子结构搜索

Cc1cnc(N)cn1

COc1cc(Nc2nc(-c3cccc(NC(C)=O)c3)cnc2NC(C)=O)cc(OC)c1OC
Reaction #44552
title compound
收率 17.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(NC(=O)c2cc(Oc3ccc(C(=O)O)cc3)cc(O[C@@H](C)CO)c2)cn1
Reaction #48838
desired compound
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(Oc2cc(O[C@@H](C)CO)cc(C(=O)Nc3cnc(C)cn3)c2)cc1
Reaction #48839
desired compound
收率 3.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1N1CCN(CCCNc2cnc(C(=O)NCCNC(=O)OC(C)(C)C)cn2)CC1
Reaction #65472
1,1-Dimethylethyl 2-[[[2-[[3-[4-(5-chloro-2-methoxyphenyl)piperazin-1-yl]propyl]amino]pyrazin-5-yl]carbonyl]amino]ethylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc2cc(OCc3cnc(Nc4ccc(Cl)c(Cl)c4)cn3)ccc2[nH]1
Reaction #164656
6-((5-(3,4-dichlorophenylamino)pyrazin-2-yl)methoxy)quinolin-2(1H)-one
收率 13.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(C(=O)NN)n2)cc1
Reaction #165773
4-(5-amino-6-(hydrazinecarbonyl)pyrazin-2-yl)-N,N-dimethylbenzamide
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(-c3nnc(NCc4ccccc4)o3)n2)cc1
Reaction #165774
4-(5-amino-6-(5-(benzylamino)-1,3,4-oxadiazol-2-yl)pyrazin-2-yl)-N,N-dimethylbenzamide
收率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(C(=O)NNC(=S)Nc3ccccc3Cl)n2)cc1
Reaction #165790
4-[5-amino-6-[[(2 chlorophenyl)carbamothioylamino]carbamoyl]pyrazin-2-yl]-N,N-dimethyl-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2nnc(-c3nc(-c4ccc(C(=O)N(C)C)cc4)cnc3N)o2)cc1
Reaction #165791
product
收率 24.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(-c3nnc(N4CCC4)o3)n2)cc1
Reaction #165792
product
收率 15.8%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccccc1-c1nnc(-c2nc(-c3ccc(C(=O)N(C)C)cc3)cnc2N)o1
Reaction #165796
product
收率 53.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1-c1nnc(-c2nc(-c3ccc(C(=O)N(C)C)cc3)cnc2N)o1
Reaction #165801
product
收率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(-c3nnc(-c4ccccc4N)o3)n2)cc1
Reaction #165802
product
收率 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(C(=O)NNC(=O)c3cccc(N)n3)n2)cc1
Reaction #165803
4-(5-amino-6-(2-(6-aminopyridine-2-carbonyl)hydrazinecarbonyl)pyrazin-2-yl)-N,N-dimethylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(-c3nnc(-c4cccc(CN)c4)o3)n2)cc1
Reaction #165806
product
收率 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(-c3nnc(-c4ccccc4OCCN)o3)n2)cc1
Reaction #165807
product
收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccsc1C(=O)NNC(=O)c1nc(-c2ccc(C(=O)N(C)C)cc2)cnc1N
Reaction #165808
4-[5-amino-6-[[(3-methoxythiophene-2-carbonyl)amino]carbamoyl]pyrazin-2-yl]-N,N-dimethyl-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(-c3nnc(-c4ccccc4-c4ccsc4)o3)n2)cc1
Reaction #165815
product
收率 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCc1ccc(-c2nnc(-c3nc(-c4ccc(C(=O)N(C)C)cc4)cnc3N)o2)cc1
Reaction #165823
solid
收率 78.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)c1ccc(-c2cnc(N)c(-c3nnc(-c4ccc(CO)cc4)o3)n2)cc1
Reaction #165824
product
收率 71.7%DOI: 10.6084/m9.figshare.5104873.v1
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