Displaying retention index compounds 651 - 675 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Tetrahydrobiopterin,3TMS,isomer#13JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)CTMS457.2361Semi standard non polar2490.953
Tetrahydrobiopterin,3TMS,isomer#14JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2TMS457.2361Semi standard non polar2509.686
Tetrahydrobiopterin,3TMS,isomer#15JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS457.2361Semi standard non polar2477.3042
Tetrahydrobiopterin,3TMS,isomer#16JsmolC[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)N2[Si](C)(C)CTMS457.2361Semi standard non polar2455.689
Tetrahydrobiopterin,3TMS,isomer#17JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N)[NH]2)N1[Si](C)(C)CTMS457.2361Semi standard non polar2369.1624
Tetrahydrobiopterin,3TMS,isomer#18JsmolC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1[Si](C)(C)CTMS457.2361Semi standard non polar2474.805
Tetrahydrobiopterin,3TMS,isomer#19JsmolC[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)N2[Si](C)(C)CTMS457.2361Semi standard non polar2479.2776
Tetrahydrobiopterin,3TMS,isomer#20JsmolC[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)[Si](C)(C)C)[NH]2TMS457.2361Semi standard non polar2473.945
Tetrahydrobiopterin,3TMS,isomer#21JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS457.2361Semi standard non polar2424.8335
Tetrahydrobiopterin,3TMS,isomer#22JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(N1)C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)N2[Si](C)(C)CTMS457.2361Semi standard non polar2546.8945
Tetrahydrobiopterin,3TMS,isomer#23JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS457.2361Semi standard non polar2474.2195
Tetrahydrobiopterin,3TMS,isomer#24JsmolC[C@H](O)[C@H](O)[C@H]1CNC2=C(C(=O)N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS457.2361Semi standard non polar2476.176
Tetrahydrobiopterin,3TMS,isomer#25JsmolC[C@H](O)[C@H](O)[C@H]1CN([Si](C)(C)C)C2=C(C(=O)N=C(N)N2[Si](C)(C)C)N1[Si](C)(C)CTMS457.2361Semi standard non polar2435.5552
Tetrahydrobiopterin,4TMS,isomer#1JsmolC[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[Si](C)(C)C)[NH]2TMS529.2756Semi standard non polar2475.0142
Tetrahydrobiopterin,4TMS,isomer#2JsmolC[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)N2[Si](C)(C)CTMS529.2756Semi standard non polar2514.2478
Tetrahydrobiopterin,4TMS,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([Si](C)(C)C)[Si](C)(C)C)[NH]2TMS529.2756Semi standard non polar2525.2097
Tetrahydrobiopterin,4TMS,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[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS529.2756Semi standard non polar2510.9048
Tetrahydrobiopterin,4TMS,isomer#5JsmolC[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)N2[Si](C)(C)CTMS529.2756Semi standard non polar2509.265
Tetrahydrobiopterin,4TMS,isomer#6JsmolC[C@H](O[Si](C)(C)C)[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)CTMS529.2756Semi standard non polar2412.803
Tetrahydrobiopterin,4TMS,isomer#7JsmolC[C@H](O[Si](C)(C)C)[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)CTMS529.2756Semi standard non polar2514.7517
Tetrahydrobiopterin,4TMS,isomer#8JsmolC[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)N2[Si](C)(C)CTMS529.2756Semi standard non polar2513.8235
Tetrahydrobiopterin,4TMS,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([Si](C)(C)C)[Si](C)(C)C)[NH]2TMS529.2756Semi standard non polar2472.9001
Tetrahydrobiopterin,4TMS,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[Si](C)(C)C)[NH]2)N1[Si](C)(C)CTMS529.2756Semi standard non polar2457.2185
Tetrahydrobiopterin,4TMS,isomer#11JsmolC[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)N2[Si](C)(C)CTMS529.2756Semi standard non polar2552.5237
Tetrahydrobiopterin,4TMS,isomer#12JsmolC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1CNC2=C(C(=O)N=C(N[Si](C)(C)C)N2[Si](C)(C)C)N1[Si](C)(C)CTMS529.2756Semi standard non polar2528.1287
Displaying retention index compounds 651 - 675 of 1722868 in total