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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 2876 - 2900 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01721301Phe-Phe-Pro-Arg,4TMS,isomer#44JsmolC[Si](C)(C)N=C(NCCCC(N=C(O[Si](C)(C)C)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(N)CC1=CC=CC=C1)C(=O)O)N([Si](C)(C)C)[Si](C)(C)CTMS853.4594Standard polar7300.134
RI01721300Phe-Phe-Pro-Arg,4TMS,isomer#43JsmolC[Si](C)(C)OC(=NC(CCCN(C(=N)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(N)CC1=CC=CC=C1TMS853.4594Standard polar7427.2505
RI01721299Phe-Phe-Pro-Arg,4TMS,isomer#42JsmolC[Si](C)(C)NC(=N)NCCCC(N=C(O[Si](C)(C)C)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)OTMS853.4594Standard polar6976.107
RI01721298Phe-Phe-Pro-Arg,4TMS,isomer#41JsmolC[Si](C)(C)NC(=N)N(CCCC(N=C(O[Si](C)(C)C)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 polar6999.379
RI01721297Phe-Phe-Pro-Arg,4TMS,isomer#40JsmolC[Si](C)(C)N=C(NCCCC(N=C(O[Si](C)(C)C)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)CTMS853.4594Standard polar6957.2715
RI01721296Phe-Phe-Pro-Arg,4TMS,isomer#39JsmolC[Si](C)(C)NC(CC1=CC=CC=C1)C(O)=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)CTMS853.4594Standard polar6971.7
RI01721295Phe-Phe-Pro-Arg,4TMS,isomer#38JsmolC[Si](C)(C)N=C(N)N(CCCC(N=C(O[Si](C)(C)C)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 polar7808.109
RI01721294Phe-Phe-Pro-Arg,4TMS,isomer#37JsmolC[Si](C)(C)N=C(N)NCCCC(N=C(O[Si](C)(C)C)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 polar7241.4844
RI01721293Phe-Phe-Pro-Arg,4TMS,isomer#36JsmolC[Si](C)(C)NC(CC1=CC=CC=C1)C(O)=NC(CC1=CC=CC=C1)C(=O)N1CCCC1C(=NC(CCCN(C(=N)N)[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS853.4594Standard polar7228.159
RI01721292Phe-Phe-Pro-Arg,4TMS,isomer#35JsmolC[Si](C)(C)OC(=O)C(CCCNC(=N)N)N=C(O[Si](C)(C)C)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 polar7246.2847
RI01721291Phe-Phe-Pro-Arg,4TMS,isomer#34JsmolC[Si](C)(C)NC(=N)N(CCCC(N=C(O[Si](C)(C)C)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 polar7356.2437
RI01721290Phe-Phe-Pro-Arg,4TMS,isomer#33JsmolC[Si](C)(C)N=C(NCCCC(N=C(O[Si](C)(C)C)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)CTMS853.4594Standard polar7309.531
RI01721289Phe-Phe-Pro-Arg,4TMS,isomer#32JsmolC[Si](C)(C)OC(=O)C(CCCNC(=N)N([Si](C)(C)C)[Si](C)(C)C)N=C(O[Si](C)(C)C)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O)C(N)CC1=CC=CC=C1TMS853.4594Standard polar7328.3745
RI01721288Phe-Phe-Pro-Arg,4TMS,isomer#31JsmolC[Si](C)(C)NC(=N)NCCCC(N=C(O[Si](C)(C)C)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 polar6811.081
RI01721287Phe-Phe-Pro-Arg,4TMS,isomer#30JsmolC[Si](C)(C)N=C(N)N(CCCC(N=C(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)C(=O)O)[Si](C)(C)CTMS853.4594Standard polar7357.575
RI01721286Phe-Phe-Pro-Arg,4TMS,isomer#29JsmolC[Si](C)(C)N=C(N)NCCCC(N=C(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)C)C(=O)OTMS853.4594Standard polar7341.5737
RI01721285Phe-Phe-Pro-Arg,4TMS,isomer#28JsmolC[Si](C)(C)OC(=NC(CC1=CC=CC=C1)C(=O)N1CCCC1C(O)=NC(CCCN(C(=N)N)[Si](C)(C)C)C(=O)O)C(CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)CTMS853.4594Standard polar7324.459
RI01721284Phe-Phe-Pro-Arg,4TMS,isomer#27JsmolC[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[Si](C)(C)C)C(N)CC1=CC=CC=C1)C(=O)O)[Si](C)(C)CTMS853.4594Standard polar7258.6714
RI01721283Phe-Phe-Pro-Arg,4TMS,isomer#26JsmolC[Si](C)(C)N=C(NCCCC(N=C(O)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)C)[Si](C)(C)CTMS853.4594Standard polar7274.27
RI01721282Phe-Phe-Pro-Arg,4TMS,isomer#25JsmolC[Si](C)(C)OC(=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)O)C(N)CC1=CC=CC=C1TMS853.4594Standard polar7399.507
RI01721281Phe-Phe-Pro-Arg,4TMS,isomer#24JsmolC[Si](C)(C)NC(=N)NCCCC(N=C(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)C)C(=O)OTMS853.4594Standard polar6950.5156
RI01721280Phe-Phe-Pro-Arg,4TMS,isomer#23JsmolC[Si](C)(C)NC(=N)N(CCCC(N=C(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)C(=O)O)[Si](C)(C)CTMS853.4594Standard polar6961.7607
RI01721279Phe-Phe-Pro-Arg,4TMS,isomer#22JsmolC[Si](C)(C)N=C(NCCCC(N=C(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)C(=O)O)N[Si](C)(C)CTMS853.4594Standard polar6919.37
RI01721278Phe-Phe-Pro-Arg,4TMS,isomer#21JsmolC[Si](C)(C)NC(CC1=CC=CC=C1)C(=NC(CC1=CC=CC=C1)C(=O)N1CCCC1C(O)=NC(CCCNC(=N)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)O[Si](C)(C)CTMS853.4594Standard polar6933.821
RI01721277Phe-Phe-Pro-Arg,4TMS,isomer#20JsmolC[Si](C)(C)N=C(N)N(CCCC(N=C(O)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)C)[Si](C)(C)CTMS853.4594Standard polar7783.334
Displaying retention index compounds 2876 - 2900 of 1722868 in total