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320099

N#Cc1ccc(CN([C@H]2CCCCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7141
titled compound
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)[C@@H]1CCCCC[C@@H]1N(Cc1ccc(C(F)(F)F)cc1)S(=O)(=O)c1ccc(Cl)cc1
Reaction #7142
titled compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)c1ccc(CN([C@H]2CCCCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7144
titled compound
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)[C@H](CC2CCCCC2)N2CC(Oc3c(F)ccc(Cl)c3F)=CC2=O)nc1
Reaction #47289
6-{(S)-2-[4-(3-chloro-2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionylamino}-nicotinic acid methyl ester
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(Nc1ccn(C[C@@H](O)CO)n1)[C@H](CC1CCCCC1)N1CC(Oc2c(F)ccc(Cl)c2F)=CC1=O
Reaction #47291
(S)-2-[4-(3-chloro-2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-propionamide hydrochloride
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CCCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53881
trans-N-{4-[5-(Allyl-methyl-amino)-pentyl]-cyclohexyl}-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53904
trans-N-{4-[4-(Allyl-methyl-amino)-butyl]-cyclohexyl}-N-methyl-4-trifluoromethyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCF)CCCCC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53936
trans-N-(4-{5-[Ethyl-(2-fluoro-ethyl)-amino]-pentyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)[C@@H]1CCCC[C@H]1NC(=O)c1sc(C)nc1C(F)(F)F
Reaction #64996
2-methyl-4-trifluoromethyl-thiazole-5-carboxylic acid-trans-2-sec-butylcyclohexylamide
Ausbeute 44.6%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)CC1CCC(n2cc(-c3ccc(Oc4ccccc4)cc3)c3c(N)ncnc32)CC1
Reaction #79878
N1-methyl-2-{4-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]cyclohexyl}acetamide
Ausbeute 26.2%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
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CCCc1ccccc1)[C@H](O)CC[C@H]1CC(F)(F)C(=O)N1CCCc1ccc(C(=O)O)s1
Reaction #87987
title compound
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)N3CCN([C@@H]4COC[C@H]4N(C)C)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172740
title compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NNC(=O)C(CC2CCCC2)CN(O)C=O)c(F)c(N2CCN(C)CC2C)n1
Reaction #173765
DOI: 10.1039/C8SC04228D
CC(C)Sc1ccc(C(CC2CCCC2)C(=O)O)cc1
Reaction #176655
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(C(CC2CCCC2)C(=O)Nc2nccs2)cc1C(F)(F)F
Reaction #183816
DOI: 10.1039/C8SC04228D
CN(C)Cc1cnc(NC(=O)C(CC2CCCC2)c2ccc(S(C)(=O)=O)c(Cl)c2)cn1
Reaction #192777
DOI: 10.1039/C8SC04228D
Cc1nc(NNC(=O)C(CC2CCCC2)CN(C=O)OCc2ccccc2)c(F)c(N2CCN(C)C(C)C2)n1
Reaction #194092
DOI: 10.1039/C8SC04228D
Cc1nc(NNC(=O)C(CC2CCCC2)CN(O)C=O)c(F)c(N2CCN(C)C(C)C2)n1
Reaction #196529
DOI: 10.1039/C8SC04228D
O=C1CCC(CC(C(=O)Nc2cnc(OCCO)cn2)c2ccc(S(=O)(=O)C3CC3)c(C3CC3)c2)C1
Reaction #197826
DOI: 10.1039/C8SC04228D
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