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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 5751 - 5775 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01718426Histidinyl-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 polar3931.2805
RI01718425Histidinyl-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 polar3800.9824
RI01718424Histidinyl-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 polar3692.16
RI01718423Histidinyl-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 polar3700.5742
RI01718422Histidinyl-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 polar3787.686
RI01718421Histidinyl-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 polar3810.8591
RI01718420Histidinyl-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 polar3700.3997
RI01718419Histidinyl-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 polar4182.7427
RI01718418Histidinyl-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 polar3562.7712
RI01718417Histidinyl-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 polar3687.2788
RI01718416Histidinyl-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 polar3572.387
RI01718415Histidinyl-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 polar4123.3784
RI01718414Histidinyl-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 polar4040.8877
RI01718413Histidinyl-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 polar3959.0654
RI01718412Histidinyl-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 polar3991.7861
RI01718411Histidinyl-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 polar3995.237
RI01718410Histidinyl-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 polar4041.8489
RI01718409Histidinyl-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 polar3953.0195
RI01718408Histidinyl-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 polar4335.5527
RI01718407Histidinyl-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 polar3869.2124
RI01718406Histidinyl-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 polar3960.3325
RI01718405Histidinyl-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 polar3909.2344
RI01718404Histidinyl-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)OTBDMS725.4583Standard polar4009.3909
RI01718403Histidinyl-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)CTBDMS725.4583Standard polar3943.7385
RI01718402Histidinyl-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)OTBDMS725.4583Standard polar3977.9756
Displaying retention index compounds 5751 - 5775 of 1722868 in total