Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14876 - 14900 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017093014alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#10JsmolCC(O[Si](C)(C)C(C)(C)C)C(O)C1CNC2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard polar4894.2007
RI017093004alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#9JsmolCC(O[Si](C)(C)C(C)(C)C)C(O)C1CNC2=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard polar5175.7544
RI017092994alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#8JsmolCC(O[Si](C)(C)C(C)(C)C)C(O)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard polar5175.8755
RI017092984alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#7JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N)=NC(=O)C2(O)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard polar4432.029
RI017092974alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#6JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CNC2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard polar4596.247
RI017092964alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#5JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CNC2=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1TBDMS713.4583Standard polar4677.376
RI017092954alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#4JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1TBDMS713.4583Standard polar4648.8936
RI017092944alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#3JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CNC2=NC(N)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard polar4708.153
RI017092934alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#2JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard polar4727.9233
RI017092924alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#1JsmolCC(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1CNC2=NC(N[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard polar5482.571
RI017092914alpha-hydroxy-tetrahydrobiopterin,7TMS,isomer#1JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS761.3891Standard polar3677.703
RI017092904alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#6JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS689.3496Standard polar3890.2976
RI017092894alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#5JsmolCC(O[Si](C)(C)C)C(O)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS689.3496Standard polar3897.3235
RI017092884alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#4JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS689.3496Standard polar3845.2737
RI017092874alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#3JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS689.3496Standard polar4204.163
RI017092864alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#2JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS689.3496Standard polar4133.8286
RI017092854alpha-hydroxy-tetrahydrobiopterin,6TMS,isomer#1JsmolCC(O[Si](C)(C)C)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS689.3496Standard polar4549.1274
RI017092844alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#16JsmolCC(O)C(O)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS617.31Standard polar4099.5425
RI017092834alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#15JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS617.31Standard polar4037.6582
RI017092824alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#14JsmolCC(O)C(O[Si](C)(C)C)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS617.31Standard polar4406.4443
RI017092814alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#13JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS617.31Standard polar4330.015
RI017092804alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#12JsmolCC(O)C(O[Si](C)(C)C)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1TMS617.31Standard polar4713.687
RI017092794alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#11JsmolCC(O[Si](C)(C)C)C(O)C1CN([Si](C)(C)C)C2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)CTMS617.31Standard polar4052.2095
RI017092784alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#10JsmolCC(O[Si](C)(C)C)C(O)C1CNC2=NC(N([Si](C)(C)C)[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS617.31Standard polar4393.354
RI017092774alpha-hydroxy-tetrahydrobiopterin,5TMS,isomer#9JsmolCC(O[Si](C)(C)C)C(O)C1CN([Si](C)(C)C)C2=NC(N[Si](C)(C)C)=NC(=O)C2(O[Si](C)(C)C)N1[Si](C)(C)CTMS617.31Standard polar4327.524
Displaying retention index compounds 14876 - 14900 of 1722868 in total