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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14326 - 14350 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017098515-androstene-3,17-dione,2TBDMS,isomer#1JsmolCC12CC=C(O[Si](C)(C)C(C)(C)C)CC1=CCC1C2CCC2(C)C(O[Si](C)(C)C(C)(C)C)=CCC12TBDMS514.3662Standard non polar2844.5974
RI017098505-androstene-3,17-dione,1TBDMS,isomer#3JsmolCC12CCC(=O)CC1=CCC1C2CCC2(C)C(O[Si](C)(C)C(C)(C)C)=CCC12TBDMS400.2798Standard non polar2591.9773
RI017098495-androstene-3,17-dione,1TBDMS,isomer#2JsmolCC12CCC3C(CC=C4C=C(O[Si](C)(C)C(C)(C)C)CCC43C)C1CCC2=OTBDMS400.2798Standard non polar2816.3225
RI017098485-androstene-3,17-dione,1TBDMS,isomer#1JsmolCC12CCC3C(CC=C4CC(O[Si](C)(C)C(C)(C)C)=CCC43C)C1CCC2=OTBDMS400.2798Standard non polar2724.7915
RI017098475-androstene-3,17-dione,2TMS,isomer#2JsmolCC12CCC(O[Si](C)(C)C)=CC1=CCC1C2CCC2(C)C(O[Si](C)(C)C)=CCC12TMS430.2723Standard non polar2636.679
RI017098465-androstene-3,17-dione,2TMS,isomer#1JsmolCC12CC=C(O[Si](C)(C)C)CC1=CCC1C2CCC2(C)C(O[Si](C)(C)C)=CCC12TMS430.2723Standard non polar2554.7852
RI017098455-androstene-3,17-dione,1TMS,isomer#3JsmolCC12CCC(=O)CC1=CCC1C2CCC2(C)C(O[Si](C)(C)C)=CCC12TMS358.2328Standard non polar2428.9448
RI017098445-androstene-3,17-dione,1TMS,isomer#2JsmolCC12CCC3C(CC=C4C=C(O[Si](C)(C)C)CCC43C)C1CCC2=OTMS358.2328Standard non polar2573.0254
RI017098435-androstene-3,17-dione,1TMS,isomer#1JsmolCC12CCC3C(CC=C4CC(O[Si](C)(C)C)=CCC43C)C1CCC2=OTMS358.2328Standard non polar2498.8623
RI017098425-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#25JsmolCC(C)(C)[Si](C)(C)NC1=C(N(C2OC(COP(=O)([O-])[O-])C(O)C2O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS808.389Standard polar4237.392
RI017098415-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#24JsmolCC(C)(C)[Si](C)(C)N(C1=C(NC2OC(COP(=O)([O-])[O-])C(O)C2O)N([Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)C1=O)[Si](C)(C)C(C)(C)CTBDMS808.389Standard polar4155.6743
RI017098405-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#23JsmolCC(C)(C)[Si](C)(C)N(C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)C(=O)[NH]1)C1OC(COP(=O)([O-])[O-])C(O)C1OTBDMS808.389Standard polar4074.1526
RI017098395-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#22JsmolCC(C)(C)[Si](C)(C)N(C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[NH]C(=O)N1[Si](C)(C)C(C)(C)C)C1OC(COP(=O)([O-])[O-])C(O)C1OTBDMS808.389Standard polar4057.3572
RI017098385-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#21JsmolCC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)([O-])[O-])OC1N(C1=C(N)C(=O)N([Si](C)(C)C(C)(C)C)C(=O)N1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS808.389Standard polar4647.1797
RI017098375-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#20JsmolCC(C)(C)[Si](C)(C)NC1=C(NC2OC(COP(=O)([O-])[O-])C(O)C2O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS808.389Standard polar4217.0225
RI017098365-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#19JsmolCC(C)(C)[Si](C)(C)NC1=C(N(C2OC(COP(=O)([O-])[O-])C(O)C2O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS808.389Standard polar4198.8906
RI017098355-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#18JsmolCC(C)(C)[Si](C)(C)NC1=C(N(C2OC(COP(=O)([O-])[O-])C(O)C2O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C(=O)[NH]C1=OTBDMS808.389Standard polar4274.376
RI017098345-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#17JsmolCC(C)(C)[Si](C)(C)OC1C(NC2=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)C(=O)[NH]2)OC(COP(=O)([O-])[O-])C1OTBDMS808.389Standard polar4064.8257
RI017098335-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#16JsmolCC(C)(C)[Si](C)(C)OC1C(NC2=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[NH]C(=O)N2[Si](C)(C)C(C)(C)C)OC(COP(=O)([O-])[O-])C1OTBDMS808.389Standard polar4012.6516
RI017098325-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#15JsmolCC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)([O-])[O-])OC1N(C1=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[NH]C(=O)[NH]1)[Si](C)(C)C(C)(C)CTBDMS808.389Standard polar3948.4387
RI017098315-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#14JsmolCC(C)(C)[Si](C)(C)OC1C(COP(=O)([O-])[O-])OC(N(C2=C(N)C(=O)N([Si](C)(C)C(C)(C)C)C(=O)N2[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C1OTBDMS808.389Standard polar4637.883
RI017098305-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#13JsmolCC(C)(C)[Si](C)(C)NC1=C(NC2OC(COP(=O)([O-])[O-])C(O[Si](C)(C)C(C)(C)C)C2O)N([Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS808.389Standard polar4217.821
RI017098295-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#12JsmolCC(C)(C)[Si](C)(C)NC1=C(N(C2OC(COP(=O)([O-])[O-])C(O[Si](C)(C)C(C)(C)C)C2O)[Si](C)(C)C(C)(C)C)[NH]C(=O)N([Si](C)(C)C(C)(C)C)C1=OTBDMS808.389Standard polar4195.3037
RI017098285-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#11JsmolCC(C)(C)[Si](C)(C)NC1=C(N(C2OC(COP(=O)([O-])[O-])C(O[Si](C)(C)C(C)(C)C)C2O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)C(=O)[NH]C1=OTBDMS808.389Standard polar4271.407
RI017098275-amino-6-(5-phospho-D-ribosylamino)uracil,4TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)OC1C(COP(=O)([O-])[O-])OC(NC2=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)N([Si](C)(C)C(C)(C)C)C(=O)[NH]2)C1OTBDMS808.389Standard polar4077.0942
Displaying retention index compounds 14326 - 14350 of 1722868 in total