JPS6445391A - Novel method for measuring alpha-amylase activity - Google Patents

Novel method for measuring alpha-amylase activity

Info

Publication number
JPS6445391A
JPS6445391A JP20112187A JP20112187A JPS6445391A JP S6445391 A JPS6445391 A JP S6445391A JP 20112187 A JP20112187 A JP 20112187A JP 20112187 A JP20112187 A JP 20112187A JP S6445391 A JPS6445391 A JP S6445391A
Authority
JP
Japan
Prior art keywords
halogen
formula
amylase activity
nitro
lower alkoxy
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
JP20112187A
Other languages
Japanese (ja)
Other versions
JPH0676430B2 (en
Inventor
Tokuji Ikenaka
Kaoru Omichi
Shinji Satomura
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.)
Fujifilm Wako Pure Chemical Corp
Original Assignee
Wako Pure Chemical Industries 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 Wako Pure Chemical Industries Ltd filed Critical Wako Pure Chemical Industries Ltd
Priority to JP20112187A priority Critical patent/JPH0676430B2/en
Publication of JPS6445391A publication Critical patent/JPS6445391A/en
Publication of JPH0676430B2 publication Critical patent/JPH0676430B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

NEW MATERIAL:A compound expressed by formula I [R<1> is formula II-IV (R<2>-R<5> are H, lower alkyl, lower alkoxy, nitro, carboxyl, sulfonic acid, halogen, etc.; R<6> is H, lower alkoxy, halogen or nitro; R<7> is H, methyl or trifluoromethyl; R<8> is H or halogen)]. USE:A substrate for measuring alpha-amylase activity applicable also to dry quantitative methods, since measurement can be made by colorimetry. PREPARATION:An oligosaccharide derivative expressed by formula V is reacted with acetals, such as benzaldehyde dimethyl acetal, to form a cyclic acetal group between the 4- and the 6-positions of nonreducing terminal glucose. The resultant cyclic acetalized substance is then acylated to modify other OH groups. The modified compound is subsequently subjected to a reduction step and then deacylated.
JP20112187A 1987-08-12 1987-08-12 New method for measuring α-amylase activity Expired - Lifetime JPH0676430B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20112187A JPH0676430B2 (en) 1987-08-12 1987-08-12 New method for measuring α-amylase activity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20112187A JPH0676430B2 (en) 1987-08-12 1987-08-12 New method for measuring α-amylase activity

Publications (2)

Publication Number Publication Date
JPS6445391A true JPS6445391A (en) 1989-02-17
JPH0676430B2 JPH0676430B2 (en) 1994-09-28

Family

ID=16435758

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20112187A Expired - Lifetime JPH0676430B2 (en) 1987-08-12 1987-08-12 New method for measuring α-amylase activity

Country Status (1)

Country Link
JP (1) JPH0676430B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0391496A (en) * 1989-09-04 1991-04-17 Boehringer Mannheim Gmbh Method and reagent for specific measurement of pancreas alpha amylase

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0391496A (en) * 1989-09-04 1991-04-17 Boehringer Mannheim Gmbh Method and reagent for specific measurement of pancreas alpha amylase

Also Published As

Publication number Publication date
JPH0676430B2 (en) 1994-09-28

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