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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 14826 - 14850 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI017093515,10-methylenetetrahydrofolate,4TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)C1=CC=C(N2CC3CNC4=C(C(=O)N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=N4)N3C2)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS743.3145Standard non polar4414.744
RI017093505,10-methylenetetrahydrofolate,3TMS,isomer#7JsmolC[Si](C)(C)N1CC2CN(C3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)CN2C2=C1N=C(N)N([Si](C)(C)C)C2=OTMS671.275Standard non polar4202.719
RI017093495,10-methylenetetrahydrofolate,3TMS,isomer#6JsmolC[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N1CN(C3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)CC1CN2[Si](C)(C)CTMS671.275Standard non polar4224.3726
RI017093485,10-methylenetetrahydrofolate,3TMS,isomer#5JsmolC[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N1CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CC1CN2[Si](C)(C)CTMS671.275Standard non polar4325.718
RI017093475,10-methylenetetrahydrofolate,3TMS,isomer#4JsmolC[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N1CN(C3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)CC1CN2TMS671.275Standard non polar4309.425
RI017093465,10-methylenetetrahydrofolate,3TMS,isomer#3JsmolC[Si](C)(C)N1CC2CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CN2C2=C1N=C(N([Si](C)(C)C)[Si](C)(C)C)[NH]C2=OTMS671.275Standard non polar4361.9517
RI017093455,10-methylenetetrahydrofolate,3TMS,isomer#2JsmolC[Si](C)(C)N(C(=O)C1=CC=C(N2CC3CNC4=C(C(=O)[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=N4)N3C2)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS671.275Standard non polar4348.7153
RI017093445,10-methylenetetrahydrofolate,3TMS,isomer#1JsmolC[Si](C)(C)N(C1=NC2=C(C(=O)N1[Si](C)(C)C)N1CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CC1CN2)[Si](C)(C)CTMS671.275Standard non polar4475.5728
RI017093435,10-methylenetetrahydrofolate,2TMS,isomer#7JsmolC[Si](C)(C)N(C(=O)C1=CC=C(N2CC3CNC4=C(C(=O)N([Si](C)(C)C)C(N)=N4)N3C2)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS599.2355Standard non polar4216.035
RI017093425,10-methylenetetrahydrofolate,2TMS,isomer#6JsmolC[Si](C)(C)N1CC2CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CN2C2=C1N=C(N)N([Si](C)(C)C)C2=OTMS599.2355Standard non polar4255.712
RI017093415,10-methylenetetrahydrofolate,2TMS,isomer#5JsmolC[Si](C)(C)N1CC2CN(C3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)CN2C2=C1N=C(N)[NH]C2=OTMS599.2355Standard non polar4146.315
RI017093405,10-methylenetetrahydrofolate,2TMS,isomer#4JsmolC[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N1CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CC1CN2[Si](C)(C)CTMS599.2355Standard non polar4307.68
RI017093395,10-methylenetetrahydrofolate,2TMS,isomer#3JsmolC[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N1CN(C3=CC=C(C(=O)N(C(CCC(=O)[O-])C(=O)[O-])[Si](C)(C)C)C=C3)CC1CN2TMS599.2355Standard non polar4288.9683
RI017093385,10-methylenetetrahydrofolate,2TMS,isomer#2JsmolC[Si](C)(C)NC1=NC2=C(C(=O)N1[Si](C)(C)C)N1CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CC1CN2TMS599.2355Standard non polar4402.47
RI017093375,10-methylenetetrahydrofolate,2TMS,isomer#1JsmolC[Si](C)(C)N(C1=NC2=C(C(=O)[NH]1)N1CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CC1CN2)[Si](C)(C)CTMS599.2355Standard non polar4471.8
RI017093365,10-methylenetetrahydrofolate,1TMS,isomer#4JsmolC[Si](C)(C)N1C(N)=NC2=C(C1=O)N1CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CC1CN2TMS527.196Standard non polar4339.362
RI017093355,10-methylenetetrahydrofolate,1TMS,isomer#3JsmolC[Si](C)(C)N(C(=O)C1=CC=C(N2CC3CNC4=C(C(=O)[NH]C(N)=N4)N3C2)C=C1)C(CCC(=O)[O-])C(=O)[O-]TMS527.196Standard non polar4170.453
RI017093345,10-methylenetetrahydrofolate,1TMS,isomer#2JsmolC[Si](C)(C)N1CC2CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CN2C2=C1N=C(N)[NH]C2=OTMS527.196Standard non polar4214.6616
RI017093335,10-methylenetetrahydrofolate,1TMS,isomer#1JsmolC[Si](C)(C)NC1=NC2=C(C(=O)[NH]1)N1CN(C3=CC=C(C(=O)NC(CCC(=O)[O-])C(=O)[O-])C=C3)CC1CN2TMS527.196Standard non polar4451.602
RI017093324alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#16JsmolCC(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)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard polar4171.9805
RI017093314alpha-hydroxy-tetrahydrobiopterin,5TBDMS,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)[Si](C)(C)C(C)(C)C)=NC(=O)C2(O)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard polar4172.8696
RI017093304alpha-hydroxy-tetrahydrobiopterin,5TBDMS,isomer#14JsmolCC(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)N1[Si](C)(C)C(C)(C)CTBDMS827.5448Standard polar4420.9097
RI017093294alpha-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 polar4394.3906
RI017093284alpha-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 polar4707.4297
RI017093274alpha-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 polar4191.8784
Displaying retention index compounds 14826 - 14850 of 1722868 in total