JP2010508362A - Ｃ型肝炎ウイルスの阻害剤 - Google Patents
Ｃ型肝炎ウイルスの阻害剤 Download PDFInfo
- Publication number
- JP2010508362A JP2010508362A JP2009535436A JP2009535436A JP2010508362A JP 2010508362 A JP2010508362 A JP 2010508362A JP 2009535436 A JP2009535436 A JP 2009535436A JP 2009535436 A JP2009535436 A JP 2009535436A JP 2010508362 A JP2010508362 A JP 2010508362A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hcv
- mmol
- compound
- tert
- 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.)
- Withdrawn
Links
- 0 CClCCCC(C=*)Cl Chemical compound CClCCCC(C=*)Cl 0.000 description 7
- SUCWJUHYGRQSDQ-TYNCELHUSA-N CC(C)(C)[C@@H](C(N(C[C@H](COc1cccc(Br)n1)C1)[C@@H]1C(O)=O)=O)NC(OC)=O Chemical compound CC(C)(C)[C@@H](C(N(C[C@H](COc1cccc(Br)n1)C1)[C@@H]1C(O)=O)=O)NC(OC)=O SUCWJUHYGRQSDQ-TYNCELHUSA-N 0.000 description 2
- PEXWJYDPDXUVSV-BQYQJAHWSA-N C/C(/c1ccccc1)=C\C(O)=O Chemical compound C/C(/c1ccccc1)=C\C(O)=O PEXWJYDPDXUVSV-BQYQJAHWSA-N 0.000 description 1
- QKZNLCCNHYFLFW-HWKANZROSA-N C=CCOCC/C=C/C(N=O)=O Chemical compound C=CCOCC/C=C/C(N=O)=O QKZNLCCNHYFLFW-HWKANZROSA-N 0.000 description 1
- FVVKCIUZDXQPKF-UHFFFAOYSA-N CC(C)(C)NS(C1(C)CC1)(=O)=O Chemical compound CC(C)(C)NS(C1(C)CC1)(=O)=O FVVKCIUZDXQPKF-UHFFFAOYSA-N 0.000 description 1
- XUKYDWPZQQADAO-UHFFFAOYSA-N CC(C)(C)NS(CC(c1ccccc1)=O)(=O)=O Chemical compound CC(C)(C)NS(CC(c1ccccc1)=O)(=O)=O XUKYDWPZQQADAO-UHFFFAOYSA-N 0.000 description 1
- STZSRXXIIYYNGM-DAFXYXGESA-N CC(C)(C)OC(N(CC(C1)Oc2c3[o]nc(C)c3nc(-c3cccc(OC)c3)c2)[C@@H]1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CC(C1)Oc2c3[o]nc(C)c3nc(-c3cccc(OC)c3)c2)[C@@H]1C(O)=O)=O STZSRXXIIYYNGM-DAFXYXGESA-N 0.000 description 1
- ZQEBQGAAWMOMAI-ZETCQYMHSA-N CC(C)(C)OC(N(CCC1)[C@@H]1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)[C@@H]1C(O)=O)=O ZQEBQGAAWMOMAI-ZETCQYMHSA-N 0.000 description 1
- LFKDJXLFVYVEFG-UHFFFAOYSA-N CC(C)(C)OC(N)=O Chemical compound CC(C)(C)OC(N)=O LFKDJXLFVYVEFG-UHFFFAOYSA-N 0.000 description 1
- KIEPKKVYVRBQKN-UHFFFAOYSA-N CC(C)(C)OC(NS(CC(Nc1c(C)[o]nc1C)=O)(=O)=O)=O Chemical compound CC(C)(C)OC(NS(CC(Nc1c(C)[o]nc1C)=O)(=O)=O)=O KIEPKKVYVRBQKN-UHFFFAOYSA-N 0.000 description 1
- OHDICOMXWDSWMR-LKUPVBHCSA-N CC(C)(C)[C@@H](C(N(C[C@H](COc1cccc(-c2ccccc2)n1)C1)[C@@H]1C(O)=O)=O)NC(OC)=O Chemical compound CC(C)(C)[C@@H](C(N(C[C@H](COc1cccc(-c2ccccc2)n1)C1)[C@@H]1C(O)=O)=O)NC(OC)=O OHDICOMXWDSWMR-LKUPVBHCSA-N 0.000 description 1
- KPYGCSBRQQGMHY-DKSSEZFCSA-N CC(C)(C)[C@@H](C(N(C[C@H](COc1nc(-c2c[o]cc2)ccc1)C1)[C@@H]1C(O)=O)=O)NC(OC)=O Chemical compound CC(C)(C)[C@@H](C(N(C[C@H](COc1nc(-c2c[o]cc2)ccc1)C1)[C@@H]1C(O)=O)=O)NC(OC)=O KPYGCSBRQQGMHY-DKSSEZFCSA-N 0.000 description 1
- QTMDNWRHSMJECC-UHFFFAOYSA-N CC(c1ccccc11)=CNC1=O Chemical compound CC(c1ccccc11)=CNC1=O QTMDNWRHSMJECC-UHFFFAOYSA-N 0.000 description 1
- VKRQARSDOYRXGA-FPPTUBEUSA-N CC/C=C(\c(cccc1)c1N)/OC[C@H](C1)CN[C@@H]1C(OC)=O Chemical compound CC/C=C(\c(cccc1)c1N)/OC[C@H](C1)CN[C@@H]1C(OC)=O VKRQARSDOYRXGA-FPPTUBEUSA-N 0.000 description 1
- FBCCQFAXNAYAHV-XKGDQIHQSA-N CCCC/C=C(\C)/C=C\c(c(OC(C[C@H]1C(O)=O)CN1C(OC(C)(C)C)=O)c1)c(C)nc1-c1ccccc1 Chemical compound CCCC/C=C(\C)/C=C\c(c(OC(C[C@H]1C(O)=O)CN1C(OC(C)(C)C)=O)c1)c(C)nc1-c1ccccc1 FBCCQFAXNAYAHV-XKGDQIHQSA-N 0.000 description 1
- KHEZKDIWDCVMTL-UHFFFAOYSA-N CCCNC(C1(CC1)S(N)(=O)=O)=O Chemical compound CCCNC(C1(CC1)S(N)(=O)=O)=O KHEZKDIWDCVMTL-UHFFFAOYSA-N 0.000 description 1
- CDXKRTQZEPXTCV-UHFFFAOYSA-N CCNS(C(C)C)(=O)=O Chemical compound CCNS(C(C)C)(=O)=O CDXKRTQZEPXTCV-UHFFFAOYSA-N 0.000 description 1
- YVGNQEXUWUKGNK-IONNQARKSA-N CCOC([C@@](C1)([C@@H]1C(C)C)N)=O Chemical compound CCOC([C@@](C1)([C@@H]1C(C)C)N)=O YVGNQEXUWUKGNK-IONNQARKSA-N 0.000 description 1
- CAYSNGVIYCONAV-UHFFFAOYSA-N CCc(cc1Cl)nc2c1[o]nc2C Chemical compound CCc(cc1Cl)nc2c1[o]nc2C CAYSNGVIYCONAV-UHFFFAOYSA-N 0.000 description 1
- WXUCBUGUUVYAAN-YNODCEANSA-N COC(C(C1)NC[C@@H]1Oc1c(cc(c(OC)c2)OC)c2nc(C2CC2)n1)=O Chemical compound COC(C(C1)NC[C@@H]1Oc1c(cc(c(OC)c2)OC)c2nc(C2CC2)n1)=O WXUCBUGUUVYAAN-YNODCEANSA-N 0.000 description 1
- MOVTXYVMTFUFHJ-UHFFFAOYSA-N COc(c(OC)cc1nc(C(F)(F)F)n2)cc1c2O Chemical compound COc(c(OC)cc1nc(C(F)(F)F)n2)cc1c2O MOVTXYVMTFUFHJ-UHFFFAOYSA-N 0.000 description 1
- VQGCJKJYRGWVHE-UHFFFAOYSA-N Cc(cn1)c(cccc2)c2c1Cl Chemical compound Cc(cn1)c(cccc2)c2c1Cl VQGCJKJYRGWVHE-UHFFFAOYSA-N 0.000 description 1
- MNQLTIDCYJRXOK-UHFFFAOYSA-N Cc1n[o]c(c(Cl)c2)c1nc2-c1cc(OC)ccc1 Chemical compound Cc1n[o]c(c(Cl)c2)c1nc2-c1cc(OC)ccc1 MNQLTIDCYJRXOK-UHFFFAOYSA-N 0.000 description 1
- OFUFXTHGZWIDDB-UHFFFAOYSA-N Clc1nc(cccc2)c2cc1 Chemical compound Clc1nc(cccc2)c2cc1 OFUFXTHGZWIDDB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Molecular Biology (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Genetics & Genomics (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86385706P | 2006-11-01 | 2006-11-01 | |
| PCT/US2007/083131 WO2008057875A2 (en) | 2006-11-01 | 2007-10-31 | Inhibitors of hepatitis c virus |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010508362A true JP2010508362A (ja) | 2010-03-18 |
| JP2010508362A5 JP2010508362A5 (enExample) | 2010-10-28 |
Family
ID=39365223
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009535436A Withdrawn JP2010508362A (ja) | 2006-11-01 | 2007-10-31 | Ｃ型肝炎ウイルスの阻害剤 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20080107623A1 (enExample) |
| EP (1) | EP2086994B1 (enExample) |
| JP (1) | JP2010508362A (enExample) |
| CN (1) | CN101578294A (enExample) |
| NO (1) | NO20091706L (enExample) |
| WO (1) | WO2008057875A2 (enExample) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003007697A (ja) * | 2001-06-21 | 2003-01-10 | Hitachi Kokusai Electric Inc | 半導体装置の製造方法、基板処理方法および基板処理装置 |
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| US7491794B2 (en) * | 2003-10-14 | 2009-02-17 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
| RU2008152171A (ru) | 2006-07-05 | 2010-08-10 | Интермьюн, Инк. (Us) | Новые ингибиторы вирусной репликации гепатита с |
| US8343477B2 (en) * | 2006-11-01 | 2013-01-01 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
| AP2009005053A0 (en) * | 2007-05-03 | 2009-12-31 | Intermune Inc | Novel macrocyclic inhibitors of hepatitis c virus replication |
| MX2009012093A (es) | 2007-05-10 | 2010-01-25 | Intermune Inc | Nuevos peptidos inhibidores de la replicacion del virus de la hepatitis c. |
| TW200918524A (en) * | 2007-06-29 | 2009-05-01 | Gilead Sciences Inc | Antiviral compounds |
| ES2437147T3 (es) * | 2008-02-04 | 2014-01-09 | Idenix Pharmaceuticals, Inc. | Inhibidores de serina proteasa macrocíclicos |
| US8207341B2 (en) | 2008-09-04 | 2012-06-26 | Bristol-Myers Squibb Company | Process or synthesizing substituted isoquinolines |
| UY32099A (es) * | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| US8044087B2 (en) * | 2008-09-29 | 2011-10-25 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| AR075584A1 (es) * | 2009-02-27 | 2011-04-20 | Intermune Inc | COMPOSICIONES TERAPEUTICAS QUE COMPRENDEN beta-D-2'-DESOXI-2'-FLUORO-2'-C-METILCITIDINA Y UN DERIVADO DE ACIDO ISOINDOL CARBOXILICO Y SUS USOS. COMPUESTO. |
| CA2758072A1 (en) | 2009-04-08 | 2010-10-14 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors |
| MX2011012155A (es) | 2009-05-13 | 2012-02-28 | Enanta Pharm Inc | Compuestos macrociclicos como inhibidores del virus de hepatitis c. |
| US8703700B2 (en) * | 2009-05-22 | 2014-04-22 | Sequoia Pharmaceuticals, Inc. | Bimacrocylic HCV NS3 protease inhibitors |
| US8232246B2 (en) * | 2009-06-30 | 2012-07-31 | Abbott Laboratories | Anti-viral compounds |
| AR077712A1 (es) | 2009-08-05 | 2011-09-14 | Idenix Pharmaceuticals Inc | Inhibidores de serina proteasa macrociclica |
| TW201119667A (en) * | 2009-10-19 | 2011-06-16 | Enanta Pharm Inc | Bismacrocyclic compounds as hepatitis C virus inhibitors |
| KR20130036201A (ko) * | 2010-02-22 | 2013-04-11 | 메르크 파텐트 게엠베하 | 헤타릴아미노나프티리딘 |
| WO2012087833A1 (en) | 2010-12-22 | 2012-06-28 | Abbott Laboratories | Hepatitis c inhibitors and uses thereof |
| JP2014502620A (ja) | 2010-12-30 | 2014-02-03 | エナンタ ファーマシューティカルズ インコーポレイテッド | 大環状ｃ型肝炎セリンプロテアーゼ阻害剤 |
| US8951964B2 (en) | 2010-12-30 | 2015-02-10 | Abbvie Inc. | Phenanthridine macrocyclic hepatitis C serine protease inhibitors |
| WO2012109398A1 (en) | 2011-02-10 | 2012-08-16 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors, pharmaceutical compositions thereof, and their use for treating hcv infections |
| US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
| US8691757B2 (en) | 2011-06-15 | 2014-04-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| JP6154474B2 (ja) | 2012-10-19 | 2017-06-28 | ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ | Ｃ型肝炎ウイルス阻害剤 |
| US9643999B2 (en) | 2012-11-02 | 2017-05-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US9334279B2 (en) | 2012-11-02 | 2016-05-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US9598433B2 (en) | 2012-11-02 | 2017-03-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| WO2014070974A1 (en) | 2012-11-05 | 2014-05-08 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
| JP6342922B2 (ja) | 2013-03-07 | 2018-06-13 | ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ | Ｃ型肝炎ウイルス阻害剤 |
| CN103396351B (zh) * | 2013-08-09 | 2015-10-21 | 山东大学 | 吡咯烷类Bcl-2蛋白小分子抑制剂化合物及其制备、药物组合物与制药用途 |
| WO2015103490A1 (en) | 2014-01-03 | 2015-07-09 | Abbvie, Inc. | Solid antiviral dosage forms |
| JP6863981B2 (ja) | 2015-07-31 | 2021-04-21 | ザ・ジョンズ・ホプキンス・ユニバーシティー | グルタミン類似体のプロドラッグ |
| JP2020506233A (ja) | 2017-02-01 | 2020-02-27 | ザ・ジョンズ・ホプキンス・ユニバーシティー | グルタミン類似体のプロドラッグ |
| WO2018172250A1 (en) | 2017-03-21 | 2018-09-27 | Bayer Pharma Aktiengesellschaft | 2-methyl-quinazolines |
| WO2019201848A1 (en) | 2018-04-18 | 2019-10-24 | Bayer Pharma Aktiengesellschaft | 2-methyl-aza-quinazolines |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7119072B2 (en) * | 2002-01-30 | 2006-10-10 | Boehringer Ingelheim (Canada) Ltd. | Macrocyclic peptides active against the hepatitis C virus |
| MY140680A (en) * | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| US20060199773A1 (en) * | 2002-05-20 | 2006-09-07 | Sausker Justin B | Crystalline forms of (1R,2S)-N-[(1,1-dimethylethoxy)carbonyl]-3-methyl-L-valyl-(4R)-4-[(6-methoxy-1-isoquinolinyl)oxy]-L-prolyl-1-amino-N-(cyclopropylsulfonyl)-2-ethenyl-cyclopropanecarboxamide, monopotassium salt |
| US7601709B2 (en) * | 2003-02-07 | 2009-10-13 | Enanta Pharmaceuticals, Inc. | Macrocyclic hepatitis C serine protease inhibitors |
| ES2320771T3 (es) * | 2003-04-16 | 2009-05-28 | Bristol-Myers Squibb Company | Inhibidores peptidicos de isoquinolina macrociclicos del virus de la hepatitis c. |
| PL1615613T3 (pl) * | 2003-04-18 | 2010-04-30 | Enanta Pharm Inc | Chinoksalinylowe makrocykliczne inhibitory proteazy serynowej zapalenia wątroby typu C |
| JP4682155B2 (ja) * | 2004-01-21 | 2011-05-11 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ｃ型肝炎ウイルスに対して活性な大環状ペプチド |
| CA2556917C (en) * | 2004-03-15 | 2013-07-09 | Boehringer Ingelheim International, Gmbh | Process for preparing macrocyclic compounds |
| US20070249637A1 (en) * | 2004-10-21 | 2007-10-25 | Collins Michael R | Inhibitors Of Hepatitis C Virus Protease, And Compositions And Treatments Using The Same |
| TW200738742A (en) * | 2005-07-14 | 2007-10-16 | Gilead Sciences Inc | Antiviral compounds |
| US7741281B2 (en) * | 2005-11-03 | 2010-06-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US7635683B2 (en) * | 2006-08-04 | 2009-12-22 | Enanta Pharmaceuticals, Inc. | Quinoxalinyl tripeptide hepatitis C virus inhibitors |
| US7605126B2 (en) * | 2006-08-11 | 2009-10-20 | Enanta Pharmaceuticals, Inc. | Acylaminoheteroaryl hepatitis C virus protease inhibitors |
| WO2008022006A2 (en) * | 2006-08-11 | 2008-02-21 | Enanta Pharmaceuticals, Inc. | Arylalkoxyl hepatitis c virus protease inhibitors |
| US7582605B2 (en) * | 2006-08-11 | 2009-09-01 | Enanta Pharmaceuticals, Inc. | Phosphorus-containing hepatitis C serine protease inhibitors |
-
2007
- 2007-10-25 US US11/923,977 patent/US20080107623A1/en not_active Abandoned
- 2007-10-31 CN CNA2007800490456A patent/CN101578294A/zh active Pending
- 2007-10-31 EP EP07863706.3A patent/EP2086994B1/en active Active
- 2007-10-31 WO PCT/US2007/083131 patent/WO2008057875A2/en not_active Ceased
- 2007-10-31 JP JP2009535436A patent/JP2010508362A/ja not_active Withdrawn
-
2009
- 2009-04-29 NO NO20091706A patent/NO20091706L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP2086994A2 (en) | 2009-08-12 |
| CN101578294A (zh) | 2009-11-11 |
| EP2086994B1 (en) | 2014-11-26 |
| WO2008057875A3 (en) | 2008-07-31 |
| NO20091706L (no) | 2009-07-21 |
| US20080107623A1 (en) | 2008-05-08 |
| WO2008057875A2 (en) | 2008-05-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100907 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20100907 |
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| A761 | Written withdrawal of application |
Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20110215 |