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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 15026 - 15050 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017091514alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#13JsmolCC(O)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[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3504.2458
RI017091504alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#12JsmolCC(O)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)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS827.5448Standard non polar3444.292
RI017091494alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#11JsmolCC(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)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3500.6707
RI017091484alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#10JsmolCC(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)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3492.6907
RI017091474alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#9JsmolCC(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)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3498.9487
RI017091464alpha-hydroxy-tetrahydrobiopterin,5TBDMS,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)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1TBDMS827.5448Standard non polar3435.2185
RI017091454alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#7JsmolCC(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)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3466.4797
RI017091444alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#6JsmolCC(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)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3451.423
RI017091434alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#5JsmolCC(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)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1TBDMS827.5448Standard non polar3396.817
RI017091424alpha-hydroxy-tetrahydrobiopterin,5TBDMS,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)=NC(=O)C2(O[Si](C)(C)C(C)(C)C)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3488.8364
RI017091414alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#3JsmolCC(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)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard non polar3460.206
RI017091404alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#2JsmolCC(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[Si](C)(C)C(C)(C)C)N1TBDMS827.5448Standard non polar3357.866
RI017091394alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#1JsmolCC(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[Si](C)(C)C(C)(C)C)N1TBDMS827.5448Standard non polar3421.92
RI017091384alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#25JsmolCC(O)C(O)C1CN([Si](C)(C)C(C)(C)C)C2=NC(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3360.5242
RI017091374alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#24JsmolCC(O)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)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3364.9558
RI017091364alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#23JsmolCC(O)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)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3355.8123
RI017091354alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#22JsmolCC(O)C(O)C1CN([Si](C)(C)C(C)(C)C)C2=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 non polar3295.7615
RI017091344alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#21JsmolCC(O)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)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3334.559
RI017091334alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#20JsmolCC(O)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)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3299.5518
RI017091324alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#19JsmolCC(O)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)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1TBDMS713.4583Standard non polar3250.699
RI017091314alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#18JsmolCC(O)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)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3341.8638
RI017091304alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#17JsmolCC(O)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)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3336.3582
RI017091294alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#16JsmolCC(O)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[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard non polar3221.1963
RI017091284alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#15JsmolCC(O)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[Si](C)(C)C(C)(C)C)N1TBDMS713.4583Standard non polar3265.3857
RI017091274alpha-hydroxy-tetrahydrobiopterin,4TBDMS,isomer#14JsmolCC(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)N1[Si](C)(C)C(C)(C)CTBDMS713.4583Standard non polar3343.3853
Displaying retention index compounds 15026 - 15050 of 1722868 in total