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Displaying retention index compounds 5526 - 5550 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass
GC Column/Stationary Phase Retention Index
Histidinyl-Proline,3TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N([Si](C)(C)C)[Si](C)(C)CTMS468.2408Standard polar3143.5002
Histidinyl-Proline,2TMS,isomer#4JsmolC[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)OTMS396.2013Standard polar3540.0122
Histidinyl-Proline,2TMS,isomer#3JsmolC[Si](C)(C)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)O)[Si](C)(C)CTMS396.2013Standard polar3597.9155
Histidinyl-Proline,2TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C1CCCN1C(=O)C(N)CC1=CN=CN1[Si](C)(C)CTMS396.2013Standard polar3613.504
Histidinyl-Proline,2TMS,isomer#1JsmolC[Si](C)(C)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)O[Si](C)(C)CTMS396.2013Standard polar3371.4856
Histidinyl-Proline,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS708.4681Semi standard non polar3591.814
Histidinyl-Proline,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)O)[Si](C)(C)C(C)(C)CTBDMS594.3817Semi standard non polar3432.1265
Histidinyl-Proline,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)O[Si](C)(C)C(C)(C)CTBDMS594.3817Semi standard non polar3291.5635
Histidinyl-Proline,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS594.3817Semi standard non polar3259.8228
Histidinyl-Proline,2TBDMS,isomer#4JsmolCC(C)(C)[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)OTBDMS480.2952Semi standard non polar3113.8337
Histidinyl-Proline,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)O)[Si](C)(C)C(C)(C)CTBDMS480.2952Semi standard non polar3047.0051
Histidinyl-Proline,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CCCN1C(=O)C(N)CC1=CN=CN1[Si](C)(C)C(C)(C)CTBDMS480.2952Semi standard non polar3041.312
Histidinyl-Proline,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)O[Si](C)(C)C(C)(C)CTBDMS480.2952Semi standard non polar2980.0615
Histidinyl-Proline,4TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)CTMS540.2803Semi standard non polar2765.4048
Histidinyl-Proline,3TMS,isomer#3JsmolC[Si](C)(C)N(C(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)O)[Si](C)(C)CTMS468.2408Semi standard non polar2749.337
Histidinyl-Proline,3TMS,isomer#2JsmolC[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)O[Si](C)(C)CTMS468.2408Semi standard non polar2623.9358
Histidinyl-Proline,3TMS,isomer#1JsmolC[Si](C)(C)OC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N([Si](C)(C)C)[Si](C)(C)CTMS468.2408Semi standard non polar2609.6853
Histidinyl-Proline,2TMS,isomer#4JsmolC[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C)C(=O)N1CCCC1C(=O)OTMS396.2013Semi standard non polar2642.6582
Histidinyl-Proline,2TMS,isomer#3JsmolC[Si](C)(C)N(C(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)O)[Si](C)(C)CTMS396.2013Semi standard non polar2621.7498
Histidinyl-Proline,2TMS,isomer#2JsmolC[Si](C)(C)OC(=O)C1CCCN1C(=O)C(N)CC1=CN=CN1[Si](C)(C)CTMS396.2013Semi standard non polar2564.3477
Histidinyl-Proline,2TMS,isomer#1JsmolC[Si](C)(C)NC(CC1=CN=C[NH]1)C(=O)N1CCCC1C(=O)O[Si](C)(C)CTMS396.2013Semi standard non polar2521.6685
Histidinyl-Proline,4TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CCCN1C(=O)C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS708.4681Standard non polar3388.5208
Histidinyl-Proline,3TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)O)[Si](C)(C)C(C)(C)CTBDMS594.3817Standard non polar3227.9402
Histidinyl-Proline,3TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)NC(CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)N1CCCC1C(=O)O[Si](C)(C)C(C)(C)CTBDMS594.3817Standard non polar3109.571
Histidinyl-Proline,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)OC(=O)C1CCCN1C(=O)C(CC1=CN=C[NH]1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)CTBDMS594.3817Standard non polar3125.0225
Displaying retention index compounds 5526 - 5550 of 1722868 in total