بحث البنية الفرعية

C1CSCN1

O=[N+]([O-])N=C1SCCN1Cc1ccc(Cl)nc1
Reaction #50494
3-(2-chloro-5-pyridylmethyl)-2-(nitroimino)thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCN1C(=O)CSC1CCCc1ccc(C(=O)OCC)cc1
Reaction #56482
title compound
المردود 31.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCN1C(=O)CSC1CCCc1ccc(C(=O)O)cc1
Reaction #56483
desired title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C)c1NC(=O)C(C)N1CSCC1=O
Reaction #63186
N-(2,6-dimethylphenyl)-2-(4-oxo-3-thiazolidinyl)propionamide
المردود 45.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(C#Cc3ccc(-c4cnc(C5N(C(=O)C(NC(=O)OC)C(C)C)CSC5(C)C)[nH]4)cc3)cc2)[nH]1)C(C)C
Reaction #159070
[1-(4-{5-[4-(4-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-phenylethynyl)-phenyl]-1H-imidazol-2-yl}-5,5-dimethyl-thiazolidine-3-carbonyl)-2-methyl-propyl]-carbamic acid methyl ester
المردود 23.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(C#Cc3ccc(-c4cnc(C5N(C(=O)C(NC(=O)OC)C(C)C)CSC5(C)C)[nH]4)cc3)cc2)[nH]1)C(C)C
Reaction #167017
[1-(4-{5-[4-(4-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-phenylethynyl)-phenyl]-1H-imidazol-2-yl}-5,5-dimethyl-thiazolidine-3-carbonyl)-2-methyl-propyl]-carbamic acid methyl ester
المردود 23.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N=C2SCC3(CCCC3)N2C2CCCC2)c(C)c1
Reaction #176121
DOI: 10.1039/C8SC04228D
CCc1cc(C(C)=O)ccc1N=C1SCC2(CCCC2)N1C1CCCC1
Reaction #177534
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C1SC(c2ccccc2)N(CCC(C)C)C1=O
Reaction #177765
DOI: 10.1039/C8SC04228D
COc1ccc(CC2SC(=O)NC2=O)c2c1N(Cc1ccc(N)cc1)C(=O)CC2
Reaction #179901
DOI: 10.1039/C8SC04228D
COC(=O)C1CSC2CC(NC(=O)OC(C)(C)C)(c3ccccc3)C(=O)N21
Reaction #180097
DOI: 10.1039/C8SC04228D
Cc1onc(-c2ccccc2Cl)c1C(=O)NC1C(=O)N2C1SC(C)(CSc1nnnn1C)C2C(=O)OCC(Cl)(Cl)Cl
Reaction #187841
DOI: 10.1039/C8SC04228D
CC(COc1ccc(CC2SC(=O)NC2=O)cc1)NCC(O)Cc1ccccc1
Reaction #212177
DOI: 10.1039/C8SC04228D
COC(=O)C(C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])C(C)(C)S[C@H]12)=C1SCCS1.[Na+]
Reaction #215683
title compound
المردود 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)N[C@@H]1C(=O)N2C(C(=O)O)C(C)(C)S[C@H]12)=C1SCCS1
Reaction #215685
title compound
المردود 73982.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)NC1C(=O)N2C1SC1(CCN(Cc3ccccc3)CC1)C2C(=O)O
Reaction #224947
DOI: 10.1039/C8SC04228D
COc1ccc(COC(=O)C2N3C(=O)C(N4C(=O)c5ccccc5C4=O)C3SCC2(C)O)cc1
Reaction #231835
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(CC#Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)(S(=O)(=O)c2ccccn2)S1
Reaction #246374
DOI: 10.1039/C8SC04228D
CC(=O)N1C(C(=O)c2cn(C(=O)N(C)C)c3ccccc23)CSC1c1cccnc1
Reaction #253372
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(Cc1ccccc1)C(=O)N1CCSC1
Reaction #253966
DOI: 10.1039/C8SC04228D
الصفحة 1التالي