Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 2151 - 2175 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01722026Pralsetinib,1TMS,isomer#2JsmolCO[C@]1(C(=O)N[C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)CC[C@@H](C2=NC(C)=CC(NC3=NN([Si](C)(C)C)C(C)=C3)=N2)CC1TMS605.3058Semi standard non polar4771.348
RI01722025Pralsetinib,1TMS,isomer#1JsmolCO[C@]1(C(=O)N[C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)CC[C@@H](C2=NC(C)=CC(N(C3=N[NH]C(C)=C3)[Si](C)(C)C)=N2)CC1TMS605.3058Semi standard non polar4481.8066
RI01722024Pralsetinib,3TBDMS,isomer#1JsmolCO[C@]1(C(=O)N([C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)[Si](C)(C)C(C)(C)C)CC[C@@H](C2=NC(C)=CC(N(C3=NN([Si](C)(C)C(C)(C)C)C(C)=C3)[Si](C)(C)C(C)(C)C)=N2)CC1TBDMS875.5257Standard non polar4582.61
RI01722023Pralsetinib,2TBDMS,isomer#3JsmolCO[C@]1(C(=O)N([C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)[Si](C)(C)C(C)(C)C)CC[C@@H](C2=NC(C)=CC(NC3=NN([Si](C)(C)C(C)(C)C)C(C)=C3)=N2)CC1TBDMS761.4393Standard non polar4408.8013
RI01722022Pralsetinib,2TBDMS,isomer#2JsmolCO[C@]1(C(=O)N[C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)CC[C@@H](C2=NC(C)=CC(N(C3=NN([Si](C)(C)C(C)(C)C)C(C)=C3)[Si](C)(C)C(C)(C)C)=N2)CC1TBDMS761.4393Standard non polar4372.429
RI01722021Pralsetinib,2TBDMS,isomer#1JsmolCO[C@]1(C(=O)N([C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)[Si](C)(C)C(C)(C)C)CC[C@@H](C2=NC(C)=CC(N(C3=N[NH]C(C)=C3)[Si](C)(C)C(C)(C)C)=N2)CC1TBDMS761.4393Standard non polar4312.9043
RI01722020Pralsetinib,1TBDMS,isomer#3JsmolCO[C@]1(C(=O)N([C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)[Si](C)(C)C(C)(C)C)CC[C@@H](C2=NC(C)=CC(NC3=N[NH]C(C)=C3)=N2)CC1TBDMS647.3528Standard non polar4164.562
RI01722019Pralsetinib,1TBDMS,isomer#2JsmolCO[C@]1(C(=O)N[C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)CC[C@@H](C2=NC(C)=CC(NC3=NN([Si](C)(C)C(C)(C)C)C(C)=C3)=N2)CC1TBDMS647.3528Standard non polar4231.6787
RI01722018Pralsetinib,1TBDMS,isomer#1JsmolCO[C@]1(C(=O)N[C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)CC[C@@H](C2=NC(C)=CC(N(C3=N[NH]C(C)=C3)[Si](C)(C)C(C)(C)C)=N2)CC1TBDMS647.3528Standard non polar4107.3335
RI01722017Pralsetinib,3TMS,isomer#1JsmolCO[C@]1(C(=O)N([C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)[Si](C)(C)C)CC[C@@H](C2=NC(C)=CC(N(C3=NN([Si](C)(C)C)C(C)=C3)[Si](C)(C)C)=N2)CC1TMS749.3849Standard non polar3983.2463
RI01722016Pralsetinib,2TMS,isomer#3JsmolCO[C@]1(C(=O)N([C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)[Si](C)(C)C)CC[C@@H](C2=NC(C)=CC(NC3=NN([Si](C)(C)C)C(C)=C3)=N2)CC1TMS677.3454Standard non polar3984.7866
RI01722015Pralsetinib,2TMS,isomer#2JsmolCO[C@]1(C(=O)N[C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)CC[C@@H](C2=NC(C)=CC(N(C3=NN([Si](C)(C)C)C(C)=C3)[Si](C)(C)C)=N2)CC1TMS677.3454Standard non polar3962.2607
RI01722014Pralsetinib,2TMS,isomer#1JsmolCO[C@]1(C(=O)N([C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)[Si](C)(C)C)CC[C@@H](C2=NC(C)=CC(N(C3=N[NH]C(C)=C3)[Si](C)(C)C)=N2)CC1TMS677.3454Standard non polar3895.0261
RI01722013Pralsetinib,1TMS,isomer#3JsmolCO[C@]1(C(=O)N([C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)[Si](C)(C)C)CC[C@@H](C2=NC(C)=CC(NC3=N[NH]C(C)=C3)=N2)CC1TMS605.3058Standard non polar3925.259
RI01722012Pralsetinib,1TMS,isomer#2JsmolCO[C@]1(C(=O)N[C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)CC[C@@H](C2=NC(C)=CC(NC3=NN([Si](C)(C)C)C(C)=C3)=N2)CC1TMS605.3058Standard non polar4014.2427
RI01722011Pralsetinib,1TMS,isomer#1JsmolCO[C@]1(C(=O)N[C@@H](C)C2=CC=C(N3C=C(F)C=N3)N=C2)CC[C@@H](C2=NC(C)=CC(N(C3=N[NH]C(C)=C3)[Si](C)(C)C)=N2)CC1TMS605.3058Standard non polar3899.1206
RI01722010Risdiplam,1TBDMS,isomer#1JsmolCC1=CN2N=C(C3=CC(=O)N4C=C(N5CCN([Si](C)(C)C(C)(C)C)C6(CC6)C5)C=CC4=N3)C=C(C)C2=N1TBDMS515.2829Standard polar5399.8965
RI01722009Risdiplam,1TMS,isomer#1JsmolCC1=CN2N=C(C3=CC(=O)N4C=C(N5CCN([Si](C)(C)C)C6(CC6)C5)C=CC4=N3)C=C(C)C2=N1TMS473.2359Standard polar5378.1973
RI01722008Risdiplam,1TBDMS,isomer#1JsmolCC1=CN2N=C(C3=CC(=O)N4C=C(N5CCN([Si](C)(C)C(C)(C)C)C6(CC6)C5)C=CC4=N3)C=C(C)C2=N1TBDMS515.2829Semi standard non polar4483.923
RI01722007Risdiplam,1TMS,isomer#1JsmolCC1=CN2N=C(C3=CC(=O)N4C=C(N5CCN([Si](C)(C)C)C6(CC6)C5)C=CC4=N3)C=C(C)C2=N1TMS473.2359Semi standard non polar4283.795
RI01722006Risdiplam,1TBDMS,isomer#1JsmolCC1=CN2N=C(C3=CC(=O)N4C=C(N5CCN([Si](C)(C)C(C)(C)C)C6(CC6)C5)C=CC4=N3)C=C(C)C2=N1TBDMS515.2829Standard non polar4337.7754
RI01722005Risdiplam,1TMS,isomer#1JsmolCC1=CN2N=C(C3=CC(=O)N4C=C(N5CCN([Si](C)(C)C)C6(CC6)C5)C=CC4=N3)C=C(C)C2=N1TMS473.2359Standard non polar4164.587
RI01722004Avapritinib,2TBDMS,isomer#1JsmolCN1C=C(C2=CN3N=CN=C(N4CCN(C5=NC=C([C@](C)(C6=CC=C(F)C=C6)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=N5)CC4)C3=C2)C=N1TBDMS726.4134Standard polar5890.703
RI01722003Avapritinib,1TBDMS,isomer#1JsmolCN1C=C(C2=CN3N=CN=C(N4CCN(C5=NC=C([C@@](C)(N[Si](C)(C)C(C)(C)C)C6=CC=C(F)C=C6)C=N5)CC4)C3=C2)C=N1TBDMS612.3269Standard polar6115.5537
RI01722002Avapritinib,2TMS,isomer#1JsmolCN1C=C(C2=CN3N=CN=C(N4CCN(C5=NC=C([C@](C)(C6=CC=C(F)C=C6)N([Si](C)(C)C)[Si](C)(C)C)C=N5)CC4)C3=C2)C=N1TMS642.3195Standard polar5977.068
Displaying retention index compounds 2151 - 2175 of 1722868 in total