Displaying retention index compounds 451 - 475 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Ureidopropionic acid,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(CCC(=O)O)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS474.3129Standard polar2223.2847
Ureidopropionic acid,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)CCN(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS588.3994Standard polar2209.513
Tetrahydrobiopterin,1TMS,isomer#1JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N)[NH]2TMS313.157Semi standard non polar2576.166
Tetrahydrobiopterin,1TMS,isomer#2JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N)[NH]2TMS313.157Semi standard non polar2606.1763
Tetrahydrobiopterin,1TMS,isomer#3JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N[Si](C)(C)C)[NH]2TMS313.157Semi standard non polar2673.9941
Tetrahydrobiopterin,1TMS,isomer#4JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N)[NH]2TMS313.157Semi standard non polar2498.7903
Tetrahydrobiopterin,1TMS,isomer#5JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N)[NH]2)N1[Si](C)(C)CTMS313.157Semi standard non polar2485.8284
Tetrahydrobiopterin,1TMS,isomer#6JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N)N2[Si](C)(C)CTMS313.157Semi standard non polar2554.3755
Tetrahydrobiopterin,2TMS,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)[NH]2TMS385.1965Semi standard non polar2536.5642
Tetrahydrobiopterin,2TMS,isomer#2JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N[Si](C)(C)C)[NH]2TMS385.1965Semi standard non polar2517.2812
Tetrahydrobiopterin,2TMS,isomer#3JsmolC[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)[NH]2TMS385.1965Semi standard non polar2417.1108
Tetrahydrobiopterin,2TMS,isomer#4JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N)N2[Si](C)(C)CTMS385.1965Semi standard non polar2497.0322
Tetrahydrobiopterin,2TMS,isomer#5JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N)[NH]2)N1[Si](C)(C)CTMS385.1965Semi standard non polar2418.5002
Tetrahydrobiopterin,2TMS,isomer#6JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N[Si](C)(C)C)[NH]2TMS385.1965Semi standard non polar2537.4277
Tetrahydrobiopterin,2TMS,isomer#7JsmolC[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)[NH]2TMS385.1965Semi standard non polar2439.7322
Tetrahydrobiopterin,2TMS,isomer#8JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N)N2[Si](C)(C)CTMS385.1965Semi standard non polar2509.1978
Tetrahydrobiopterin,2TMS,isomer#9JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N)[NH]2)N1[Si](C)(C)CTMS385.1965Semi standard non polar2452.9941
Tetrahydrobiopterin,2TMS,isomer#10JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N[Si](C)(C)C)[NH]2TMS385.1965Semi standard non polar2497.7883
Tetrahydrobiopterin,2TMS,isomer#11JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)CTMS385.1965Semi standard non polar2542.6873
Tetrahydrobiopterin,2TMS,isomer#12JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2TMS385.1965Semi standard non polar2607.9136
Tetrahydrobiopterin,2TMS,isomer#13JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS385.1965Semi standard non polar2480.9048
Tetrahydrobiopterin,2TMS,isomer#14JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(N1)C(=O)N=C(N)N2[Si](C)(C)CTMS385.1965Semi standard non polar2455.9216
Tetrahydrobiopterin,2TMS,isomer#15JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N)[NH]2)N1[Si](C)(C)CTMS385.1965Semi standard non polar2357.6416
Tetrahydrobiopterin,2TMS,isomer#16JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1[Si](C)(C)CTMS385.1965Semi standard non polar2429.5645
Tetrahydrobiopterin,1TBDMS,isomer#1JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1CNC2=C(N1)C(=O)N=C(N)[NH]2TBDMS355.204Semi standard non polar2842.5393
Displaying retention index compounds 451 - 475 of 1722868 in total