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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 22326 - 22350 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01701851Isorhamnetin 3-sophoroside 7-rhamnoside,1TMS,isomer#4JsmolCOC1=CC(C2=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3OC3OC(CO)C(O)C(O)C3O)C(=O)C3=C(O)C=C(OC4OC(C)C(O)C(O)C4O)C=C3O2)=CC=C1OTMS858.2614Standard non polar5831.1323
RI01701850Niazicin A,3TBDMS,isomer#2JsmolCO/C(=N\CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1)S[Si](C)(C)C(C)(C)CTBDMS727.379Standard polar3805.632
RI01701849Niazicin A,3TBDMS,isomer#1JsmolCOC(=S)N(CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)CTBDMS727.379Standard polar3798.985
RI01701848Niazicin A,3TMS,isomer#2JsmolCO/C(=N\CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1)S[Si](C)(C)CTMS601.2381Standard polar3613.2642
RI01701847Niazicin A,3TMS,isomer#1JsmolCOC(=S)N(CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1)[Si](C)(C)CTMS601.2381Standard polar3586.9763
RI01701846Niazicin A,3TBDMS,isomer#2JsmolCO/C(=N\CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1)S[Si](C)(C)C(C)(C)CTBDMS727.379Semi standard non polar3521.113
RI01701845Niazicin A,3TBDMS,isomer#1JsmolCOC(=S)N(CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)CTBDMS727.379Semi standard non polar3592.1152
RI01701844Niazicin A,3TMS,isomer#2JsmolCO/C(=N\CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1)S[Si](C)(C)CTMS601.2381Semi standard non polar2918.6172
RI01701843Niazicin A,3TMS,isomer#1JsmolCOC(=S)N(CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1)[Si](C)(C)CTMS601.2381Semi standard non polar2919.5808
RI01701842Niazicin A,3TBDMS,isomer#2JsmolCO/C(=N\CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1)S[Si](C)(C)C(C)(C)CTBDMS727.379Standard non polar3069.5007
RI01701841Niazicin A,3TBDMS,isomer#1JsmolCOC(=S)N(CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)CTBDMS727.379Standard non polar3158.281
RI01701840Niazicin A,3TMS,isomer#2JsmolCO/C(=N\CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1)S[Si](C)(C)CTMS601.2381Standard non polar2645.5923
RI01701839Niazicin A,3TMS,isomer#1JsmolCOC(=S)N(CC1=CC=C(OC2OC(C)C(OC(C)=O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C=C1)[Si](C)(C)CTMS601.2381Standard non polar2650.4763
RI01701838Citrusin II,1TBDMS,isomer#6JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CNC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C(CC2=CC=CC=C2)N([Si](C)(C)C(C)(C)C)C(=O)C2CCCN2C1=OTBDMS826.4198Standard polar10881.205
RI01701837Citrusin II,1TBDMS,isomer#5JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CNC(=O)C(CC2=C[NH]C3=CC=CC=C23)N([Si](C)(C)C(C)(C)C)C(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C1=OTBDMS826.4198Standard polar10767.069
RI01701836Citrusin II,1TBDMS,isomer#4JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CNC(=O)C(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=CC=C23)NC(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C1=OTBDMS826.4198Standard polar11356.721
RI01701835Citrusin II,1TBDMS,isomer#3JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CN([Si](C)(C)C(C)(C)C)C(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C1=OTBDMS826.4198Standard polar10687.275
RI01701834Citrusin II,1TBDMS,isomer#2JsmolCC1NC(=O)C2CCCN2C(=O)CN([Si](C)(C)C(C)(C)C)C(=O)CNC(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C1=OTBDMS826.4198Standard polar10885.064
RI01701833Citrusin II,1TBDMS,isomer#1JsmolCC1C(=O)N2CCCC2C(=O)NC(CC2=CC=CC=C2)C(=O)NC(CC2=C[NH]C3=CC=CC=C23)C(=O)NCC(=O)NCC(=O)N2CCCC2C(=O)N1[Si](C)(C)C(C)(C)CTBDMS826.4198Standard polar10957.213
RI01701832Citrusin II,2TMS,isomer#15JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CNC(=O)C(CC2=C[NH]C3=CC=CC=C23)N([Si](C)(C)C)C(=O)C(CC2=CC=CC=C2)N([Si](C)(C)C)C(=O)C2CCCN2C1=OTMS856.4123Standard polar10256.425
RI01701831Citrusin II,2TMS,isomer#14JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CNC(=O)C(CC2=CN([Si](C)(C)C)C3=CC=CC=C23)NC(=O)C(CC2=CC=CC=C2)N([Si](C)(C)C)C(=O)C2CCCN2C1=OTMS856.4123Standard polar10749.746
RI01701830Citrusin II,2TMS,isomer#13JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CNC(=O)C(CC2=CN([Si](C)(C)C)C3=CC=CC=C23)N([Si](C)(C)C)C(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C1=OTMS856.4123Standard polar10654.339
RI01701829Citrusin II,2TMS,isomer#12JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CN([Si](C)(C)C)C(=O)C(CC2=C[NH]C3=CC=CC=C23)NC(=O)C(CC2=CC=CC=C2)N([Si](C)(C)C)C(=O)C2CCCN2C1=OTMS856.4123Standard polar10016.586
RI01701828Citrusin II,2TMS,isomer#11JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CN([Si](C)(C)C)C(=O)C(CC2=C[NH]C3=CC=CC=C23)N([Si](C)(C)C)C(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C1=OTMS856.4123Standard polar10061.931
RI01701827Citrusin II,2TMS,isomer#10JsmolCC1NC(=O)C2CCCN2C(=O)CNC(=O)CN([Si](C)(C)C)C(=O)C(CC2=CN([Si](C)(C)C)C3=CC=CC=C23)NC(=O)C(CC2=CC=CC=C2)NC(=O)C2CCCN2C1=OTMS856.4123Standard polar10534.348
Displaying retention index compounds 22326 - 22350 of 1722868 in total