C233/16 ,  C07C323/25 ,  C07D213/32 ,  C07D213/70 ,  C07D213/81 ,  C07D295/08 ,  C07D295/088 ,  C07D295/21 ,  C07D307/10 ,  C07D307/38 ,  C07D307/54 ,  C07D317/56 ,  C11D3/48 ,  A61K31/16

公开(公告)号：FR2332760A1

公开(公告)日：1977-06-24

申请号：FR7635644

申请日：1976-11-26

Applicant: OREAL

Inventor： BERREBI CLAUDINE ,  MANOUSSOS GEORGES

IPC: A61K8/98 ,  A61K35/36 ,  A61K35/48 ,  A61Q19/00 ,  A61K35/64

公开(公告)号：CA965008A

公开(公告)日：1975-03-25

申请号：CA88893

申请日：1970-07-22

Applicant: OREAL

Inventor： KALOPISSIS GREGOIRE ,  BOUILLON CLAUDE ,  MANOUSSOS GEORGES ,  BERREBI CLAUDINE

IPC: A61K8/67 ,  A61K31/44 ,  A61Q5/00 ,  A61Q5/02 ,  A61Q19/00 ,  C07D213/66 ,  C07D491/04 ,  C11D1/00

Abstract: 1310559 Pyridoxine derivatives L'OREAL 23 July 1970 [23 July 1969] 35797/70 Heading C2C [Also in Divisions A5, C4 and D1] Dermatological compounds II (including salts thereof) where R signifies an organic radical containing at least one amine group and optionally a carboxylic acid, ester or amide group and wherein the amine group may be substituted by an acyl or sulphonyl radical or by one or two alkyl radicals which can contain acid, ester, amide, amine, alcohol or guanidine groups (R signifies, e.g. -CH 2 CH 2 NH 2 or -CH 2 CHNH 2 CO 2 H), are made: (a) by converting pyridoxine hydrochloride into a ketal (i.e. the phenolic hydroxy in the 3-position and the alcohol group in the 4- position are blocked by ketalization, utilizing, e.g. acetone), thereafter chlorinating the 5- hydroxymethyl group to afford the corresponding 5-chloromethyl compound, which is, in turn, reacted with a thiol or alkali metal thiolate, A.S.R (A is H or an alkali metal atom) and subsequently hydrolysing the product so obtained to remove the protecting ketal group, or (b) by reacting R.halogen with an appropriate thiol derived from pyridoxine.