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4-Hydroxy-2-alkylquinoline

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Luckner, M.; Ritter, C. (1965). "Biosynthesis of the 2-n-alkyl-4-hydroxyquinolines by Pseudomonas aeruginosa".
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The overproduction of these molecules, with their pro-oxidative effects, leads to antibiotic properties.
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Chemical structure of 4-hydroxy-2-heptylquinoline, a common form of HAQ
39: 42:. HAQs are produced by various types of bacteria, such as 71: 107: 18: 108: 13: 14: 127: 34:) are a class of intracellular 65: 1: 88:10.1016/s0040-4039(01)83977-0 58: 7: 28:4-Hydroxy-2-alkylquinolines 16:Class of chemical compounds 10: 132: 48:, and are involved in 45:Pseudomonas aeruginosa 24: 38:associated with iron 22: 75:Tetrahedron Letters 36:signaling molecules 25: 123: 100: 99: 69: 131: 130: 126: 125: 124: 122: 121: 120: 106: 105: 104: 103: 70: 66: 61: 17: 12: 11: 5: 129: 119: 118: 102: 101: 63: 62: 60: 57: 50:quorum sensing 15: 9: 6: 4: 3: 2: 128: 117: 114: 113: 111: 97: 93: 89: 85: 81: 77: 76: 68: 64: 56: 53: 51: 47: 46: 41: 37: 33: 29: 21: 79: 73: 67: 54: 43: 31: 27: 26: 116:Quinolinols 82:: 741–744. 59:References 40:chelation 110:Category 96:14291872 94:  92:PMID 32:HAQs 84:doi 112:: 90:. 80:12 78:. 52:. 98:. 86:: 30:(

Index


signaling molecules
chelation
Pseudomonas aeruginosa
quorum sensing
Tetrahedron Letters
doi
10.1016/s0040-4039(01)83977-0
PMID
14291872
Category
Quinolinols

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