Urea or thiourea substituted 1,4-pyrazine compounds useful as anti-cancer agents and for inhibiting Chk1
7 7 1-33-8Compounds of the formula wherein: Y′ is O or S, W′ is optionally substituted, Z′ is selected from the group consisting of wherein Q′ is ORand Ris CalkyleneCheterocycloalkyl useful in the treatment of diseases and conditions related to DNA damage or lesions in DNA replication are disclosed....
Saved in:
Main Authors | , , , , |
---|---|
Format | Patent |
Language | English |
Published |
27.10.2009
|
Online Access | Get full text |
Cover
Loading…
Abstract | 7 7 1-33-8Compounds of the formula wherein: Y′ is O or S, W′ is optionally substituted, Z′ is selected from the group consisting of wherein Q′ is ORand Ris CalkyleneCheterocycloalkyl useful in the treatment of diseases and conditions related to DNA damage or lesions in DNA replication are disclosed. Methods of making the compounds, and their use as therapeutic agents, for example, in treating cancer and other diseases characterized by defects in DNA replication, chromosome segregation, or cell division also are disclosed. |
---|---|
AbstractList | 7 7 1-33-8Compounds of the formula wherein: Y′ is O or S, W′ is optionally substituted, Z′ is selected from the group consisting of wherein Q′ is ORand Ris CalkyleneCheterocycloalkyl useful in the treatment of diseases and conditions related to DNA damage or lesions in DNA replication are disclosed. Methods of making the compounds, and their use as therapeutic agents, for example, in treating cancer and other diseases characterized by defects in DNA replication, chromosome segregation, or cell division also are disclosed. |
Author | Cook, Adam Wade Gaudino, John Joseph Kesicki, Edward A Cowen, Scott Douglas Burgess, Laurence Edward |
Author_xml | – sequence: 1 givenname: Edward A surname: Kesicki fullname: Kesicki, Edward A – sequence: 2 givenname: John Joseph surname: Gaudino fullname: Gaudino, John Joseph – sequence: 3 givenname: Adam Wade surname: Cook fullname: Cook, Adam Wade – sequence: 4 givenname: Scott Douglas surname: Cowen fullname: Cowen, Scott Douglas – sequence: 5 givenname: Laurence Edward surname: Burgess fullname: Burgess, Laurence Edward |
BookMark | eNqNjEsOgkAQRGehC3936ANIAtEge6LxALo2DTRMB-whMz0LPb1O4gFcvUrlVa3NQpzQyti7JwTnQS27mHKITVDWqNRBsT9m88vjm4Wgdc_ZRekCxEB9nAADoChnLUpLHnAg0VR10H8PWSw3rCwD1HYstmbZ4xRo9-PGwOV8q69ZDDNqWj4Gjwn5qcyrsqgOfygftSpCTw |
ContentType | Patent |
CorporateAuthor | Icos Corporation |
CorporateAuthor_xml | – name: Icos Corporation |
DBID | EFH |
DatabaseName | USPTO Issued Patents |
DatabaseTitleList | |
Database_xml | – sequence: 1 dbid: EFH name: USPTO Issued Patents url: http://www.uspto.gov/patft/index.html sourceTypes: Open Access Repository |
DeliveryMethod | fulltext_linktorsrc |
ExternalDocumentID | 07608618 |
GroupedDBID | EFH |
ID | FETCH-uspatents_grants_076086183 |
IEDL.DBID | EFH |
IngestDate | Sun Mar 05 22:31:26 EST 2023 |
IsOpenAccess | true |
IsPeerReviewed | false |
IsScholarly | false |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-uspatents_grants_076086183 |
OpenAccessLink | https://image-ppubs.uspto.gov/dirsearch-public/print/downloadPdf/7608618 |
ParticipantIDs | uspatents_grants_07608618 |
PatentNumber | 7608618 |
PublicationCentury | 2000 |
PublicationDate | 20091027 |
PublicationDateYYYYMMDD | 2009-10-27 |
PublicationDate_xml | – month: 10 year: 2009 text: 20091027 day: 27 |
PublicationDecade | 2000 |
PublicationYear | 2009 |
References | (WO 99/32463) 19990700 (WO 99/11621) 19990300 Heinisch, et al., "Synthesis of N-aryl-N'-heteroaryl-substituted urea and thiourea derivatives and evaluation of their anticonvulsant activity" Archiv Der Pharmazie, VCH Verlagsgesellschaft MBH, Weinheim, DE, vol. 330, No. 7, Jul. 1, 1997, pp. 207-210. Lee et al. (5041653) 19910800 Chaplin et al, Chemical Abstract DN 114:77895, also cited as British J. Of Cancer, 62/4, 561-6(1990). (WO 99/32436) 19990700 (WO 00/26203) 20000500 PubMed Abstract 8384080, also cited as Cancer Res. 43/7, 1599-601 (1993). (2132771) 19950900 Keegan et al. (7067506) 20060600 (WO 99/32433) 19990700 Chemical Abstract DN:4609659, also cited as U.S.P. 4609659, 1986. S.P. Dutta et al., J. Carbohydrates Nucleosides Nucleotides, 7(4), 217-240 (1980). Chemical Abstract DN 127:277898, also cited as Magnetic Reson. in Chem., 35/9, 653-55 (1997). Chemical Abstract DN 124:75535, also cited as. Med. Chem., 39/1, 304-13 (1996). (1 054 004) 20001100 PubMed Abstract 12554671, also cited as EMBO J. 22/3, 713-23(2003). Luo et al. (6211164) 20010400 Verlinden, et al., Cancer Res. 67, 6574-6581, Jun. 15, 2007. Chemical Abstract DN 91:117865, also cited as Acta Poloniae Pharm. 35/5, 615-18 (19878). (1621447) 19960200 Chemical Abstract DN 131:44827, also cited as WO 9929674. Cecil Textbook of Medicine, 20th edition, vol. 1, pp. 1104-1010 (1996). (WO 00/18738) 20000400 (WO 01/57034) 20010800 Jin, et al., Genes & Devel. 17:3062-3074, 2003. Sturgeon, et al., Cell Cycle, 2007, vol. 6 # 5, 572-575. (WO 00/03005) 20000100 (WO 99/00357) 19990100 Sanchez et al., Science, vol. 277, 1497-1501 (1997). PCT/US1993/03539, Apr. 20, 1993. Chemical Abstract DN 112:216860, also cited as Acta Poloniae Pharm. 46/2, 101-13 (1989). (1624949) 19960200 Lee et al. (5215738) 19930600 McBride (6051218) 20000400 Chemical Abstract DN 123:143653, also cited as CA 2132771 (1995). Uckun et al., Current Cancer Drug Targets, 1, 59-71 (2001). Kim, et al., Eur. J. Surg. Oncol., vol. 33, # 5, Jun. 2007, 580-585. Elledge et al. (6218109) 20010400 (WO 94/26715) 19941100 Basso et al. (2762743) 19560400 (WO 96/11930) 19960400 Salituro et al. (6093742) 20000700 Tabernero, et al., Ann. Oncol. 2005 16(11):1740-1748. (WO 99/29674) 19990600 Carter et al., Chemotherapy of Cancer, second edition, 362-65 (1981). (1 096 014) 20010500 Hartman (4609659) 19860900 Chemical Abstract DN 130:209605, also cited as WO 9911621. PubMed Abstract 12576328, also cited as Blood, 101/11,4589-97 (2003). (WO 00/56725) 20000900 (WO 00/75120) 20001200 (1 143 920) 20011100 PubMed Abstract 14593735, also cited as Prog. Cell Cycle Res., 4, 413-21 (2003). Chemical Abstract DN 128:13243, also cited as Arch. der Pharm. (Weinheim, Germany) 330/7, 207-10 (1997). (1 199 306) 20020400 (WO 93/07128) 19930400 |
References_xml | – year: 20060600 ident: 7067506 contributor: fullname: Keegan et al. – year: 19860900 ident: 4609659 contributor: fullname: Hartman – year: 19990700 ident: WO 99/32436 – year: 19990700 ident: WO 99/32463 – year: 20001100 ident: 1 054 004 – year: 19990700 ident: WO 99/32433 – year: 20000400 ident: 6051218 contributor: fullname: McBride – year: 20000100 ident: WO 00/03005 – year: 19960400 ident: WO 96/11930 – year: 20010800 ident: WO 01/57034 – year: 20000900 ident: WO 00/56725 – year: 20000700 ident: 6093742 contributor: fullname: Salituro et al. – year: 20020400 ident: 1 199 306 – year: 20010400 ident: 6211164 contributor: fullname: Luo et al. – year: 19941100 ident: WO 94/26715 – year: 20010400 ident: 6218109 contributor: fullname: Elledge et al. – year: 19930600 ident: 5215738 contributor: fullname: Lee et al. – year: 20001200 ident: WO 00/75120 – year: 19950900 ident: 2132771 – year: 19990100 ident: WO 99/00357 – year: 20000400 ident: WO 00/18738 – year: 19930400 ident: WO 93/07128 – year: 19560400 ident: 2762743 contributor: fullname: Basso et al. – year: 20000500 ident: WO 00/26203 – year: 20010500 ident: 1 096 014 – year: 19960200 ident: 1624949 – year: 19990600 ident: WO 99/29674 – year: 19910800 ident: 5041653 contributor: fullname: Lee et al. – year: 20011100 ident: 1 143 920 – year: 19960200 ident: 1621447 – year: 19990300 ident: WO 99/11621 |
Score | 2.7506542 |
Snippet | 7 7 1-33-8Compounds of the formula wherein: Y′ is O or S, W′ is optionally substituted, Z′ is selected from the group consisting of wherein Q′ is ORand Ris... |
SourceID | uspatents |
SourceType | Open Access Repository |
Title | Urea or thiourea substituted 1,4-pyrazine compounds useful as anti-cancer agents and for inhibiting Chk1 |
URI | https://image-ppubs.uspto.gov/dirsearch-public/print/downloadPdf/7608618 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3fS8MwED62IahPiorzF_fgo9F2rU33PFaKoOzBwd5Gm6S2ONvRtIj_vXetDF_09QLJccclX7gvXwBulRdInSSuCDztCF9KJgE4jlAmmBoZEsDuWJXPL0G89J9Wj6sBxLu3MB9URmJLvtj71m6bqiNX0vbeJ1704s-sEViy-sBnuakSvdDZgwwInLvhEIahw9S-eRQfwj5NQZCtbOyvQyM6gr1FZz2GgSlPIF8SPsOqxiYvKuaCo6Xl-069RvfOF9uvuhN7RuZ583dHFltrsnaDiUWKQCEU56jGhN9DsUkjYU4syrxIC-Yv4yx_d08Bo_nrLBY7t9ZvNdNd1s6P-94ZjOjab84Bw9RVmVKp5sKSyksDOQlNaLxk6mdOlo1h_Oc0F_-MXcJB1xGh_Xcir2DU1K25poO1SW-6qH0D6YCFiA |
link.rule.ids | 230,309,783,805,888,64367 |
linkProvider | USPTO |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1LT8MwDLbGQDxOIECMpw8cCbRrSbrzoCqvaQcm7Ta1aUorRjs1rRD_HidDExe4OlLkxLL9WfnsAFxKj4s0jl3GvdRhvhCGBOA4TCo-UCIggG1ZlS8jHk38x-nttAPRqhfmg9yILUgXfd3qRVNZciWF96Xh2XL4s5kRWJrpA5_lvIrTcZrdCE7g3A3WYJ1yLLclWRjtwBZtQqCtbPSvtBHuwsbYSvego8p9yCeE0LCqscmLyrDBUZMCy7f6FN0rny2-ajvuGQ3T23x4pLHVKmvnGGukOyiYNFaqMTYdUUaUIqFOLMq8SArDYMZh_u4eAIb3r8OIrdSavdWG8DJzfg7gHUKXCn91BBgkrsykTFLjWkJ6CRf9QAXKiwd-5mRZD3p_bnP8z9oFbI7vwtnzw-jpBLbt8wgF4744hW5Tt-qMsmyTnNsL_AabqoiF |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Apatent&rft.title=Urea+or+thiourea+substituted+1%2C4-pyrazine+compounds+useful+as+anti-cancer+agents+and+for+inhibiting+Chk1&rft.inventor=Kesicki%2C+Edward+A&rft.inventor=Gaudino%2C+John+Joseph&rft.inventor=Cook%2C+Adam+Wade&rft.inventor=Cowen%2C+Scott+Douglas&rft.inventor=Burgess%2C+Laurence+Edward&rft.number=7608618&rft.date=2009-10-27&rft.externalDBID=n%2Fa&rft.externalDocID=07608618 |