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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 4826 - 4850 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01719351Lysyl-Lysine,4TMS,isomer#19JsmolC[Si](C)(C)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(O)=NC(CCCCN)C(=O)O[Si](C)(C)CTMS562.3586Standard polar3877.8474
RI01719350Lysyl-Lysine,4TMS,isomer#18JsmolC[Si](C)(C)NCCCCC(N)C(O)=NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS562.3586Standard polar4168.6167
RI01719349Lysyl-Lysine,4TMS,isomer#17JsmolC[Si](C)(C)NCCCCC(N=C(O)C(N)CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS562.3586Standard polar4169.5215
RI01719348Lysyl-Lysine,4TMS,isomer#16JsmolC[Si](C)(C)NCCCCC(N=C(O)C(CCCCN)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS562.3586Standard polar3817.8916
RI01719347Lysyl-Lysine,4TMS,isomer#15JsmolC[Si](C)(C)NC(CCCCN)C(O)=NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS562.3586Standard polar3878.5032
RI01719346Lysyl-Lysine,4TMS,isomer#14JsmolC[Si](C)(C)NCCCCC(N=C(O)C(CCCCN[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS562.3586Standard polar3495.9993
RI01719345Lysyl-Lysine,4TMS,isomer#13JsmolC[Si](C)(C)NCCCCC(C(=NC(CCCCN)C(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS562.3586Standard polar3799.5762
RI01719344Lysyl-Lysine,4TMS,isomer#12JsmolC[Si](C)(C)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=NC(CCCCN)C(=O)O)O[Si](C)(C)CTMS562.3586Standard polar3836.8987
RI01719343Lysyl-Lysine,4TMS,isomer#11JsmolC[Si](C)(C)NCCCCC(N)C(=NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)O[Si](C)(C)CTMS562.3586Standard polar4098.856
RI01719342Lysyl-Lysine,4TMS,isomer#10JsmolC[Si](C)(C)NCCCCC(N=C(O[Si](C)(C)C)C(N)CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS562.3586Standard polar4100.024
RI01719341Lysyl-Lysine,4TMS,isomer#9JsmolC[Si](C)(C)NCCCCC(N=C(O[Si](C)(C)C)C(CCCCN)N([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS562.3586Standard polar3800.5583
RI01719340Lysyl-Lysine,4TMS,isomer#8JsmolC[Si](C)(C)NC(CCCCN)C(=NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)O[Si](C)(C)CTMS562.3586Standard polar3837.2815
RI01719339Lysyl-Lysine,4TMS,isomer#7JsmolC[Si](C)(C)NCCCCC(N=C(O[Si](C)(C)C)C(CCCCN[Si](C)(C)C)N[Si](C)(C)C)C(=O)OTMS562.3586Standard polar3467.869
RI01719338Lysyl-Lysine,4TMS,isomer#6JsmolC[Si](C)(C)OC(=O)C(CCCCN)N=C(O[Si](C)(C)C)C(N)CCCCN([Si](C)(C)C)[Si](C)(C)CTMS562.3586Standard polar4483.631
RI01719337Lysyl-Lysine,4TMS,isomer#5JsmolC[Si](C)(C)OC(=O)C(CCCCN)N=C(O[Si](C)(C)C)C(CCCCN)N([Si](C)(C)C)[Si](C)(C)CTMS562.3586Standard polar4205.745
RI01719336Lysyl-Lysine,4TMS,isomer#4JsmolC[Si](C)(C)NCCCCC(N[Si](C)(C)C)C(=NC(CCCCN)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS562.3586Standard polar3719.6802
RI01719335Lysyl-Lysine,4TMS,isomer#3JsmolC[Si](C)(C)OC(=O)C(CCCCN([Si](C)(C)C)[Si](C)(C)C)N=C(O[Si](C)(C)C)C(N)CCCCNTMS562.3586Standard polar4454.8945
RI01719334Lysyl-Lysine,4TMS,isomer#2JsmolC[Si](C)(C)NCCCCC(N)C(=NC(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS562.3586Standard polar4052.4844
RI01719333Lysyl-Lysine,4TMS,isomer#1JsmolC[Si](C)(C)NCCCCC(N=C(O[Si](C)(C)C)C(CCCCN)N[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS562.3586Standard polar3720.3804
RI01719332Lysyl-Lysine,3TMS,isomer#22JsmolC[Si](C)(C)NCCCCC(N=C(O)C(CCCCN)N([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS490.3191Standard polar4092.1882
RI01719331Lysyl-Lysine,3TMS,isomer#21JsmolC[Si](C)(C)NC(CCCCN)C(O)=NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS490.3191Standard polar4145.2466
RI01719330Lysyl-Lysine,3TMS,isomer#20JsmolC[Si](C)(C)NCCCCC(N)C(O)=NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS490.3191Standard polar4383.829
RI01719329Lysyl-Lysine,3TMS,isomer#19JsmolC[Si](C)(C)NCCCCC(N=C(O)C(N)CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS490.3191Standard polar4384.7563
RI01719328Lysyl-Lysine,3TMS,isomer#18JsmolC[Si](C)(C)NCCCCC(C(O)=NC(CCCCN)C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS490.3191Standard polar4091.74
RI01719327Lysyl-Lysine,3TMS,isomer#17JsmolC[Si](C)(C)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(O)=NC(CCCCN)C(=O)OTMS490.3191Standard polar4144.258
Displaying retention index compounds 4826 - 4850 of 1722868 in total