Knowledge (XXG)

Alkyl-lysophospholipids

Source 📝

17: 96:
Munder, PG; Modolell M; Adreesen R; Weltzien HU; Westphal O (1979). "Lysophosphatidylcholine (Lysolecithin) and its Synthetic Analogues. Immunemodulating and Other Biologic Effects".
179:
van Blitterswijk, W; Verheij M (2008). "Anticancer alkylphospholipids: mechanisms of action, cellular sensitivity and resistance, and clinical prospects".
220: 36: 39:(LPCs), also called lysolecithins. They are synthesized by replacing the acyl-group within the LPC with an 54:
effects. Their anti-tumor effects are due to modulation of intracellular signalling pathways, inducing
161: 113: 32: 196: 153: 51: 188: 145: 105: 71: 225: 24:, an alkyl-lysophospholipid being studied for its potential use as a pharmaceutical drug 47: 136:
Houlihan, W; Lohmeyer M; Workman P; Cheon SH (1995). "Phospholipid antitumor agents".
214: 117: 165: 63: 40: 192: 67: 59: 21: 58:. It is highly selective, sparing healthy cells. Several examples including 55: 200: 149: 157: 109: 16: 15: 43:. In contrast to LPCs, ALPs are metabolically very stable. 131: 129: 127: 91: 89: 87: 8: 74:as drugs against cancer and other diseases. 46:ALPs are being studied for their potential 83: 7: 98:Springer Seminars in Immunopathology 14: 1: 181:Current Pharmaceutical Design 242: 193:10.2174/138161208785294636 138:Medicinal Research Reviews 221:Experimental cancer drugs 37:lysophosphatidylcholines 150:10.1002/med.2610150302 29:Alky-lysophospholipids 25: 20:Chemical structure of 31:(ALPs) are synthetic 19: 110:10.1007/BF01891668 50:(anti-cancer) and 26: 52:immune-modulating 233: 205: 204: 176: 170: 169: 133: 122: 121: 93: 241: 240: 236: 235: 234: 232: 231: 230: 211: 210: 209: 208: 187:(21): 2061–74. 178: 177: 173: 135: 134: 125: 95: 94: 85: 80: 12: 11: 5: 239: 237: 229: 228: 223: 213: 212: 207: 206: 171: 144:(3): 157–223. 123: 104:(2): 187–203. 82: 81: 79: 76: 48:antineoplastic 13: 10: 9: 6: 4: 3: 2: 238: 227: 224: 222: 219: 218: 216: 202: 198: 194: 190: 186: 182: 175: 172: 167: 163: 159: 155: 151: 147: 143: 139: 132: 130: 128: 124: 119: 115: 111: 107: 103: 99: 92: 90: 88: 84: 77: 75: 73: 69: 65: 61: 57: 53: 49: 44: 42: 38: 34: 30: 23: 18: 184: 180: 174: 141: 137: 101: 97: 45: 28: 27: 72:development 64:miltefosine 41:alkyl group 215:Categories 78:References 70:are under 68:perifosine 60:edelfosine 22:edelfosine 56:apoptosis 201:18691116 118:42907729 166:6997551 158:7658750 33:analogs 226:Lipids 199:  164:  156:  116:  66:, and 162:S2CID 114:S2CID 197:PMID 154:PMID 189:doi 146:doi 106:doi 102:203 35:of 217:: 195:. 185:14 183:. 160:. 152:. 142:15 140:. 126:^ 112:. 100:. 86:^ 62:, 203:. 191:: 168:. 148:: 120:. 108::

Index


edelfosine
analogs
lysophosphatidylcholines
alkyl group
antineoplastic
immune-modulating
apoptosis
edelfosine
miltefosine
perifosine
development



doi
10.1007/BF01891668
S2CID
42907729



doi
10.1002/med.2610150302
PMID
7658750
S2CID
6997551
doi
10.2174/138161208785294636

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