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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 4701 - 4725 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01719476Lysyl-Phenylalanine,3TMS,isomer#7JsmolC[Si](C)(C)OC(=O)C(CC1=CC=CC=C1)N=C(O)C(CCCCN)N([Si](C)(C)C)[Si](C)(C)CTMS509.2925Standard non polar2701.3225
RI01719475Lysyl-Phenylalanine,3TMS,isomer#6JsmolC[Si](C)(C)NCCCCC(N[Si](C)(C)C)C(O)=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)CTMS509.2925Standard non polar2657.7478
RI01719474Lysyl-Phenylalanine,3TMS,isomer#5JsmolC[Si](C)(C)OC(=NC(CC1=CC=CC=C1)C(=O)O)C(N)CCCCN([Si](C)(C)C)[Si](C)(C)CTMS509.2925Standard non polar2712.38
RI01719473Lysyl-Phenylalanine,3TMS,isomer#4JsmolC[Si](C)(C)OC(=NC(CC1=CC=CC=C1)C(=O)O)C(CCCCN)N([Si](C)(C)C)[Si](C)(C)CTMS509.2925Standard non polar2640.3645
RI01719472Lysyl-Phenylalanine,3TMS,isomer#3JsmolC[Si](C)(C)NCCCCC(N[Si](C)(C)C)C(=NC(CC1=CC=CC=C1)C(=O)O)O[Si](C)(C)CTMS509.2925Standard non polar2637.4377
RI01719471Lysyl-Phenylalanine,3TMS,isomer#2JsmolC[Si](C)(C)NCCCCC(N)C(=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS509.2925Standard non polar2599.6536
RI01719470Lysyl-Phenylalanine,3TMS,isomer#1JsmolC[Si](C)(C)NC(CCCCN)C(=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS509.2925Standard non polar2537.5027
RI01719469Lysyl-Lysine,5TBDMS,isomer#22JsmolCC(C)(C)[Si](C)(C)NCCCCC(N=C(O)C(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS844.6329Standard polar3731.8618
RI01719468Lysyl-Lysine,5TBDMS,isomer#21JsmolCC(C)(C)[Si](C)(C)NCCCCC(C(O)=NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3731.709
RI01719467Lysyl-Lysine,5TBDMS,isomer#20JsmolCC(C)(C)[Si](C)(C)NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)=NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS844.6329Standard polar3772.1418
RI01719466Lysyl-Lysine,5TBDMS,isomer#19JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CCCCN)N=C(O)C(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3866.4285
RI01719465Lysyl-Lysine,5TBDMS,isomer#18JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=C(O)C(N)CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar4132.0576
RI01719464Lysyl-Lysine,5TBDMS,isomer#17JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=C(O)C(CCCCN)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3868.0898
RI01719463Lysyl-Lysine,5TBDMS,isomer#16JsmolCC(C)(C)[Si](C)(C)NCCCCC(N=C(O)C(CCCCN[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3606.881
RI01719462Lysyl-Lysine,5TBDMS,isomer#15JsmolCC(C)(C)[Si](C)(C)NCCCCC(N=C(O)C(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3655.5684
RI01719461Lysyl-Lysine,5TBDMS,isomer#14JsmolCC(C)(C)[Si](C)(C)NCCCCC(N[Si](C)(C)C(C)(C)C)C(O)=NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3656.3032
RI01719460Lysyl-Lysine,5TBDMS,isomer#13JsmolCC(C)(C)[Si](C)(C)OC(=NC(CCCCN)C(=O)O)C(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3816.9934
RI01719459Lysyl-Lysine,5TBDMS,isomer#12JsmolCC(C)(C)[Si](C)(C)OC(=NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)C(N)CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar4049.5996
RI01719458Lysyl-Lysine,5TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)OC(=NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)C(CCCCN)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3817.6035
RI01719457Lysyl-Lysine,5TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)NCCCCC(N=C(O[Si](C)(C)C(C)(C)C)C(CCCCN[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS844.6329Standard polar3573.6104
RI01719456Lysyl-Lysine,5TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)NCCCCC(N=C(O[Si](C)(C)C(C)(C)C)C(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)OTBDMS844.6329Standard polar3605.5303
RI01719455Lysyl-Lysine,5TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)NCCCCC(N[Si](C)(C)C(C)(C)C)C(=NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3606.3403
RI01719454Lysyl-Lysine,5TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)NCCCCC(C(=NC(CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3707.2556
RI01719453Lysyl-Lysine,5TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=NC(CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar3746.425
RI01719452Lysyl-Lysine,5TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)NCCCCC(N)C(=NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS844.6329Standard polar4018.8613
Displaying retention index compounds 4701 - 4725 of 1722868 in total