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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 10151 - 10175 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01714026phosphoadenosine-5'-phosphosulfate,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(C1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(=O)([O-])OS(=O)(=O)[O-])[C@@H](OP(=O)([O-])[O-])[C@H]1O)[Si](C)(C)C(C)(C)CTBDMS731.1301Standard non polar4454.04
RI01714025phosphoadenosine-5'-phosphosulfate,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(=O)([O-])OS(=O)(=O)[O-])[C@@H](OP(=O)([O-])[O-])[C@H]1O[Si](C)(C)C(C)(C)CTBDMS731.1301Standard non polar4406.7603
RI01714024phosphoadenosine-5'-phosphosulfate,3TMS,isomer#1JsmolC[Si](C)(C)O[C@@H]1[C@H](OP(=O)([O-])[O-])[C@@H](COP(=O)([O-])OS(=O)(=O)[O-])O[C@H]1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21TMS719.0757Standard non polar4058.77
RI01714023phosphoadenosine-5'-phosphosulfate,2TMS,isomer#2JsmolC[Si](C)(C)N(C1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(=O)([O-])OS(=O)(=O)[O-])[C@@H](OP(=O)([O-])[O-])[C@H]1O)[Si](C)(C)CTMS647.0362Standard non polar3988.751
RI01714022phosphoadenosine-5'-phosphosulfate,2TMS,isomer#1JsmolC[Si](C)(C)NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(=O)([O-])OS(=O)(=O)[O-])[C@@H](OP(=O)([O-])[O-])[C@H]1O[Si](C)(C)CTMS647.0362Standard non polar3867.951
RI01714021phenylacetohydroximoyl-glutathione,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS664.2788Standard polar5190.159
RI01714020phenylacetohydroximoyl-glutathione,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)NC(=O)CCC([N+])C(=O)[O-]TBDMS550.1923Standard polar5515.2695
RI01714019phenylacetohydroximoyl-glutathione,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CSC(CC1=CC=CC=C1)=NO)C(=O)NCC(=O)[O-]TBDMS550.1923Standard polar5536.6978
RI01714018phenylacetohydroximoyl-glutathione,2TMS,isomer#1JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)CTMS580.1849Standard polar5242.821
RI01714017phenylacetohydroximoyl-glutathione,1TMS,isomer#2JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)NC(=O)CCC([N+])C(=O)[O-]TMS508.1453Standard polar5550.012
RI01714016phenylacetohydroximoyl-glutathione,1TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CSC(CC1=CC=CC=C1)=NO)C(=O)NCC(=O)[O-]TMS508.1453Standard polar5614.922
RI01714015phenylacetohydroximoyl-glutathione,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS664.2788Semi standard non polar3962.2356
RI01714014phenylacetohydroximoyl-glutathione,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)NC(=O)CCC([N+])C(=O)[O-]TBDMS550.1923Semi standard non polar3826.0217
RI01714013phenylacetohydroximoyl-glutathione,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CSC(CC1=CC=CC=C1)=NO)C(=O)NCC(=O)[O-]TBDMS550.1923Semi standard non polar3814.0632
RI01714012phenylacetohydroximoyl-glutathione,2TMS,isomer#1JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)CTMS580.1849Semi standard non polar3438.333
RI01714011phenylacetohydroximoyl-glutathione,1TMS,isomer#2JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)NC(=O)CCC([N+])C(=O)[O-]TMS508.1453Semi standard non polar3576.4878
RI01714010phenylacetohydroximoyl-glutathione,1TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CSC(CC1=CC=CC=C1)=NO)C(=O)NCC(=O)[O-]TMS508.1453Semi standard non polar3537.2927
RI01714009phenylacetohydroximoyl-glutathione,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)C(C)(C)CTBDMS664.2788Standard non polar3755.0874
RI01714008phenylacetohydroximoyl-glutathione,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)NC(=O)CCC([N+])C(=O)[O-]TBDMS550.1923Standard non polar3523.6265
RI01714007phenylacetohydroximoyl-glutathione,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CSC(CC1=CC=CC=C1)=NO)C(=O)NCC(=O)[O-]TBDMS550.1923Standard non polar3569.6042
RI01714006phenylacetohydroximoyl-glutathione,2TMS,isomer#1JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)N(C(=O)CCC([N+])C(=O)[O-])[Si](C)(C)CTMS580.1849Standard non polar3391.3813
RI01714005phenylacetohydroximoyl-glutathione,1TMS,isomer#2JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C(CSC(CC1=CC=CC=C1)=NO)NC(=O)CCC([N+])C(=O)[O-]TMS508.1453Standard non polar3331.5396
RI01714004phenylacetohydroximoyl-glutathione,1TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CCC([N+])C(=O)[O-])C(CSC(CC1=CC=CC=C1)=NO)C(=O)NCC(=O)[O-]TMS508.1453Standard non polar3375.372
RI01714003phenylacetohydroximoyl-cysteinylglycine,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(CC(=O)[O-])C(=O)C([N+])CSC(CC1=CC=CC=C1)=NOTBDMS422.157Standard polar3810.6555
RI01714002phenylacetohydroximoyl-cysteinylglycine,1TMS,isomer#1JsmolC[Si](C)(C)N(CC(=O)[O-])C(=O)C([N+])CSC(CC1=CC=CC=C1)=NOTMS380.11Standard polar3767.909
Displaying retention index compounds 10151 - 10175 of 1722868 in total