子结构搜索

c1cnoc1

CN1CCN(Cc2ccc(-c3cc4onc(-c5ccccc5)c4c(=O)n3C)cc2)CC1
Reaction #8404
5-methyl-6-[4-(4-methyl-piperazin-1-ylmethyl)-phenyl]-3-phenyl-5H-isoxazolo[4,5-c]pyridin-4-one
收率 41.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(-c2ccc(-c3ccc(C4(C(=O)NS(C)(=O)=O)CC4)cc3)cc2)c1NC(=O)OC(C)(C)C
Reaction #73878
{5-[4′-(1-Methanesulfonylaminocarbonyl-cyclopropyl)-biphenyl-4-yl]-3-methyl-isoxazol-4-yl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1noc(-c2ccc(-c3ccc(C4(C(=O)NS(C)(=O)=O)CC4)cc3)cc2)c1N
Reaction #73879
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2cncc(Nc3c(C)noc3-c3ccc(-c4ccc(C5(C(=O)NS(C)(=O)=O)CC5)cc4)cc3)c2)c1
Reaction #73883
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccccc2c(=O)n1CCN1CCC(c2noc3cc(F)ccc23)CC1
Reaction #83965
3-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-2-methyl-3H-quinazolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCC(c2noc3cc(F)ccc23)CC1)N1c2ccccc2CCc2ccccc21.O=C(O)/C=C/C(=O)O
Reaction #83982
white crystals
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C(=O)C[N+]23CCC(CC2)[C@@H](OC(=O)C(NCc2ccccc2)c2ccccc2)C3)on1.[Br-]
Reaction #164223
title compound
收率 35.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164303
(R/S)-2-hydroxy-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetic acid
收率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCO)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164366
(R/S)-2-hydroxy-N-(2-hydroxyethyl)-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
收率 68.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)CNC(=O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164367
(R/S)-2-hydroxy-N—((S)-2-hydroxypropyl)-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
收率 47.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)CNC(=O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164368
(R/S)-2-hydroxy-N-(2-hydroxy-2-methylpropyl)-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
收率 52.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCn1ccnc1)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1.O=C(O)C(F)(F)F
Reaction #164369
(R/S)-N-(3-(1H-imidazol-1-yl)propyl)-2-hydroxy-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide TFA
收率 42.3%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CNC(=O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164370
(R/S)-N-(2-amino-2-oxoethyl)-2-hydroxy-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
收率 42.2%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164371
(R/S)-N-ethyl-2-hydroxy-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cccnc1)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1.O=C(O)C(F)(F)F
Reaction #164372
(R/S)-2-hydroxy-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)-N-(pyridin-3-ylmethyl)acetamide TFA
收率 41.8%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)CNC(=O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164373
(R/S)-2-hydroxy-N-(2-(methylamino)-2-oxoethyl)-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
收率 9.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)CNC(=O)C(O)c1ccc(-c2noc(-c3noc(-c4ccccc4)c3C(F)(F)F)n2)cc1
Reaction #164374
(R/S)-N-(2-(ethylamino)-2-oxoethyl)-2-hydroxy-2-(4-(5-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-1,2,4-oxadiazol-3-yl)phenyl)acetamide
收率 15.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N)cc1-c1c(C)noc1C.COc1ccc(N)cc1-c1c(C)noc1C
Reaction #169155
[3-(3,5-dimethyl-4-isoxazolyl)-4-(methyloxy)phenyl]amine 3-(3,5-dimethyl-4-isoxazolyl)-4-(methyloxy)aniline
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(c2ccc(-c3ccc(-c4onc(C)c4NC(=O)OC(C)c4ccccc4OC)cc3)cc2)CC1
Reaction #187714
DOI: 10.1039/C8SC04228D
Cc1cccc(C)c1OCc1noc(C(C)C)c1COc1ccc(-c2ccc3nc(C(=O)O)ccc3c2)cc1
Reaction #189453
DOI: 10.1039/C8SC04228D
第 1 页下一页