Substructure Search

CCC(=O)NC

N#CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCC(=O)N1
Reaction #4594
15
Yield 42.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC1CCCN1C(=O)C(Cc1ccccc1)N(C)C(=O)C(Cc1ccc2ccccc2c1)N(C)C(=O)C=CCC(C)(C)NC(=O)OC(C)(C)C
Reaction #173998
DOI: 10.1039/C8SC04228D
CC(NC(=O)Cc1cc(F)cc(F)c1)C(=O)NC(C)C(=O)N1CCSC1
Reaction #181905
DOI: 10.1039/C8SC04228D
CC(C)C(CCNC(=N)N)CC(O)C(CC1CCCCC1)NC(=O)C(Cc1c[nH]cn1)NC(=O)C(Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #188495
DOI: 10.1039/C8SC04228D
CC(C)(C)N1C(=O)CC(c2ccc(CC(NC(=O)OCc3ccccc3)C(N)=O)cc2)S1(=O)=O
Reaction #200412
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(CNC(=O)C(C)(C)C)ccc1Cl
Reaction #200922
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
CC(C)(C)OC(=O)C1CC2(CN(c3cccc(Cl)c3)C(=O)O2)CN1C(=O)C(NC(=O)CC1CCCCC1)C(C)(C)C
Reaction #206669
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCCCCC(=O)NCCCCCC(=O)N1CC(OC(=O)CCC(=O)O)CC1C(OCc1ccc(OC)cc1)(c1ccccc1)c1ccc(OC)cc1
Reaction #212606
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1CCCCC1C(=O)N1CCCC2C(c3ccccc3)Nc3ccccc3C21
Reaction #231558
DOI: 10.1039/C8SC04228D
CCCN(CCC)C(=O)c1cccc(C(=O)NC(Cc2ccccc2)C(O)([PH2]=O)C(CC(=O)O)C(=O)Nc2ccccc2)c1
Reaction #232121
DOI: 10.1039/C8SC04228D
CCC(C(=O)NC(CC(=O)O)C(=O)COc1c(F)c(F)cc(F)c1F)n1cccc(NC(C)=O)c1=O
Reaction #233584
DOI: 10.1039/C8SC04228D
C[NH-]
Reaction #244879
DOI: 10.1039/C8SC04228D
CC(C)(c1ccccc1)n1nnc(C(Oc2ccc(CC(NC(=O)c3ccccc3)C(=O)NCCCCc3ccccc3)cc2)C(=O)O)n1
Reaction #244962
DOI: 10.1039/C8SC04228D
CN(C)CC1CCN(C(=O)C(Cc2ccccc2)N(C)C(=O)C(Cc2ccc3ccccc3c2)N(C)C(=O)C=CCC(C)(C)NC(=O)OC(C)(C)C)CC1
Reaction #265591
DOI: 10.1039/C8SC04228D
Cl
Reaction #283813
DOI: 10.1039/C8SC04228D
CC(NC(=O)Cc1cc(F)cc(F)c1)C(=O)NC(C)C(=O)N1CCCC1
Reaction #286016
DOI: 10.1039/C8SC04228D
CC(C)C(CCCC(=O)NCCc1ccccc1)CC(O)C(CC1CCCCC1)NC(=O)C(Cc1c[nH]cn1)NC(=O)C(Cc1ccccc1)NC(=O)OC(C)(C)C
Reaction #288632
DOI: 10.1039/C8SC04228D
CCCC(=O)N[C@H](C(=O)N[C@@H](CCC(=O)O)C(=O)O)C(C)C
Reaction #323681
N-(N-butanoyl-L-valyl)-L-glutamic acid
Yield 87.8%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CC[C@H](NC(=O)COc1ccc([C@@H]2[C@@H](SCC(O)c3ccc(F)cc3)C(=O)N2c2ccc(F)cc2)cc1)C(=O)O
Reaction #337481
N2-{[4-((2R,3R)-1-(4-fluorophenyl)-3-{[2-(4-fluorophenyl)-2-hydroxyethyl]thio}-4-oxoazetidin-2-yl)phenoxy]acetyl}-L-glutamine
DOI: 10.6084/m9.figshare.5104873.v1
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