CN102015717A - 趋化因子受体调节剂 - Google Patents
趋化因子受体调节剂 Download PDFInfo
- Publication number
- CN102015717A CN102015717A CN2009801150516A CN200980115051A CN102015717A CN 102015717 A CN102015717 A CN 102015717A CN 2009801150516 A CN2009801150516 A CN 2009801150516A CN 200980115051 A CN200980115051 A CN 200980115051A CN 102015717 A CN102015717 A CN 102015717A
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- Prior art keywords
- formula
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- Prior art date
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- 0 CC1=*C([C@](*CC2C(CC(*3)C=C)C3=CC*2)CCC2)=C2C1=N Chemical compound CC1=*C([C@](*CC2C(CC(*3)C=C)C3=CC*2)CCC2)=C2C1=N 0.000 description 30
- JNTHBIUSFJMMIA-UHFFFAOYSA-N CC(CCC1)c2c1cccn2 Chemical compound CC(CCC1)c2c1cccn2 JNTHBIUSFJMMIA-UHFFFAOYSA-N 0.000 description 3
- HYFLWBNQFMXCPA-UHFFFAOYSA-N CCc1c(C)cccc1 Chemical compound CCc1c(C)cccc1 HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 2
- ZXTRMHOUGKPHHM-UHFFFAOYSA-N CNC1c2ncccc2CCC1 Chemical compound CNC1c2ncccc2CCC1 ZXTRMHOUGKPHHM-UHFFFAOYSA-N 0.000 description 2
- JQGOUNFVDYUKMM-UHFFFAOYSA-N NC1c2ncccc2CCC1 Chemical compound NC1c2ncccc2CCC1 JQGOUNFVDYUKMM-UHFFFAOYSA-N 0.000 description 2
- YQDGQEKUTLYWJU-UHFFFAOYSA-N C1Cc2cccnc2CC1 Chemical compound C1Cc2cccnc2CC1 YQDGQEKUTLYWJU-UHFFFAOYSA-N 0.000 description 1
- NRDWTJRFRDNIQK-AWEZNQCLSA-N CC(C)(C)OC(NCCCC[C@@H](C(NCc1ccccn1)=O)N)=O Chemical compound CC(C)(C)OC(NCCCC[C@@H](C(NCc1ccccn1)=O)N)=O NRDWTJRFRDNIQK-AWEZNQCLSA-N 0.000 description 1
- YLYPWESVKQZFEK-KEKNWZKVSA-N CC(C)(C)OC(NCCCC[C@@H](C(NCc1ncccc1)=O)NC1c2ncccc2CCC1)=O Chemical compound CC(C)(C)OC(NCCCC[C@@H](C(NCc1ncccc1)=O)NC1c2ncccc2CCC1)=O YLYPWESVKQZFEK-KEKNWZKVSA-N 0.000 description 1
- XMGUWUWWBBKFBI-UHFFFAOYSA-N CC(C)(C)OC(NCCNc1c(CN(C)C2c3ncccc3CCC2)cnc(S(C)=O)n1)=O Chemical compound CC(C)(C)OC(NCCNc1c(CN(C)C2c3ncccc3CCC2)cnc(S(C)=O)n1)=O XMGUWUWWBBKFBI-UHFFFAOYSA-N 0.000 description 1
- KUKIKOMOOMKASH-UHFFFAOYSA-N CC(C)(C)OC(NCCNc1nc(N(C)C)ncc1CN(C)C1c2ncccc2CCC1)=O Chemical compound CC(C)(C)OC(NCCNc1nc(N(C)C)ncc1CN(C)C1c2ncccc2CCC1)=O KUKIKOMOOMKASH-UHFFFAOYSA-N 0.000 description 1
- XBIMRZKFAPJBFF-UHFFFAOYSA-N CC(C)(C)OC(NCCNc1nc(SC)ncc1CN(C)C1c2ncccc2CCC1)=O Chemical compound CC(C)(C)OC(NCCNc1nc(SC)ncc1CN(C)C1c2ncccc2CCC1)=O XBIMRZKFAPJBFF-UHFFFAOYSA-N 0.000 description 1
- RCIFXWXZJUCFCW-UHFFFAOYSA-N CC(C)(C)OC(NCc1ccccc1-[n]1nnc(C=O)c1)=O Chemical compound CC(C)(C)OC(NCc1ccccc1-[n]1nnc(C=O)c1)=O RCIFXWXZJUCFCW-UHFFFAOYSA-N 0.000 description 1
- URLZGMRQTXRHKJ-UHFFFAOYSA-N CC(C)(C)OC(NCc1ccccc1-[n]1nnc(CO)c1)=O Chemical compound CC(C)(C)OC(NCc1ccccc1-[n]1nnc(CO)c1)=O URLZGMRQTXRHKJ-UHFFFAOYSA-N 0.000 description 1
- QSIQJZBBKBXYFR-UHFFFAOYSA-N CC(C)C(CCC1)c2c1cccn2 Chemical compound CC(C)C(CCC1)c2c1cccn2 QSIQJZBBKBXYFR-UHFFFAOYSA-N 0.000 description 1
- LKOUOYVTSCDVPA-UHFFFAOYSA-N CC(C)C1C2=NCCC=C2OCC1 Chemical compound CC(C)C1C2=NCCC=C2OCC1 LKOUOYVTSCDVPA-UHFFFAOYSA-N 0.000 description 1
- UWRWHOKKUJISAM-UHFFFAOYSA-N CC(C)c1ccccc1SC Chemical compound CC(C)c1ccccc1SC UWRWHOKKUJISAM-UHFFFAOYSA-N 0.000 description 1
- PFYPDUUXDADWKC-UHFFFAOYSA-N CC(C)c1ncccc1 Chemical compound CC(C)c1ncccc1 PFYPDUUXDADWKC-UHFFFAOYSA-N 0.000 description 1
- CHWJBMPGMPUBCD-UHFFFAOYSA-N CC(c1ncccc1)c1ccccn1 Chemical compound CC(c1ncccc1)c1ccccn1 CHWJBMPGMPUBCD-UHFFFAOYSA-N 0.000 description 1
- LPTKNKRCUZFOGS-UHFFFAOYSA-N CC1c(nccc2)c2OCC1 Chemical compound CC1c(nccc2)c2OCC1 LPTKNKRCUZFOGS-UHFFFAOYSA-N 0.000 description 1
- HXZINZDOBKUJIU-UHFFFAOYSA-N CC1c2ncccc2SCC1 Chemical compound CC1c2ncccc2SCC1 HXZINZDOBKUJIU-UHFFFAOYSA-N 0.000 description 1
- FRWGSFWIPPNVJB-RMKNXTFCSA-N CCC(/C(/C)=N/C=C)N Chemical compound CCC(/C(/C)=N/C=C)N FRWGSFWIPPNVJB-RMKNXTFCSA-N 0.000 description 1
- ILKRUJZSVMGEDI-UHFFFAOYSA-N CCOC(c1c2[o]c(cccc3)c3c2ccn1)=O Chemical compound CCOC(c1c2[o]c(cccc3)c3c2ccn1)=O ILKRUJZSVMGEDI-UHFFFAOYSA-N 0.000 description 1
- WEBZMGHVGASLFJ-UHFFFAOYSA-N CCc(cccc1)c1SC Chemical compound CCc(cccc1)c1SC WEBZMGHVGASLFJ-UHFFFAOYSA-N 0.000 description 1
- XCIZVKSCLVSDHN-UHFFFAOYSA-N CCc1nc(cccc2)c2cc1 Chemical compound CCc1nc(cccc2)c2cc1 XCIZVKSCLVSDHN-UHFFFAOYSA-N 0.000 description 1
- UBDYMAZEEMMDCG-UHFFFAOYSA-N CCc1nccc2c1cccc2 Chemical compound CCc1nccc2c1cccc2 UBDYMAZEEMMDCG-UHFFFAOYSA-N 0.000 description 1
- NRGGMCIBEHEAIL-UHFFFAOYSA-N CCc1ncccc1 Chemical compound CCc1ncccc1 NRGGMCIBEHEAIL-UHFFFAOYSA-N 0.000 description 1
- MEBNLBHILOYVPC-UHFFFAOYSA-N CCc1ncccc1Br Chemical compound CCc1ncccc1Br MEBNLBHILOYVPC-UHFFFAOYSA-N 0.000 description 1
- FTKZKUSQFCXEEL-UHFFFAOYSA-N CCc1ncccc1C Chemical compound CCc1ncccc1C FTKZKUSQFCXEEL-UHFFFAOYSA-N 0.000 description 1
- QCFGLRNIVWMMQC-UHFFFAOYSA-N CCc1ncccc1C(F)(F)F Chemical compound CCc1ncccc1C(F)(F)F QCFGLRNIVWMMQC-UHFFFAOYSA-N 0.000 description 1
- BFTNBGARNXDMEQ-UHFFFAOYSA-N CCc1ncccc1Cl Chemical compound CCc1ncccc1Cl BFTNBGARNXDMEQ-UHFFFAOYSA-N 0.000 description 1
- FYZHRGLUMOYIGB-UHFFFAOYSA-N CCc1ncccc1F Chemical compound CCc1ncccc1F FYZHRGLUMOYIGB-UHFFFAOYSA-N 0.000 description 1
- HOYXCWDNGCBQGG-UHFFFAOYSA-N CCc1ncccc1I Chemical compound CCc1ncccc1I HOYXCWDNGCBQGG-UHFFFAOYSA-N 0.000 description 1
- JPMRBTQVUWKUDU-UHFFFAOYSA-N CCc1ncccc1OC Chemical compound CCc1ncccc1OC JPMRBTQVUWKUDU-UHFFFAOYSA-N 0.000 description 1
- SUGRPPSHXYZOAN-UHFFFAOYSA-N CN(C)c1ncc(CN(C)C2c3ncccc3CCC2)c(NCCN)n1 Chemical compound CN(C)c1ncc(CN(C)C2c3ncccc3CCC2)c(NCCN)n1 SUGRPPSHXYZOAN-UHFFFAOYSA-N 0.000 description 1
- PHEIKCKEDOLYRP-UHFFFAOYSA-N CN(Cc1c[n](-c2ccccc2)nn1)C1c2ncccc2CCC1 Chemical compound CN(Cc1c[n](-c2ccccc2)nn1)C1c2ncccc2CCC1 PHEIKCKEDOLYRP-UHFFFAOYSA-N 0.000 description 1
- KPFMFRBMIIVDNL-UHFFFAOYSA-N CN(Cc1cccc2c1[nH]cc2)C1c2ncccc2CCC1 Chemical compound CN(Cc1cccc2c1[nH]cc2)C1c2ncccc2CCC1 KPFMFRBMIIVDNL-UHFFFAOYSA-N 0.000 description 1
- JNTHBIUSFJMMIA-MRVPVSSYSA-N C[C@H](CCC1)c2c1cccn2 Chemical compound C[C@H](CCC1)c2c1cccn2 JNTHBIUSFJMMIA-MRVPVSSYSA-N 0.000 description 1
- VMCXNOFFTMPRMM-MRVPVSSYSA-N C[C@H](COC)c1ncccc1 Chemical compound C[C@H](COC)c1ncccc1 VMCXNOFFTMPRMM-MRVPVSSYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N Cc1c(C)cccc1 Chemical compound Cc1c(C)cccc1 CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- GUAWMXYQZKVRCW-UHFFFAOYSA-N Cc1ccccc1NC Chemical compound Cc1ccccc1NC GUAWMXYQZKVRCW-UHFFFAOYSA-N 0.000 description 1
- HSHCUUAQVINMJK-UHFFFAOYSA-N NCCCCN(Cc1c2[nH]ccc2ccc1)C1c2ncccc2CCC1 Chemical compound NCCCCN(Cc1c2[nH]ccc2ccc1)C1c2ncccc2CCC1 HSHCUUAQVINMJK-UHFFFAOYSA-N 0.000 description 1
- ZGIHVBKQAQIYMQ-UHFFFAOYSA-N NCCCCN(Cc1nccc2c1[nH]c1ccccc21)C1c2ncccc2CCC1 Chemical compound NCCCCN(Cc1nccc2c1[nH]c1ccccc21)C1c2ncccc2CCC1 ZGIHVBKQAQIYMQ-UHFFFAOYSA-N 0.000 description 1
- JIAKIQWNYAZUJD-UHFFFAOYSA-N O=C(CCC1)c2c1cccn2 Chemical compound O=C(CCC1)c2c1cccn2 JIAKIQWNYAZUJD-UHFFFAOYSA-N 0.000 description 1
- VKJCJJYNVIYVQR-UHFFFAOYSA-N O=C(c1c2cccc1)N(CCCBr)C2=O Chemical compound O=C(c1c2cccc1)N(CCCBr)C2=O VKJCJJYNVIYVQR-UHFFFAOYSA-N 0.000 description 1
- FYJBXSJCQWYLKL-UHFFFAOYSA-N O=Cc1c2[o]c(cccc3)c3c2ccn1 Chemical compound O=Cc1c2[o]c(cccc3)c3c2ccn1 FYJBXSJCQWYLKL-UHFFFAOYSA-N 0.000 description 1
- AQBWYVZHTYJMES-UHFFFAOYSA-N O=Cc1c[n](-c2ccccc2)nn1 Chemical compound O=Cc1c[n](-c2ccccc2)nn1 AQBWYVZHTYJMES-UHFFFAOYSA-N 0.000 description 1
Classifications
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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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- 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
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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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
- A61P35/04—Antineoplastic agents specific for metastasis
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- A—HUMAN NECESSITIES
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- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4051608P | 2008-03-28 | 2008-03-28 | |
| US61/040,516 | 2008-03-28 | ||
| PCT/US2009/038805 WO2009121063A2 (en) | 2008-03-28 | 2009-03-30 | Chemokine receptor modulators |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102015717A true CN102015717A (zh) | 2011-04-13 |
Family
ID=41114825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009801150516A Pending CN102015717A (zh) | 2008-03-28 | 2009-03-30 | 趋化因子受体调节剂 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US8338448B2 (https=) |
| EP (2) | EP2262808B1 (https=) |
| JP (1) | JP5690715B2 (https=) |
| KR (1) | KR20110005819A (https=) |
| CN (1) | CN102015717A (https=) |
| AU (1) | AU2009228034A1 (https=) |
| BR (1) | BRPI0909375A2 (https=) |
| CA (1) | CA2718618A1 (https=) |
| DK (1) | DK2262808T3 (https=) |
| IL (1) | IL208185A0 (https=) |
| MX (1) | MX2010010619A (https=) |
| NZ (1) | NZ587929A (https=) |
| SG (1) | SG189723A1 (https=) |
| WO (1) | WO2009121063A2 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109553604A (zh) * | 2017-09-25 | 2019-04-02 | 苏州云轩医药科技有限公司 | 4-氨基嘧啶衍生物作cxcr4抑制剂及其应用 |
| CN110669036A (zh) * | 2018-07-02 | 2020-01-10 | 苏州云轩医药科技有限公司 | 一类具有cxcr4信号通路抑制活性的杂环化合物及其应用 |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100518160B1 (ko) * | 1996-11-05 | 2006-09-18 | 닛폰 프라파렛트 가부시키가이샤 | 합성수지팔레트 |
| AU2009228034A1 (en) | 2008-03-28 | 2009-10-01 | Altiris Therapeutics | Chemokine receptor modulators |
| EP3153510B1 (en) | 2010-12-03 | 2020-05-06 | Emory University | Fused azines as chemokine cxcr4 receptor modulators and uses related thereto |
| CN105120863B (zh) * | 2013-03-14 | 2021-06-04 | 奥斯特克有限公司 | 促进骨生长的烷基胺骆驼蓬碱衍生物 |
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- 2009-03-30 CN CN2009801150516A patent/CN102015717A/zh active Pending
- 2009-03-30 EP EP09724705.0A patent/EP2262808B1/en not_active Not-in-force
- 2009-03-30 JP JP2011502132A patent/JP5690715B2/ja not_active Expired - Fee Related
- 2009-03-30 MX MX2010010619A patent/MX2010010619A/es active IP Right Grant
- 2009-03-30 EP EP13174241.3A patent/EP2664618A3/en not_active Withdrawn
- 2009-03-30 CA CA2718618A patent/CA2718618A1/en not_active Abandoned
- 2009-03-30 KR KR1020107023643A patent/KR20110005819A/ko not_active Ceased
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- 2009-03-30 BR BRPI0909375-3A patent/BRPI0909375A2/pt not_active IP Right Cessation
- 2009-03-30 US US12/414,352 patent/US8338448B2/en not_active Expired - Fee Related
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| CN109553604A (zh) * | 2017-09-25 | 2019-04-02 | 苏州云轩医药科技有限公司 | 4-氨基嘧啶衍生物作cxcr4抑制剂及其应用 |
| CN109553604B (zh) * | 2017-09-25 | 2021-08-27 | 盛世泰科生物医药技术(苏州)有限公司 | 4-氨基嘧啶衍生物作cxcr4抑制剂及其应用 |
| CN110669036A (zh) * | 2018-07-02 | 2020-01-10 | 苏州云轩医药科技有限公司 | 一类具有cxcr4信号通路抑制活性的杂环化合物及其应用 |
| CN110669036B (zh) * | 2018-07-02 | 2022-02-11 | 盛世泰科生物医药技术(苏州)有限公司 | 一类具有cxcr4信号通路抑制活性的杂环化合物及其应用 |
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| DK2262808T3 (da) | 2013-11-04 |
| SG189723A1 (en) | 2013-05-31 |
| KR20110005819A (ko) | 2011-01-19 |
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| US20100029634A1 (en) | 2010-02-04 |
| WO2009121063A3 (en) | 2010-01-07 |
| BRPI0909375A2 (pt) | 2015-08-04 |
| EP2664618A3 (en) | 2014-05-07 |
| EP2262808A2 (en) | 2010-12-22 |
| US9314468B2 (en) | 2016-04-19 |
| EP2664618A2 (en) | 2013-11-20 |
| WO2009121063A2 (en) | 2009-10-01 |
| EP2262808A4 (en) | 2011-11-16 |
| JP2011516427A (ja) | 2011-05-26 |
| NZ587929A (en) | 2012-10-26 |
| EP2262808B1 (en) | 2013-08-14 |
| CA2718618A1 (en) | 2009-10-01 |
| US8338448B2 (en) | 2012-12-25 |
| IL208185A0 (en) | 2010-12-30 |
| MX2010010619A (es) | 2010-12-17 |
| US20130172330A1 (en) | 2013-07-04 |
| AU2009228034A1 (en) | 2009-10-01 |
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