Substructure Search

18704

CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCC(=O)C(C)C)[C@@]4(C)CC[C@@H]32)C1
Reaction #3186
3β-acetoxy-24-oxo-5-cholestene
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC[C@@]1(O)CC[C@@H]2[C@@H]3CCC4=CC(=O)CCC4=C3[C@@H](c3ccc(C(C)=O)cc3)C[C@@]21C
Reaction #5434
title compound
Yield 69.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.OC1CCCCC1C(CN1CCNCC1)c1cccc(Cl)c1
Reaction #57108
2-[1-(3-chlorophenyl)-2-piperazin-1-ylethyl]cyclohexanol dihydrochloride
Yield 274.6%DOI: 10.6084/m9.figshare.5104873.v1
C[N+](C)(C)CC(O)(CC(=O)[O-])C(=O)CCC1CCCC1.[Cl-]
Reaction #63652
cyclopentanpropionyl carnitine chloride
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81458
title compound
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(c3cccnc3)=CC[C@@H]12
Reaction #81467
17-(3-Pyridyl)androsta-5,16-dien-3β-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@@H]3[C@@H]2CC[C@]2(C)C(c4cccnc4)=CC[C@@H]32)C1
Reaction #81468
title compound
Yield 84.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(n3cnc4ccccc43)=CC[C@@H]12
Reaction #87333
3β-Hydroxy-17-(1H-benzimidazol-1-yl)-androsta-5,16-diene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)OC(C)(C)C)C1CC1CCO
Reaction #157673
title compound
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)C(=O)OC1CC(C)C=C2C=CC(C)C(CCC(O)CC(CC(=O)NCc3ccccc3)O[Si](C)(C)C(C)(C)C)C21
Reaction #177844
DOI: 10.1039/C8SC04228D
CC1CC(CC(=O)O)CC(C)(C)C1
Reaction #182473
DOI: 10.1039/C8SC04228D
CC(CCC(O[SiH](C)C)C(C)(C)C)C1CCC2C3C(=O)C=C4CC(OC5CCCCO5)CCC4(C)C3CCC12C
Reaction #198520
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCC(C(C)=O)C(=O)c1ccc(F)cc1
Reaction #199911
DOI: 10.1039/C8SC04228D
CCCC(NOCC)=C1C(=O)CC(C2CCOC(C(C)C)OC2)CC1=O
Reaction #202667
DOI: 10.1039/C8SC04228D
CCC(C)(C)C(=O)OC1CC(C)C=C2C=CC(C)C(CCC3CC(O)CC(=O)O3)C21
Reaction #203193
DOI: 10.1039/C8SC04228D
CCC(Oc1ccc(Br)cc1)C(=O)OC1CC(C(C)(C)C)C=C2C=CC(C)C(CCC3CC(C(C)(C)C)C(O[SiH](C)C)C(=O)O3)(O[SiH](C)C)C21
Reaction #211947
DOI: 10.1039/C8SC04228D
CC(=O)O[C@H]1C[C@H](O)CC2=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)C)[C@@]4(C)CC[C@@H]3[C@]21C
Reaction #213852
1α-acetoxycholesterol
Yield 107.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #215382
oil
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccccc1OC(CC)C(=O)OC1CC(C(C)(C)C)C=C2C=CC(C)C(CCC3CC(C(C)(C)C)C(O[SiH](C)C)C(=O)O3)(O[SiH](C)C)C21
Reaction #222398
DOI: 10.1039/C8SC04228D
C=CC(=O)OCCCCCCOc1ccc(-c2ccc(C3CCC(CCC4OCCO4)CC3)cc2)cc1
Reaction #224757
DOI: 10.1039/C8SC04228D
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