部分構造検索

608434

CC(C)(C)OC(=O)CC(=O)c1cnc(NC(=O)C(C)(C)C)cn1
Reaction #40276
3-[5-(2,2-dimethylpropionylamino)-pyrazin-2-yl]-3-oxo-propionic acid-tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(Br)C(=O)c1cnc(NC(=O)C(C)(C)C)cn1
Reaction #40277
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)c1cnc(NC(=O)C(C)(C)C)cn1
Reaction #40278
title compound
収率 90.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1cnc([C@H](O)CO)cn1
Reaction #40279
(S)—N-[5-(1,2-dihydroxy-ethyl)-pyrazin-yl]-2,2-dimethyl-propionamide
収率 105.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40845
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40846
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cnc2nnn(Cc3ccc4ncccc4c3)c2n1
Reaction #44276
1-(3-quinolin-6-ylmethyl-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl)-ethanone
収率 104.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)c1cnc2nnn(Cc3ccc4ncccc4c3)c2n1
Reaction #44277
2-(3-quinolin-6-ylmethyl-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl)-propan-2-ol
収率 4.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)c1cnc2nnn(Cc3ccc4ncccc4c3)c2n1
Reaction #44278
1-(3-quinolin-6-ylmethyl-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl)-ethanol
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1cnccn1
Reaction #46485
2-(2-bromoacetyl)pyrazine
収率 38.3%DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@@H](O)c1cnccn1
Reaction #51985
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2cnccn2)cc1
Reaction #57856
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)c1cnccn1
Reaction #88076
1-pyrazin-2-yl-ethylamine
収率 749.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2nc3c(nc12)C=CCC3=O
Reaction #93049
4-keto-9-methylphenazine
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2nc3c(nc12)C=CCC3=O
Reaction #93050
4-keto-9-methylphenazine
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)c1cnccn1
Reaction #164943
1-pyrazin-2-yl-ethylamine
収率 2374.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(-c2ccc3[nH]ccc3c2)nc1C(=O)c1cccnc1
Reaction #168642
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCNc1ncc(-c2cccc(NC(C)=O)c2)nc1C(=O)c1cccnc1
Reaction #168643
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCNS(=O)(=O)c1cccc(-c2cnc(N)c(C(=O)c3cccnc3)n2)c1
Reaction #168644
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(-c2ccc(Cl)c(Cl)c2)nc1C(=O)c1ccc(CN2CCCCC2)cc1
Reaction #168645
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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