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CCCCCCCCCCC1CO1

C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1
Reaction #42642
epothilone B
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CCC45OC4C(=O)CC[C@H]35)[C@@H]1CC/C2=C\Cl
Reaction #52574
E-17-Chloromethylene-4ξ,5ξ-epoxy-estran-3-one
DOI: 10.6084/m9.figshare.5104873.v1
C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1
Reaction #53255
epothilone B
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C[C@@H]4O[C@@]45C[C@@H](O)CC[C@]35C)[C@@H]1CCC2=O
Reaction #70359
3β-hydroxy-5α,6α-epoxyandrostane-17-one
Ausbeute 47115.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CC[C@@]4(O)C[C@@H](O)CC[C@]34C)[C@@H]1CC[C@@H]2O
Reaction #70360
androstane-3β,5α,17β-triol
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C[C@@H]4O[C@@]45CCCC[C@]35C)[C@@H]1CCC2=O
Reaction #70379
5α,6α-epoxyandrostan-17-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](CC(=O)[C@@]4(O)CC(=O)CC[C@]34C)[C@@H]1CCC2=O
Reaction #70380
5α-hydroxyandrostane-3,6,17-trione
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C(Cl)=C1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)C[C@@H]3C[C@]312
Reaction #78035
4-chloro-17β-hydroxy-14α,15α-methylene-androst-4-ene-3-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)C(O)=C1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](O)C[C@@H]3C[C@]312
Reaction #78036
4,17β-Dihydroxy-14α,15α-methylene-androst-4-ene-3-one
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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 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
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #92666
solid
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #92667
solid
Ausbeute 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
Ausbeute 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
Ausbeute 59.0%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
Ausbeute 60.4%DOI: 10.6084/m9.figshare.5104873.v1
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