部分構造検索

C#CCN1CCNCC1

CC(CC#CCN1CCN(C)CC1)C(=O)N1c2ccccc2C(=O)Nc2cccnc21
Reaction #4271
5,11-Dihydro-11-[1-oxo-2-methyl-6-(4-methyl-1-piperazinyl)-4-hexynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(CC#CCN1CCN(C)CC1)C(=O)N1c2ccccc2C(=O)Nc2cccnc21.Cl.Cl
Reaction #4272
5,11-Dihydro-11-[1-oxo-2-methyl-6-(4-methyl-1-piperazinyl)-4-hexynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCN(C(=O)OC(C)(C)C)CC1
Reaction #44338
yellow oil
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCNCC1
Reaction #44340
product
DOI: 10.6084/m9.figshare.5104873.v1
C#CC(=O)N1CCN(C(=O)OC2C3=C(OCCS3)C(=O)N2c2ccc3ccc(Cl)nc3n2)CC1
Reaction #55360
6-(7-Chloro-1,8-naphthyridin-2-yl)-7-oxo-5-(4-propioloylpiperazin-1-yl)carbonyloxy-2,3,6,7-tetrahydro-5H-1,4-oxathiino[2,3-c]pyrrole
収率 23.9%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCN(c2ccccc2C2CC(C)(C)CC(C)(C)C2)CC1
Reaction #60478
1-prop-2-ynyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1
CC#CCN1CCN(c2ccccc2C2CC(C)(C)CC(C)(C)C2)CC1
Reaction #60479
1-but-2-ynyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine
DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCN(c2ccc(-n3c(C)nc(C)cc3=O)cc2F)CC1
Reaction #84474
title compound
収率 44.1%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(C)N1CCN(c2cc3c(cc2C(C)=O)C(=O)c2c([nH]c4cc(C#N)ccc24)C3(C)C)CC1
Reaction #90074
title compound
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CCCN2CCN(C)CC2)cc2c1C(=O)N(Cc1ccc(Oc3ccccc3)cc1)C2
Reaction #183412
DOI: 10.1039/C8SC04228D
C#CCN1CCN(C(C)C)CC1
Reaction #195619
DOI: 10.1039/C8SC04228D
CCN1CCN(CC#CC(=O)Nc2ccc3ncc(C#N)c(Nc4cccc(Br)c4)c3c2)CC1
Reaction #195876
DOI: 10.1039/C8SC04228D
CN1CCN(CC#Cc2cc3nccc(Oc4ccc(N)cc4F)c3s2)CC1
Reaction #203590
DOI: 10.1039/C8SC04228D
C#CCN1CCN(CC)CC1
Reaction #205943
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccncc1C#CCN1CCN(Cc2ccc3c(N)ncnc3c2)C(=O)C1
Reaction #223580
DOI: 10.1039/C8SC04228D
CCN1CCN(CC#CC(=O)Nc2ccc3ncc(C#N)c(Nc4cccc(Br)c4)c3c2)CC1
Reaction #224019
DOI: 10.1039/C8SC04228D
CN1CCN(CC#Cc2cc(Cl)c3c(c2)CN(Cc2ccc(Cl)cc2)C3=O)CC1
Reaction #229078
DOI: 10.1039/C8SC04228D
CN1CCN(CC#CC(=O)Nc2ccc3ncnc(Nc4cccc(Br)c4)c3c2)CC1
Reaction #230955
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
Cc1ccc(CC2CN(CC#CCO)CCN2C(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc1C
Reaction #244859
DOI: 10.1039/C8SC04228D
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