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1231077

N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #965
title compound
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1c(OC)ccc(S(=O)(=O)N[C@@H](CCCNC(=N)N)C(=O)N2CCC(C)CC2C(=O)O)c1OC
Reaction #74759
1-[N2 -(3-butoxy2,4-dimethoxyphenylsulfonyl)-L-arginyl]-4-methyl-2-piperidinecarboxylic acid
Ausbeute 79.6%DOI: 10.6084/m9.figshare.5104873.v1
NC(=N[N+](=O)[O-])NCCC[C@@H](N)C(=O)NC(c1ccccc1)c1ccccc1.O=C([O-])C(F)(F)F
Reaction #80875
(R)-N5 -[Amino(nitroimino)methyl]-N-(diphenylmethyl)-ornithinamide trifluoroacetate
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)NCCC[C@@H](NC(=O)C(c1ccccc1)c1ccccc1)C(=O)NCc1ccc(CCO)cc1
Reaction #80880
(R)-N2 -(Diphenylacetyl)-N-[[4-(2-hydroxyethyl)-phenyl]methyl]-argininamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[O-].N=C(N)NCCC[C@@H](NC(=O)C1c2ccccc2-c2ccccc21)C(=O)NCc1ccccc1O
Reaction #80881
(R)-N2 -[(9-Fluorenyl)carbonyl]-N-[(hydroxyphenyl)methyl]-argininamide acetate
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N[C@@H](CCCNC(=N)N)C(=O)N2CCC(C)CC2C(=O)O)cc1C1CCCCC1
Reaction #94591
1-[N2 -(3-cyclohexyl-4-methoxyphenylsulfonyl)-L-arginyl]-4-methyl-2-piperidinecarboxylic acid
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(C)CCN1C(=O)[C@H](CCCNC(=N)N)NS(=O)(=O)c1ccc2c(c1)Sc1ccccc1O2
Reaction #94593
ethyl 1-[N2 -(2-phenoxathiinylsulfonyl)-L-arginyl]-4-methyl-2-piperidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(C(=O)[C@H](CCCNC(=N)N)NS(=O)(=O)c2ccc3c(c2)Sc2ccccc2O3)C(C(=O)O)C1
Reaction #94594
1-[N2 -(2-phenoxathiinylsulfonyl)-L-arginyl]-4-methyl-2-piperidinecarboxylic acid
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CN=C(NN)N(C)C1CCC(N)CC1
Reaction #173495
DOI: 10.1039/C8SC04228D
O=C(O)CC(c1ccccc1)n1cnc2c(N3CCC(C(=O)NC4=NCCCN4)CC3)cccc21
Reaction #190277
DOI: 10.1039/C8SC04228D
COc1ccc(C(=O)NCC2CCN(C(=N)N)CC2)cc1OCCc1ccc(Cl)cc1Cl
Reaction #212323
DOI: 10.1039/C8SC04228D
Nc1nc(N)c(C(=O)N=C2NCC3(CC4CCC(C3)N4C(=O)CCc3ccc(OCc4ccccc4)cc3)N2)nc1Cl
Reaction #241202
DOI: 10.1039/C8SC04228D
CCNC(=NS(=O)(=O)c1ccc(N)cc1)N1CC2(C=N1)CCN(Cc1ccccc1)CC2
Reaction #254640
DOI: 10.1039/C8SC04228D
N=C(N)NCCCC(N)C(=O)OCc1ccccc1
Reaction #254761
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCC(=O)OC(=O)C(N)CCCNC(=N)N
Reaction #267967
DOI: 10.1039/C8SC04228D
COc1ccc2cc(S(=O)(=O)NC(CCCNC(=N)N)C(=O)Cl)ccc2c1
Reaction #291614
DOI: 10.1039/C8SC04228D
N=C(N)NCCCC(NS(=O)(=O)c1ccc2sc3ccccc3c2c1)C(=O)Cl
Reaction #297712
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O
Reaction #310497
product ( 3 )
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](Cc1ccccc1)NC(C)=O
Reaction #311949
Ac-Phe-Arg OEt
DOI: 10.6084/m9.figshare.5104873.v1
N=C(NCCC[C@H](NC(=O)OCc1ccccc1)C(=O)NCC(=O)OCc1ccccc1)N[N+](=O)[O-]
Reaction #334105
Z-Arg(NO2)-Gly-OBzl
DOI: 10.6084/m9.figshare.5104873.v1
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