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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 22076 - 22100 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01702101Nicotinamide ascorbate,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC1=C(O[Si](C)(C)C(C)(C)C)C(C(CO)O[Si](C)(C)C(C)(C)C)OC1=OTBDMS518.2915Standard non polar2464.6982
RI01702100Nicotinamide ascorbate,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OCC(O)C1OC(=O)C(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)CTBDMS518.2915Standard non polar2479.9417
RI01702099Nicotinamide ascorbate,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)C1OC(=O)C(O)=C1O[Si](C)(C)C(C)(C)CTBDMS518.2915Standard non polar2521.3374
RI01702098Nicotinamide ascorbate,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OCC(O[Si](C)(C)C(C)(C)C)C1OC(=O)C(O[Si](C)(C)C(C)(C)C)=C1OTBDMS518.2915Standard non polar2468.5881
RI01702097Nicotinamide ascorbate,2TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)N(C(=O)C1=CC=CN=C1)[Si](C)(C)C(C)(C)CTBDMS350.221Standard non polar1956.1785
RI01702096Nicotinamide ascorbate,4TMS,isomer#1JsmolC[Si](C)(C)OCC(O[Si](C)(C)C)C1OC(=O)C(O[Si](C)(C)C)=C1O[Si](C)(C)CTMS464.1902Standard non polar1912.9502
RI01702095Nicotinamide ascorbate,3TMS,isomer#4JsmolC[Si](C)(C)OC1=C(O[Si](C)(C)C)C(C(CO)O[Si](C)(C)C)OC1=OTMS392.1507Standard non polar1828.744
RI01702094Nicotinamide ascorbate,3TMS,isomer#3JsmolC[Si](C)(C)OCC(O)C1OC(=O)C(O[Si](C)(C)C)=C1O[Si](C)(C)CTMS392.1507Standard non polar1833.9103
RI01702093Nicotinamide ascorbate,3TMS,isomer#2JsmolC[Si](C)(C)OCC(O[Si](C)(C)C)C1OC(=O)C(O)=C1O[Si](C)(C)CTMS392.1507Standard non polar1847.4108
RI01702092Nicotinamide ascorbate,3TMS,isomer#1JsmolC[Si](C)(C)OCC(O[Si](C)(C)C)C1OC(=O)C(O[Si](C)(C)C)=C1OTMS392.1507Standard non polar1808.2534
RI01702091Nicotinamide ascorbate,2TMS,isomer#7JsmolC[Si](C)(C)N(C(=O)C1=CC=CN=C1)[Si](C)(C)CTMS266.1271Standard non polar1567.1189
RI01702090Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#8JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CNC(=O)C(C)NC(=O)C(C)N([Si](C)(C)C)C1=OTMS893.5195Standard polar12572.666
RI01702089Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#7JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CNC(=O)C(C)N([Si](C)(C)C)C(=O)C(C)NC1=OTMS893.5195Standard polar12633.833
RI01702088Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#6JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CN([Si](C)(C)C)C(=O)C(C)NC(=O)C(C)NC1=OTMS893.5195Standard polar12591.832
RI01702087Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#5JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)N([Si](C)(C)C)C(=O)CNC(=O)C(C)NC(=O)C(C)NC1=OTMS893.5195Standard polar12701.311
RI01702086Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#4JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)N([Si](C)(C)C)C(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CNC(=O)C(C)NC(=O)C(C)NC1=OTMS893.5195Standard polar12679.3545
RI01702085Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#3JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=CN([Si](C)(C)C)C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CNC(=O)C(C)NC(=O)C(C)NC1=OTMS893.5195Standard polar13218.309
RI01702084Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#2JsmolCCC(C)C1NC(=O)C(CC(C)C)N([Si](C)(C)C)C(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CNC(=O)C(C)NC(=O)C(C)NC1=OTMS893.5195Standard polar12539.295
RI01702083Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#1JsmolCCC(C)C1C(=O)NC(C)C(=O)NC(C)C(=O)NCC(=O)NC(CC(C)C)C(=O)N2CCCC2C(=O)NC(CC2=C[NH]C3=CC=CC=C23)C(=O)NC(CC(C)C)C(=O)N1[Si](C)(C)CTMS893.5195Standard polar12612.532
RI01702082Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#8JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CNC(=O)C(C)NC(=O)C(C)N([Si](C)(C)C)C1=OTMS893.5195Semi standard non polar6793.798
RI01702081Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#7JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CNC(=O)C(C)N([Si](C)(C)C)C(=O)C(C)NC1=OTMS893.5195Semi standard non polar6837.505
RI01702080Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#6JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CN([Si](C)(C)C)C(=O)C(C)NC(=O)C(C)NC1=OTMS893.5195Semi standard non polar6852.8887
RI01702079Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#5JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)N([Si](C)(C)C)C(=O)CNC(=O)C(C)NC(=O)C(C)NC1=OTMS893.5195Semi standard non polar6851.0254
RI01702078Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#4JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=C[NH]C3=CC=CC=C23)N([Si](C)(C)C)C(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CNC(=O)C(C)NC(=O)C(C)NC1=OTMS893.5195Semi standard non polar6801.6567
RI01702077Cyclo(alanylalanylglycylleucylprolyltryptophylleucylisoleucyl),1TMS,isomer#3JsmolCCC(C)C1NC(=O)C(CC(C)C)NC(=O)C(CC2=CN([Si](C)(C)C)C3=CC=CC=C23)NC(=O)C2CCCN2C(=O)C(CC(C)C)NC(=O)CNC(=O)C(C)NC(=O)C(C)NC1=OTMS893.5195Semi standard non polar6978.611
Displaying retention index compounds 22076 - 22100 of 1722868 in total