Busqueda de Subestructura

4257

C[C@H](C[C@H](N)C(=O)O)C(=O)O
Reaction #2979
(2S, 4R)-4-Methyl Glutamic Acid
DOI: 10.6084/m9.figshare.5104873.v1
NCCC#Cc1ccccc1
Reaction #6820
4-phenyl-but-3-ynylamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC1)c1cc(NCc2cnc(Nc3ccccn3)s2)c(F)cc1F
Reaction #6972
title compound
Rendimiento 47.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CNC(=O)c1cnc(N2CCc3ccccc32)nc1OCc1ccc(F)cc1
Reaction #7532
title compound
Rendimiento 82.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2nc(Nc3ccc(N)cc3)nc3ccccc23)[nH]n1
Reaction #7718
[2-(4-Aminophenylamino)-quinazolin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Nc2ccc(N3CCNCC3)cc2)sc1C(=O)c1cccc(F)c1
Reaction #10898
[4-amino-2-[[4-(1-piperazinyl)phenyl]amino]-5-thiazolyl](3-fluorophenyl)methanone
Rendimiento 100.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C(=O)O)CCc2ncc(NC(=O)OCc3ccccc3)c(=O)n21
Reaction #11069
intermediate 19b
Rendimiento 105.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c3cc(N)c4c(c3c2c1)C(=O)NC4=O
Reaction #11110
4-amino-9-methoxypyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Rendimiento 93.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1Oc2ccccc2NC(=O)[C@H]1N.O=C(O)C(F)(F)F
Reaction #11690
(2S,3S)-3-amino-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one trifluoroacetate salt
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1Oc2ccccc2NC(=O)[C@@H]1N.O=C(O)C(F)(F)F
Reaction #11691
(2S,3R)-3-amino-2-methyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one trifluoroacetate salt
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)[C@@H](C)N)c1.O=C(O)C(F)(F)F
Reaction #41494
(R)-2-amino-N-((1R,2S)-1-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-1-(3-methoxyphenyl)propan-2-yl)propanamide trifluoroacetic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccc(NC(=O)CCN2CCC(OC(=O)Nc3ccccc3-c3ccccc3)CC2)cc1
Reaction #42138
title intermediate
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc2c(Br)c(F)cnc2cc1F
Reaction #43411
product
Rendimiento 57.4%DOI: 10.6084/m9.figshare.5104873.v1
COCC1(S(N)(=O)=O)CC1
Reaction #46081
1-methoxymethylcyclopropysulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(O)/C=C/c1cnc2c(c1)CCC(=O)N2
Reaction #46536
title compound
Rendimiento 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)[C@@H](NC(=O)n1nc(-c2cc(F)c(F)cc2F)c2c1CCN(C)C2)C(C)(C)C
Reaction #46749
(S)—N-(3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl)-5-methyl-3-(2,4,5-trifluoro-phenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-1-carboxamide
Rendimiento 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](N)C(=O)Nc1cnccn1
Reaction #47679
(S)-2-amino-4-methyl-pentanoic acid pyrazin-2-ylamide
Rendimiento 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@]1(O)C[C@H]2CN(CCc3c([nH]c4c(I)cccc34)[C@@](C(=O)OC)(c3cc4c(cc3OC)N(C)[C@H]3[C@@](O)(C(=O)OC)[C@H](OC(C)=O)[C@]5(CC)C=CCN6CC[C@]43[C@@H]65)C2)C1
Reaction #48763
12′-iodovinblastine
Rendimiento 112.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(=O)n(C[C@H](N)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #56774
2a
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)NC(OC2CCCCC2)[C@H](O)[C@H](Cc2ccccc2)NC(=O)O[C@H]2CCOC2)cc1
Reaction #57456
white solid
Rendimiento 67.5%DOI: 10.6084/m9.figshare.5104873.v1
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