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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 5826 - 5850 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01718351Histidinyl-Asparagine,4TMS,isomer#9JsmolC[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C)C(=NC(CC(=N)O)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS557.2705Standard polar3716.3376
RI01718350Histidinyl-Asparagine,4TMS,isomer#8JsmolC[Si](C)(C)OC(=O)C(CC(=N)O)N=C(O[Si](C)(C)C)C(CC1=CN=C[NH]1)N([Si](C)(C)C)[Si](C)(C)CTMS557.2705Standard polar3687.5386
RI01718349Histidinyl-Asparagine,4TMS,isomer#7JsmolC[Si](C)(C)N=C(CC(N=C(O[Si](C)(C)C)C(N)CC1=CN=CN1[Si](C)(C)C)C(=O)O)O[Si](C)(C)CTMS557.2705Standard polar4257.669
RI01718348Histidinyl-Asparagine,4TMS,isomer#6JsmolC[Si](C)(C)N=C(CC(N=C(O[Si](C)(C)C)C(CC1=CN=C[NH]1)N[Si](C)(C)C)C(=O)O)O[Si](C)(C)CTMS557.2705Standard polar3788.8047
RI01718347Histidinyl-Asparagine,4TMS,isomer#5JsmolC[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C)C(=NC(CC(=N)O[Si](C)(C)C)C(=O)O)O[Si](C)(C)CTMS557.2705Standard polar3892.0837
RI01718346Histidinyl-Asparagine,4TMS,isomer#4JsmolC[Si](C)(C)OC(=N)CC(N=C(O[Si](C)(C)C)C(CC1=CN=C[NH]1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS557.2705Standard polar3887.2566
RI01718345Histidinyl-Asparagine,4TMS,isomer#3JsmolC[Si](C)(C)OC(=N)CC(N=C(O[Si](C)(C)C)C(N)CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS557.2705Standard polar4352.9126
RI01718344Histidinyl-Asparagine,4TMS,isomer#2JsmolC[Si](C)(C)N=C(CC(N=C(O[Si](C)(C)C)C(N)CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS557.2705Standard polar4246.7856
RI01718343Histidinyl-Asparagine,4TMS,isomer#1JsmolC[Si](C)(C)NC(CC1=CN=C[NH]1)C(=NC(CC(=N)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS557.2705Standard polar3680.4172
RI01718342Histidinyl-Asparagine,5TBDMS,isomer#16JsmolCC(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)O[Si](C)(C)C(C)(C)CTBDMS839.5448Semi standard non polar4000.8806
RI01718341Histidinyl-Asparagine,5TBDMS,isomer#15JsmolCC(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)[Si](C)(C)C(C)(C)C)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS839.5448Semi standard non polar3990.0352
RI01718340Histidinyl-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)CTBDMS839.5448Semi standard non polar3774.319
RI01718339Histidinyl-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)CTBDMS839.5448Semi standard non polar4002.5244
RI01718338Histidinyl-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)CTBDMS839.5448Semi standard non polar3858.6072
RI01718337Histidinyl-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)OTBDMS839.5448Semi standard non polar3997.6055
RI01718336Histidinyl-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)CTBDMS839.5448Semi standard non polar3756.1143
RI01718335Histidinyl-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)CTBDMS839.5448Semi standard non polar3961.0254
RI01718334Histidinyl-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)CTBDMS839.5448Semi standard non polar3873.6128
RI01718333Histidinyl-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)CTBDMS839.5448Semi standard non polar3772.5127
RI01718332Histidinyl-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)OTBDMS839.5448Semi standard non polar4021.5198
RI01718331Histidinyl-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)CTBDMS839.5448Semi standard non polar3878.605
RI01718330Histidinyl-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)CTBDMS839.5448Semi standard non polar3748.6836
RI01718329Histidinyl-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)CTBDMS839.5448Semi standard non polar3622.8137
RI01718328Histidinyl-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)CTBDMS839.5448Semi standard non polar3790.0571
RI01718327Histidinyl-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)CTBDMS839.5448Semi standard non polar3873.9695
Displaying retention index compounds 5826 - 5850 of 1722868 in total