RI01723901 | Nordeoxycholic acid,2TMS,isomer#2 | JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C | TMS | 522.3561 | Semi standard non polar | 3240.6062 |
RI01723900 | Nordeoxycholic acid,2TMS,isomer#1 | JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C | TMS | 522.3561 | Semi standard non polar | 3350.067 |
RI01723899 | Nordeoxycholic acid,1TMS,isomer#3 | JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C | TMS | 450.3165 | Semi standard non polar | 3335.8723 |
RI01723898 | Nordeoxycholic acid,1TMS,isomer#2 | JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C | TMS | 450.3165 | Semi standard non polar | 3383.1619 |
RI01723897 | Nordeoxycholic acid,1TMS,isomer#1 | JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C | TMS | 450.3165 | Semi standard non polar | 3305.9175 |
RI01723896 | Nordeoxycholic acid,3TBDMS,isomer#1 | JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12C | TBDMS | 720.5364 | Standard non polar | 3796.2224 |
RI01723895 | Nordeoxycholic acid,2TBDMS,isomer#3 | JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12C | TBDMS | 606.45 | Standard non polar | 3548.9795 |
RI01723894 | Nordeoxycholic acid,2TBDMS,isomer#2 | JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12C | TBDMS | 606.45 | Standard non polar | 3655.8958 |
RI01723893 | Nordeoxycholic acid,2TBDMS,isomer#1 | JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O)C12C | TBDMS | 606.45 | Standard non polar | 3653.2747 |
RI01723892 | Nordeoxycholic acid,1TBDMS,isomer#3 | JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C(C)(C)C)C12C | TBDMS | 492.3635 | Standard non polar | 3289.413 |
RI01723891 | Nordeoxycholic acid,1TBDMS,isomer#2 | JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C(C)(C)C)CCC4(C)C3CC(O)C12C | TBDMS | 492.3635 | Standard non polar | 3298.3032 |
RI01723890 | Nordeoxycholic acid,1TBDMS,isomer#1 | JsmolCC(CC(=O)O[Si](C)(C)C(C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C | TBDMS | 492.3635 | Standard non polar | 3382.0862 |
RI01723889 | Nordeoxycholic acid,3TMS,isomer#1 | JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C | TMS | 594.3956 | Standard non polar | 3092.0159 |
RI01723888 | Nordeoxycholic acid,2TMS,isomer#3 | JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O[Si](C)(C)C)C12C | TMS | 522.3561 | Standard non polar | 3025.3079 |
RI01723887 | Nordeoxycholic acid,2TMS,isomer#2 | JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C | TMS | 522.3561 | Standard non polar | 3114.2507 |
RI01723886 | Nordeoxycholic acid,2TMS,isomer#1 | JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C | TMS | 522.3561 | Standard non polar | 3124.2585 |
RI01723885 | Nordeoxycholic acid,1TMS,isomer#3 | JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O[Si](C)(C)C)C12C | TMS | 450.3165 | Standard non polar | 3004.602 |
RI01723884 | Nordeoxycholic acid,1TMS,isomer#2 | JsmolCC(CC(=O)O)C1CCC2C3CCC4CC(O[Si](C)(C)C)CCC4(C)C3CC(O)C12C | TMS | 450.3165 | Standard non polar | 3028.661 |
RI01723883 | Nordeoxycholic acid,1TMS,isomer#1 | JsmolCC(CC(=O)O[Si](C)(C)C)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C | TMS | 450.3165 | Standard non polar | 3105.0322 |
RI01723882 | Indole-3-acetic acid ethyl ester,1TBDMS,isomer#1 | JsmolCCOC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12 | TBDMS | 317.1811 | Standard polar | 2413.374 |
RI01723881 | Indole-3-acetic acid ethyl ester,1TMS,isomer#1 | JsmolCCOC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12 | TMS | 275.1342 | Standard polar | 2303.6804 |
RI01723880 | Indole-3-acetic acid ethyl ester,1TBDMS,isomer#1 | JsmolCCOC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12 | TBDMS | 317.1811 | Semi standard non polar | 2148.2441 |
RI01723879 | Indole-3-acetic acid ethyl ester,1TMS,isomer#1 | JsmolCCOC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12 | TMS | 275.1342 | Semi standard non polar | 1919.7465 |
RI01723878 | Indole-3-acetic acid ethyl ester,1TBDMS,isomer#1 | JsmolCCOC(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12 | TBDMS | 317.1811 | Standard non polar | 2087.455 |
RI01723877 | Indole-3-acetic acid ethyl ester,1TMS,isomer#1 | JsmolCCOC(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12 | TMS | 275.1342 | Standard non polar | 1876.4521 |