子结构搜索

1228119

CC(C)(C)OC(=O)NC(C)(C)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)OCc1ccccc1
Reaction #2003
(R)-α-[(2-t-Butoxycarbonylamino-2-methyl-1-oxopropyl)amino]-1H-indole-3-propanoic acid, benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(C)(C)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)O
Reaction #2004
product
收率 102.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)C(C)(C)NC(=O)OCc1ccccc1
Reaction #2015
desired product
收率 84.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CC(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)OCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2016
(R)-α-[(3-t-Butoxycarbonylamino-3-methyl-1-oxobutyl)amino]-1-H-indole-3-propanoic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)C#Cc1ccc(S(=O)(=O)N[C@H](Cc2c[nH]c3ccccc23)C(=O)O)s1
Reaction #68772
(R)-3-(1H-Indol-3-yl)-2-(5-trimethylsilanylethynyl-thiophene-2-sulfonylamino)-propionic acid
收率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(S(=O)(=O)N[C@H](Cc2c[nH]c3ccccc23)C(=O)O)s1
Reaction #68773
(R)-2-(5-Ethynyl-thiophene-2-sulfonylamino)-3-(1H-indol-3-yl)-propionic acid
收率 49.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@@H]1N[C@H](C(=O)OC)Cc2c1[nH]c1ccccc21.Cl
Reaction #93358
methyl (1RS, 3RS)-cis-1-butyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate hydrochloride
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H]1N[C@H](C(=O)OC)Cc2c1[nH]c1ccccc21.Cl
Reaction #93359
methyl (1RS, 3RS)-cis-1-n-propyl-1,2,3,4-tetrahydro-β-carboline-3-carboxylate hydrochloride
收率 38.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CCCN)CSC(C)=O.O=C(O)C(F)(F)F
Reaction #94148
N-(2-acetylthiomethyl-5-aminopentanoyl)-L-tryptophane methyl ester trifluoroacetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)Cc1cc(C)cc(C)c1
Reaction #158207
(S)-methyl 2-(2-(3,5-dimethylphenyl)acetamido)-3-(1H-indol-3-yl)propanoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)cc(CC(=O)N[C@@H](Cc2c[nH]c3ccccc23)C(=O)O)c1
Reaction #158208
(S)-2-(2-(3,5-dimethylphenyl)acetamido)-3-(1H-indol-3-yl)propionic acid
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(Cc1c[nH]c2ccccc12)(C(=O)O)C(=O)c1cccnc1
Reaction #169660
product
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)NCc1cc(F)cc(F)c1)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)OC(C)(C)C
Reaction #192153
DOI: 10.1039/C8SC04228D
O=C(CCC(=O)C(Cc1ccccc1)NC(=O)c1ccccc1)NC(Cc1ccccc1)C(=O)O
Reaction #198194
DOI: 10.1039/C8SC04228D
CSC(=S)N1Cc2[nH]c3ccccc3c2CC1C(=O)O
Reaction #213361
DOI: 10.1039/C8SC04228D
CCOC(=O)[C@H](Cc1c[nH]c2cc(Br)cc(Br)c12)NC(=O)OCc1ccccc1
Reaction #217033
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(S(=O)(=O)NC(Cc2c[nH]c3ccccc23)C(=O)O)s1
Reaction #239481
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)C=C1CCC(c2ccccc2)(N(C)C)CC1
Reaction #243498
DOI: 10.1039/C8SC04228D
CSCSC(=S)N1Cc2[nH]c3ccccc3c2CC1C(=O)O
Reaction #244923
DOI: 10.1039/C8SC04228D
COC(=O)C1Cc2c(n(C(=S)SCc3cccs3)c3ccccc23)CN1C(=S)SCc1cccs1
Reaction #277595
DOI: 10.1039/C8SC04228D
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