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Displaying retention index compounds 5251 - 5275 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
L-Cystathionine,2TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)N([C@@H](CSCC[C@H](N)C(=O)O)C(=O)O)[Si](C)(C)C(C)(C)CTBDMS450.2404Semi standard non polar2746.6414
L-CystathionineJsmolN[C@@H](CCSC[C@H](N)C(O)=O)C(O)=OUnderivatized222.0674Standard polar3020.9333
L-Cystathionine,3TMS,isomer#1JsmolC[Si](C)(C)N[C@@H](CCSC[C@H](N)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS438.186Standard non polar2202.3
L-Cystathionine,3TMS,isomer#2JsmolC[Si](C)(C)N[C@@H](CSCC[C@H](N)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS438.186Standard non polar2221.0005
L-Cystathionine,3TMS,isomer#3JsmolC[Si](C)(C)N[C@@H](CCSC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)OTMS438.186Standard non polar2216.3723
L-Cystathionine,3TMS,isomer#4JsmolC[Si](C)(C)OC(=O)[C@H](CSCC[C@H](N)C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS438.186Standard non polar2261.6116
L-Cystathionine,3TMS,isomer#5JsmolC[Si](C)(C)OC(=O)[C@@H](N)CSCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS438.186Standard non polar2272.4248
L-Cystathionine,3TMS,isomer#6JsmolC[Si](C)(C)N[C@@H](CCSC[C@H](N[Si](C)(C)C)C(=O)O)C(=O)O[Si](C)(C)CTMS438.186Standard non polar2217.169
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 non polar2229.2957
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 non polar2305.0679
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 non polar2254.0662
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 non polar2269.6128
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 non polar2275.9321
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 non polar2321.9067
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 non polar2357.202
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 non polar2348.4854
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 non polar2335.3645
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 non polar2324.178
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 non polar2361.1619
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 non polar2420.1692
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 non polar2372.932
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 non polar2385.85
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 non polar2470.3098
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 non polar2469.406
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 non polar2486.155
Displaying retention index compounds 5251 - 5275 of 1722868 in total