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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 3026 - 3050 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01721151Phe-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 non polar3761.9805
RI01721150Phe-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 non polar4125.172
RI01721149Phe-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 non polar4081.067
RI01721148Phe-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 non polar4031.6858
RI01721147Phe-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 non polar3814.6697
RI01721146Phe-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 non polar4083.0269
RI01721145Phe-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 non polar3630.16
RI01721144Phe-Phe-Pro-Arg,4TMS,isomer#19JsmolC[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)C(=O)O[Si](C)(C)CTMS853.4594Standard non polar3795.8733
RI01721143Phe-Phe-Pro-Arg,4TMS,isomer#18JsmolC[Si](C)(C)NC(CC1=CC=CC=C1)C(=NC(CC1=CC=CC=C1)C(=O)N1CCCC1C(O)=NC(CCCN(C(=N)N)[Si](C)(C)C)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS853.4594Standard non polar3901.71
RI01721142Phe-Phe-Pro-Arg,4TMS,isomer#17JsmolC[Si](C)(C)OC(=O)C(CCCNC(=N)N)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)CTMS853.4594Standard non polar3937.3296
RI01721141Phe-Phe-Pro-Arg,4TMS,isomer#16JsmolC[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(N)CC1=CC=CC=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)CTMS853.4594Standard non polar3946.4492
RI01721140Phe-Phe-Pro-Arg,4TMS,isomer#15JsmolC[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[Si](C)(C)C)N[Si](C)(C)CTMS853.4594Standard non polar3733.445
RI01721139Phe-Phe-Pro-Arg,4TMS,isomer#14JsmolC[Si](C)(C)OC(=O)C(CCCNC(=N)N([Si](C)(C)C)[Si](C)(C)C)N=C(O)C1CCCN1C(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(N)CC1=CC=CC=C1TMS853.4594Standard non polar4004.9822
RI01721138Phe-Phe-Pro-Arg,4TMS,isomer#13JsmolC[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)C(=O)O[Si](C)(C)CTMS853.4594Standard non polar3918.5728
RI01721137Phe-Phe-Pro-Arg,4TMS,isomer#12JsmolC[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[Si](C)(C)C)C(N)CC1=CC=CC=C1)C(=O)O)[Si](C)(C)CTMS853.4594Standard non polar3494.9048
RI01721136Phe-Phe-Pro-Arg,4TMS,isomer#11JsmolC[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(CC1=CC=CC=C1)N[Si](C)(C)C)C(=O)OTMS853.4594Standard non polar3653.127
RI01721135Phe-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)CTMS853.4594Standard non polar3764.1233
RI01721134Phe-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)CTMS853.4594Standard non polar3796.3328
RI01721133Phe-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)CTMS853.4594Standard non polar3814.5337
RI01721132Phe-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)CTMS853.4594Standard non polar3583.2205
RI01721131Phe-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=C1TMS853.4594Standard non polar3869.3604
RI01721130Phe-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)OTMS853.4594Standard non polar3788.163
RI01721129Phe-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)CTMS853.4594Standard non polar3588.9976
RI01721128Phe-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=C1TMS853.4594Standard non polar3695.7205
RI01721127Phe-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)CTMS853.4594Standard non polar3648.0515
Displaying retention index compounds 3026 - 3050 of 1722868 in total