Substructure Search

13022

Cl.NCCCC[C@@H](N)C(=O)O
Reaction #891
D-lysine monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCCC[C@@H](N)C(=O)O
Reaction #892
D-lysine monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCCC1C(=O)O
Reaction #6710
N-methyl-piperidine-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCCCC1C(=O)O)N1CC[C@H](NS(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7406
title compound
Yield 21.9%DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8947
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8949
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8952
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8954
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O
Reaction #8956
L-lysine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCCCN2C(=O)N1c1c(F)cc(Cl)c2nc(Cl)sc12
Reaction #50004
N-(2,4-dichloro-6-fluorobenzothiazol-7-yl)-perhydroimidazo[1,5-a]pyridine-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #55889
2,3-dehydro-1-(3-acetylthio-1-oxopropyl)-5-methoxypipecolic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCN1C(=O)c1cc2ncnc(NC(C)c3nc4cc(Cl)ccc4[nH]3)c2cc1Cl
Reaction #62455
6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-[(2R/S)-2-ethoxycarbonyl-piperidin-1-yl-carbonyl]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCCN1C(=O)c1cc2ncnc(NC(C)c3nc4cc(Cl)ccc4[nH]3)c2cc1Cl
Reaction #62490
6-chloro-4-[(1R/S)-1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-[(2R/S)-2-ethoxycarbonyl-piperidin-1-yl-carbonyl]-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)[C@H]2CCCCN2c2nc(Cl)ncc21
Reaction #73085
Intermediate D
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(N)=O.NCCCC[C@H](N)C(=O)O
Reaction #76728
Lysine-methacrylamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCCc2c(Cc3ccccc3)c3cccc(OC)c3n21
Reaction #79744
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)CCC2CC=CC=C2N1C(=O)C(F)(F)F
Reaction #80816
2-methyl-N-trifluoroacetyl-2-methoxycarbonyltetrahydroquinoline
Yield 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CO)CCC2CC=CC=C2N1
Reaction #80817
2-hydroxymethyl-2-methyltetrahydroquinoline
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCCC[C@H](N)C(=O)O.O=C([O-])CCC(=O)[O-].[Li+].[Li+]
Reaction #81349
Lithium Lysine Succinate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCCC[C@H](N)C(=O)O.NCCCC[C@H](N)C(=O)O.O=C([O-])CCC(=O)[O-].[Na+].[Na+]
Reaction #81350
Sodium Dilysine Succinate Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
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