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1.
公开(公告)号:WO0126693A3
公开(公告)日:2001-12-27
申请号:PCT/US0028109
申请日:2000-10-12
Applicant: CELL THERAPEUTICS INC , KUMAR ANIL M , KLEIN J PETER , BHATT RAMA , VAWTER EDWARD
Inventor: KUMAR ANIL M , KLEIN J PETER , BHATT RAMA , VAWTER EDWARD
IPC: A61K31/337 , A61K31/427 , A61K31/4745 , A61K47/42 , A61K47/48 , A61P35/00
CPC classification number: A61K47/645
Abstract: The invention provides new processes for preparing polyglutamic acid-therapeutic agent conjugates for clinical development and pharmaceutical use, and polyglutamic acid-therapeutic agent conjugates prepared by these processes.
Abstract translation: 本发明提供了用于制备用于临床开发和药物用途的聚谷氨酸治疗剂缀合物的新方法,以及通过这些方法制备的聚谷氨酸治疗剂缀合物。
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公开(公告)号:ES2254163T3
公开(公告)日:2006-06-16
申请号:ES00921774
申请日:2000-04-07
Applicant: CELL THERAPEUTICS INC
Inventor: KLEIN J PETER , KLAUS STEPHEN J , KUMAR ANIL M , GONG BAOQING
IPC: C07D473/06 , A61K31/522 , A61P1/04 , A61P1/16 , A61P7/00 , A61P7/06 , A61P9/14 , A61P11/00 , A61P11/06 , A61P17/06 , A61P19/02 , A61P25/00 , A61P25/16 , A61P25/28 , A61P29/00 , A61P31/04 , A61P35/00 , A61P37/00 , A61P37/02 , A61P43/00 , C07D209/00 , C07D235/00 , C07D239/00 , C07D249/00 , C07D285/00 , C07D333/00 , C07D473/04 , C07D473/10 , C07D487/04 , C07D495/04 , C07D513/04 , C07D519/00
Abstract: Un compuesto, incluyendo enantiómeros resueltos, diastereómeros, tautómeros, sales y solvatos de los mismos, que tienen la siguiente **fórmula** en donde: X, Y y Z son independientemente seleccionados de un miembro del grupo formado por C(R3), N, N(R3) y S; R1 se selecciona de un miembro del grupo formado por hidrógeno, metil sustituido, C(5-9)alquilo sustituido o no sustituido, C(5-9)alquenilo sustituido o no sustituido, C(5- 9)alquinilo sustituido o no sustituido, , C(5- 9)hidroxialquilo sustituido o no sustituido, C(3-8)alcoxilo sustituido o no sustituido, C(5-9)alcoxialquilo sustituido o no sustituido, en donde cuando es sustituido R1, es sustituido con un miembro del grupo formado por N-OH, acilamino, grupo ciano, sulfo, sulfonilo, sulfinilo, sulfhidrilo (mercapto), sulfeno, sulfanililo, sulfamilo, sulfamino, y fosfino, fosfinilo, fosfo, fosfono y ¿NRaRb, en donde cada uno de Ra y Rb pueden ser los mismos o diferentes y cada uno se selecciona del grupo formado por hidrógeno, alquilo opcionalmente sustituido, cicloalquilo, alquenilo, cicloalquenilo, alquinilo, arilo, heteroarilo y grupo heterocíclico.
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公开(公告)号:BR0014652A
公开(公告)日:2003-06-10
申请号:BR0014652
申请日:2000-10-12
Applicant: CELL THERAPEUTICS INC
Inventor: KUMAR ANIL M , KLEIN J PETER , BHATT RAMA , VANTER EDWARD
IPC: A61K31/337 , A61K31/427 , A61K31/4745 , A61K47/42 , A61K47/48 , A61P35/00
Abstract: The present invention relates to conjugates comprising a polyglutamic acid polymer covalently bonded to a camptothecin molecule selected from the group consisting of 20(S)(+)-camptothecin, 9-aminocamptothecin, 9-nitrocamptothecin, 7-ethyl-10-hydroxycamptothecin, 9-dimethyl-aminomethyl-10-hydroxycamptothecin and 7-methylpiperizinomethyl-10,11-ethylenedioxy-camptothecin. The present invention also relates to such compounds as medicaments, in particular for the treatment of cancer.
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公开(公告)号:CA2387611A1
公开(公告)日:2001-04-19
申请号:CA2387611
申请日:2000-10-12
Applicant: CELL THERAPEUTICS INC
Inventor: BHATT RAMA , VAWTER EDWARD , KUMAR ANIL M , KLEIN J PETER
IPC: A61K31/337 , A61K31/427 , A61K31/4745 , A61K47/42 , A61K47/48 , A61P35/00
Abstract: The invention provides new processes for preparing polyglutamic acid- therapeutic agent conjugates for clinical development and pharmaceutical use , and polyglutamic acid-therapeutic agent conjugates prepared by these process es.
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公开(公告)号:AU4205000A
公开(公告)日:2000-11-14
申请号:AU4205000
申请日:2000-04-07
Applicant: CELL THERAPEUTICS INC
Inventor: KLEIN J PETER , KLAUS STEPHEN J , KUMAR ANIL M , GONG BAOQING
IPC: C07D473/06 , A61K31/522 , A61P1/04 , A61P1/16 , A61P7/00 , A61P7/06 , A61P9/14 , A61P11/00 , A61P11/06 , A61P17/06 , A61P19/02 , A61P25/00 , A61P25/16 , A61P25/28 , A61P29/00 , A61P31/04 , A61P35/00 , A61P37/00 , A61P37/02 , A61P43/00 , C07D209/00 , C07D235/00 , C07D239/00 , C07D249/00 , C07D285/00 , C07D333/00 , C07D473/04 , C07D473/10 , C07D487/04 , C07D495/04 , C07D513/04 , C07D519/00
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公开(公告)号:AU2098799A
公开(公告)日:1999-08-02
申请号:AU2098799
申请日:1998-12-30
Applicant: CELL THERAPEUTICS INC
Inventor: KLAUS STEPHEN J , KLEIN PETER J , KUMAR ANIL M
IPC: A61K31/00 , C07D473/04 , C07D473/06 , C07D487/04 , C07D495/04 , C07D513/04 , A61K31/52
Abstract: Novel heterocyclic compounds having a six membered ring structure fused to a five membered ring structure are found to be useful for the treatment and prevention of symptoms or manifestations associated with disorders affected by Interleukin-12 ("IL-12") intracellular signaling, such as, for example, Th1 cell-mediated disorders. The therapeutic compounds, pharmaceutically acceptable derivatives (e.g., resolved enantiomers, diastereomers, tautomers, salts and solvates thereof) or prodrugs thereof, have the following general formula: Each X, Y and Z are independently selected from a member of the group consisting of C(R3), N,N(R3) and S. Each R1, R2 and R3 is substituted or unsubstituted and is independently selected from a member of the group consisting of hydrogen, halo, oxo, C(1-20)alkyl, C(1-20)hydroxyalkyl, C(1-20)thioalkyl, C(1-20)alkylamino, C(1-20)alkylaminoalkyl, C(1-20)aminoalkyl, C(1-20)aminoalkoxyalkenyl, C(1-20)aminoalkoxyalkynyl, C(1-20)diaminoalkyl, C(1-20)triaminoalkyl, C(1-20)tetraminoalkyl, C(5-15)aminotrialkoxyamino, C(1-20)alkylamido, C(1-20)alkylamidoalkyl, C(1-20)amidoalkyl, C(1-20)acetamidoalkyl, C(1-20)alkenyl, C(1-20)alkynyl, C(3-8)alkoxyl, C(1-11)alkoxyalkyl, and C(1-20)dialkoxyalkyl.
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公开(公告)号:CA2159640A1
公开(公告)日:1994-10-13
申请号:CA2159640
申请日:1994-03-31
Applicant: CELL THERAPEUTICS INC
Inventor: KLEIN J PETER , MICHNICK JOHN , RICE GLENN C , UNDERINER GAIL E , KUMAR ANIL M
IPC: A61K31/13 , A61K31/135 , A61K31/165 , A61K31/40 , A61K31/4015 , A61K31/403 , A61K31/4035 , A61K31/445 , A61K31/45 , A61K31/47 , A61K31/472 , A61K31/505 , A61K31/513 , A61K31/517 , A61K31/519 , A61K31/52 , A61K31/522 , A61P29/00 , A61P31/04 , A61P35/00 , A61P37/06 , C07C215/08 , C07C215/56 , C07C217/62 , C07C229/22 , C07C233/36 , C07C233/78 , C07C233/91 , C07C237/06 , C07D207/40 , C07D207/404 , C07D207/408 , C07D209/48 , C07D211/40 , C07D211/76 , C07D211/88 , C07D217/24 , C07D239/54 , C07D239/90 , C07D239/96 , C07D295/13 , C07D473/10 , C07D519/00 , C07K5/06 , A61K31/00 , A61K38/05 , C07D239/88 , C07D473/06
Abstract: The invention provides a group of compounds that are effective agents to inhibit specific cellular signaling events often induced by inflammatory stimuli, to act as anti-inflammatory or immunosupressive agents, to act as cytotoxic agents for treatment of cancers, or to be directly or indirectly antimicrobial to yeast or fungal infections. More specifically, the inventive compounds have at least one amino alcohol (or derivative thereof) functional group on a side chain attached to a core moiety. The inventive compounds are useful antagonists to control intracellular levels of specific sn-2 unsaturated phosphatidic acids and corresponding acid-derived diacylglycerols, intracellular cell signaling messengers which occur in response to pro-inflammatory and selectively proliferative stimuli.
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公开(公告)号:AT312102T
公开(公告)日:2005-12-15
申请号:AT00921774
申请日:2000-04-07
Applicant: CELL THERAPEUTICS INC
Inventor: KLEIN J PETER , KLAUS STEPHEN J , KUMAR ANIL M , GONG BAOQING
IPC: C07D473/06 , A61K31/522 , A61P1/04 , A61P1/16 , A61P7/00 , A61P7/06 , A61P9/14 , A61P11/00 , A61P11/06 , A61P17/06 , A61P19/02 , A61P25/00 , A61P25/16 , A61P25/28 , A61P29/00 , A61P31/04 , A61P35/00 , A61P37/00 , A61P37/02 , A61P43/00 , C07D209/00 , C07D235/00 , C07D239/00 , C07D249/00 , C07D285/00 , C07D333/00 , C07D473/04 , C07D473/10 , C07D487/04 , C07D495/04 , C07D513/04 , C07D519/00
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公开(公告)号:AU781735B2
公开(公告)日:2005-06-09
申请号:AU1079301
申请日:2000-10-12
Applicant: CELL THERAPEUTICS INC
Inventor: KUMAR ANIL M , KLEIN J PETER , BHATT RAMA , VAWTER EDWARD
IPC: A61K31/337 , A61K31/427 , A61K31/4745 , A61K47/42 , A61K47/48 , A61P35/00
Abstract: The present invention relates to conjugates comprising a polyglutamic acid polymer covalently bonded to a camptothecin molecule selected from the group consisting of 20(S)(+)-camptothecin, 9-aminocamptothecin, 9-nitrocamptothecin, 7-ethyl-10-hydroxycamptothecin, 9-dimethyl-aminomethyl-10-hydroxycamptothecin and 7-methylpiperizinomethyl-10,11-ethylenedioxy-camptothecin. The present invention also relates to such compounds as medicaments, in particular for the treatment of cancer.
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公开(公告)号:NZ529789A
公开(公告)日:2005-04-29
申请号:NZ52978900
申请日:2000-10-12
Applicant: CELL THERAPEUTICS INC
Inventor: KUMAR ANIL M , KLEIN PETER J , BHATT RAMA , VAWTER EDWARD
IPC: A61K31/337 , A61K31/427 , A61K31/4745 , A61K47/42 , A61K47/48 , A61P35/00
Abstract: A process for preparing a polyglutamic acid-20(S)-campotothecin conjugate and the conjugate produced is disclosed. A pharmaceutical composition for the treatment of cancer comprising an effective amount of the polyglutamic acid-camptothecin conjugate is also disclosed. (62) Divided out of 518262
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