Displaying retention index compounds 626 - 650 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Tetrahydrobiopterin,5TBDMS,isomer#6JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3729.1775
Tetrahydrobiopterin,5TBDMS,isomer#7JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3622.1252
Tetrahydrobiopterin,5TBDMS,isomer#8JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3783.2568
Tetrahydrobiopterin,5TBDMS,isomer#9JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3692.244
Tetrahydrobiopterin,5TBDMS,isomer#10JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3834.2202
Tetrahydrobiopterin,5TBDMS,isomer#11JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3690.4707
Tetrahydrobiopterin,5TBDMS,isomer#12JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(N1)C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3755.6099
Tetrahydrobiopterin,5TBDMS,isomer#13JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3673.5725
Tetrahydrobiopterin,5TBDMS,isomer#14JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[NH]2)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3822.0007
Tetrahydrobiopterin,5TBDMS,isomer#15JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3660.1292
Tetrahydrobiopterin,5TBDMS,isomer#16JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C(C)(C)C)C2=C(C(=O)N=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N2[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS811.5499Standard non polar3792.474
TetrahydrobiopterinJsmol[H][C@@]1(CNC2=C(N1)C(=O)N=C(N)N2)[C@@H](O)[C@H](C)OUnderivatized241.1175Standard non polar2702.632
TetrahydrobiopterinJsmol[H][C@@]1(CNC2=C(N1)C(=O)N=C(N)N2)[C@@H](O)[C@H](C)OUnderivatized241.1175Semi standard non polar2903.146
Tetrahydrobiopterin,3TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N[Si](C)(C)C)[NH]2TMS457.2361Semi standard non polar2459.623
Tetrahydrobiopterin,3TMS,isomer#2JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N)[NH]2TMS457.2361Semi standard non polar2408.1987
Tetrahydrobiopterin,3TMS,isomer#3JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N)N2[Si](C)(C)CTMS457.2361Semi standard non polar2495.9465
Tetrahydrobiopterin,3TMS,isomer#4JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N)[NH]2)N1[Si](C)(C)CTMS457.2361Semi standard non polar2420.3823
Tetrahydrobiopterin,3TMS,isomer#5JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N[Si](C)(C)C)[NH]2TMS457.2361Semi standard non polar2429.4272
Tetrahydrobiopterin,3TMS,isomer#6JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)CTMS457.2361Semi standard non polar2489.7915
Tetrahydrobiopterin,3TMS,isomer#7JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2TMS457.2361Semi standard non polar2483.2327
Tetrahydrobiopterin,3TMS,isomer#8JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS457.2361Semi standard non polar2457.536
Tetrahydrobiopterin,3TMS,isomer#9JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N)N2[Si](C)(C)CTMS457.2361Semi standard non polar2456.6982
Tetrahydrobiopterin,3TMS,isomer#10JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N)[NH]2)N1[Si](C)(C)CTMS457.2361Semi standard non polar2347.2192
Tetrahydrobiopterin,3TMS,isomer#11JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1[Si](C)(C)CTMS457.2361Semi standard non polar2462.948
Tetrahydrobiopterin,3TMS,isomer#12JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N[Si](C)(C)C)[NH]2TMS457.2361Semi standard non polar2441.8757
Displaying retention index compounds 626 - 650 of 1722868 in total