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Kinamycin

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Woo, C. M.; Lu, L.; Gholap, S. L.; Smith, D. R.; Herzon, S. B. (2010). "Development of a Convergent Entry to the Diazofluorene Antitumor Antibiotics: Enantioselective Synthesis of Kinamycin F".
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synthesize kinamycins C, F, and J were discovered. In 2010 a method was found to allow easier synthesis of these compounds in fewer steps, making research into their properties more feasible.
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O'Hara, K. A.; Wu, X.; Patel, D.; Liang, H.; Yalowich, J. C.; Chen, N.; Goodfellow, V.; Adedayo, O.; Dmitrienko, G. I.; Hasinoff, B. B. (2007).
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Nicolaou, K. C.; Li, H.; Nold, A. L.; Pappo, D.; Lenzen, A. (2007). "Total Synthesis of Kinamycins C, F, and J".
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Lei, X.; Porco Ja, J. (2006). "Total synthesis of the diazobenzofluorene antibiotic (-)-kinamycin C1".
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Ballard, T. E.; Melander, C. (2008). "Kinamycin-mediated DNA cleavage under biomimetic conditions".
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EMBL-EBI listing—includes links to structural formula and other properties of group members
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Description of Porco(2006) and Nicolaou(2007) synthesis on University of Pittsburgh site
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and are considered of interest for potential use in anti-cancer therapies.
19: 232: 197: 162: 38: 18: 8: 53:In 2006 and 2007 the means to totally and 125: 221:Journal of the American Chemical Society 186:Journal of the American Chemical Society 151:Journal of the American Chemical Society 65: 41:group. Kinamycins are known for their 7: 118:10.1016/j.freeradbiomed.2007.07.005 288:Nucleic acid inhibitor antibiotics 14: 106:Free Radical Biology and Medicine 23:Chemical structure of kinamycin A 1: 87:10.1016/j.tetlet.2008.03.019 16:Group of chemical compounds 304: 30:are a group of bacterial 258:kinamycin (CHEBI:48207) 278:Polyketide antibiotics 24: 35:secondary metabolites 22: 157:(46): 14790–14791. 75:Tetrahedron Letters 55:enantioselectively 25: 233:10.1021/ja910769j 198:10.1021/ja074297d 163:10.1021/ja066621v 295: 245: 244: 216: 210: 209: 181: 175: 174: 146: 140: 139: 129: 112:(8): 1132–1144. 97: 91: 90: 70: 303: 302: 298: 297: 296: 294: 293: 292: 283:Diazo compounds 268: 267: 253: 248: 218: 217: 213: 192:(34): 10356–7. 183: 182: 178: 148: 147: 143: 99: 98: 94: 72: 71: 67: 63: 51: 17: 12: 11: 5: 301: 299: 291: 290: 285: 280: 270: 269: 266: 265: 260: 252: 251:External links 249: 247: 246: 211: 176: 141: 92: 64: 62: 59: 50: 47: 15: 13: 10: 9: 6: 4: 3: 2: 300: 289: 286: 284: 281: 279: 276: 275: 273: 264: 261: 259: 255: 254: 250: 242: 238: 234: 230: 227:(8): 2540–1. 226: 222: 215: 212: 207: 203: 199: 195: 191: 187: 180: 177: 172: 168: 164: 160: 156: 152: 145: 142: 137: 133: 128: 123: 119: 115: 111: 107: 103: 96: 93: 88: 84: 80: 76: 69: 66: 60: 58: 56: 48: 46: 44: 40: 37:containing a 36: 33: 29: 21: 224: 220: 214: 189: 185: 179: 154: 150: 144: 109: 105: 95: 81:(19): 3157. 78: 74: 68: 52: 43:cytotoxicity 27: 26: 272:Categories 61:References 32:polyketide 28:Kinamycins 49:Synthesis 241:20141138 206:17676854 171:17105273 136:17854709 127:2753228 239:  204:  169:  134:  124:  39:diazo 237:PMID 202:PMID 167:PMID 132:PMID 229:doi 225:132 194:doi 190:129 159:doi 155:128 122:PMC 114:doi 83:doi 274:: 235:. 223:. 200:. 188:. 165:. 153:. 130:. 120:. 110:43 108:. 104:. 79:49 77:. 243:. 231:: 208:. 196:: 173:. 161:: 138:. 116:: 89:. 85::

Index


polyketide
secondary metabolites
diazo
cytotoxicity
enantioselectively
doi
10.1016/j.tetlet.2008.03.019
"Mechanism of the cytotoxicity of the diazoparaquinone antitumor antibiotic kinamycin F"
doi
10.1016/j.freeradbiomed.2007.07.005
PMC
2753228
PMID
17854709
doi
10.1021/ja066621v
PMID
17105273
doi
10.1021/ja074297d
PMID
17676854
doi
10.1021/ja910769j
PMID
20141138
kinamycin (CHEBI:48207)
Description of Porco(2006) and Nicolaou(2007) synthesis on University of Pittsburgh site
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