部分構造検索

803188

Reaction #48498

title compound

収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #48505

title compound

収率 37.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #48506

title compound

収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #48507

title compound

DOI: 10.6084/m9.figshare.5104873.v1

O=C([C@H](O)CS(=O)(=O)c1ccc2cc(Cl)ccc2c1)N1CCN(N2CCCNC2=O)CC1

Reaction #48508

title compound

収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #48510

title compound

DOI: 10.6084/m9.figshare.5104873.v1

Cn1c(CCc2ccc(C#N)cc2)nc2cc(C(=O)NN3CCN(CC=Cc4ccccc4)CC3)ccc21

Reaction #52189

2-[2-(4-Cyanophenyl)-ethyl]-1-methyl-benzimidazole-5-yl-carboxylic acid-[4-(3-phenyl-allyl)-piperazinyl]-amide

DOI: 10.6084/m9.figshare.5104873.v1

CN1CCN(NC(=O)c2ccccc2C(=C2CN(C(c3ccc(Cl)cc3)c3ccc(Cl)cc3)C2)S(C)(=O)=O)CC1

Reaction #53468

1-[bis(4-chlorophenyl)methyl]-3-{(methylsulfonyl)[(N-4-methylpiperazinylcarbamoyl)phenyl]methylene}azetidine

DOI: 10.6084/m9.figshare.5104873.v1

$CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C$

Reaction #74993

rifampicin

DOI: 10.6084/m9.figshare.5104873.v1

$CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C$

Reaction #74994

rifampicin

DOI: 10.6084/m9.figshare.5104873.v1

$CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C$

Reaction #74995

rifampicin

DOI: 10.6084/m9.figshare.5104873.v1