Substructure Search

CCCCCCCCCCCCCCCCC(CN)O

CCCCCCC(O)CCCCCCCCCCCCC(O)C[N+](C)(C)CC(C)O.[Br-]
Reaction #1203
title compound
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)CNCCO
Reaction #1204
title compound
Yield 74.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)CN(C)CCO
Reaction #1205
title compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)CN
Reaction #1218
title compound
Yield 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=C[C@@H](NCCCNCCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92660
Dendrogenin B
Yield 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C[C@@H](NCCCCNCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92661
5α-Hydroxy-6β-[4-(3-aminopropylamino)-butylamino]-cholestan-3β-ol
Yield 50.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C[C@@H](NCCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92662
5α-Hydroxy-6β-(4-aminobutylamino)-cholestan-3β-ol
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C[C@@H](NCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92663
5α-Hydroxy-6β-(3-aminopropylamino)-cholestan-3β-ol
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN[C@@H]1C[C@H]2[C@@H]3CC[C@H]([C@H](C)CCCC(C)C)[C@@]3(C)CC[C@@H]2[C@@]2(C)CC[C@H](O)C[C@]12O
Reaction #92664
5α-Hydroxy-6β-(3-propylamino)-cholestan-3β-ol
Yield 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=C[C@@H](NCCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92665
5α-Hydroxy-6β-(4-aminobutylamino)-cholest-7-en-3β-ol
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #92666
solid
Yield 49.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #92667
solid
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=C[C@@H](NCCCN)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92668
5α-Hydroxy-6β-(3-aminopropylamino)-cholest-7-en-3β-ol
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCN[C@@H]1C=C2[C@@H]3CC[C@H]([C@H](C)CCCC(C)C)[C@@]3(C)CC[C@@H]2[C@@]2(C)CC[C@H](O)C[C@]12O
Reaction #92669
5α-Hydroxy-6β-(3-propylamino)-cholest-7-en-3β-ol
Yield 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@H]4[C@@H]3C[C@@H](NCCc3c[nH]cn3)[C@@]2(O)C1
Reaction #92670
5α-Hydroxy-6β-[2-(1H-imidazol-4-yl)-ethylamino]-cholestan-3β-yl acetate
Yield 61.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)O[C@H]1CC[C@]2(C)[C@H]3CC[C@]4(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@H]4[C@@H]3C[C@@H](NCCc3c[nH]cn3)[C@@]2(O)C1
Reaction #92671
5α-Hydroxy-6β-[2-(1H-imidazol-4-yl)-ethylamino]-cholestan-3β-yl butyrate
Yield 60.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3C[C@@H](NCCO)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92672
5α-Hydroxy-6β-[2-hydroxyethylamino]-cholestan-3β-ol
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC(O)C(O)C(N)(CO)CO
Reaction #179810
DOI: 10.1039/C8SC04228D
CC12CCC(O)CC1CCC1C2CCC2(C)C(N)C(O)CC12
Reaction #223775
DOI: 10.1039/C8SC04228D
Cl
Reaction #228032
DOI: 10.1039/C8SC04228D
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