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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 8301 - 8325 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01715876trans-zeatin riboside triphosphate,4TMS,isomer#1JsmolCC(=CCNC1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)CO[Si](C)(C)CTMS876.1895Standard non polar3991.1353
RI01715875trans-zeatin riboside monophosphate,4TBDMS,isomer#1JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])[O-])C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[Si](C)(C)C(C)(C)CTBDMS885.452Standard polar4384.5923
RI01715874trans-zeatin riboside monophosphate,4TMS,isomer#1JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])[O-])C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS717.2642Standard polar4299.238
RI01715873trans-zeatin riboside monophosphate,4TBDMS,isomer#1JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])[O-])C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[Si](C)(C)C(C)(C)CTBDMS885.452Semi standard non polar4062.3171
RI01715872trans-zeatin riboside monophosphate,4TMS,isomer#1JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])[O-])C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS717.2642Semi standard non polar3344.903
RI01715871trans-zeatin riboside monophosphate,4TBDMS,isomer#1JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])[O-])C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[Si](C)(C)C(C)(C)CTBDMS885.452Standard non polar4143.2075
RI01715870trans-zeatin riboside monophosphate,4TMS,isomer#1JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])[O-])C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS717.2642Standard non polar3392.531
RI01715869trans-zeatin riboside diphosphate,4TMS,isomer#1JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])[O-])C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS796.2232Standard polar4798.2905
RI01715868trans-zeatin riboside diphosphate,4TMS,isomer#1JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])[O-])C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS796.2232Semi standard non polar3609.529
RI01715867trans-zeatin riboside diphosphate,4TMS,isomer#1JsmolCC(=CCN(C1=NC=NC2=C1N=CN2C1OC(COP(=O)([O-])OP(=O)([O-])[O-])C(O[Si](C)(C)C)C1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS796.2232Standard non polar3606.0356
RI01715866trans-zeatin riboside,5TMS,isomer#1JsmolC/C(=C\CN(C1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS711.3519Standard polar3703.7273
RI01715865trans-zeatin riboside,5TMS,isomer#1JsmolC/C(=C\CN(C1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS711.3519Semi standard non polar3064.077
RI01715864trans-zeatin riboside,5TMS,isomer#1JsmolC/C(=C\CN(C1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)[Si](C)(C)C)CO[Si](C)(C)CTMS711.3519Standard non polar2950.828
RI01715863tetrahydropteroyl tri-L-glutamate,1TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)N1C(N)=NC2=C(NC(CNC3=CC=C(C(=O)NC(CCC(=O)NC(CCC(=O)NC(CCC(=O)[O-])C(=O)[O-])C(=O)[O-])C(=O)[O-])C=C3)CN2)C1=OTBDMS813.3135Standard polar10018.028
RI01715862tetrahydropteroyl tri-L-glutamate,1TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)NC(CCC(=O)NC(CCC(=O)[O-])C(=O)[O-])C(=O)[O-])C(=O)[O-])C=C2)NC2=C1N=C(N)[NH]C2=OTBDMS813.3135Standard polar9821.602
RI01715861tetrahydropteroyl tri-L-glutamate,1TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC(NC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(=O)[NH]C(N)=N3)C=C1)C(=O)[O-])C(=O)[O-])C(CCC(=O)[O-])C(=O)[O-]TBDMS813.3135Standard polar9993.302
RI01715860tetrahydropteroyl tri-L-glutamate,1TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(=O)[NH]C(N)=N3)C=C1)C(=O)[O-])C(CCC(=O)NC(CCC(=O)[O-])C(=O)[O-])C(=O)[O-]TBDMS813.3135Standard polar9989.957
RI01715859tetrahydropteroyl tri-L-glutamate,1TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)N(C(=O)C1=CC=C(NCC2CNC3=C(N2)C(=O)[NH]C(N)=N3)C=C1)C(CCC(=O)NC(CCC(=O)NC(CCC(=O)[O-])C(=O)[O-])C(=O)[O-])C(=O)[O-]TBDMS813.3135Standard polar9913.544
RI01715858tetrahydropteroyl tri-L-glutamate,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(CC1CNC2=C(N1)C(=O)[NH]C(N)=N2)C1=CC=C(C(=O)NC(CCC(=O)NC(CCC(=O)NC(CCC(=O)[O-])C(=O)[O-])C(=O)[O-])C(=O)[O-])C=C1TBDMS813.3135Standard polar9908.185
RI01715857tetrahydropteroyl tri-L-glutamate,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1C2=C(N=C(N)[NH]C2=O)NCC1CNC1=CC=C(C(=O)NC(CCC(=O)NC(CCC(=O)NC(CCC(=O)[O-])C(=O)[O-])C(=O)[O-])C(=O)[O-])C=C1TBDMS813.3135Standard polar9590.239
RI01715856tetrahydropteroyl tri-L-glutamate,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC1=NC2=C(NC(CNC3=CC=C(C(=O)NC(CCC(=O)NC(CCC(=O)NC(CCC(=O)[O-])C(=O)[O-])C(=O)[O-])C(=O)[O-])C=C3)CN2)C(=O)[NH]1TBDMS813.3135Standard polar10659.417
RI01715855tetrahydropteroyl tri-L-glutamate,2TMS,isomer#29JsmolC[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)NC(CCC(=O)NC(CCC(=O)[O-])C(=O)[O-])C(=O)[O-])C(=O)[O-])C=C2)NC2=C1N=C(N)N([Si](C)(C)C)C2=OTMS843.3061Standard polar9554.033
RI01715854tetrahydropteroyl tri-L-glutamate,2TMS,isomer#28JsmolC[Si](C)(C)N(C(=O)CCC(NC(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(=O)N([Si](C)(C)C)C(N)=N3)C=C1)C(=O)[O-])C(=O)[O-])C(CCC(=O)[O-])C(=O)[O-]TMS843.3061Standard polar9784.179
RI01715853tetrahydropteroyl tri-L-glutamate,2TMS,isomer#27JsmolC[Si](C)(C)N1CC(CNC2=CC=C(C(=O)NC(CCC(=O)NC(CCC(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C(=O)[O-])C(=O)[O-])C=C2)NC2=C1N=C(N)[NH]C2=OTMS843.3061Standard polar9529.259
RI01715852tetrahydropteroyl tri-L-glutamate,2TMS,isomer#26JsmolC[Si](C)(C)N(C(=O)CCC(C(=O)[O-])N(C(=O)CCC(NC(=O)C1=CC=C(NCC2CNC3=C(N2)C(=O)[NH]C(N)=N3)C=C1)C(=O)[O-])[Si](C)(C)C)C(CCC(=O)[O-])C(=O)[O-]TMS843.3061Standard polar9785.103
Displaying retention index compounds 8301 - 8325 of 1722868 in total