子结构搜索

CC(=S)N

CN1CC(CCCl)Sc2ncccc2C1=S
Reaction #4909
2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-thiazepine-5(4H)-thione
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(CCN(C)c2ccccc2)Oc2ncccc2C1=S
Reaction #4941
2,3-Dihydro-4-methyl-2-[2-(methylphenylamino)ethyl]pyrido[3,2-f][1,4]oxazepin-5(4H)-thione
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=S)C(C#N)(CCCc1ccccc1)c1ccc(Cl)cc1
Reaction #6035
N-methyl-2-(4-chlorophenyl)-2-cyano-5-phenylthiovaleroamide
收率 52.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=S)N1CC(C)(C)CSC1=Nc1ccccc1C(C)C
Reaction #57299
3-(ethylthiocarbonyl)-2-(2-isopropylphenyl)imino-5,5-dimethyl-1,3-thiazine
收率 57.6%DOI: 10.6084/m9.figshare.5104873.v1
N
Reaction #58765
NH3
收率 1.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C(=S)CCCc1nnnn1C1CCCCC1OC)C1CCCCC1
Reaction #63535
N-ethyl-N-cyclohexyl-4-[1-(2-methoxycyclohexyl)-1,2,3,4-tetrazol-5-yl]thiobutyramide
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-n2nnnc2CCCC(=S)N(CC)C2CCCCC2)cc1
Reaction #63536
N-ethyl-N-cyclohexyl-4-[1-(4-ethylphenyl)-1,2,3,4-tetrazol-5-yl]thio-butyramide
收率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1=C(CCl)CS[C@@H]2[C@H](NC(=S)Cc3cc(Cl)ccc3Cl)C(=O)N12
Reaction #81888
(6R)-trans-3-chloromethyl-7-[(2,5-dichlorophenyl)-thioacetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
收率 72.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(-c3ccc(-c4nc(=O)[nH]s4)cc3)ccc2c1
Reaction #84092
product
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158107
solid
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158113
solid
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158120
solid
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158135
solid
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158157
solid
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=S)Nc2ccc(-c3cccc(F)c3)cc21
Reaction #182969
DOI: 10.1039/C8SC04228D
CCc1cccc(C)c1C(=S)NC(Cc1ccc(N2C(=O)C(Cc3cccnc3)N(C(C)=O)C2c2ccccc2)cc1)C(=O)OC
Reaction #188355
DOI: 10.1039/C8SC04228D
C=CCNC(=S)C(CN1CCOCC1)(OC)c1ccccn1
Reaction #194263
DOI: 10.1039/C8SC04228D
COCC(=S)Nc1c(Cl)c(Cl)cc2nc(OC)c(OC)nc12
Reaction #195302
DOI: 10.1039/C8SC04228D
—
Reaction #216009
XV
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=S)C(C(=O)c2ccccc2)c2ccccc21
Reaction #227604
DOI: 10.1039/C8SC04228D
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