Tyrphostins. 5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins.
about
11H-Indeno-[1,2-b]quinoxalin-11-one5-hydroxytryptamine 2B receptor regulates cell-cycle progression: cross-talk with tyrosine kinase pathwaysCrystal structure of 2-aza-niumyl-3-bromo-6-oxo-5,6-di-hydro-pyrido[1,2-a]quinoxalin-11-ium dibromide.FLT3: ITDoes matter in leukemia.Emerging treatments in acute myeloid leukaemia.Copper-catalyzed aerobic oxidative coupling: From ketone and diamine to pyrazineUnusual Friedlander reactions: a route to novel quinoxaline-based heterocycles.Crystal structure of methyl 3'-benzamido-4'-(4-meth-oxy-phen-yl)-1'-methyl-spiro-[indeno-[1,2-b]quinoxaline-11,2'-pyrrolidine]-3'-carboxyl-ateBis[(l)prolinate-N,O]Zn: A water-soluble and recycle catalyst for various organic transformations.FMS-like tyrosine kinase 3 inhibitors: a patent review.Quinoxaline-Based Scaffolds Targeting Tyrosine Kinases and Their Potential Anticancer Activity.Screening of the 'Stasis Box' identifies two kinase inhibitors under pharmaceutical development with activity against Haemonchus contortus.Intrinsic regulation of hemangioma involution by platelet-derived growth factor.rac-(2R,3S)-2-Phenyl-3-(3-phenyl-1,2,3,4-tetra-hydro-quinoxalin-2-yl)quinoxaline.A single amino acid exchange inverts susceptibility of related receptor tyrosine kinases for the ATP site inhibitor STI-571.Synthesis and antibacterial activity of some glucosyl- and ribosyl-pyridazin-3-ones.Facile, eco-friendly, catalyst-free synthesis of polyfunctionalized quinoxalines.Accelerated generation of (protonated) imines and quinoxalines by formation of C=N bonds in the microdroplets of a nebuliser.Highly efficient synthesis of quinoxaline derivatives from 1,2-benzenediamine and α-aminoxylated 1,3-dicarbonyl compounds.Design of Organic Transformations at Ambient Conditions: Our Sincere Efforts to the Cause of Green Chemistry Practice.An efficient lactamisation/N-acyliminium Pictet-Spengler domino strategy for the diasteroselective synthesis of polyhydroxylated quinoxalinone, β-carboline and quinazolinone derivatives.Design for carbon–carbon bond forming reactions under ambient conditionsMagnetically separable MnFe2O4 nano-material: an efficient and reusable heterogeneous catalyst for the synthesis of 2-substituted benzimidazoles and the extended synthesis of quinoxalines at room temperature under aerobic conditions
P2860
Q34302426-5D235C5D-4D6F-482B-9BBB-742CD488094AQ35077547-0577F930-4FDF-4CAC-B619-53745F211C6DQ35093387-C0909268-AAF8-4D76-83DF-1CE7C1F05ECEQ35217399-FF7FD6E2-D0CE-4186-B949-01CF3047044FQ35779278-16DAFCF1-567B-415B-AC81-CB415CB96F90Q36284842-E0B1D129-9DB8-4E30-A2F7-A71D73E2608CQ36381436-8DB56064-6CCD-43A7-892C-719531545324Q37432461-DA0FF26B-BD2A-4971-B8E0-83103814354CQ37682706-A9150B5B-572C-4F9B-8509-495146991099Q37842585-AFCED2CE-B8A2-4E24-B057-EC518B31E973Q38803278-98095722-E349-44BD-85D3-017474B362F9Q40146751-83F8CA68-70CB-408F-B19D-EA4022AB65CDQ42222851-B4CD0060-87D7-40CA-A2D8-EBBD30EB91B7Q42402337-D86E7C40-771B-4873-8BB6-F19FA2D091A4Q44219205-6287DCDE-F563-4B32-829D-5C20D1856B96Q46067957-E32DF11D-2E80-4750-BE60-A202F5A205BCQ47600003-FB33477F-C767-40CA-89C3-3D123448D192Q50098848-CDC0A1C5-2E66-4D27-B619-E8BE90C701C6Q50234637-C8951888-EA67-44C2-9470-4ED2D2E735DBQ50239124-7CD18E44-3406-4A07-B5DC-60BC79E01042Q50861208-3D615F16-F8FE-414B-ADAD-58066F28A9CAQ57631372-61DD00F6-67EF-4937-ACC4-DCBEE7C361E6Q57631434-E5F33F1E-B87B-4B0C-9E53-A92F4C6E4E1B
P2860
Tyrphostins. 5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Tyrphostins. 5. Potent inhibit ...... lines, and indole tyrphostins.
@en
Tyrphostins. 5. Potent inhibit ...... lines, and indole tyrphostins.
@nl
type
label
Tyrphostins. 5. Potent inhibit ...... lines, and indole tyrphostins.
@en
Tyrphostins. 5. Potent inhibit ...... lines, and indole tyrphostins.
@nl
prefLabel
Tyrphostins. 5. Potent inhibit ...... lines, and indole tyrphostins.
@en
Tyrphostins. 5. Potent inhibit ...... lines, and indole tyrphostins.
@nl
P2093
P356
P1476
Tyrphostins. 5. Potent inhibit ...... lines, and indole tyrphostins.
@en
P2093
P304
P356
10.1021/JM950727B
P407
P577
1996-05-01T00:00:00Z