Substructure Search

On1nnc2cccnc21

O=C1COc2ccc(Cl)cc2CNC(=O)[C@@H]2CCCN2C(=O)[C@@H](C2CCCCC2)NC(=O)CN1
Reaction #6783
(6R,20aS)-16-chloro-6-cyclohexyl-2,3,6,7,9,10,18,19-octahydro-1H-pyrrolo[1,2-j][1,4,7,10,13] benzoxatetraazacyclohexadecine-5,8,11,20 (12H,20aH)-tetrone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1cn2c(n1)C(CCSC(c1ccccc1)(c1ccccc1)c1ccccc1)N(C(=O)C(CSC(c1ccccc1)(c1ccccc1)c1ccccc1)NC(=O)OC(C)(C)C)CC2
Reaction #6871
foam
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
NCC(F)(F)CNC(=O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
Reaction #6980
title compound
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(=O)NC1CCCN(C(=O)[C@H](C)N2CC[C@H](NS(=O)(=O)c3ccc4cc(Cl)ccc4c3)C2=O)C1
Reaction #7399
title compound
Yield 115.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=O)C1(NC(=O)CC(F)(F)F)CC1)c1ccc(-c2cccc(F)c2C(=O)O)cc1
Reaction #10165
3-fluoro-4′-{(1R)-1-[({1-[(3,3,3-trifluoropropanoyl)amino]cyclopropyl}carbonyl)-amino]ethyl}-1,1′-biphenyl-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)Nc1ccccc1)CC2
Reaction #11064
18b
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)NCc1ccc(C(=N)NC(=O)OCc3ccccc3)cc1)C[C@@]2(C)N=[N+]=[N-]
Reaction #11067
intermediate
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(N(Cc4cccc(C(F)(F)F)c4)C(=O)OCc4ccccc4)c(=O)n32)cc1
Reaction #11083
intermediate 25b
Yield 79.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H]1C[C@@H](C(=O)NCc2ccc(C(=N)NC(=O)OCc3ccccc3)cc2)n2c1ncc(N(CC=C)C(=O)OCc1ccccc1)c2=O
Reaction #11087
intermediate 28e
Yield 20.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1Cc2ccccc2NC1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11670
title compound
Yield 81.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11674
title compound
Yield 26.3%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11684
title compound
Yield 53.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1COc2ccccc2NC1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11687
title compound
Yield 88.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1Cc2ccccc2CNC1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11693
title compound
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1Cc2ccccc2CNC1=O
Reaction #11695
(S)-4-(t-butyloxycarbonylamino)-2,3,4,5-tetrahydro-2-benzazepin-3(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1Cc2ccccc2CNC1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11697
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@H]1c2ccccc2NC(=O)[C@@H]1NC(=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11700
title compound
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)c1ccc2[nH]c(-c3cc(-c4ccncc4)n[nH]c3=O)nc2c1
Reaction #40544
2-(3-Oxo-6-pyridin-4-yl-2,3-dihydropyridazin-4-yl)-1H-benzimidazole-5-carboxylic acid (2-diethylaminoethyl)amide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/c1ccc(-c2ccc(O)c(Cl)c2)cc1)NO
Reaction #41267
title compound
Yield 9.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(C(=O)N[C@@H](C)[C@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)c2ccccc2)o1
Reaction #41420
N-{(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenylpropan-2-yl}-5-methyl-[1,3,4]oxadiazol-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
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