子结构搜索

CNC.Cl

NC(=O)N1CCOCC1.O=C(O)CCl
Reaction #2799
chloroacetic acid morpholine carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c(=O)n(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1C(F)(F)F
Reaction #41036
title compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c(=O)n(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1C(F)(F)F
Reaction #41037
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(CCN(Cc2ccc(C(C)(C)C)cc2)C(=O)c2cc(C(F)(F)F)cc(Cl)c2F)ccc1F
Reaction #48092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN[C@@H]1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)C[C@H]1SC
Reaction #64995
8-chloro-1-cyclopropyl-7-(trans-3-ethylamino-4-methylthio-1-pyrrolidinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccc(CCNC(=O)C2CCN(C(=O)c3cc4ccccc4n3Cc3ccc(Cl)cc3)CC2)cc1
Reaction #170817
1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)-N-(4-isopropylphenethyl)piperidine-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NC(=O)CCCN(C)C)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172752
title compound
收率 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC=O)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CNS(=O)(=O)C2CC2)C2CC2)C1=O
Reaction #186555
DOI: 10.1039/C8SC04228D
CN(CCO)C(=O)CC1CCN(C(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)CC1
Reaction #192114
DOI: 10.1039/C8SC04228D
CC(O)(CNC(=O)c1nc(-c2ccc(Cl)cc2)c(OCC2CC2)nc1C(F)(F)F)C1CC1
Reaction #192280
DOI: 10.1039/C8SC04228D
CCc1cc(CCN(Cc2ccc(C(C)(C)C)cc2)C(=O)c2cc(C(F)(F)F)cc(Cl)c2F)ccc1F
Reaction #193009
DOI: 10.1039/C8SC04228D
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3-c3ccc(C(F)(F)F)cc3)CC2)ccc1Cl
Reaction #194841
DOI: 10.1039/C8SC04228D
O=C(NCc1cn(-c2ccccc2)c2cc(Cl)ccc2c1=O)c1cccc(F)c1F
Reaction #196039
DOI: 10.1039/C8SC04228D
CC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC1N
Reaction #196765
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)OCCC2(c3ccc(Cl)c(Cl)c3)CN(C(=O)Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)CCO2)cc1
Reaction #198209
DOI: 10.1039/C8SC04228D
CN1CCN(C(=O)CCc2ccc3c(c2)N(Cc2ccc(C(=O)N4CC=CC4)cc2)C(=O)CN(C(=O)c2ccc(Cl)cc2)C3)CC1
Reaction #204696
DOI: 10.1039/C8SC04228D
CC(C)[Si](OCCC1(CCN2CCCC2)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(CC2CC2)C1=O)(C(C)C)C(C)C
Reaction #205296
DOI: 10.1039/C8SC04228D
CNC(=O)C1CN(CC(=O)Nc2c(Cl)cc(C(C)=O)cc2Cl)CCN1CCCCN(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #208901
DOI: 10.1039/C8SC04228D
O=C(O)c1cn(C2CC2F)c2c(Cl)c(N3CCN(CC(=O)N4CCOCC4)CC3)c(F)cc2c1=O
Reaction #209856
DOI: 10.1039/C8SC04228D
CN(Cc1ccc(Cl)c(Cl)c1)C1CC(C(=O)N2CCN(c3ccccc3C#N)CC2)N(Cc2ccccc2)C1
Reaction #210349
DOI: 10.1039/C8SC04228D
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