Displaying retention index compounds 1401 - 1425 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Dihydrobiopterin,4TMS,isomer#10JsmolC[C@H](O)[C@H](O[Si](C)(C)C)C1=NC2=C([NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)N([Si](C)(C)C)C1TMS527.2599Semi standard non polar2342.7283
Dihydrobiopterin,4TMS,isomer#11JsmolC[C@H](O)[C@H](O)C1=NC2=C(N([Si](C)(C)C)C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS527.2599Semi standard non polar2393.7854
Dihydrobiopterin,5TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS599.2995Semi standard non polar2492.1904
Dihydrobiopterin,5TMS,isomer#2JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C1=NC2=C(N([Si](C)(C)C)C1)N([Si](C)(C)C)C(N[Si](C)(C)C)=NC2=OTMS599.2995Semi standard non polar2432.3962
Dihydrobiopterin,5TMS,isomer#3JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C1=NC2=C([NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=O)N([Si](C)(C)C)C1TMS599.2995Semi standard non polar2450.2415
Dihydrobiopterin,5TMS,isomer#4JsmolC[C@H](O[Si](C)(C)C)[C@H](O)C1=NC2=C(N([Si](C)(C)C)C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS599.2995Semi standard non polar2456.5767
Dihydrobiopterin,5TMS,isomer#5JsmolC[C@H](O)[C@H](O[Si](C)(C)C)C1=NC2=C(N([Si](C)(C)C)C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS599.2995Semi standard non polar2449.255
Dihydrobiopterin,6TMS,isomer#1JsmolC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C1=NC2=C(N([Si](C)(C)C)C1)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC2=OTMS671.339Semi standard non polar2537.527
Dihydrobiopterin,3TBDMS,isomer#1JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)[NH]C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Semi standard non polar2941.5837
Dihydrobiopterin,3TBDMS,isomer#2JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS581.3613Semi standard non polar2985.8853
Dihydrobiopterin,3TBDMS,isomer#3JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS581.3613Semi standard non polar2846.9414
Dihydrobiopterin,3TBDMS,isomer#4JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Semi standard non polar2985.9932
Dihydrobiopterin,3TBDMS,isomer#5JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C(NC1)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Semi standard non polar2940.021
Dihydrobiopterin,3TBDMS,isomer#6JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C([NH]C(N[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS581.3613Semi standard non polar2886.293
Dihydrobiopterin,3TBDMS,isomer#7JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS581.3613Semi standard non polar2934.3425
Dihydrobiopterin,3TBDMS,isomer#8JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Semi standard non polar2968.2422
Dihydrobiopterin,3TBDMS,isomer#9JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Semi standard non polar2912.4255
Dihydrobiopterin,3TBDMS,isomer#10JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS581.3613Semi standard non polar2880.4087
Dihydrobiopterin,3TBDMS,isomer#11JsmolC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N)=NC2=OTBDMS581.3613Semi standard non polar2919.8223
Dihydrobiopterin,3TBDMS,isomer#12JsmolC[C@H](O)[C@H](O)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Semi standard non polar2989.3955
Dihydrobiopterin,3TBDMS,isomer#13JsmolC[C@H](O)[C@H](O)C1=NC2=C(N([Si](C)(C)C(C)(C)C)C1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS581.3613Semi standard non polar2936.1255
Dihydrobiopterin,3TBDMS,isomer#14JsmolC[C@H](O)[C@H](O)C1=NC2=C([NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS581.3613Semi standard non polar2887.5051
Dihydrobiopterin,4TBDMS,isomer#1JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Semi standard non polar3176.17
Dihydrobiopterin,4TBDMS,isomer#2JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C(NC1)[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC2=OTBDMS695.4477Semi standard non polar3115.1895
Dihydrobiopterin,4TBDMS,isomer#3JsmolC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)C1=NC2=C([NH]C(N[Si](C)(C)C(C)(C)C)=NC2=O)N([Si](C)(C)C(C)(C)C)C1TBDMS695.4477Semi standard non polar3082.5498
Displaying retention index compounds 1401 - 1425 of 1722868 in total