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Browsing Retention Index for different Chemical Structures

Displaying retention index compounds 11101 - 11125 of 1722868 in total
RIpred ID Structure Name Chemical Structure Derivatization Type
Base compound Mass 		GC Column/Stationary Phase Retention Index
RI01713076indole-3-acetyl-tryptophan,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(CC1=C[NH]C2=CC=CC=C12)C(=O)[O-]TBDMS588.3083Semi standard non polar3986.0098
RI01713075indole-3-acetyl-tryptophan,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1C=C(CC(=O)NC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TBDMS588.3083Semi standard non polar3961.868
RI01713074indole-3-acetyl-tryptophan,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)[O-]TBDMS588.3083Semi standard non polar4001.472
RI01713073indole-3-acetyl-tryptophan,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1C=C(CC(=O)NC(CC2=C[NH]C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TBDMS474.2218Semi standard non polar3785.0
RI01713072indole-3-acetyl-tryptophan,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)C(CC1=C[NH]C2=CC=CC=C12)C(=O)[O-]TBDMS474.2218Semi standard non polar3817.38
RI01713071indole-3-acetyl-tryptophan,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C=C(CC(NC(=O)CC2=C[NH]C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TBDMS474.2218Semi standard non polar3786.12
RI01713070indole-3-acetyl-tryptophan,3TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)[O-]TMS576.2539Semi standard non polar3544.8506
RI01713069indole-3-acetyl-tryptophan,2TMS,isomer#3JsmolC[Si](C)(C)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(CC1=C[NH]C2=CC=CC=C12)C(=O)[O-]TMS504.2144Semi standard non polar3516.39
RI01713068indole-3-acetyl-tryptophan,2TMS,isomer#2JsmolC[Si](C)(C)N1C=C(CC(=O)NC(CC2=CN([Si](C)(C)C)C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TMS504.2144Semi standard non polar3530.4194
RI01713067indole-3-acetyl-tryptophan,2TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)[O-]TMS504.2144Semi standard non polar3528.0732
RI01713066indole-3-acetyl-tryptophan,1TMS,isomer#3JsmolC[Si](C)(C)N1C=C(CC(=O)NC(CC2=C[NH]C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TMS432.1749Semi standard non polar3558.0771
RI01713065indole-3-acetyl-tryptophan,1TMS,isomer#2JsmolC[Si](C)(C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)C(CC1=C[NH]C2=CC=CC=C12)C(=O)[O-]TMS432.1749Semi standard non polar3522.5889
RI01713064indole-3-acetyl-tryptophan,1TMS,isomer#1JsmolC[Si](C)(C)N1C=C(CC(NC(=O)CC2=C[NH]C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TMS432.1749Semi standard non polar3553.1582
RI01713063indole-3-acetyl-tryptophan,3TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)[O-]TBDMS702.3948Standard non polar3971.1265
RI01713062indole-3-acetyl-tryptophan,2TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N(C(=O)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(CC1=C[NH]C2=CC=CC=C12)C(=O)[O-]TBDMS588.3083Standard non polar3822.5918
RI01713061indole-3-acetyl-tryptophan,2TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N1C=C(CC(=O)NC(CC2=CN([Si](C)(C)C(C)(C)C)C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TBDMS588.3083Standard non polar3778.1616
RI01713060indole-3-acetyl-tryptophan,2TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)[O-]TBDMS588.3083Standard non polar3831.633
RI01713059indole-3-acetyl-tryptophan,1TBDMS,isomer#3JsmolCC(C)(C)[Si](C)(C)N1C=C(CC(=O)NC(CC2=C[NH]C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TBDMS474.2218Standard non polar3553.203
RI01713058indole-3-acetyl-tryptophan,1TBDMS,isomer#2JsmolCC(C)(C)[Si](C)(C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)C(CC1=C[NH]C2=CC=CC=C12)C(=O)[O-]TBDMS474.2218Standard non polar3574.1653
RI01713057indole-3-acetyl-tryptophan,1TBDMS,isomer#1JsmolCC(C)(C)[Si](C)(C)N1C=C(CC(NC(=O)CC2=C[NH]C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TBDMS474.2218Standard non polar3571.2397
RI01713056indole-3-acetyl-tryptophan,3TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)[O-]TMS576.2539Standard non polar3440.666
RI01713055indole-3-acetyl-tryptophan,2TMS,isomer#3JsmolC[Si](C)(C)N(C(=O)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(CC1=C[NH]C2=CC=CC=C12)C(=O)[O-]TMS504.2144Standard non polar3420.0598
RI01713054indole-3-acetyl-tryptophan,2TMS,isomer#2JsmolC[Si](C)(C)N1C=C(CC(=O)NC(CC2=CN([Si](C)(C)C)C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TMS504.2144Standard non polar3405.189
RI01713053indole-3-acetyl-tryptophan,2TMS,isomer#1JsmolC[Si](C)(C)N(C(=O)CC1=C[NH]C2=CC=CC=C12)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)[O-]TMS504.2144Standard non polar3435.0667
RI01713052indole-3-acetyl-tryptophan,1TMS,isomer#3JsmolC[Si](C)(C)N1C=C(CC(=O)NC(CC2=C[NH]C3=CC=CC=C23)C(=O)[O-])C2=CC=CC=C21TMS432.1749Standard non polar3363.3655
Displaying retention index compounds 11101 - 11125 of 1722868 in total