WO1991004754A3 - Illudin analogs as anti-tumor agents - Google Patents

Illudin analogs as anti-tumor agents Download PDF

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Publication number
WO1991004754A3
WO1991004754A3 PCT/US1990/005614 US9005614W WO9104754A3 WO 1991004754 A3 WO1991004754 A3 WO 1991004754A3 US 9005614 W US9005614 W US 9005614W WO 9104754 A3 WO9104754 A3 WO 9104754A3
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WO
WIPO (PCT)
Prior art keywords
illudin
tumor agents
illudin analogs
analog
subject
Prior art date
Application number
PCT/US1990/005614
Other languages
French (fr)
Other versions
WO1991004754A2 (en
Inventor
Michael J Kelner
Trevor C Mcmorris
Raymond Taetle
Original Assignee
Univ California
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 Univ California filed Critical Univ California
Priority to EP90916968A priority Critical patent/EP0565519B1/en
Priority to CA002067365A priority patent/CA2067365C/en
Priority to DE69028320T priority patent/DE69028320T2/en
Publication of WO1991004754A2 publication Critical patent/WO1991004754A2/en
Publication of WO1991004754A3 publication Critical patent/WO1991004754A3/en

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    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/12—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/12—Ketones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/27—Esters, e.g. nitroglycerine, selenocyanates of carbamic or thiocarbamic acids, meprobamate, carbachol, neostigmine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
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    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
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    • C07C45/673—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton
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    • C07C49/657—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings
    • C07C49/665—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings a keto group being part of a condensed ring system
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    • C07C49/703—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups
    • C07C49/723—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups polycyclic
    • C07C49/727—Unsaturated compounds containing a keto groups being part of a ring containing hydroxy groups polycyclic a keto group being part of a condensed ring system
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    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/753—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups
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    • C07—ORGANIC CHEMISTRY
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    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
    • C07C49/753—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups
    • C07C49/755—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups a keto group being part of a condensed ring system with two or three rings, at least one ring being a six-membered aromatic ring
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Abstract

A method of inhibiting certain tumor cell growth in a subject is provided comprising contacting the tumor with a therapeutic amount of an illudin S or illudin M analog having the structure <IMAGE> wherein the analog is capable of inhibiting tumor cell growth without excessive toxicity to the subject and wherein R1 is hydrogen; R2 is methyl; and R3 is hydroxy.
PCT/US1990/005614 1989-10-03 1990-10-02 Illudin analogs as anti-tumor agents WO1991004754A2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP90916968A EP0565519B1 (en) 1989-10-03 1990-10-02 Illudin analogs as anti-tumor agents
CA002067365A CA2067365C (en) 1989-10-03 1990-10-02 Illudin analogs as anti-tumor agents
DE69028320T DE69028320T2 (en) 1989-10-03 1990-10-02 ILLUDINE ANALOG, USED AS AN ANTI-TUMOR MEDICINE

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US41639589A 1989-10-03 1989-10-03
US416,395 1989-10-03

Publications (2)

Publication Number Publication Date
WO1991004754A2 WO1991004754A2 (en) 1991-04-18
WO1991004754A3 true WO1991004754A3 (en) 1991-12-12

Family

ID=23649800

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1990/005614 WO1991004754A2 (en) 1989-10-03 1990-10-02 Illudin analogs as anti-tumor agents

Country Status (11)

Country Link
US (1) US5439942A (en)
EP (1) EP0565519B1 (en)
JP (1) JPH05503077A (en)
AT (1) ATE141802T1 (en)
AU (1) AU6729590A (en)
CA (2) CA2067365C (en)
DE (1) DE69028320T2 (en)
DK (1) DK0565519T3 (en)
ES (1) ES2091249T3 (en)
IL (1) IL95875A (en)
WO (1) WO1991004754A2 (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5439936A (en) * 1989-10-03 1995-08-08 The Regents Of The University Of California Method of treating certain tumors using illudin analogs
US5932553A (en) * 1996-07-18 1999-08-03 The Regents Of The University Of California Illudin analogs useful as antitumor agents
US5723632A (en) 1996-08-08 1998-03-03 Mgi Pharma, Inc. Total synthesis of antitumor acylfulvenes
US7141603B2 (en) 1999-02-19 2006-11-28 The Regents Of The University California Antitumor agents
US6025328A (en) 1998-02-20 2000-02-15 The Regents Of The University Of California Antitumor agents
US7655695B2 (en) 2005-08-03 2010-02-02 The Regents Of The University Of California Illudin analogs useful as anticancer agents
US20080065083A1 (en) * 2006-09-07 2008-03-13 Csaba Truckai Bone treatment systems and methods
US11135182B2 (en) 2014-04-10 2021-10-05 Af Chemicals, Llc Affinity medicant conjugates
US10285955B2 (en) 2014-04-10 2019-05-14 Af Chemicals, Llc Affinity medicant conjugate
CA2944699C (en) 2014-04-10 2023-05-23 Af Chemicals, Llc Affinity medicant conjugates
CN106083953A (en) * 2016-06-15 2016-11-09 成都医学院 A kind of from fiddlehead, extract former pteroside and the method preparing high purity raw pteroside
JP2021536492A (en) * 2018-09-04 2021-12-27 ランタン ファーマ インコーポレイテッド Illudin analogs, their use, and how to synthesize them
US11160807B1 (en) 2018-12-11 2021-11-02 Af Chemicals, Llc Methods, compositions and devices for treating cancer with illudofulvenes
US11591295B2 (en) 2019-11-25 2023-02-28 Af Chemicals Llc Affinity illudofulvene conjugates

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62234040A (en) * 1986-04-02 1987-10-14 Kyowa Hakko Kogyo Co Ltd Substance dc1043 and production thereof

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
Cancer Research, vol. 45, no. 11, November 1985, R.O. Dillman et al.: "Athymic mouse model of a human T-cell tumor", pages 5632-5636, see abstract; page 5634, discussion (cited in the application) *
Cancer Research, vol. 47, 15 June 1987, M.J. Kelner et al.: "Preclinical evaluation of illudins as anticancer agents", pages 3186-3189, see abstract; page 3189, left-hand column, last paragraph; page 3189 (cited in the application) *
STN File Server CAS Chemical Abstracts, vol. 90, S. Shinozawa et al.: "The antitumor effect of illudin S (lampterol) entrapped in liposome for mice inoculated with Ehrlich ascites tumor cells", see abstract no. 197682, & Igaku no Ayumi (IGAYAY, 03677826); 79; vol. 108 (7), pages 414-416 *
STN File Server, File Medline, Ass. no. 2, I. Hirono et al.: "Reproduction of acute bracken poisoning in a calf with ptaquiloside, a bracken constituent", see abstract no. 85067284, & Vet Rec, (1984 Oct 13) 115(15), 375-8, see the abstract *
Tetrahedron Letters, vol. 38, 1971, Pergamon Press, (GB), S.M. Weinreb: "Fulvenes derived from illudin S", pages 3489-3491, see page 3490, compositions 3,2 *
Tetrahedron, vol. 45, no. 17, 1989, Pergamon Press plc, (GB), T.C. McMorris et al.: "Structure and reactivity of illudins", pages 5433-5440, see page 5433, paragraphs 1,2; page 5437, last paragraph *

Also Published As

Publication number Publication date
CA2530543C (en) 2008-04-01
ATE141802T1 (en) 1996-09-15
US5439942A (en) 1995-08-08
IL95875A (en) 1994-10-21
JPH05503077A (en) 1993-05-27
CA2067365A1 (en) 1991-04-04
DK0565519T3 (en) 1996-09-23
ES2091249T3 (en) 1996-11-01
CA2067365C (en) 2006-01-31
CA2530543A1 (en) 1991-04-18
EP0565519B1 (en) 1996-08-28
DE69028320T2 (en) 1997-03-06
AU6729590A (en) 1991-04-28
DE69028320D1 (en) 1996-10-02
IL95875A0 (en) 1991-07-18
EP0565519A1 (en) 1993-10-20
WO1991004754A2 (en) 1991-04-18

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