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Displaying retention index compounds 5351 - 5375 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
L-Cystathionine,3TMS,isomer#7JsmolC[Si](C)(C)OC(=O)[C@H](CCSC[C@H](N)C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS438.186Standard polar3450.0547
L-Cystathionine,3TMS,isomer#8JsmolC[Si](C)(C)OC(=O)[C@@H](N)CCSC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS438.186Standard polar3343.138
L-Cystathionine,3TMS,isomer#9JsmolC[Si](C)(C)N[C@@H](CSCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS438.186Standard polar3152.0532
L-Cystathionine,3TMS,isomer#10JsmolC[Si](C)(C)N[C@@H](CCSC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS438.186Standard polar3108.194
L-Cystathionine,4TMS,isomer#1JsmolC[Si](C)(C)N[C@@H](CCSC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS510.2255Standard polar2605.5361
L-Cystathionine,4TMS,isomer#2JsmolC[Si](C)(C)OC(=O)[C@H](CCSC[C@H](N)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS510.2255Standard polar3061.0615
L-Cystathionine,4TMS,isomer#3JsmolC[Si](C)(C)OC(=O)[C@@H](N)CCSC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS510.2255Standard polar3116.2642
L-Cystathionine,4TMS,isomer#4JsmolC[Si](C)(C)N[C@@H](CSCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS510.2255Standard polar2756.4646
L-Cystathionine,4TMS,isomer#5JsmolC[Si](C)(C)N[C@@H](CCSC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS510.2255Standard polar2774.7185
L-Cystathionine,4TMS,isomer#6JsmolC[Si](C)(C)N[C@@H](CSCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS510.2255Standard polar2806.8335
L-Cystathionine,4TMS,isomer#7JsmolC[Si](C)(C)N[C@@H](CCSC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS510.2255Standard polar2724.135
L-Cystathionine,4TMS,isomer#8JsmolC[Si](C)(C)N([C@@H](CCSC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)CTMS510.2255Standard polar2874.256
L-Cystathionine,5TMS,isomer#1JsmolC[Si](C)(C)N[C@@H](CSCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS582.2651Standard polar2478.0308
L-Cystathionine,5TMS,isomer#2JsmolC[Si](C)(C)N[C@@H](CCSC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS582.2651Standard polar2445.0693
L-Cystathionine,5TMS,isomer#3JsmolC[Si](C)(C)OC(=O)[C@H](CSCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS582.2651Standard polar2577.8535
L-Cystathionine,5TMS,isomer#4JsmolC[Si](C)(C)OC(=O)[C@H](CCSC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS582.2651Standard polar2578.0437
L-Cystathionine,6TMS,isomer#1JsmolC[Si](C)(C)OC(=O)[C@H](CCSC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS654.3046Standard polar2389.8804
L-Cystathionine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N[C@@H](CCSC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS564.3269Standard polar3247.7944
L-Cystathionine,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N[C@@H](CSCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)CTBDMS564.3269Standard polar3307.515
L-Cystathionine,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N[C@@H](CCSC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)OTBDMS564.3269Standard polar3116.2244
L-Cystathionine,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@H](CSCC[C@H](N)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS564.3269Standard polar3450.0928
L-Cystathionine,3TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CSCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS564.3269Standard polar3279.463
L-Cystathionine,3TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)N[C@@H](CCSC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)O[Si](C)(C)C(C)(C)CTBDMS564.3269Standard polar3116.6619
L-Cystathionine,3TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@H](CCSC[C@H](N)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS564.3269Standard polar3390.968
L-Cystathionine,3TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCSC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS564.3269Standard polar3332.8708
Displaying retention index compounds 5351 - 5375 of 1722868 in total