Busqueda de Subestructura

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Reaction #40262
foam
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@H](C)NC(=O)CC1=CCCCC1
Reaction #51394
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CNCCC1=CCCCC1
Reaction #51875
methyl 2-[N-(2-cyclohex-1-enyl)ethylamino]acetate
Rendimiento 78.0%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #54545
diacetate ester, hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCC2SCC(=O)N2CCC2=CCCCC2)cc1
Reaction #56486
4-{3-[3-[2-(1-Cyclohexenyl)ethyl]-4-oxo-2-thiazolidinyl]propyl}benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Reaction #56487
4-{3-[3-[2-(1-Hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl]propyl}benzoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(CCCC2SCC(=O)N2CCC2=CCCCC2)cc1Cl
Reaction #56491
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC2=C(C#Cc3ccccc3)CCCC21
Reaction #71255
(±)-(RS)-4-phenylethynyl-2,3,5,6,7,7a-hexahydro-indole-1-carboxylic acid ethyl ester
Rendimiento 1.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](CO)NC(=O)CN2CCOCC2)C(=O)N[C@@H](CC2=CCCCC2)C(=O)[C@@]2(C)CO2)cc1O
Reaction #87070
(S)-N-((S)-3-(cyclohex-1-en-1-yl)-1-((R)-2-methyloxiran-2-yl)-1-oxopropan-2-yl)-2-((S)-3-hydroxy-2-(2-morpholinoacetamido)propanamido)-3-(3-hydroxy-4-methoxyphenyl)propanamide
Rendimiento 35.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]1(C(=O)[C@H](CC2=CCCCC2)NC(=O)[C@H](Cc2ccc(S(C)(=O)=O)cc2)NC(=O)[C@H](CO)NC(=O)CN2CCOCC2)CO1
Reaction #87071
(S)-N-((S)-3-(cyclohex-1-en-1-yl)-1-((R)-2-methyloxiran-2-yl)-1-oxopropan-2-yl)-2-((S)-3-hydroxy-2-(2-morpholinoacetamido)propanamido)-3-(4-(methylsulfonyl)phenyl)propanamide
Rendimiento 35.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([C@@H](O)[C@H](NC(=O)[C@H](CO)NC(=O)CN2CCOCC2)C(=O)N[C@@H](CC2=CCCCC2)C(=O)[C@@]2(C)CO2)cc1
Reaction #87091
(2S,3R)-N-((S)-3-(cyclohex-1-en-1-yl)-1-((R)-2-methyloxiran-2-yl)-1-oxopropan-2-yl)-3-hydroxy-2-((S)-3-hydroxy-2-(2-morpholinoacetamido)propanamido)-3-(4-methoxyphenyl)propanamide
Rendimiento 68.7%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](N=[N+]=[N-])CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92529
3α-azidocholest-5-ene
Rendimiento 67.0%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](N)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #92530
3α-Aminocholest-5-ene
Rendimiento 93.0%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](N)CC[C@]4(C)[C@H]3CC[C@]12C.Cl
Reaction #92531
3α-aminocholest-5-ene hydrochloride
Rendimiento 46.0%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](N)CC[C@]4(C)[C@H]3CC[C@]12C.O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #92532
3α-aminocholest-5-ene citrate
Rendimiento 63.0%DOI: 10.6084/m9.figshare.5104873.v1
C#C[C@]1(O)C(=C)C[C@H]2[C@@H]3CC(=C)C4=CC(=O)CC[C@]4(C)[C@H]3CC[C@@]21C
Reaction #93683
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #94678
diacetate ester, hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(S(=O)(=O)N2CCC3=CC(=O)CCC3(Cc3ccc(-c4ccncc4)cc3)C2)cc1
Reaction #176399
DOI: 10.1039/C8SC04228D
OC(CNCCC1=CCCCC1)COc1cccc(-c2noc3cc(F)ccc23)c1
Reaction #200101
DOI: 10.1039/C8SC04228D
O=C1C2CC2C(=O)N1CCC1=CCCCC1
Reaction #201627
DOI: 10.1039/C8SC04228D
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