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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 2951 - 2975 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01721226Phe-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)CTMS853.4594Semi standard non polar4825.8516
RI01721225Phe-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)CTMS853.4594Semi standard non polar4732.209
RI01721224Phe-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)CTMS853.4594Semi standard non polar4624.557
RI01721223Phe-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=C1TMS853.4594Semi standard non polar4735.867
RI01721222Phe-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)CTMS853.4594Semi standard non polar4850.6064
RI01721221Phe-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)CTMS853.4594Semi standard non polar4679.604
RI01721220Phe-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)OTMS853.4594Semi standard non polar4772.278
RI01721219Phe-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)CTMS853.4594Semi standard non polar4895.389
RI01721218Phe-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)CTMS853.4594Semi standard non polar4684.829
RI01721217Phe-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)CTMS853.4594Semi standard non polar4707.3423
RI01721216Phe-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=C1TMS853.4594Semi standard non polar4776.8867
RI01721215Phe-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)OTMS853.4594Semi standard non polar4961.511
RI01721214Phe-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)CTMS853.4594Semi standard non polar4844.492
RI01721213Phe-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)CTMS853.4594Semi standard non polar4761.118
RI01721212Phe-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)CTMS853.4594Semi standard non polar4840.4805
RI01721211Phe-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)CTMS853.4594Semi standard non polar4565.459
RI01721210Phe-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)CTMS853.4594Semi standard non polar4626.8
RI01721209Phe-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)CTMS853.4594Semi standard non polar4720.2427
RI01721208Phe-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)CTMS853.4594Semi standard non polar4809.6895
RI01721207Phe-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)CTMS853.4594Semi standard non polar4716.2295
RI01721206Phe-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)CTMS853.4594Semi standard non polar4631.5693
RI01721205Phe-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=C1TMS853.4594Semi standard non polar4724.7646
RI01721204Phe-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)CTMS853.4594Semi standard non polar4843.19
RI01721203Phe-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)CTMS853.4594Semi standard non polar4539.5635
RI01721202Phe-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)OTMS853.4594Semi standard non polar4587.056
Displaying retention index compounds 2951 - 2975 of 1722868 in total