Recherche de Sous-structure

306216

CCCCCCCCCCCCCCCCC[C@@H](C[C@@H]1OC(=O)[C@H]1CC)OC(=O)[C@H](CC(C)C)NC=O
Reaction #6163
N-formyl-(S)-leucine (S)-1-[[(2S,3S)-3-ethyl-4-oxo-2-oxetanyl]methyl]octadecyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(O)CCC4(C)C3CCC12C
Reaction #49204
amide
Rendement 93.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(O)CCC4(C)C3CCC12C
Reaction #49207
amide
Rendement 172.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #54631
Sodium behenate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #56601
sodium behenate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #59235
sodium behenate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #61373
sodium behenate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #61375
sodium behenate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@@]43C)[C@@H]1CC(C(C(=O)O)C(=O)O)[C@@H]2C(=O)CO
Reaction #63002
21-acetoxy-16α-methoxycarbonyl-11β-hydroxy-3,20-dioxo-1,4-pregnadiene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #65344
CHOLESTEROL
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #75459
sodium behenate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #75460
sodium behenate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #78806
Sodium Behenate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #78807
Sodium Behenate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCCCC(=O)[O-].[Na+]
Reaction #96220
sodium behenate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172729
title compound
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CCC(=O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172730
title compound
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(N=C=O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172944
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-isocyanato-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-ol
Rendement 78.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1ccccc1Br
Reaction #181629
DOI: 10.1039/C8SC04228D
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #215679
CHOLESTEROL
DOI: 10.6084/m9.figshare.5104873.v1
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