部分構造検索

CN(C)CC#C

C#CCN1C(=O)C2CC(c3ccc([N+](=O)[O-])cc3)(C2)C1=O
Reaction #63374
1-(4-nitrophenyl)-3-propargyl-3-azabicyclo[3.1.1]heptane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCCc1ccc(CCCN2C(=O)c3ccccc3C2=O)nc1
Reaction #77852
11-1
収率 63.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CCN(CC#Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1.CS(=O)(=O)O
Reaction #96204
1-(3,5-bistrifluoromethylphenyl)-3-(4-tert-butylpiperidino)prop-1-yne methanesulphonate
収率 95.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CCN(CC#Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1.O=S(=O)(O)CCO
Reaction #96205
1-(3,5-bistrifluoromethylphenyl)-3-(4-tert-butylpiperidino)prop-1-yne 2-hydroxyethanesulphonate
収率 1475.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CCN(CC#Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)CC1.O=S(=O)(O)O
Reaction #96206
1-(3,5-bistrifluoromethylphenyl)-3-(4-tert-butylpiperidino)prop-1-yne hydrogensulphate
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cnc(C(=O)N2CCc3cc(F)ccc32)cc1N1CCC(N2CCc3cc(OC)ccc3NC2=O)CC1
Reaction #161868
3-[5′-ethynyl-2′-(5-fluoro-2,3-dihydro-indole-1-carbonyl)-3,4,5,6-tetrahydro-2H-[1,4′]-bipyridinyl-4-yl]-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)(C)c2cnc(SCc3c(F)cc(C#CCN(C)C)cc3F)n2-c2ccc(F)cc2)ccc1Cl
Reaction #171022
3-(4-((5-(2-(4-chloro-3-methoxyphenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazol-2-ylthio)methyl)-3,5-difluorophenyl)-N,N-dimethylprop-2-yn-1-amine
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)(C)c2cnc(SCc3c(F)cc(C#CC[N+](C)(C)C)cc3F)n2-c2ccc(F)cc2)ccc1Cl.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #171023
3-(4-((5-(2-(4-chloro-3-methoxyphenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazol-2-ylthio)methyl)-3,5-difluorophenyl)-N,N,N-trimethylprop-2-yn-1-aminium 4-methylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(OCC#Cc2cc(C#CCN3CCOCC3)cc(C#Cc3ccc(S(C)(=O)=O)cc3)c2)cc1C
Reaction #184633
DOI: 10.1039/C8SC04228D
Nc1ccnc(SCC#CCN2C(=O)c3ccccc3C2=O)n1
Reaction #195568
DOI: 10.1039/C8SC04228D
CCN1CCN(CC#CC(=O)Nc2ccc3ncc(C#N)c(Nc4cccc(Br)c4)c3c2)CC1
Reaction #195876
DOI: 10.1039/C8SC04228D
C#CCN(C)C(=O)c1ccccc1Nc1nc(Cl)ncc1Cl
Reaction #198174
DOI: 10.1039/C8SC04228D
C#CCN1CCN(CC)CC1
Reaction #205943
DOI: 10.1039/C8SC04228D
COC(=O)COc1ccc(OCC=C(c2ccc(C#CCN(C)C)cc2)c2cccc(C(F)(F)F)c2)cc1C
Reaction #212855
DOI: 10.1039/C8SC04228D
CCN1CCN(CC#CC(=O)Nc2ccc3ncc(C#N)c(Nc4cccc(Br)c4)c3c2)CC1
Reaction #224019
DOI: 10.1039/C8SC04228D
CS(=O)(=O)O
Reaction #224433
DOI: 10.1039/C8SC04228D
C#CCN(C)C(=O)c1ccccc1Nc1nc(Nc2ccc3c(c2)CCCC(=O)N3C)ncc1Cl
Reaction #225960
DOI: 10.1039/C8SC04228D
Cc1cc(OCC#Cc2cc(Br)cc(C#CCN3CCOCC3)c2)ccc1OCC(=O)O
Reaction #227239
DOI: 10.1039/C8SC04228D
C#Cc1cc(CNC(=O)C=Cc2ccc(C(F)(F)F)cc2C#CCN(CC)CC)cc(F)c1NS(C)(=O)=O
Reaction #233997
DOI: 10.1039/C8SC04228D
CN1CCN(CC#Cc2cc(Cl)c3c(c2)CN(Cc2ccc(C(F)(F)F)cc2)C3=O)CC1
Reaction #239707
DOI: 10.1039/C8SC04228D
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