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CSCCC(N)C(=O)NCCCc1ccccc1

CSCCC(NC(=O)C(Cc1ccc(OC(C)(C)C)cc1)N(C)C(=O)OC(C)(C)C)C(=O)NCCCc1ccccc1
Reaction #231776
DOI: 10.1039/C8SC04228D
CSCCC(NC(=O)C(Cc1ccc(OC(C)(C)C)cc1)NC(=O)OC(C)(C)C)C(=O)N(C)CCCc1ccccc1
Reaction #252323
DOI: 10.1039/C8SC04228D
CSCCC(NC(=O)C(Cc1ccc(OC(C)(C)C)cc1)NC(=O)OC(C)(C)C)C(=O)NCCCc1ccccc1
Reaction #404258
DOI: 10.1039/C8SC04228D
Cl
Reaction #767471
DOI: 10.1039/C8SC04228D
O=C(O)Cc1cccc(NC(=O)NCC(=O)N2C(C(=O)N3CCCc4ccccc43)CC(S(=O)(=O)c3ccccc3)C2c2ccccc2F)c1
Reaction #780019
DOI: 10.1039/C8SC04228D
O=C(O)Cc1cccc(NC(=O)NCC(=O)N2C(C(=O)N3CCCc4ccccc43)CC(S(=O)(=O)c3ccccc3)C2c2ccccc2F)c1
Reaction #813058
(2RS,4RS,5SR)-3-{3-[2-(5-(2-fluorophenyl)-2-(1,2,3,4-tetrahydro-1-quinolylcarbonyl)-4-(phenylsulphonyl)-1-pyrrolidinyl)-2-oxoethyl]ureido}phenylacetic acid
المردود 66.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CC(S(=O)(=O)c2ccccc2)C(c2ccccc2F)N1C(=O)CNC(=O)Nc1cccc(-c2nnn[nH]2)c1
Reaction #813059
(2RS,4SR,5RS)-5-{3-[3-(2-(2-tert-butoxycarbonyl-5-(2-flurophenyl)-4-phenylsulphonyl-1-pyrrolidinyl)-2-oxoethyl)ureido]phenyl}tetrazole
DOI: 10.6084/m9.figshare.5104873.v1
CSCCC(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1
Reaction #911467
DOI: 10.1039/C8SC04228D
—
Reaction #932510
solid
DOI: 10.6084/m9.figshare.5104873.v1
CSCCC(NC(=O)c1ccccc1)C(=O)N1CCC(O)(c2ccc(Cl)cc2)CC1
Reaction #1103288
N-(1-(4-(4-Chlorophenyl)-4-hydroxypiperidin-1-yl)-4-(methylthio)-1-oxobutan-2-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@@H](N)C(=O)NCCCc1ccccc1.Cl
Reaction #1350057
N-(3-phenylpropyl)-D-methioninamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@@H](NC(=O)[C@H](Cc1ccc(OC(C)(C)C)cc1)NC(=O)OC(C)(C)C)C(=O)NCCCc1ccccc1
Reaction #1350058
[N-(tert-butyloxycarbonyl)-O-(tert-butyl)-L-tyrosyl]-N-(3-phenylpropyl)-D-methioninamide
DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCCCc1ccccc1.Cl.O
Reaction #1350059
L-tyrosyl-N-(3-phenylpropyl)-D-methioninamide monohydrochloride monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)CC[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCCCc1ccccc1.CS(=O)CC[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCCCc1ccccc1.Cl.Cl.O.O.O
Reaction #1350060
L-tyrosyl-N-(3-phenylpropyl)-D-methioninamide S-oxide monohydrochloride sesquihydrate
المردود 244.2%DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@@H](N)C(=O)N(C)CCCc1ccccc1
Reaction #1350061
N-methyl-N-(3-phenylpropyl)-D-methioninamide
المردود 112.3%DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@@H](NC(=O)[C@H](Cc1ccc(OC(C)(C)C)cc1)NC(=O)OC(C)(C)C)C(=O)N(C)CCCc1ccccc1
Reaction #1350062
[N-(tert-butyloxycarbonyl)-O-(tert-butyl)-L-tyrosyl]-N-methyl-N-(3-phenylpropyl)-D-methioninamide
المردود 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N(C)CCCc1ccccc1.Cl
Reaction #1350063
L-tyrosyl-N-methyl-N-(3-phenylpropyl)-D-methioninamide monohydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCc1ccccc1)C(=O)[C@@H](CCS(C)=O)NC(=O)[C@@H](N)Cc1ccc(O)cc1.Cl.O
Reaction #1350064
L-tyrosyl-N-methyl-N-(3-phenylpropyl)-D-methioninamide S-oxide monohydrochloride monohydrate
DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@@H](NC(=O)[C@H](Cc1ccc(OC(C)(C)C)cc1)N(C)C(=O)OC(C)(C)C)C(=O)NCCCc1ccccc1
Reaction #1350065
[N-(tert-butyloxycarbonyl)-O-(tert-butyl)-N-methyl-L-tyrosyl]-N-(3-phenylpropyl)-D-methioninamide
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCSC)C(=O)NCCCc1ccccc1.Cl.O
Reaction #1350066
N-methyl-L-tyrosyl-N-(3-phenylpropyl)-L-methioninamide monohydrochloride hydrate
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي