部分構造検索

C1=CSC=C1

Cc1ccc(S(=O)(=O)OCC2CN(Cc3ccccc3)CC2c2cc(Br)cs2)cc1
Reaction #58577
subtitle compound
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCC1CN(Cc2ccccc2)CC1c1cc(Br)cs1
Reaction #58578
subtitle compound
収率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2sc(-c3c(-c4ccccc4)ncn3C3CC3)cc12
Reaction #60861
title compound
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ncnc2sc(-c3c(-c4ccccc4)ncn3C3CC3)cc12
Reaction #60862
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(-c2cccs2)nn(Cc2cc(-c3ccc(Cl)s3)on2)c1C(=O)O
Reaction #61518
2-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-4-cyano-5-thiophen-2-yl-2H-pyrazole-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccco2)n(Cc2cc(-c3ccc(Cl)s3)on2)n1
Reaction #61526
1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-furan-2-yl-1H-pyrazole-3-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(-c2ccco2)n(Cc2cc(-c3ccc(Cl)s3)on2)n1
Reaction #61527
1-[5-(5-Chloro-thiophen-2-yl)-isoxazol-3-ylmethyl]-5-furan-2-yl-1H-pyrazole-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ncc(/C=C(/C(=O)O)C(Cc2ccccc2)c2cccs2)n1Cc1ccccc1Cl
Reaction #65273
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)Nc2ccc3c(CC)c(C(=O)O)sc3c2)nc1Cl
Reaction #72079
title compound
収率 87.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccsc1-c1nnc(-c2nc(-c3ccc(C(=O)N(C)C)cc3)cnc2N)o1
Reaction #165809
product
収率 23.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Oc2ccnc3cc(-c4ccc(C5OCCO5)cn4)sc23)c(F)c1
Reaction #171564
title compound 139
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1(C(=O)N(c2ccccc2)c2ccc(Oc3ccnc4cc(-c5ccc(C6OCCO6)cn5)sc34)c(F)c2)CC1
Reaction #171565
140
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1nc(-c2sccc2Cl)cs1)c1cc(Cl)c(Cl)cc1Cl
Reaction #177681
DOI: 10.1039/C8SC04228D
N#Cc1ccc2nc3sc(-c4ccccc4)cc3c(=O)n2c1
Reaction #178131
DOI: 10.1039/C8SC04228D
Cc1nc(N2CCN(Cc3ncoc3-c3ccccc3)C2=O)sc1C(=O)NCc1cccnc1
Reaction #179585
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccc(C(=O)c3ccccc3)s2)noc1C(F)(F)F
Reaction #182443
DOI: 10.1039/C8SC04228D
OCCNc1cc2nc(-c3cccc4[nH]ncc34)nc(N3CCOCC3)c2s1
Reaction #189421
DOI: 10.1039/C8SC04228D
O=CCn1cnc(-c2cc3nccc(Oc4ccc(NC(=O)NC5CC5)cc4F)c3s2)c1
Reaction #191649
DOI: 10.1039/C8SC04228D
O=C(NCCN1CCOCC1)c1cc2nc(-c3cccc4[nH]ncc34)nc(N3CCOCC3)c2s1
Reaction #203431
DOI: 10.1039/C8SC04228D
Cc1nc(N2CCN(Cc3ccc4nsnc4c3)C2=O)sc1C(=O)NCc1cccnc1
Reaction #210896
DOI: 10.1039/C8SC04228D
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