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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 5851 - 5875 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01718326Histidinyl-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)OTBDMS725.4583Semi standard non polar3840.5044
RI01718325Histidinyl-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)CTBDMS725.4583Semi standard non polar3671.8755
RI01718324Histidinyl-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)CTBDMS725.4583Semi standard non polar3830.1802
RI01718323Histidinyl-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)CTBDMS725.4583Semi standard non polar3718.9316
RI01718322Histidinyl-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)CTBDMS725.4583Semi standard non polar3646.8271
RI01718321Histidinyl-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)OTBDMS725.4583Semi standard non polar3858.997
RI01718320Histidinyl-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)CTBDMS725.4583Semi standard non polar3706.4753
RI01718319Histidinyl-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)CTBDMS725.4583Semi standard non polar3613.9058
RI01718318Histidinyl-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)CTBDMS725.4583Semi standard non polar3541.1875
RI01718317Histidinyl-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)CTBDMS725.4583Semi standard non polar3666.7065
RI01718316Histidinyl-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)CTBDMS725.4583Semi standard non polar3726.4246
RI01718315Histidinyl-Asparagine,4TBDMS,isomer#14JsmolCC(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)OTBDMS725.4583Semi standard non polar3641.4019
RI01718314Histidinyl-Asparagine,4TBDMS,isomer#13JsmolCC(C)(C)[Si](C)(C)OC(=NC(CC(=N)O)C(=O)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)CTBDMS725.4583Semi standard non polar3847.614
RI01718313Histidinyl-Asparagine,4TBDMS,isomer#12JsmolCC(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)OTBDMS725.4583Semi standard non polar3722.4258
RI01718312Histidinyl-Asparagine,4TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)N=C(O)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)CTBDMS725.4583Semi standard non polar3624.3513
RI01718311Histidinyl-Asparagine,4TBDMS,isomer#10JsmolCC(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)C(=O)O[Si](C)(C)C(C)(C)CTBDMS725.4583Semi standard non polar3536.61
RI01718310Histidinyl-Asparagine,4TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=NC(CC(=N)O)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS725.4583Semi standard non polar3629.6165
RI01718309Histidinyl-Asparagine,4TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC(=N)O)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)CTBDMS725.4583Semi standard non polar3687.809
RI01718308Histidinyl-Asparagine,4TBDMS,isomer#7JsmolCC(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)O[Si](C)(C)C(C)(C)CTBDMS725.4583Semi standard non polar3639.394
RI01718307Histidinyl-Asparagine,4TBDMS,isomer#6JsmolCC(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)O[Si](C)(C)C(C)(C)CTBDMS725.4583Semi standard non polar3539.8174
RI01718306Histidinyl-Asparagine,4TBDMS,isomer#5JsmolCC(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)O[Si](C)(C)C(C)(C)CTBDMS725.4583Semi standard non polar3678.692
RI01718305Histidinyl-Asparagine,4TBDMS,isomer#4JsmolCC(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)OTBDMS725.4583Semi standard non polar3741.711
RI01718304Histidinyl-Asparagine,4TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=N)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)CTBDMS725.4583Semi standard non polar3657.4387
RI01718303Histidinyl-Asparagine,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N=C(CC(N=C(O[Si](C)(C)C(C)(C)C)C(N)CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS725.4583Semi standard non polar3510.3857
RI01718302Histidinyl-Asparagine,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC(CC1=CN=C[NH]1)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)CTBDMS725.4583Semi standard non polar3575.2742
Displaying retention index compounds 5851 - 5875 of 1722868 in total