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

Displaying retention index compounds 10826 - 10850 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
L-histidinol-phosphate,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N([C@H](COP(=O)(O)O)CC1=C[NH]C=N1)[Si](C)(C)C(C)(C)CTBDMS449.2295Standard polar3423.072
L-histidinol-phosphate,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1TBDMS449.2295Standard polar3306.5483
L-histidinol-phosphate,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)CC1=C[NH]C=N1TBDMS449.2295Standard polar3149.6418
L-histidinol-phosphate,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OP(=O)(OC[C@@H](N)CC1=C[NH]C=N1)O[Si](C)(C)C(C)(C)CTBDMS449.2295Standard polar3134.2893
L-histidinol-phosphate,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1C=NC(C[C@H](N)COP(=O)(O)O)=C1TBDMS335.143Standard polar3810.3909
L-histidinol-phosphate,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N[C@H](COP(=O)(O)O)CC1=C[NH]C=N1TBDMS335.143Standard polar3623.0657
L-histidinol-phosphate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@@H](N)CC1=C[NH]C=N1TBDMS335.143Standard polar3483.121
L-histidinol-phosphate,5TMS,isomer#1JsmolC[Si](C)(C)OP(=O)(OC[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)CTMS581.2542Standard polar2570.8228
L-histidinol-phosphate,4TMS,isomer#3JsmolC[Si](C)(C)OP(=O)(O)OC[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)CTMS509.2146Standard polar2832.5405
L-histidinol-phosphate,4TMS,isomer#2JsmolC[Si](C)(C)N[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)CC1=CN([Si](C)(C)C)C=N1TMS509.2146Standard polar2599.8845
L-histidinol-phosphate,4TMS,isomer#1JsmolC[Si](C)(C)OP(=O)(OC[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)CTMS509.2146Standard polar2541.3096
L-histidinol-phosphate,3TMS,isomer#5JsmolC[Si](C)(C)N([C@H](COP(=O)(O)O)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)CTMS437.1751Standard polar3243.1152
L-histidinol-phosphate,3TMS,isomer#4JsmolC[Si](C)(C)N[C@H](COP(=O)(O)O[Si](C)(C)C)CC1=CN([Si](C)(C)C)C=N1TMS437.1751Standard polar2922.5125
L-histidinol-phosphate,3TMS,isomer#3JsmolC[Si](C)(C)OP(=O)(O)OC[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)CTMS437.1751Standard polar2877.7976
L-histidinol-phosphate,3TMS,isomer#2JsmolC[Si](C)(C)OP(=O)(OC[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)O[Si](C)(C)CTMS437.1751Standard polar2902.0105
L-histidinol-phosphate,3TMS,isomer#1JsmolC[Si](C)(C)N[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)CC1=C[NH]C=N1TMS437.1751Standard polar2612.7776
L-histidinol-phosphate,2TMS,isomer#5JsmolC[Si](C)(C)N[C@H](COP(=O)(O)O)CC1=CN([Si](C)(C)C)C=N1TMS365.1356Standard polar3396.5955
L-histidinol-phosphate,2TMS,isomer#4JsmolC[Si](C)(C)N([C@H](COP(=O)(O)O)CC1=C[NH]C=N1)[Si](C)(C)CTMS365.1356Standard polar3410.4927
L-histidinol-phosphate,2TMS,isomer#3JsmolC[Si](C)(C)OP(=O)(O)OC[C@@H](N)CC1=CN([Si](C)(C)C)C=N1TMS365.1356Standard polar3194.8804
L-histidinol-phosphate,2TMS,isomer#2JsmolC[Si](C)(C)N[C@H](COP(=O)(O)O[Si](C)(C)C)CC1=C[NH]C=N1TMS365.1356Standard polar2990.5186
L-histidinol-phosphate,2TMS,isomer#1JsmolC[Si](C)(C)OP(=O)(OC[C@@H](N)CC1=C[NH]C=N1)O[Si](C)(C)CTMS365.1356Standard polar2994.6775
L-histidinol-phosphate,1TMS,isomer#3JsmolC[Si](C)(C)N1C=NC(C[C@H](N)COP(=O)(O)O)=C1TMS293.0961Standard polar3770.73
L-histidinol-phosphate,1TMS,isomer#2JsmolC[Si](C)(C)N[C@H](COP(=O)(O)O)CC1=C[NH]C=N1TMS293.0961Standard polar3629.8997
L-histidinol-phosphate,1TMS,isomer#1JsmolC[Si](C)(C)OP(=O)(O)OC[C@@H](N)CC1=C[NH]C=N1TMS293.0961Standard polar3389.324
L-histidinol-phosphate,5TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OP(=O)(OC[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS791.4889Semi standard non polar3537.328
Displaying retention index compounds 10826 - 10850 of 1722868 in total