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JPS57142987A - N-acyl c-15003pnd and its preparation - Google Patents

N-acyl c-15003pnd and its preparation

Info

Publication number
JPS57142987A
JPS57142987A JP56028977A JP2897781A JPS57142987A JP S57142987 A JPS57142987 A JP S57142987A JP 56028977 A JP56028977 A JP 56028977A JP 2897781 A JP2897781 A JP 2897781A JP S57142987 A JPS57142987 A JP S57142987A
Authority
JP
Japan
Prior art keywords
reaction
compound
formula
preparation
formulai
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.)
Pending
Application number
JP56028977A
Other languages
Japanese (ja)
Inventor
Mikio Izawa
Mitsuko Asai
Seiichi Tanida
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.)
Takeda Pharmaceutical Co Ltd
Original Assignee
Takeda 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 Takeda Chemical Industries Ltd filed Critical Takeda Chemical Industries Ltd
Priority to JP56028977A priority Critical patent/JPS57142987A/en
Publication of JPS57142987A publication Critical patent/JPS57142987A/en
Pending legal-status Critical Current

Links

Landscapes

  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

NEW MATERIAL:A maytansinoid of formulaI(R1 is lower alkyl; R2 is lower alkyl, aryl).
EXAMPLE: PND-3-N-acetate.
USE: Antitumor agent, antiprotozoal agent: it is low-toxicity and can be administered orally or parenterally.
PREPARATION: The reaction of a compound of formula II with a carboxylic acid of formula III or its reactive derivative gives a compound of formulaI. The reaction is preferably effected in the presence of a basic or acidic catalyst such as a tertiary amine or Lewis acid. When necessary, the reaction is conducted in the presence of a condensation reagent and a solvent at -40W100°C. The compound of formula II is obtained from the culture mixture of a microorganism such as Nocardia.
COPYRIGHT: (C)1982,JPO&Japio
JP56028977A 1981-02-27 1981-02-27 N-acyl c-15003pnd and its preparation Pending JPS57142987A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56028977A JPS57142987A (en) 1981-02-27 1981-02-27 N-acyl c-15003pnd and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56028977A JPS57142987A (en) 1981-02-27 1981-02-27 N-acyl c-15003pnd and its preparation

Publications (1)

Publication Number Publication Date
JPS57142987A true JPS57142987A (en) 1982-09-03

Family

ID=12263472

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56028977A Pending JPS57142987A (en) 1981-02-27 1981-02-27 N-acyl c-15003pnd and its preparation

Country Status (1)

Country Link
JP (1) JPS57142987A (en)

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