RIpred (Beta) is still undergoing development. Please feel free to explore and use the predictor. Please provide us with your feedback..

Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 63101 - 63125 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI00063101Cytidine 5'-monophosphate-N-acetylneuraminic acid,2TBDMS,isomer#44JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](OP(=O)(OC[C@H]2O[C@@H](N3C=CC(N)=NC3=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)CTBDMS842.3202Semi standard non polar4992.9365
RI00063102Cytidine 5'-monophosphate-N-acetylneuraminic acid,2TBDMS,isomer#45JsmolCC(=O)N([C@@H]1[C@@H](O)C[C@@](OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N[Si](C)(C)C(C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)CTBDMS842.3202Semi standard non polar5137.901
RI00063103Cytidine 5'-monophosphate-N-acetylneuraminic acid,2TBDMS,isomer#46JsmolCC(=O)N[C@@H]1[C@@H](O)C[C@@](OP(=O)(O)OC[C@H]2O[C@@H](N3C=CC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC3=O)[C@H](O)[C@@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)COTBDMS842.3202Semi standard non polar5036.6772
RI00063104Cytidine 5'-monophosphate-N-acetylneuraminic acidJsmol[H][C@]1(O[C@](C[C@H](O)[C@H]1NC(C)=O)(OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(N)=NC1=O)C(O)=O)[C@H](O)[C@H](O)COUnderivatized614.1473Standard polar4816.0312
RI00063105Cytidine 5'-monophosphate-N-acetylneuraminic acidJsmol[H][C@]1(O[C@](C[C@H](O)[C@H]1NC(C)=O)(OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(N)=NC1=O)C(O)=O)[C@H](O)[C@H](O)COUnderivatized614.1473Standard non polar3975.0938
RI00063106Cytidine 5'-monophosphate-N-acetylneuraminic acidJsmol[H][C@]1(O[C@](C[C@H](O)[C@H]1NC(C)=O)(OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(N)=NC1=O)C(O)=O)[C@H](O)[C@H](O)COUnderivatized614.1473Semi standard non polar5314.0386
RI00063107(S)-Succinyldihydrolipoamide,1TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(N)=OTMS379.1307Semi standard non polar2659.7183
RI00063108(S)-Succinyldihydrolipoamide,1TMS,isomer#2JsmolC[Si](C)(C)SCC[C@@H](CCCCC(N)=O)SC(=O)CCC(=O)OTMS379.1307Semi standard non polar2781.6858
RI00063109(S)-Succinyldihydrolipoamide,1TMS,isomer#3JsmolC[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)OTMS379.1307Semi standard non polar2722.5544
RI00063110(S)-Succinyldihydrolipoamide,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(N)=OTBDMS421.1777Semi standard non polar2950.1191
RI00063111(S)-Succinyldihydrolipoamide,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)SCC[C@@H](CCCCC(N)=O)SC(=O)CCC(=O)OTBDMS421.1777Semi standard non polar3044.4756
RI00063112(S)-Succinyldihydrolipoamide,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)OTBDMS421.1777Semi standard non polar2979.3125
RI00063113(S)-SuccinyldihydrolipoamideJsmolNC(=O)CCCC[C@H](CCS)SC(=O)CCC(O)=OUnderivatized307.0912Standard polar4050.8271
RI00063114(S)-Succinyldihydrolipoamide,2TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(N)=O)CCS[Si](C)(C)CTMS451.1703Standard non polar2773.4475
RI00063115(S)-Succinyldihydrolipoamide,2TMS,isomer#2JsmolC[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O[Si](C)(C)CTMS451.1703Standard non polar2719.2463
RI00063116(S)-Succinyldihydrolipoamide,2TMS,isomer#3JsmolC[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C)SC(=O)CCC(=O)OTMS451.1703Standard non polar2846.574
RI00063117(S)-Succinyldihydrolipoamide,2TMS,isomer#4JsmolC[Si](C)(C)N(C(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O)[Si](C)(C)CTMS451.1703Standard non polar2702.6301
RI00063118(S)-Succinyldihydrolipoamide,3TMS,isomer#1JsmolC[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C)SC(=O)CCC(=O)O[Si](C)(C)CTMS523.2098Standard non polar2905.3657
RI00063119(S)-Succinyldihydrolipoamide,3TMS,isomer#2JsmolC[Si](C)(C)OC(=O)CCC(=O)S[C@@H](CCS)CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)CTMS523.2098Standard non polar2811.0955
RI00063120(S)-Succinyldihydrolipoamide,3TMS,isomer#3JsmolC[Si](C)(C)SCC[C@@H](CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C)SC(=O)CCC(=O)OTMS523.2098Standard non polar2934.7104
RI00063121(S)-Succinyldihydrolipoamide,4TMS,isomer#1JsmolC[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(=O)N([Si](C)(C)C)[Si](C)(C)C)CCS[Si](C)(C)CTMS595.2493Standard non polar2969.1597
RI00063122(S)-Succinyldihydrolipoamide,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCC(=O)S[C@H](CCCCC(N)=O)CCS[Si](C)(C)C(C)(C)CTBDMS535.2642Standard non polar3192.896
RI00063123(S)-Succinyldihydrolipoamide,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O[Si](C)(C)C(C)(C)CTBDMS535.2642Standard non polar3078.652
RI00063124(S)-Succinyldihydrolipoamide,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NC(=O)CCCC[C@H](CCS[Si](C)(C)C(C)(C)C)SC(=O)CCC(=O)OTBDMS535.2642Standard non polar3200.7083
RI00063125(S)-Succinyldihydrolipoamide,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCCC[C@H](CCS)SC(=O)CCC(=O)O)[Si](C)(C)C(C)(C)CTBDMS535.2642Standard non polar3067.6982
Displaying retention index compounds 63101 - 63125 of 1722868 in total