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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 5926 - 5950 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01718251Histidinyl-Asparagine,5TBDMS,isomer#14JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3372.452
RI01718250Histidinyl-Asparagine,5TBDMS,isomer#13JsmolCC(C)(C)[Si](C)(C)OC(=N)CC(N=C(O)C(CC1=CN=CN1[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)CTBDMS839.5448Standard non polar3555.7607
RI01718249Histidinyl-Asparagine,5TBDMS,isomer#12JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O)C(CC1=CN=C[NH]1)N([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)CTBDMS839.5448Standard non polar3352.8425
RI01718248Histidinyl-Asparagine,5TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)N=C(O)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS839.5448Standard non polar3423.8665
RI01718247Histidinyl-Asparagine,5TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)N=C(O)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3312.2473
RI01718246Histidinyl-Asparagine,5TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC(=N)O)N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3523.491
RI01718245Histidinyl-Asparagine,5TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)N=C(O)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CN=C[NH]1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3298.3132
RI01718244Histidinyl-Asparagine,5TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3252.4827
RI01718243Histidinyl-Asparagine,5TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)OC(=N)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS839.5448Standard non polar3467.1199
RI01718242Histidinyl-Asparagine,5TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CN=C[NH]1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3239.2395
RI01718241Histidinyl-Asparagine,5TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O[Si](C)(C)C(C)(C)C)C(N)CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3244.1052
RI01718240Histidinyl-Asparagine,5TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CN=C[NH]1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3151.7378
RI01718239Histidinyl-Asparagine,5TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=NC(CC(=N)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3360.1943
RI01718238Histidinyl-Asparagine,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=N)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CN=C[NH]1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS839.5448Standard non polar3336.9768
RI01718237Histidinyl-Asparagine,4TBDMS,isomer#25JsmolCC(C)(C)[Si](C)(C)N=C(O)CC(N=C(O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS725.4583Standard non polar3411.6719
RI01718236Histidinyl-Asparagine,4TBDMS,isomer#24JsmolCC(C)(C)[Si](C)(C)N=C(O)CC(N=C(O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS725.4583Standard non polar3276.7715
RI01718235Histidinyl-Asparagine,4TBDMS,isomer#23JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC(=N)O)N=C(O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS725.4583Standard non polar3445.7917
RI01718234Histidinyl-Asparagine,4TBDMS,isomer#22JsmolCC(C)(C)[Si](C)(C)N=C(O)CC(N=C(O)C(CC1=CN=C[NH]1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS725.4583Standard non polar3281.5076
RI01718233Histidinyl-Asparagine,4TBDMS,isomer#21JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS725.4583Standard non polar3234.261
RI01718232Histidinyl-Asparagine,4TBDMS,isomer#20JsmolCC(C)(C)[Si](C)(C)OC(=N)CC(N=C(O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)OTBDMS725.4583Standard non polar3412.409
RI01718231Histidinyl-Asparagine,4TBDMS,isomer#19JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O)C(CC1=CN=C[NH]1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS725.4583Standard non polar3235.4673
RI01718230Histidinyl-Asparagine,4TBDMS,isomer#18JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O)C(N)CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS725.4583Standard non polar3221.8066
RI01718229Histidinyl-Asparagine,4TBDMS,isomer#17JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O)C(CC1=CN=C[NH]1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS725.4583Standard non polar3127.5193
RI01718228Histidinyl-Asparagine,4TBDMS,isomer#16JsmolCC(C)(C)[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(O)=NC(CC(=N)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS725.4583Standard non polar3287.0217
RI01718227Histidinyl-Asparagine,4TBDMS,isomer#15JsmolCC(C)(C)[Si](C)(C)OC(=N)CC(N=C(O)C(CC1=CN=C[NH]1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS725.4583Standard non polar3285.1748
Displaying retention index compounds 5926 - 5950 of 1722868 in total