Busqueda de Subestructura

574619

Cl.O=C(O)C1CN(Cc2ccccc2)CCO1
Reaction #58591
4-Benzyl-morpholine-2-carboxylic acid hydrochloride
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(C1CN(Cc2ccccc2)CCO1)N1CCOCC1
Reaction #58592
92
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCN(CCCC(c2ccc(F)cc2)c2ccc(F)cc2)C(C(=O)O)C1)Nc1c(Cl)cccc1Cl
Reaction #63625
1-[4,4-bis(4-fluorophenyl)butyl]-4-[2-[(2,6-dichlorophenyl)amino]-2-oxoethyl]-2-piperazinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCC(=O)N1CCc2c(ncnc2Oc2ccc3c(ccn3C(=O)Nc3cccc(C(F)(F)F)c3)c2)C1
Reaction #73350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCN(CCC(=O)OCC)C(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1)n2C.Cl
Reaction #78620
1-Methyl-2-[N-(4-amidinophenyl)aminomethyl]benzimidazol-5-yl-carboxylic acid-N-propargyl-N-(2-ethoxycarbonylethyl)amide hydrochloride
Rendimiento 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCN1CCC(c2nsc3cc(F)ccc23)CC1.Cl
Reaction #83938
desired compound
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1c[nH]c2ccc(Cl)cc12)[C@H]1CCN(Cc2ccccc2)C1
Reaction #86968
(S)-1-benzyl-N-(2-(5-chloro-1H-indol-3-yl)ethyl)pyrrolidine-3-carboxamide
Rendimiento 22.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCc1c[nH]c2ccc(Cl)cc12)[C@@H]1CCN(Cc2ccccc2)C1
Reaction #86969
(R)-1-benzyl-N-(2-(5-chloro-1H-indol-3-yl)ethyl)pyrrolidine-3-carboxamide
Rendimiento 34.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@H]1CN(C(=O)C2Cc3ccc(Cl)cc3CN2C(=O)OC(C)(C)C)C[C@@]1(N=[N+]=[N-])C(=O)OCC(=O)c1ccccc1
Reaction #89682
tert-butyl 3-({(3R,4S)-4-allyl-3-azido-3-[(2-oxo-2-phenylethoxy)carbonyl]pyrrolidin-1-yl}carbonyl)-7-chloro-3,4-dihydroisoquinoline-2(1H)-carboxylate
Rendimiento 54.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCl)CN(Cc1ccccc1)[C@@H](CC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
Reaction #89694
(2S)-[benzyl-(2-chloromethyl-allyl)-amino]-succinic acid 1-benzyl ester 4-tert-butyl ester
Rendimiento 58.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(C2CCN(C)CC2)CCN1C(=O)C(Cc1cc(Cl)c(N)c(C(F)(F)F)c1)OC(=O)N1CCC(N2CCc3ccccc3NC2=O)CC1
Reaction #182917
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(COc2ccc(-c3ccc(Cl)cc3)nc2)CCN(C(=O)c2ccc(Cl)cc2)C1
Reaction #228052
DOI: 10.1039/C8SC04228D
O=C1CC(N2CCN(CCOc3cc4ncnc(Nc5ccc(F)c(Cl)c5)c4cc3OCC3CCCC3)CC2)CO1
Reaction #233185
DOI: 10.1039/C8SC04228D
CC(CCN1CCSC1C(=O)O)N(c1cc(Cl)ccc1Cl)S(=O)(=O)c1ccc(Cl)cc1
Reaction #236941
DOI: 10.1039/C8SC04228D
CN1CCC(N2CCN(C(=O)C(Cc3cc(Cl)c(N)c(C(F)(F)F)c3)OC(=O)N3CCC(N4CCc5ccccc5NC4=O)CC3)CC2C(=O)O)CC1
Reaction #247778
DOI: 10.1039/C8SC04228D
COC(=O)C1(CCCCl)CC2COC(c3ccccc3)N2C1=O
Reaction #265941
DOI: 10.1039/C8SC04228D
CCc1c(CN2CCC(C(=O)O)C2)cccc1-c1nnc(-c2ccc(OC(C)C)c(Cl)c2)s1
Reaction #267430
DOI: 10.1039/C8SC04228D
CCCCCCN1CCC(NC(=O)C2(CC(=O)OC(C)(C)C)CN(Cc3c(Cl)cccc3Cl)CC2C)CC1
Reaction #273243
DOI: 10.1039/C8SC04228D
CC1C(=O)N(CCC(=O)N2CCC3(CC3)C(O)C2)CCN1C(=O)Nc1ccc(Cl)c(Cl)c1
Reaction #277228
DOI: 10.1039/C8SC04228D
Cn1ccc2cc(Sc3ccc(C=CC(=O)N4CCCC(C(=O)O)C4)c(Cl)c3Cl)ccc21
Reaction #278218
DOI: 10.1039/C8SC04228D
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