Ultraviolet light

Summarized by Plex Health
Last Updated: 05 May 2022
ultraviolet light triggers the conversion of cu2+-bound aβ42 aggregates into cytotoxic species in a copper chelation-independent manner. "ultraviolet light triggers the conversion of cu2+-bound aβ42 aggregates into cytotoxic species in a copper chelation-independent manner.", by Dong X, Zhang Z, Zhao D, Liu Y, Meng Y, Zhang Y, Zhang D, Liu C. f3: Analysis for dissociation of the Cu2+-free and -bound Aβ42 aggregates.The amount of soluble Aβ42 species in the supernatants provided by incubating 20 μM Cu2+-free and -bound Aβ42 (Cu2+/Aβ42 = 1:1) aggregates with 20 μM...

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PubChem - CovalentUnitCount

(Table source)
CIDMolecularFormulaMolecularWeightCanonicalSMILESIsomericSMILESInChIInChIKeyIUPACNameXLogPExactMassMonoisotopicMassTPSAComplexityChargeHBondDonorCountHBondAcceptorCountRotatableBondCountHeavyAtomCountIsotopeAtomCountAtomStereoCountDefinedAtomStereoCountUndefinedAtomStereoCountBondStereoCountDefinedBondStereoCountUndefinedBondStereoCountCovalentUnitCount
57392528C83H109N17O341888.8CC(C)CC(C(=O)NC(CCC(=O)O)C(=O)O)NC(=O)C(CC1=CNC2=CC=CC=C21)NC(=O)C(CCC(=O)O)NC(=O)C(CC3=CC=CC=C3)NC(=O)C(CC4=CC=C(C=C4)O)NC(=O)C(CC(=O)O)NC(=O)CNC(=O)C(CCC(=O)O)NC(=O)C(C)NC(=O)C(CCC(=O)O)NC(=O)C(CC(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(CCC(=O)N)NC(=O)C(CCC(=O)O)NC[[email protected]@H](C(=O)N[[email protected]@H](CCC(=O)O)C(=O)NCC(=O)N[[email protected]@H](CC(=O)O)C(=O)N[[email protected]@H](CC1=CC=C(C=C1)O)C(=O)N[[email protected]@H](CC2=CC=CC=C2)C(=O)N[[email protected]@H](CCC(=O)O)C(=O)N[[email protected]@H](CC3=CNC4=CC=CC=C43)C(=O)N[[email protected]@H](CC(C)C)C(=O)N[[email protected]@H](CCC(=O)O)C(=O)O)NC(=O)[[email protected]](CCC(=O)O)NC(=O)[[email protected]](CC(=O)O)NC(=O)[[email protected]](CCC(=O)O)NC(=O)[[email protected]](CCC(=O)N)NC(=O)[[email protected]](CCC(=O)O)NInChI=1S/C83H109N17O34/c1-39(2)31-54(77(127)95-53(83(133)134)23-30-67(114)115)96-80(130)57(34-43-37-86-47-12-8-7-11-45(43)47)99-75(125)52(22-29-66(112)113)94-78(128)55(32-41-9-5-4-6-10-41)97-79(129)56(33-42-13-15-44(101)16-14-42)98-81(131)58(35-68(116)117)89-61(103)38-87-72(122)48(19-26-63(106)107)90-70(120)40(3)88-73(123)50(20-27-64(108)109)93-82(132)59(36-69(118)119)100-76(126)51(21-28-65(110)111)92-74(124)49(18-24-60(85)102)91-71(121)46(84)17-25-62(104)105/h4-16,37,39-40,46,48-59,86,101H,17-36,38,84H2,1-3H3,(H2,85,102)(H,87,122)(H,88,123)(H,89,103)(H,90,120)(H,91,121)(H,92,124)(H,93,132)(H,94,128)(H,95,127)(H,96,130)(H,97,129)(H,98,131)(H,99,125)(H,100,126)(H,104,105)(H,106,107)(H,108,109)(H,110,111)(H,112,113)(H,114,115)(H,116,117)(H,118,119)(H,133,134)/t40-,46-,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-/m0/s1IBOGFXANYQFJQL-STZPQELMSA-N(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-5-amino-2-[[(2S)-2-amino-4-carboxybutanoyl]amino]-5-oxopentanoyl]amino]-4-carboxybutanoyl]amino]-3-carboxypropanoyl]amino]-4-carboxybutanoyl]amino]propanoyl]amino]-4-carboxybutanoyl]amino]acetyl]amino]-3-carboxypropanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-phenylpropanoyl]amino]-4-carboxybutanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-4-methylpentanoyl]amino]pentanedioic acid-7.21887.73228361887.7322836848418002735621340141400001
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