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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 5151 - 5175 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01719026Lysyl-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 non polar2699.5461
RI01719025Lysyl-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 non polar2767.7217
RI01719024Lysyl-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 non polar2769.634
RI01719023Lysyl-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 non polar2709.0667
RI01719022Lysyl-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 non polar2696.5635
RI01719021Lysyl-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 non polar2741.689
RI01719020Lysyl-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 non polar2682.3242
RI01719019Lysyl-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 non polar2629.1516
RI01719018Lysyl-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 non polar2622.0505
RI01719017Lysyl-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 non polar2677.5608
RI01719016Lysyl-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 non polar2689.5737
RI01719015Lysyl-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 non polar2621.196
RI01719014Lysyl-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 non polar2745.5952
RI01719013Lysyl-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 non polar2734.527
RI01719012Lysyl-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 non polar2806.7239
RI01719011Lysyl-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 non polar2809.5205
RI01719010Lysyl-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 non polar2744.8635
RI01719009Lysyl-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 non polar2736.9812
RI01719008Lysyl-Lysine,3TMS,isomer#16JsmolC[Si](C)(C)NCCCCC(N=C(O)C(CCCCN[Si](C)(C)C)N[Si](C)(C)C)C(=O)OTMS490.3191Standard non polar2772.3247
RI01719007Lysyl-Lysine,3TMS,isomer#15JsmolC[Si](C)(C)OC(=O)C(CCCCN)N=C(O)C(N)CCCCN([Si](C)(C)C)[Si](C)(C)CTMS490.3191Standard non polar2694.5657
RI01719006Lysyl-Lysine,3TMS,isomer#14JsmolC[Si](C)(C)OC(=O)C(CCCCN)N=C(O)C(CCCCN)N([Si](C)(C)C)[Si](C)(C)CTMS490.3191Standard non polar2656.12
RI01719005Lysyl-Lysine,3TMS,isomer#13JsmolC[Si](C)(C)NCCCCC(N[Si](C)(C)C)C(O)=NC(CCCCN)C(=O)O[Si](C)(C)CTMS490.3191Standard non polar2667.6243
RI01719004Lysyl-Lysine,3TMS,isomer#12JsmolC[Si](C)(C)OC(=O)C(CCCCN([Si](C)(C)C)[Si](C)(C)C)N=C(O)C(N)CCCCNTMS490.3191Standard non polar2692.0361
RI01719003Lysyl-Lysine,3TMS,isomer#11JsmolC[Si](C)(C)NCCCCC(N)C(O)=NC(CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS490.3191Standard non polar2709.7515
RI01719002Lysyl-Lysine,3TMS,isomer#10JsmolC[Si](C)(C)NCCCCC(N=C(O)C(CCCCN)N[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS490.3191Standard non polar2667.8108
Displaying retention index compounds 5151 - 5175 of 1722868 in total