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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 4626 - 4650 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01719551Lysyl-Phenylalanine,4TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=NC(CC1=CC=CC=C1)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS749.5198Semi standard non polar3642.551
RI01719550Lysyl-Phenylalanine,4TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C(C)(C)C)C(N)CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS749.5198Semi standard non polar3615.487
RI01719549Lysyl-Phenylalanine,4TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C(C)(C)C)C(CCCCN)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS749.5198Semi standard non polar3560.4463
RI01719548Lysyl-Phenylalanine,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NCCCCC(N[Si](C)(C)C(C)(C)C)C(=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS749.5198Semi standard non polar3381.255
RI01719547Lysyl-Phenylalanine,3TBDMS,isomer#10JsmolCC(C)(C)[Si](C)(C)NCCCCC(C(O)=NC(CC1=CC=CC=C1)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS635.4334Semi standard non polar3485.4714
RI01719546Lysyl-Phenylalanine,3TBDMS,isomer#9JsmolCC(C)(C)[Si](C)(C)NC(CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O)=NC(CC1=CC=CC=C1)C(=O)OTBDMS635.4334Semi standard non polar3488.8948
RI01719545Lysyl-Phenylalanine,3TBDMS,isomer#8JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC1=CC=CC=C1)N=C(O)C(N)CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS635.4334Semi standard non polar3432.148
RI01719544Lysyl-Phenylalanine,3TBDMS,isomer#7JsmolCC(C)(C)[Si](C)(C)OC(=O)C(CC1=CC=CC=C1)N=C(O)C(CCCCN)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS635.4334Semi standard non polar3344.1353
RI01719543Lysyl-Phenylalanine,3TBDMS,isomer#6JsmolCC(C)(C)[Si](C)(C)NCCCCC(N[Si](C)(C)C(C)(C)C)C(O)=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)C(C)(C)CTBDMS635.4334Semi standard non polar3293.4302
RI01719542Lysyl-Phenylalanine,3TBDMS,isomer#5JsmolCC(C)(C)[Si](C)(C)OC(=NC(CC1=CC=CC=C1)C(=O)O)C(N)CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS635.4334Semi standard non polar3443.224
RI01719541Lysyl-Phenylalanine,3TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)OC(=NC(CC1=CC=CC=C1)C(=O)O)C(CCCCN)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS635.4334Semi standard non polar3359.8137
RI01719540Lysyl-Phenylalanine,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)NCCCCC(N[Si](C)(C)C(C)(C)C)C(=NC(CC1=CC=CC=C1)C(=O)O)O[Si](C)(C)C(C)(C)CTBDMS635.4334Semi standard non polar3261.2046
RI01719539Lysyl-Phenylalanine,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NCCCCC(N)C(=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS635.4334Semi standard non polar3235.0718
RI01719538Lysyl-Phenylalanine,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC(CCCCN)C(=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)CTBDMS635.4334Semi standard non polar3151.0046
RI01719537Lysyl-Phenylalanine,6TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(CCCCN([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS725.4111Semi standard non polar3086.8867
RI01719536Lysyl-Phenylalanine,5TMS,isomer#4JsmolC[Si](C)(C)OC(=O)C(CC1=CC=CC=C1)N=C(O)C(CCCCN([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS653.3716Semi standard non polar2998.1135
RI01719535Lysyl-Phenylalanine,5TMS,isomer#3JsmolC[Si](C)(C)OC(=NC(CC1=CC=CC=C1)C(=O)O)C(CCCCN([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS653.3716Semi standard non polar3026.8618
RI01719534Lysyl-Phenylalanine,5TMS,isomer#2JsmolC[Si](C)(C)NCCCCC(C(=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS653.3716Semi standard non polar2821.2312
RI01719533Lysyl-Phenylalanine,5TMS,isomer#1JsmolC[Si](C)(C)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)C)O[Si](C)(C)CTMS653.3716Semi standard non polar2803.5957
RI01719532Lysyl-Phenylalanine,4TMS,isomer#8JsmolC[Si](C)(C)N(CCCCC(C(O)=NC(CC1=CC=CC=C1)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)CTMS581.332Semi standard non polar2972.2239
RI01719531Lysyl-Phenylalanine,4TMS,isomer#7JsmolC[Si](C)(C)NCCCCC(C(O)=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS581.332Semi standard non polar2807.8982
RI01719530Lysyl-Phenylalanine,4TMS,isomer#6JsmolC[Si](C)(C)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(O)=NC(CC1=CC=CC=C1)C(=O)O[Si](C)(C)CTMS581.332Semi standard non polar2777.2288
RI01719529Lysyl-Phenylalanine,4TMS,isomer#5JsmolC[Si](C)(C)NCCCCC(C(=NC(CC1=CC=CC=C1)C(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS581.332Semi standard non polar2808.496
RI01719528Lysyl-Phenylalanine,4TMS,isomer#4JsmolC[Si](C)(C)NC(CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=NC(CC1=CC=CC=C1)C(=O)O)O[Si](C)(C)CTMS581.332Semi standard non polar2785.724
RI01719527Lysyl-Phenylalanine,4TMS,isomer#3JsmolC[Si](C)(C)OC(=O)C(CC1=CC=CC=C1)N=C(O[Si](C)(C)C)C(N)CCCCN([Si](C)(C)C)[Si](C)(C)CTMS581.332Semi standard non polar2761.924
Displaying retention index compounds 4626 - 4650 of 1722868 in total