SG11201811590RA - [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds - Google Patents
[1,2,4]triazolo[1,5-a]pyridinyl substituted indole compoundsInfo
- Publication number
- SG11201811590RA SG11201811590RA SG11201811590RA SG11201811590RA SG11201811590RA SG 11201811590R A SG11201811590R A SG 11201811590RA SG 11201811590R A SG11201811590R A SG 11201811590RA SG 11201811590R A SG11201811590R A SG 11201811590RA SG 11201811590R A SG11201811590R A SG 11201811590RA
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- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4196—1,2,4-Triazoles
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- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property :::` , Organization MD 1101111 II DOI HIM 011101 0 011111 HH11111111111111111111111111 International Bureau (10) International Publication Number (43) International Publication Date .....•\"\"- WO 2018/005586 Al 04 January 2018 (04.01.2018) W I PO I PCT (51) International Patent Classification: dra Industrial Area IV Phase, Jigani Link Road, Bommasan- C07D 471/04 (2006.01) A61K 31/437 (2006.01) dra, Karnataka, Bangalore 560 099 (IN). HEGDE, Subra- (21) International Application Number: maya; c/o Syngene International Limited, Biocon Special Economic Zone, Biocon Park, Plot No. 2&3, Bommasan- PCT/US2017/039633 dra Industrial Area IV Phase, Jigani Link Road, Bommasan- (22) International Filing Date: dra, Karnataka, Bangalore 560 099 (IN). RAMACHAN- 28 June 2017 (28.06.2017) DRA, Anupama; c/o Syngene International Limited, Bio- con Special Economic Zone, Biocon Park, Plot No. 2&3, (25) Filing Language: English Bommasandra Industrial Area IV Phase, Jigani Link Road, (26) Publication Language: English Bommasandra, Karnataka, Bangalore 560 099 (IN). (30) Priority Data: (74) Agent: VANATTEN, Mary K. et al.; Bristol-Myers 201611022328 29 June 2016 (29.06.2016) IN Squibb Company, Route 206 and Province Line Road, 15/635,055 27 June 2017 (27.06.2017) US Princeton, New Jersey 08543 (US). (71) Applicant: BRISTOL-MYERS SQUIBB COMPANY (81) Designated States (unless otherwise indicated, for every [US/US]; Route 206 and Province Line Road, Princeton, kind of national protection available): AE, AG, AL, AM, New Jersey 08543 (US). AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, — (72) Inventors: DYCKMAN, Alaric J.; c/o Bristol-Myers DZ, EC, EE, EG, ES, FL GB, GD, GE, GH, GM, GT, HN, Squibb Company, Route 206 and Province Line Road, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, Princeton, New Jersey 08543 (US). DODD, Dharmpal KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, S.; c/o Bristol-Myers Squibb Company, Route 206 and MG, MK, MN, MW, MX, MY, MZ, NA, NG, NL NO, NZ, Province Line Road, Princeton, New Jersey 08543 (US). OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, HAQUE, Tasir Shamsul; c/o Bristol-Myers Squibb Com- SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, pany, Route 206 and Province Line Road, Princeton, New TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. — = = _ Jersey 08543 (US). LOMBARDO, Louis J.; c/o Bris- tol-Myers Squibb Company, Route 206 and Province Line (84) Designated States (unless otherwise indicated, for every Road, Princeton, New Jersey 08543 (US). MACOR, John kind of regional protection available): ARIPO (BW, GH, E.; 55 Commanders Drive, Washington Crossing, Pennsyl- GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, vania 18977 (US). MUSSARI, Christopher P.; c/o Bris- UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, tol-Myers Squibb Company, Route 206 and Province Line TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, Road, Princeton, New Jersey 08543 (US). PASUNOORI, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, Laxman; c/o Syngene International Limited, Biocon Spe- MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, cial Economic Zone, Biocon Park, Plot No. 2&3, Bom- TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, masandra Industrial Area IV Phase, Jigani Link Road, Bom- KM, ML, MR, NE, SN, TD, TG). = = = — = = = masandra, Karnataka, Bangalore 560 099 (IN). RATNA KUMAR, Sreekantha; c/o Syngene International Limit- Declarations under Rule 4.17: = ed, Biocon Special Economic Zone, Biocon Park, Plot No. — as to applicant's entitlement to apply for and be a granted _ 2&3, Bommasandra Industrial Area IV Phase, Jigani Link patent (Rule 4.17(ii)) = Road, Bommasandra, Karnataka, Bangalore 560 099 (IN). — as to the applicant's entitlement to claim the priority of the = SHERWOOD, Trevor C.; c/o Bristol-Myers Squibb Com- earlier application (Rule 4.17(iii)) = — pany, Route 206 and Province Line Road, Princeton, New — of inventorship (Rule 4.17(iv)) = Jersey 08543 (US). POSY, Shoshana L.; c/o Bristol-My- Published: = ers Squibb Company, Route 206 and Province Line Road, — with international search report (Art. 21(3)) Princeton, New Jersey 08543 (US). SISTLA, Ramesh Ku- mar; c/o Syngene International Limited, Biocon Special _ Economic Zone, Biocon Park, Plot No. 2&3, Bommasan- 1-1 of (54) kir) kir) Title: [1,2,4]TRIAZOLO[1,5-A]PYRIDINYL SUBSTITUTED INDOLE COMPOUNDS (IR \ , 4, rn (57) : Disclosed are compounds of Formula (I) or a salt thereof, wherein R 1 , R 2 , R 3 , © ...... © GC R 3 , Nom../. R i , R s R4, R 5 , m, n, and p are defined herein. Also disclosed are methods of using such compounds \ 2 ) P •••-•, \ -I- as inhibitors of signaling through Toll-like receptor 7, or 8, or 9, and pharmaceutical compo- 1-1 I , , sitions comprising such compounds. These compounds are useful in treating inflammatory 0 *-- ..- . - ..„^-N H and autoimmune diseases. N ( 5)° N (I) C
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN201611022328 | 2016-06-29 | ||
US15/635,055 US10071079B2 (en) | 2016-06-29 | 2017-06-27 | [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds |
PCT/US2017/039633 WO2018005586A1 (en) | 2016-06-29 | 2017-06-28 | [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds |
Publications (1)
Publication Number | Publication Date |
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SG11201811590RA true SG11201811590RA (en) | 2019-01-30 |
Family
ID=60805851
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201811590RA SG11201811590RA (en) | 2016-06-29 | 2017-06-28 | [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds |
Country Status (31)
Country | Link |
---|---|
US (8) | US10071079B2 (en) |
EP (1) | EP3478682B1 (en) |
JP (1) | JP6995067B6 (en) |
KR (1) | KR102473482B1 (en) |
CN (1) | CN109641895B (en) |
AR (1) | AR108905A1 (en) |
AU (1) | AU2017287902B2 (en) |
BR (1) | BR112018077119A2 (en) |
CA (1) | CA3029620A1 (en) |
CL (1) | CL2018003821A1 (en) |
CO (1) | CO2019000686A2 (en) |
CY (1) | CY1124514T1 (en) |
DK (1) | DK3478682T3 (en) |
EA (1) | EA037530B1 (en) |
ES (1) | ES2886964T3 (en) |
HR (1) | HRP20211261T8 (en) |
HU (1) | HUE056091T2 (en) |
IL (1) | IL263961B (en) |
LT (1) | LT3478682T (en) |
MX (1) | MX2018015422A (en) |
MY (1) | MY196474A (en) |
PE (1) | PE20190324A1 (en) |
PL (1) | PL3478682T3 (en) |
PT (1) | PT3478682T (en) |
RS (1) | RS62292B1 (en) |
SG (1) | SG11201811590RA (en) |
SI (1) | SI3478682T1 (en) |
TW (1) | TWI636053B (en) |
UY (1) | UY37310A (en) |
WO (1) | WO2018005586A1 (en) |
ZA (1) | ZA201900571B (en) |
Families Citing this family (59)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10071079B2 (en) | 2016-06-29 | 2018-09-11 | Bristol-Myers Squibb Company | [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds |
AU2017307208B2 (en) | 2016-07-30 | 2021-01-21 | Bristol-Myers Squibb Company | Dimethoxyphenyl substituted indole compounds as TLR7, TLR8 or TLR9 inhibitors |
EP3510024B1 (en) | 2016-09-09 | 2021-11-17 | Bristol-Myers Squibb Company | Pyridyl substituted indole compounds |
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WO2019028301A1 (en) * | 2017-08-04 | 2019-02-07 | Bristol-Myers Squibb Company | [1,2,4]TRIAZOLO[4,3-a]PYRIDINYL SUBSTITUTED INDOLE COMPOUNDS |
ES2909401T3 (en) | 2017-08-04 | 2022-05-06 | Bristol Myers Squibb Co | Substituted Indole Compounds Useful as Inhibitors of TLR7/8/9 |
WO2019099336A1 (en) * | 2017-11-14 | 2019-05-23 | Bristol-Myers Squibb Company | Substituted indole compounds |
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EA202091483A1 (en) | 2017-12-19 | 2020-10-28 | Бристол-Маерс Сквибб Компани | AMIDE-SUBSTITUTED INDOLIC COMPOUNDS SUITABLE AS TLR INHIBITORS |
SG11202005696YA (en) * | 2017-12-19 | 2020-07-29 | Bristol Myers Squibb Co | Substituted indole compounds useful as tlr inhibitors |
WO2019123340A1 (en) | 2017-12-20 | 2019-06-27 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3'3' cyclic dinucleotides with phosphonate bond activating the sting adaptor protein |
US11203610B2 (en) | 2017-12-20 | 2021-12-21 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 2′3′ cyclic dinucleotides with phosphonate bond activating the sting adaptor protein |
SG11202005694RA (en) | 2017-12-20 | 2020-07-29 | Bristol Myers Squibb Co | Amino indole compounds useful as tlr inhibitors |
SG11202005733QA (en) | 2017-12-20 | 2020-07-29 | Bristol Myers Squibb Co | Diazaindole compounds |
US11420958B2 (en) | 2017-12-20 | 2022-08-23 | Bristol-Myers Squibb Company | Aryl and heteroaryl substituted indole compounds |
EP3752505B1 (en) | 2018-02-12 | 2023-01-11 | F. Hoffmann-La Roche AG | Novel sulfone compounds and derivatives for the treatment and prophylaxis of virus infection |
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US10870691B2 (en) | 2018-04-05 | 2020-12-22 | Gilead Sciences, Inc. | Antibodies and fragments thereof that bind hepatitis B virus protein X |
CA3093888A1 (en) | 2018-04-06 | 2019-10-10 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3'3'-cyclic dinucleotides |
TW202005654A (en) | 2018-04-06 | 2020-02-01 | 捷克科學院有機化學與生物化學研究所 | 2'2'-cyclic dinucleotides |
TWI818007B (en) | 2018-04-06 | 2023-10-11 | 捷克科學院有機化學與生物化學研究所 | 2'3'-cyclic dinucleotides |
US11142750B2 (en) | 2018-04-12 | 2021-10-12 | Precision Biosciences, Inc. | Optimized engineered meganucleases having specificity for a recognition sequence in the Hepatitis B virus genome |
TW202014193A (en) | 2018-05-03 | 2020-04-16 | 捷克科學院有機化學與生物化學研究所 | 2’3’-cyclic dinucleotides comprising carbocyclic nucleotide |
US11713327B2 (en) | 2018-06-12 | 2023-08-01 | Hoffmann-La Roche Inc. | Heteroaryl heterocyclyl compounds for the treatment of autoimmune disease |
CN112585134A (en) * | 2018-06-13 | 2021-03-30 | 豪夫迈·罗氏有限公司 | Pyridyl heterocyclyl compounds for the treatment of autoimmune diseases |
EP3826724B1 (en) | 2018-07-23 | 2022-10-05 | F. Hoffmann-La Roche AG | Novel piperazine compounds for the treatment of autoimmune disease |
WO2020028097A1 (en) | 2018-08-01 | 2020-02-06 | Gilead Sciences, Inc. | Solid forms of (r)-11-(methoxymethyl)-12-(3-methoxypropoxy)-3,3-dimethyl-8-0x0-2,3,8,13b-tetrahydro-1h-pyrido[2,1-a]pyrrolo[1,2-c] phthalazine-7-c arboxylic acid |
WO2020048583A1 (en) | 2018-09-04 | 2020-03-12 | F. Hoffmann-La Roche Ag | Benzothiazole compounds for the treatment of autoimmune diseases |
CN112654618A (en) | 2018-09-06 | 2021-04-13 | 豪夫迈·罗氏有限公司 | Novel cyclic amidine compounds for the treatment of autoimmune diseases |
WO2020086505A1 (en) * | 2018-10-24 | 2020-04-30 | Bristol-Myers Squibb Company | Substituted indole dimer compounds |
US20210403468A1 (en) * | 2018-10-24 | 2021-12-30 | Bristol-Myers Squibb Company | Substituted indole and indazole compounds |
LT3873903T (en) | 2018-10-31 | 2024-05-10 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds as hpk1 inhibitors |
CA3116347A1 (en) | 2018-10-31 | 2020-05-07 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds having hpk1 inhibitory activity |
WO2020178768A1 (en) | 2019-03-07 | 2020-09-10 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide as sting modulator |
WO2020178769A1 (en) | 2019-03-07 | 2020-09-10 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 2'3'-cyclic dinucleotides and prodrugs thereof |
JP7350872B2 (en) | 2019-03-07 | 2023-09-26 | インスティチュート オブ オーガニック ケミストリー アンド バイオケミストリー エーエスシーアール,ヴイ.ヴイ.アイ. | 3'3'-cyclic dinucleotide and its prodrug |
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JP2022532568A (en) * | 2019-05-07 | 2022-07-15 | ブリストル-マイヤーズ スクイブ カンパニー | Prodrug compound |
WO2020237025A1 (en) | 2019-05-23 | 2020-11-26 | Gilead Sciences, Inc. | Substituted exo-methylene-oxindoles which are hpk1/map4k1 inhibitors |
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WO2021034804A1 (en) | 2019-08-19 | 2021-02-25 | Gilead Sciences, Inc. | Pharmaceutical formulations of tenofovir alafenamide |
CN117843811A (en) | 2019-09-30 | 2024-04-09 | 吉利德科学公司 | HBV vaccine and method of treating HBV |
WO2021067657A1 (en) * | 2019-10-04 | 2021-04-08 | Bristol-Myers Squibb Company | Substituted carbazole compounds |
WO2021113765A1 (en) | 2019-12-06 | 2021-06-10 | Precision Biosciences, Inc. | Optimized engineered meganucleases having specificity for a recognition sequence in the hepatitis b virus genome |
TW202200161A (en) | 2020-03-20 | 2022-01-01 | 美商基利科學股份有限公司 | Prodrugs of 4’-c-substituted-2-halo-2’-deoxyadenosine nucleosides and methods of making and using the same |
JP2023530264A (en) | 2020-06-11 | 2023-07-14 | ブリストル-マイヤーズ スクイブ カンパニー | TLR7 inhibitors in combination with prednisolone or hydroxychloroquine to treat cutaneous lupus erythematosus |
BR112022025920A2 (en) | 2020-06-22 | 2023-01-10 | Bristol Myers Squibb Co | TREATMENT OF RHEUMATOID ARTHRITIS |
TW202214632A (en) * | 2020-07-27 | 2022-04-16 | 大陸商江蘇恆瑞醫藥股份有限公司 | Indole fused ring derivatives, their preparation method and medical use |
WO2022111636A1 (en) | 2020-11-26 | 2022-06-02 | 江苏恒瑞医药股份有限公司 | Fused tricyclic compound, preparation method therefor and application thereof in medicine |
IL307203A (en) | 2021-04-16 | 2023-11-01 | Gilead Sciences Inc | Thienopyrrole compounds |
JP2024518558A (en) | 2021-05-13 | 2024-05-01 | ギリアード サイエンシーズ, インコーポレイテッド | Combination of TLR8 Modulating Compounds with Anti-HBV siRNA Therapeutics |
CN113416188B (en) * | 2021-05-31 | 2022-12-13 | 河南偶联生物科技有限公司 | Synthetic method of [1,2,4] triazolo [1,5-A ] pyridine compound |
CA3220923A1 (en) | 2021-06-23 | 2022-12-29 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
KR20240005901A (en) | 2021-06-23 | 2024-01-12 | 길리애드 사이언시즈, 인코포레이티드 | Diacylglycerol Kinase Modulating Compounds |
WO2022271684A1 (en) | 2021-06-23 | 2022-12-29 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
AU2022298639A1 (en) | 2021-06-23 | 2023-12-07 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
WO2024015825A1 (en) | 2022-07-13 | 2024-01-18 | Bristol-Myers Squibb Company | Processes for preparing 5-bromo-3,4-dimethylpyridin-2-amine and 6-bromo-7,8-dimethyl-[1,2,4]triazolo[1,5-a]pyridine |
Family Cites Families (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6867200B1 (en) | 1998-12-18 | 2005-03-15 | Axys Pharmaceuticals, Inc. | (Hetero)aryl-bicyclic heteroaryl derivatives, their preparation and their use as protease inhibitors |
EA200600069A1 (en) | 2003-06-20 | 2006-08-25 | Коли Фармасьютикал Гмбх | LOW-MOLECULAR ANTAGONISTS OF TOLL-SIMILAR RECEPTORS (TLR) |
WO2006113458A1 (en) * | 2005-04-15 | 2006-10-26 | Bristol-Myers Squibb Company | Heterocyclic inhibitors of protein arginine methyl transferases |
AU2007234399A1 (en) | 2006-04-04 | 2007-10-11 | Myriad Genetics, Inc. | Compounds for diseases and disorders |
DE102006033109A1 (en) | 2006-07-18 | 2008-01-31 | Grünenthal GmbH | Substituted heteroaryl derivatives |
US8027888B2 (en) | 2006-08-31 | 2011-09-27 | Experian Interactive Innovation Center, Llc | Online credit card prescreen systems and methods |
ATE495743T1 (en) | 2006-12-01 | 2011-02-15 | Galapagos Nv | TRIAZOLOPYRIDINE COMPOUNDS FOR THE TREATMENT OF DEGENERATIONAL AND INFLAMMATORY DISEASES |
WO2008152471A1 (en) | 2007-06-12 | 2008-12-18 | Coley Pharmaceutical Group, Inc. | Quinazoline derivative useful as toll-like receptor antagonist |
WO2009030996A1 (en) | 2007-09-05 | 2009-03-12 | Coley Pharmaceutical Group, Inc. | Triazole compounds as toll-like receptor (tlr) agonists |
FR2926556B1 (en) * | 2008-01-22 | 2010-02-19 | Sanofi Aventis | N-AZABICYCLIC CARBOXAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
EP2350032B1 (en) | 2008-09-26 | 2016-05-25 | Eisai R&D Management Co., Ltd. | Benzoxazole compounds and methods of use |
CA2738929A1 (en) | 2008-10-17 | 2010-04-22 | Boehringer Ingelheim International Gmbh | Heteroaryl substituted indole compounds useful as mmp-13 inhibitors |
RU2011137419A (en) | 2009-02-11 | 2013-03-20 | Суновион Фармасьютикалз Инк. | REVERSE AGONISTS AND HISTAMINE H3 ANTAGONISTS AND WAYS OF THEIR APPLICATION |
KR20120035183A (en) | 2009-06-10 | 2012-04-13 | 선오비온 파마슈티컬스 인코포레이티드 | Histamine h3 inverse agonists and antagonists and methods of use thereof |
TWI462920B (en) * | 2009-06-26 | 2014-12-01 | 葛萊伯格有限公司 | Novel compound useful for the treatment of degenerative and inflammatory diseases |
EP2453895B1 (en) | 2009-07-16 | 2018-05-23 | Mallinckrodt LLC | (+) - morphinans as antagonists of toll-like receptor 9 and therapeutic uses thereof |
US9241991B2 (en) | 2010-10-21 | 2016-01-26 | The Brigham And Women's Hospital, Inc. | Agents, compositions, and methods for treating pruritus and related skin conditions |
PL2663555T4 (en) | 2011-01-12 | 2017-08-31 | Ventirx Pharmaceuticals, Inc. | Substituted benzoazepines as toll-like receptor modulators |
PL2663550T4 (en) | 2011-01-12 | 2017-07-31 | Ventirx Pharmaceuticals, Inc. | Substituted benzoazepines as toll-like receptor modulators |
CA2837207A1 (en) | 2011-06-01 | 2012-12-06 | Janus Biotherapeutics, Inc. | Novel immune system modulators |
RU2606114C2 (en) | 2011-06-01 | 2017-01-10 | Джейнус Байотерапьютикс, Инк. | Novel immune system modulators related applications |
KR101913619B1 (en) | 2011-06-09 | 2018-12-28 | 리젠 파마슈티컬스 소시에떼 아노님 | Novel compounds as modulators of gpr-119 |
WO2013009140A2 (en) | 2011-07-13 | 2013-01-17 | Sk Chemicals Co., Ltd. | 2-pyridyl substituted imidazoles as alk5 and/or alk4 inhibitors |
CA2850932A1 (en) | 2011-10-04 | 2013-04-11 | Janus Biotherapeutics, Inc. | Novel imidazole quinoline-based immune system modulators |
TWI619704B (en) | 2012-05-18 | 2018-04-01 | 大日本住友製藥股份有限公司 | Carboxylic acid compounds |
JO3407B1 (en) | 2012-05-31 | 2019-10-20 | Eisai R&D Man Co Ltd | Tetrahydropyrazolopyrimidine Compounds |
AU2014334554B2 (en) | 2013-10-14 | 2018-12-06 | Eisai R&D Management Co., Ltd. | Selectively substituted quinoline compounds |
US9643967B2 (en) | 2013-12-13 | 2017-05-09 | Takeda Pharmaceutical Company Limited | Pyrrolo[3,2-c]pyridine derivatives as TLR inhibitors |
EP3398948A3 (en) | 2014-08-22 | 2018-12-05 | Janus Biotherapeutics, Inc. | 2,4,6,7-tetrasubstituted pteridine compounds and methods of synthesis and use thereof |
US9550778B2 (en) | 2014-10-03 | 2017-01-24 | Vanderbilt University | Substituted 6-aryl-imidazopyridine and 6-aryl-triazolopyridine carboxamide analogs as negative allosteric modulators of mGluR5 |
EP3334745B1 (en) | 2015-08-13 | 2024-05-15 | Merck Sharp & Dohme LLC | Cyclic di-nucleotide compounds as sting agonists |
IL263934B2 (en) | 2016-06-29 | 2023-10-01 | Hanmi Pharm Ind Co Ltd | Glucagon derivative, conjugate thereof, composition comprising same and therapeutic use thereof |
US10071079B2 (en) | 2016-06-29 | 2018-09-11 | Bristol-Myers Squibb Company | [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds |
SG11201811507YA (en) | 2016-06-29 | 2019-01-30 | Kezar Life Sciences | Crystalline salts of peptide epoxyketone immunoproteasome inhibitor |
AU2017307208B2 (en) | 2016-07-30 | 2021-01-21 | Bristol-Myers Squibb Company | Dimethoxyphenyl substituted indole compounds as TLR7, TLR8 or TLR9 inhibitors |
EP3510024B1 (en) | 2016-09-09 | 2021-11-17 | Bristol-Myers Squibb Company | Pyridyl substituted indole compounds |
ES2909401T3 (en) | 2017-08-04 | 2022-05-06 | Bristol Myers Squibb Co | Substituted Indole Compounds Useful as Inhibitors of TLR7/8/9 |
WO2019028301A1 (en) | 2017-08-04 | 2019-02-07 | Bristol-Myers Squibb Company | [1,2,4]TRIAZOLO[4,3-a]PYRIDINYL SUBSTITUTED INDOLE COMPOUNDS |
WO2019099336A1 (en) | 2017-11-14 | 2019-05-23 | Bristol-Myers Squibb Company | Substituted indole compounds |
SG11202005513TA (en) | 2017-12-15 | 2020-07-29 | Bristol Myers Squibb Co | Substituted indole ether compounds |
US10544143B2 (en) | 2017-12-18 | 2020-01-28 | Bristol-Myers Squibb Company | 4-azaindole compounds |
EA202091483A1 (en) | 2017-12-19 | 2020-10-28 | Бристол-Маерс Сквибб Компани | AMIDE-SUBSTITUTED INDOLIC COMPOUNDS SUITABLE AS TLR INHIBITORS |
SG11202005696YA (en) | 2017-12-19 | 2020-07-29 | Bristol Myers Squibb Co | Substituted indole compounds useful as tlr inhibitors |
AU2018390543A1 (en) | 2017-12-19 | 2020-08-06 | Bristol-Myers Squibb Company | 6-azaindole compounds |
SG11202005733QA (en) | 2017-12-20 | 2020-07-29 | Bristol Myers Squibb Co | Diazaindole compounds |
US11420958B2 (en) | 2017-12-20 | 2022-08-23 | Bristol-Myers Squibb Company | Aryl and heteroaryl substituted indole compounds |
SG11202005694RA (en) | 2017-12-20 | 2020-07-29 | Bristol Myers Squibb Co | Amino indole compounds useful as tlr inhibitors |
US20210403468A1 (en) | 2018-10-24 | 2021-12-30 | Bristol-Myers Squibb Company | Substituted indole and indazole compounds |
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