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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 2976 - 3000 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01721201Phe-Phe-Pro-Arg,4TMS,isomer#10JsmolC[Si](C)(C)NC(CC1=CC=CC=C1)C(=NC(CC1=CC=CC=C1)C(=O)N1CCCC1C(=NC(CCCN(C(=N)N)[Si](C)(C)C)C(=O)O)O[Si](C)(C)C)O[Si](C)(C)CTMS853.4594Semi standard non polar4696.27
RI01721200Phe-Phe-Pro-Arg,4TMS,isomer#9JsmolC[Si](C)(C)OC(=NC(CCCNC(=N)N)C(=O)O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)CTMS853.4594Semi standard non polar4793.514
RI01721199Phe-Phe-Pro-Arg,4TMS,isomer#8JsmolC[Si](C)(C)NC(=N)N(CCCC(N=C(O[Si](C)(C)C)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(N)CC1=CC=CC=C1)C(=O)O)[Si](C)(C)CTMS853.4594Semi standard non polar4687.244
RI01721198Phe-Phe-Pro-Arg,4TMS,isomer#7JsmolC[Si](C)(C)N=C(NCCCC(N=C(O[Si](C)(C)C)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(N)CC1=CC=CC=C1)C(=O)O)N[Si](C)(C)CTMS853.4594Semi standard non polar4585.7295
RI01721197Phe-Phe-Pro-Arg,4TMS,isomer#6JsmolC[Si](C)(C)OC(=NC(CC1=CC=CC=C1)C(=O)N1CCCC1C(=NC(CCCNC(=N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)O[Si](C)(C)C)C(N)CC1=CC=CC=C1TMS853.4594Semi standard non polar4685.187
RI01721196Phe-Phe-Pro-Arg,4TMS,isomer#5JsmolC[Si](C)(C)NC(=N)NCCCC(N=C(O[Si](C)(C)C)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(CC1=CC=CC=C1)N[Si](C)(C)C)C(=O)OTMS853.4594Semi standard non polar4809.912
RI01721195Phe-Phe-Pro-Arg,4TMS,isomer#4JsmolC[Si](C)(C)N=C(N)NCCCC(N=C(O[Si](C)(C)C)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(N)CC1=CC=CC=C1)C(=O)O[Si](C)(C)CTMS853.4594Semi standard non polar4442.2373
RI01721194Phe-Phe-Pro-Arg,4TMS,isomer#3JsmolC[Si](C)(C)OC(=O)C(CCCN(C(=N)N)[Si](C)(C)C)N=C(O[Si](C)(C)C)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(N)CC1=CC=CC=C1TMS853.4594Semi standard non polar4566.916
RI01721193Phe-Phe-Pro-Arg,4TMS,isomer#2JsmolC[Si](C)(C)NC(CC1=CC=CC=C1)C(=NC(CC1=CC=CC=C1)C(=O)N1CCCC1C(=NC(CCCNC(=N)N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)CTMS853.4594Semi standard non polar4638.1006
RI01721192Phe-Phe-Pro-Arg,4TMS,isomer#1JsmolC[Si](C)(C)NC(=N)NCCCC(N=C(O[Si](C)(C)C)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(N)CC1=CC=CC=C1)C(=O)O[Si](C)(C)CTMS853.4594Semi standard non polar4654.7744
RI01721191Phe-Phe-Pro-Arg,4TMS,isomer#66JsmolC[Si](C)(C)N=C(N(CCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(N)CC1=CC=CC=C1)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS853.4594Standard non polar3897.898
RI01721190Phe-Phe-Pro-Arg,4TMS,isomer#65JsmolC[Si](C)(C)N=C(N)N(CCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)CTMS853.4594Standard non polar4011.572
RI01721189Phe-Phe-Pro-Arg,4TMS,isomer#64JsmolC[Si](C)(C)NC(=N)N(CCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)CTMS853.4594Standard non polar4284.609
RI01721188Phe-Phe-Pro-Arg,4TMS,isomer#63JsmolC[Si](C)(C)N=C(NCCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)N[Si](C)(C)CTMS853.4594Standard non polar4081.7292
RI01721187Phe-Phe-Pro-Arg,4TMS,isomer#62JsmolC[Si](C)(C)N=C(N[Si](C)(C)C)N(CCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N[Si](C)(C)C)C(=O)O)[Si](C)(C)CTMS853.4594Standard non polar3863.3682
RI01721186Phe-Phe-Pro-Arg,4TMS,isomer#61JsmolC[Si](C)(C)N=C(NCCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS853.4594Standard non polar3971.5771
RI01721185Phe-Phe-Pro-Arg,4TMS,isomer#60JsmolC[Si](C)(C)NC(CC1=CC=CC=C1)C(O)=NC(CC1=CC=CC=C1)C(=O)N1CCCC1C(O)=NC(CCCN(C(=N)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)OTMS853.4594Standard non polar4274.3936
RI01721184Phe-Phe-Pro-Arg,4TMS,isomer#59JsmolC[Si](C)(C)N(C(=N)NCCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)CTMS853.4594Standard non polar4341.169
RI01721183Phe-Phe-Pro-Arg,4TMS,isomer#58JsmolC[Si](C)(C)N=C(N)N(CCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)CTMS853.4594Standard non polar3805.4702
RI01721182Phe-Phe-Pro-Arg,4TMS,isomer#57JsmolC[Si](C)(C)N=C(N)NCCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS853.4594Standard non polar4052.9092
RI01721181Phe-Phe-Pro-Arg,4TMS,isomer#56JsmolC[Si](C)(C)OC(=O)C(CCCN(C(=N)N)[Si](C)(C)C)N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)CTMS853.4594Standard non polar4160.92
RI01721180Phe-Phe-Pro-Arg,4TMS,isomer#55JsmolC[Si](C)(C)N=C(N[Si](C)(C)C)N(CCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(N)CC1=CC=CC=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)CTMS853.4594Standard non polar3766.047
RI01721179Phe-Phe-Pro-Arg,4TMS,isomer#54JsmolC[Si](C)(C)N=C(NCCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(N)CC1=CC=CC=C1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS853.4594Standard non polar3879.3203
RI01721178Phe-Phe-Pro-Arg,4TMS,isomer#53JsmolC[Si](C)(C)OC(=O)C(CCCN(C(=N)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(N)CC1=CC=CC=C1TMS853.4594Standard non polar4196.6333
RI01721177Phe-Phe-Pro-Arg,4TMS,isomer#52JsmolC[Si](C)(C)NC(=N)NCCCC(N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)CTMS853.4594Standard non polar4145.1924
Displaying retention index compounds 2976 - 3000 of 1722868 in total