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CCC(C(=O)OCC)N.Cl

CCOC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@H]1CCCCCC[C@H](CSC(C)=O)C(=O)N1
Reaction #5499
N-[[trans 3-(acetylthiomethyl)-2-oxo-1-aza-cyclodecan-10-yl]-carbonyl]-trans 4-hydroxy-L-proline ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8955
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #50254
ml,CH2Cl2
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cccc(-c3nc4c(ccc5cc(C(=O)N[C@@H](Cc6ccccc6)C(=O)O)cc(O)c54)[nH]3)c2)cc1C
Reaction #53600
(S)-2-({1-[2-(3′,4′-dimethylbiphenyl-3-yl)-9-hydroxy-3H-naphtho[1,2-d]imidazol-7-yl]-methanoyl}-amino)-3-phenylpropionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H](N)Cc1c[nH]c2ccccc12.Cl
Reaction #53601
H-Trp-OtBu HCl
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(-c2cccc(-c3nc4c(ccc5cc(C(=O)N[C@@H](Cc6ccccc6)C(=O)O)cc(O)c54)[nH]3)c2)cc1
Reaction #53602
(S)-2-({1-[2-(4′-tert-butylbiphenyl-3-yl)-9-hydroxy-3H-naphtho[1,2-d]imidazol-7-yl]-methanoyl}-amino)-3-phenylpropionic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C(NC(=O)COc2ccccc2)C1SSc1nc2ccccc2s1
Reaction #54380
2-[4-(benzthiazol-2-yldithio)-3-phenoxyacetamido-2-oxoazetidin-1-yl]-3-methylene-butyric acid 2,2,2-trichloroethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1=CC(Cl)CN1C(=O)CS
Reaction #55886
4,5-dihydro-4-chloro-1-(2-mercaptoacetyl)-1H-pyrrole-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3nc4cc(Cl)ccc4s3)cc2)cc1)C(=O)OC(C)(C)C
Reaction #57724
(S)-3-methyl-2-{4′-[(5-chloro-benzothiazole-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid tert-butyl ester
Выход 35.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NS(=O)(=O)c1ccc(-c2ccc(NC(=O)c3nc4cc(Cl)ccc4s3)cc2)cc1)C(=O)O
Reaction #57725
(S)-3-methyl-2-{4′-[(5-chloro-benzothiazole-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid
Выход 386.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2cc(C)cc(C)c2)c2c(Cl)cc(Cl)cc2N1
Reaction #75656
Compound 24
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccc(C(C)(C)C)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75657
Compound 25
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2F)c2c(Cl)cc(Cl)cc2N1
Reaction #75658
Compound 26
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2Cl)c2c(Cl)cc(Cl)cc2N1
Reaction #75665
Compound 33
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2Br)c2c(Cl)cc(Cl)cc2N1
Reaction #75668
Compound 36
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2cccc(C(F)(F)F)c2)c2c(Cl)cc(Cl)cc2N1
Reaction #75673
Compound 41
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2ccccc2)C1C
Reaction #75674
Compound 42
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2OC)c2cc(Cl)ccc2N1
Reaction #75689
Compound 58
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)O[C@]1(C(=O)C(O)OC(=O)[C@@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](C)NC(=O)[C@H](C)NS(=O)(=O)c2ccc(Cl)cc2)C(C)C)CC[C@H]2[C@@H]3C[C@H](C)C4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@@]21C
Reaction #81341
N-(N-(N-(N-(4-chlorobenzenesulfonyl)-L-alanyl)-L-alanyl)-L -prolyl)-L-valine [11β,21-dihydroxy-3,20-dioxo-6α-methyl-17-propionyloxy-pregna-1,4-dien-21-yl] ester
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC1CC1)n1ccc(-c2cc(Cl)ccc2C(F)(F)F)cc1=O
Reaction #84941
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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