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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 9801 - 9825 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01714376S-sulfanylglutathione,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSS)NC(=O)CCC([N+])C(=O)[O-]TBDMS449.1116Standard non polar3040.8784
RI01714375S-sulfanylglutathione,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CSS)C(=O)NCC(=O)[O-]TBDMS449.1116Standard non polar3049.2717
RI01714374S-sulfanylglutathione,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)SSCC(NC(=O)CCC([N+])C(=O)[O-])C(=O)NCC(=O)[O-]TBDMS449.1116Standard non polar3141.7292
RI01714373S-sulfanylglutathione,3TMS,isomer#1JsmolC[Si](C)(C)SSCC(C(=O)N(CC(=O)[O-])[Si](C)(C)C)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)CTMS551.1437Standard non polar3044.5747
RI01714372S-sulfanylglutathione,2TMS,isomer#3JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSS)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)CTMS479.1042Standard non polar2891.6296
RI01714371S-sulfanylglutathione,2TMS,isomer#2JsmolC[Si](C)(C)SSCC(NC(=O)CCC([N+])C(=O)[O-])C(=O)N(CC(=O)[O-])[Si](C)(C)CTMS479.1042Standard non polar2983.0342
RI01714370S-sulfanylglutathione,2TMS,isomer#1JsmolC[Si](C)(C)SSCC(C(=O)NCC(=O)[O-])N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)CTMS479.1042Standard non polar2995.5334
RI01714369S-sulfanylglutathione,1TMS,isomer#3JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSS)NC(=O)CCC([N+])C(=O)[O-]TMS407.0647Standard non polar2821.1567
RI01714368S-sulfanylglutathione,1TMS,isomer#2JsmolC[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CSS)C(=O)NCC(=O)[O-]TMS407.0647Standard non polar2815.6565
RI01714367S-sulfanylglutathione,1TMS,isomer#1JsmolC[Si](C)(C)SSCC(NC(=O)CCC([N+])C(=O)[O-])C(=O)NCC(=O)[O-]TMS407.0647Standard non polar2924.3892
RI01714366S-adenosyl-L-methioninamine,4TBDMS,isomer#1JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS812.5079Standard polar3732.416
RI01714365S-adenosyl-L-methioninamine,3TBDMS,isomer#3JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS698.4214Standard polar3932.2002
RI01714364S-adenosyl-L-methioninamine,3TBDMS,isomer#2JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1OTBDMS698.4214Standard polar3957.1838
RI01714363S-adenosyl-L-methioninamine,3TBDMS,isomer#1JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N[Si](C)(C)C(C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS698.4214Standard polar4161.032
RI01714362S-adenosyl-L-methioninamine,4TMS,isomer#1JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)CTMS644.3201Standard polar3589.1199
RI01714361S-adenosyl-L-methioninamine,3TMS,isomer#3JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)[C@H](O)[C@@H]1O[Si](C)(C)CTMS572.2805Standard polar3871.4927
RI01714360S-adenosyl-L-methioninamine,3TMS,isomer#2JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C)[C@@H]1OTMS572.2805Standard polar3896.6177
RI01714359S-adenosyl-L-methioninamine,3TMS,isomer#1JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N[Si](C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)CTMS572.2805Standard polar4110.764
RI01714358S-adenosyl-L-methioninamine,4TBDMS,isomer#1JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS812.5079Semi standard non polar3779.7734
RI01714357S-adenosyl-L-methioninamine,3TBDMS,isomer#3JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS698.4214Semi standard non polar3654.1133
RI01714356S-adenosyl-L-methioninamine,3TBDMS,isomer#2JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1OTBDMS698.4214Semi standard non polar3647.8333
RI01714355S-adenosyl-L-methioninamine,3TBDMS,isomer#1JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N[Si](C)(C)C(C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)CTBDMS698.4214Semi standard non polar3681.7312
RI01714354S-adenosyl-L-methioninamine,4TMS,isomer#1JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)CTMS644.3201Semi standard non polar3130.1223
RI01714353S-adenosyl-L-methioninamine,3TMS,isomer#3JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)[C@H](O)[C@@H]1O[Si](C)(C)CTMS572.2805Semi standard non polar3137.3704
RI01714352S-adenosyl-L-methioninamine,3TMS,isomer#2JsmolC[S+](CCC[NH3+])C[C@H]1O[C@@H](N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)[C@H](O[Si](C)(C)C)[C@@H]1OTMS572.2805Semi standard non polar3127.979
Displaying retention index compounds 9801 - 9825 of 1722868 in total